Half-year Report

AstraZeneca PLC
25 July 2024
 

AstraZeneca

25 July 2024

H1 and Q2 2024 results

 

Strong underlying growth supports FY 2024 guidance upgrade, with both Total Revenue and Core EPS now expected to increase by a mid teens percentage at CER[1]

 

Revenue and EPS summary

 



H1 2024

% Change

Q2 2024

% Change

 

 

$m 

Actual 

CER

$m 

Actual 

CER

- Product Sales


24,629 

15 

18 

12,452 

14 

18 

- Alliance Revenue


939 

50 

50 

482 

42 

42 

- Collaboration Revenue


49 

(78)

(78)

(98)

(98)

Total Revenue


25,617 

15 

18 

12,938 

13 

17 

Reported EPS


$2.65 

13 

23 

$1.24 

15 

Core[2] EPS


$4.03 

(1)

$1.98 

(8)

(3)

 

Financial performance for H1 2024 (Growth numbers at constant exchange rates)

 

‒    Total Revenue up 18% to $25,617m, driven by an 18% increase in Product Sales and continued growth in Alliance Revenue from partnered medicines

 

‒    Total Revenue growth from Oncology was 22%, CVRM 22%, R&I 22%, and Rare Disease 15%

 

‒    Core Product Sales Gross Margin[3] of 82%

 

‒    Core Operating Margin of 33%

 

‒    Core Tax Rate of 20%

 

‒    Core EPS increased 5% to $4.03. The increase in Core EPS was lower than Total Revenue growth principally due to gains recognised in the prior year, specifically a $241m gain on the disposal of Pulmicort Flexhaler US rights (Q1 2023), and a $712m gain relating to updates to contractual arrangements for Beyfortus (Q2 2023)

 

‒    Interim dividend increased 7c to $1.00 (77.6 pence, 10.79 SEK) has been declared

 

‒    Guidance for FY 2024 increased, with Total Revenue and Core EPS anticipated to grow by a mid teens percentage at CER (previously a low double-digit to low teens percentage). An increase in Collaboration Revenue is not assumed in the upgraded guidance

 

Pascal Soriot, Chief Executive Officer, AstraZeneca, said:

 

"Building on our strong growth in the first half of the year and continued underlying demand for our medicines we are upgrading our FY 2024 guidance for both Total Revenue and Core EPS. 

 

At our Investor Day in May we set out a new revenue ambition to deliver $80 billion of Total Revenue by 2030. This is a clear reflection of the substantial growth potential we see from both our approved medicines and those in our late-stage pipeline. Already this year we have announced five positive, potentially practice-changing Phase III studies that are anticipated to meaningfully contribute to our growth.

 

In the year to date we have continued to make encouraging progress with several disruptive technologies, including antibody drug conjugates, bispecifics, cell and gene therapies, radioconjugates, and weight management medicines, all of which have the potential to drive our growth beyond 2030."

 

Key milestones achieved since the prior results announcement

 

‒    Positive read-outs for Imfinzi in combination with chemotherapy in muscle-invasive bladder cancer (NIAGARA), Calquence in untreated mantle cell lymphoma (ECHO), Enhertu in HR-positive, HER2-low metastatic breast cancer (DESTINY-Breast06)

 

‒    US approvals for Imfinzi in combination with chemotherapy followed by Imfinzi monotherapy for primary advanced or recurrent endometrial cancer that is mismatch repair deficient (DUO-E). EU approvals for Truqap in combination with Faslodex for biomarker-positive estrogen receptor-positive, HER2negative advanced breast cancer (CAPItello-291), Tagrisso with the addition of chemotherapy for 1st‑line EGFRm NSCLC (FLAURA2). Japan and China approvals for Tagrisso with the addition of chemotherapy for the 1st--‑line EGFRm NSCLC (FLAURA2)

 

Guidance

 

Due to strong underlying growth in Product Sales and Alliance Revenue, the Company raises its Total Revenue and Core EPS guidance for FY 2024 at CER, based on the average foreign exchange rates through 2023.

 

Total Revenue is expected to increase by a mid teens percentage
(previously a low double-digit to low teens percentage) 

Core EPS is expected to increase by a mid teens percentage
(previously a low double-digit to low teens percentage)

 

‒    An increase in Collaboration Revenue is not assumed in the upgraded guidance (previously assumed a substantial increase)

 

‒    Other operating income is expected to decrease substantially (FY 2023 included a $241m gain on the disposal of Pulmicort Flexhaler US rights, and a $712m one-time gain relating to updates to contractual arrangements for Beyfortus)

 

‒    The Core Tax rate is expected to be between 18-22%

 

The Company is unable to provide guidance on a Reported basis because it cannot reliably forecast material elements of the Reported results, including any fair value adjustments arising on acquisition-related liabilities, intangible asset impairment charges and legal settlement provisions. Please refer to the cautionary statements section regarding forward-looking statements at the end of this announcement.

 

Currency impact

 

If foreign exchange rates for July 2024 to December 2024 were to remain at the average rates seen in June 2024, it is anticipated that FY 2024 Total Revenue would incur a low single-digit percentage adverse impact compared to the performance at CER, and Core EPS would incur a mid single-digit percentage adverse impact. The Company's foreign exchange rate sensitivity analysis is provided in Table 17.

 

Table 1: Key elements of Total Revenue performance in Q2 2024

 

 

% Change 

 

 

 

Revenue type 


$m 

Actual % 

CER % 

 

 

Product Sales 


12,452 

14 

18 



Alliance Revenue


482 

42 

42 


*   $344m Enhertu (Q2 2023: $255m)

*   $104m Tezspire (Q2 2023: $62m)

Collaboration Revenue 


(98)

(98)


*   Q2 2023 included $180m for COVID-19 mAbs

Total Revenue 


12,938 

13 

17 



Therapy areas 


$m 

Actual %

CER %

 

 

Oncology 


5,331 

15 

19 


*   Tagrisso up 8% (12% at CER) due to strong global demand, Calquence up 21% (22% at CER) with sustained leadership in 1L CLL. Enhertu Total Revenue up 46% (49% at CER)

CVRM 


3,160 

18 

22 

 

*   Farxiga up 29% (32% at CER), Lokelma up 36% (41% at CER)

R&I 


1,905 

23 

26 


*   Breztri up 44% (47% at CER). Saphnelo up 65%, Tezspire up 97% (>2x at CER), Symbicort up 20% (25% CER)

V&I


119 

(57)

(53)


*   The drop in V&I revenue was primarily driven by lower Collaboration Revenue from COVID-19 mAbs

*   Beyfortus revenue was $35m (Q2 2023: $2m), which more than offset a $6m decline in Synagis

Rare Disease 


2,147 

10 

14 


*   Ultomiris up 33% (36% at CER), partially offset by decline in Soliris of 14% (8% at CER)

*   Strensiq up 13% (14% at CER) and Koselugo up 43% (45% at CER)

Other Medicines 


276 

(11)

(5)



Total Revenue 


12,938 

13 

17 



Regions


$m 

Actual %

CER %

 

 

US 


5,571 

17 

17 



Emerging Markets 


3,386 

18 



- China 

 

1,630 

13 

18 

 

 

- Ex-China Emerging Markets 

 

1,756 

18 

 

 

Europe 


2,732 

24 

24 



Established RoW 


1,249 

(5)



Total Revenue


12,938 

13 

17 



 

Key partnered medicines

 

‒    Combined sales of Enhertu, recorded by Daiichi Sankyo Company Limited (Daiichi Sankyo) and AstraZeneca, amounted $1,772m in H1 2024 (H1 2023: $1,169m).

 

‒    Combined sales of Tezspire, recorded by Amgen and AstraZeneca, amounted to $507m in H1 2024 (H1 2023: $257m).

‒   

Table 2: Key elements of financial performance in Q2 2024

 

Metric

Reported

Reported change

Core

Core
change


Comments[4]

Total Revenue

$12,938m

13% Actual      17% CER

$12,938m

13% Actual      17% CER


*   See Table 1 and the Total Revenue section of this document for further details

Product Sales Gross Margin

82%

Stable Actual     
Stable CER

83%

Stable Actual     
Stable CER


*   Variations in Product Sales Gross Margin can be expected between periods due to product seasonality (e.g. FluMist and Beyfortus in H2), foreign exchange fluctuations and other effects

R&D

 expense

$3,008m

13% Actual      13% CER

$2,872m

12% Actual      13% CER


+ Increased investment in the pipeline

*   Core R&D-to-Total Revenue ratio of 22%
(Q2 2023: 22%)

SG&A expense

$4,929m

-1% Actual      1% CER

$3,735m

13% Actual      16% CER


+ Market development for recent launches and pre-launch activities

*   Core SG&A-to-Total Revenue ratio of 29%
(Q2 2023: 29%)

Other operating income and expense[5]

$60m

-92% Actual      -92% CER

$60m

-92% Actual      -92% CER


The prior year quarter included a $712m gain relating to updates to contractual arrangements for Beyfortus

Operating Margin

21%

Stable Actual      +1pp CER

32%

-6pp Actual      -5pp CER


*   See commentary above on Gross Margin, R&D, SG&A and Other operating income and expense

Net finance expense

$343m

-7% Actual      -7% CER

$285m

10% Actual      10% CER


+ Higher level of Net debt

Tax rate

20%

+7pp Actual      +7pp CER

19%

+2pp Actual      +2pp CER


*   Variations in the tax rate can be expected between periods

EPS

$1.24

6% Actual      15% CER

$1.98

-8% Actual      -3% CER


*   Further details of differences between Reported and Core are shown in Table 12

 

 

Table 3: Pipeline highlights since prior results announcement

 

Event

Medicine

Indication / Trial

 

Event

Regulatory approvals and other regulatory actions

Imfinzi

Primary advanced or recurrent endometrial cancer with mismatch repair deficiency (DUO-E)

Regulatory approval (US), CHMP positive opinion (EU)

Imfinzi + Lynparza

Primary advanced or recurrent endometrial cancer with mismatch repair proficiency (DUO-E)

CHMP positive opinion (EU)

Tagrisso

EGFRm NSCLC (1st-line)

(FLAURA2)

Regulatory approval (EU, JP, CN)

Truqap

Biomarker-positive ER-positive HER2-negative locally advanced or metastatic breast cancer (CAPItello-291)

Regulatory approval (EU)




Regulatory submissions
or acceptances*

Tagrisso

EGFRm NSCLC (Stage III unresectable) (LAURA)

sNDA acceptance and Priority Review (US)

Dato-DXd

 

Non-squamous NSCLC (2nd- and 3rd-line) (TROPION-Lung01)

Regulatory submission (EU)

sipavibart

Prevention of COVID-19

(SUPERNOVA)

Regulatory submission (EU)

 

 

 

Major Phase III data readouts and other developments

Calquence

Mantle cell lymphoma (1st‑line) (ECHO)

Primary endpoint met

Dato-DXd

Locally advanced or metastatic NSCLC (TROPION-Lung01)

Dual primary endpoint OS not met in the intention to treat population

Enhertu

HER2-low breast cancer (2nd-line) (DESTINY-Breast-06)

Primary endpoint met

Imfinzi

Muscle-invasive bladder cancer (NIAGARA)

Primary endpoint met

Imfinzi

Adjuvant use in early-stage PD-L1 ≥25%  NSCLC (Adjuvant BR.31)

Primary endpoint not met






Truqap

Locally advanced or metastatic TNBC (CAPItello-290)

Primary endpoint not met






sipavibart

Prevention of COVID-19 (SUPERNOVA)

Primary endpoint met

 

*US, EU and China regulatory submission denotes filing acceptance

 

Upcoming pipeline catalysts

 

For recent trial starts and anticipated timings of key trial readouts, please refer to the Clinical Trials Appendix, available on www.astrazeneca.com/investor-relations.html.

 

Corporate and business development

 

In May 2024, AstraZeneca announced its intention to build a $1.5 billion manufacturing facility in Singapore for antibody drug conjugates (ADCs), enhancing global supply of its ADC portfolio. ADCs are next-generation treatments that deliver highly potent cancer-killing agents directly to cancer cells through a targeted antibody. The planned greenfield facility, supported by the Singapore Economic Development Board, will be AstraZeneca's first end-to-end ADC production site, fully incorporating all steps of the manufacturing process at a commercial scale. Manufacturing of ADCs is a multi-step process that comprises antibody production, synthesis of chemotherapy drug and linker, conjugation of drug-linker to the antibody, and filling of the completed ADC substance.

 

In May 2024, AstraZeneca completed an additional $140m equity investment in Cellectis, a clinical-stage biotechnology company. The equity investment and a research collaboration agreement, announced in November 2023, will leverage the Cellectis proprietary gene editing technologies and manufacturing capabilities, to design up to 10 novel cell and gene therapy products for areas of high unmet need, including oncology, immunology and rare diseases. In Q4 2023, Cellectis received an initial payment of $105m from AstraZeneca, which comprised a $25m upfront cash payment under the terms of a research collaboration agreement and an $80m equity investment. Now that the additional $140m equity investment has closed, AstraZeneca holds a total equity stake of c.44% in Cellectis and AstraZeneca continues to treat its investment in Cellectis as an associate.

 

In June 2024, AstraZeneca completed the acquisition of Fusion Pharmaceuticals Inc., a clinical-stage biopharmaceutical company developing next-generation radioconjugates. The acquisition marks a major step forward in AstraZeneca delivering on its ambition to transform cancer treatment and outcomes for patients by replacing traditional regimens like chemotherapy and radiotherapy with more targeted treatments. The acquisition complements AstraZeneca's leading oncology portfolio with the addition of the Fusion pipeline of radioconjugates, including FPI-2265, a potential new treatment for patients with mCRPC, and brings new expertise and pioneering R&D, manufacturing and supply chain capabilities in actinium-based radioconjugates to AstraZeneca. See Note 5 for further information.

 

In July 2024, AstraZeneca completed the acquisition of Amolyt Pharma, a clinical-stage biotechnology company focused on developing novel treatments for rare endocrine diseases. The acquisition bolsters the Alexion, AstraZeneca Rare Disease late-stage pipeline and expands on its bone metabolism franchise with the notable addition of eneboparatide (AZP-3601), a Phase III investigational therapeutic peptide with a novel mechanism of action designed to meet key therapeutic goals for hypoparathyroidism. In patients with hypoparathyroidism, a deficiency in parathyroid hormone production results in significant dysregulation of calcium and phosphate, which can lead to life-altering symptoms and complications, including chronic kidney disease. See Note 7 for further information.

 

Sustainability highlights

 

At the 77th World Health Assembly in Geneva, Switzerland in May, AstraZeneca convened Ministers of Health, industry, civil society and patient groups. Areas of focus for engagement, led by Ruud Dobber, EVP BioPharmaceuticals, included the need to increase early action to prevent, diagnose and treat disease and to accelerate collaboration to build resilient, equitable and net zero health systems.

 

Conference call

 

A conference call and webcast for investors and analysts will begin today, 25 July 2024, at 11:45 UK time. Details can be accessed via astrazeneca.com.

 

Reporting calendar

 

The Company intends to publish its 9M and Q3 2024 results on 12 November 2024.

 

Conclusion of audit tender

 

Following a rigorous process, the audit tender for the Group's external audit provider has now concluded. The Audit Committee has recommended, and the Board has endorsed, the appointment of KPMG as the Group's external auditor for the financial year ending 31 December 2026. A resolution will be put to shareholders at the 2026 Annual General Meeting (AGM) to approve this appointment. It is intended that PwC, who have been the Group's auditor since the year ended 31 December 2017, will continue as the Group's auditors for the years ended 31 December 2024 and 2025 and will cease to hold office at the conclusion of the Company's 2026 AGM.

 

Operating and financial review

 

All narrative on growth and results in this section is based on actual exchange rates, and financial figures are in US$ millions ($m), unless stated otherwise. Unless stated otherwise, the performance shown in this announcement covers the six month period to 30 June 2024 ('the half year' or 'H1 2024') compared to the six month period to 30 June 2023 ('H1 2023').

 

Core financial measures, EBITDA, Net debt, Product Sales Gross Margin, Operating Margin and CER are non-GAAP financial measures because they cannot be derived directly from the Group's Condensed consolidated financial statements. Management believes that these non-GAAP financial measures, when provided in combination with Reported results, provide investors and analysts with helpful supplementary information to understand better the financial performance and position of the Group on a comparable basis from period to period. These non-GAAP financial measures are not a substitute for, or superior to, financial measures prepared in accordance with GAAP.

 

Core financial measures are adjusted to exclude certain significant items:

 

‒    Charges and provisions related to restructuring programmes, which includes charges that relate to the impact of restructuring programmes on capitalised IT assets

 

‒    Amortisation and impairment of intangible assets, including impairment reversals but excluding any charges relating to IT assets

 

‒    Other specified items, principally the imputed finance charges and fair value movements relating to contingent consideration on business combinations, imputed finance charges and remeasurement adjustments on certain Other payables arising from intangible asset acquisitions, legal settlements and remeasurement adjustments relating to Other payables assumed from the Alexion acquisition

 

‒    The tax effects of the adjustments above are excluded from the Core Tax charge

 

Details on the nature of Core financial measures are provided on page 61 of the Annual Report and Form 20-F Information 2023.

 

Reference should be made to the Reconciliation of Reported to Core financial measures table included in the financial performance section in this announcement.

 

Product Sales Gross Margin is calculated by dividing the difference between Product Sales and Cost of Sales by the Product Sales. The calculation of Reported and Core Product Sales Gross Margin excludes the impact of Alliance Revenue and Collaboration Revenue and any associated costs, thereby reflecting the underlying performance of Product Sales.

 

EBITDA is defined as Reported Profit before tax after adding back Net finance expense, results from Joint ventures and associates and charges for Depreciation, amortisation and impairment. Reference should be made to the Reconciliation of Reported Profit before tax to EBITDA included in the financial performance section in this announcement.

 

Operating margin is defined as Operating profit as a percentage of Total Revenue.

 

Net debt is defined as Interest-bearing loans and borrowings and Lease liabilities, net of Cash and cash equivalents, Other investments, and Net derivative financial instruments. Reference should be made to Note 3 'Net debt' included in the Notes to the Interim financial statements in this announcement.

 

The Company strongly encourages investors and analysts not to rely on any single financial measure, but to review AstraZeneca's financial statements, including the Notes thereto, and other available Company reports, carefully and in their entirety.

 

Due to rounding, the sum of a number of dollar values and percentages in this announcement may not agree to totals.

 

Total Revenue

 

Table 4: Total Revenue by therapy area and medicine[6]

 

 

 

H1 2024 

Q2 2024 

 

 

 

 

 

% Change 

 

 

% Change 

 

Total Revenue

 

$m 

% Total 

Actual 

CER 

$m 

% Total 

Actual 

CER 

Oncology 


10,440 

41 

19 

22 

5,331 

41 

15 

19 

- Tagrisso 


3,203 

13 

10 

13 

1,608 

12 

12 

- Imfinzi


2,259 

20 

25 

1,147 

13 

18 

- Calquence 


1,508 

27 

28 

790 

21 

22 

- Lynparza 


1,450 

744 

- Enhertu 


932 

61 

62 

472 

46 

49 

- Zoladex


567 

19 

26 

282 

17 

25 

- Imjudo


136 

35 

38 

74 

17 

19 

- Truqap


142 

n/m 

n/m 

92 

n/m 

n/m 

- Orpathys 


25 

14 

18 

13 

(5)

(1)

- Other Oncology


216 

(21)

(15)

109 

(17)

(11)

BioPharmaceuticals: CVRM 


6,220 

24 

19 

22 

3,160 

24 

18 

22 

- Farxiga 


3,836 

15 

35 

38 

1,945 

15 

29 

32 

- Brilinta 


665 

342 

- Crestor


590 

293 

11 

- Lokelma


249 

26 

30 

136 

36 

41 

- Seloken/Toprol-XL 


315 

(8)

(1)

150 

(8)

- roxadustat


167 

22 

27 

90 

20 

25 

- Andexxa


105 

18 

21 

59 

29 

35 

- Wainua


21 

n/m 

n/m 

16 

n/m 

n/m 

- Other CVRM


272 

(30)

(28)

130 

(26)

(24)

BioPharmaceuticals: R&I 


3,791 

15 

19 

22 

1,905 

15 

23 

26 

- Symbicort 


1,491 

16 

19 

722 

20 

25 

- Fasenra


781 

423 

- Breztri


454 

48 

51 

235 

44 

47 

- Pulmicort 


379 

10 

14 

155 

25 

30 

- Tezspire


280 

>2x 

>2x 

160 

97 

>2x 

- Saphnelo 


203 

77 

77 

112 

65 

65 

- Airsupra


21 

n/m 

n/m 

14 

n/m 

n/m 

- Other R&I 


181 

(26)

(25)

83 

(21)

(19)

BioPharmaceuticals: V&I 


350 

(45)

(42)

119 

(57)

(53)

- Beyfortus

 

80 

>10x 

>10x 

35 

>10x 

>10x 

- Synagis

 

253 

(11)

(6)

81 

(6)

- COVID-19 mAbs


(99)

(99)

(99)

(99)

- FluMist


(34)

(36)

(84)

(84)

- Other V&I


(79)

(80)

n/m 

n/m 

Rare Disease


4,243 

17 

11 

15 

2,147 

17 

10 

14 

- Ultomiris 


1,804 

32 

35 

946 

33 

36 

- Soliris


1,439 

(13)

(8)

700 

(14)

(8)

- Strensiq 


653 

16 

18 

340 

13 

14 

- Koselugo 


247 

55 

64 

114 

43 

45 

- Kanuma 


100 

17 

20 

47 

Other Medicines 


573 

(9)

(2)

276 

(11)

(5)

- Nexium 

 

469 

(6)

227 

(10)

(3)

- Others 


104 

(21)

(18)

49 

(16)

(12)

Total


25,617 

100 

15 

18 

12,938 

100 

13 

17 

 

Table 5: Alliance Revenue



H1 2024

Q2 2024

 





% Change

 

 

% Change

 

 


$m 

% Total 

Actual 

CER 

$m 

% Total 

Actual 

CER 

Enhertu


683 

73 

44 

44 

344 

71 

35 

36 

Tezspire


180 

19 

72 

72 

104 

22 

67 

67 

Beyfortus


26 

n/m 

n/m 

n/m 

n/m 

Other Alliance Revenue 


50 

27 

17 

17 

Total 

 

939 

100 

50 

50 

482 

100 

42 

42 

 

 

Table 6: Collaboration Revenue



H1 2024

Q2 2024

 

 

 




% Change

 

 

% Change

 

 


$m 

% Total 

Actual 

CER 

$m 

% Total 

Actual 

CER 

Farxiga: sales milestones 


49 

100 

96 

96 

100 

>5x 

>5x 

COVID-19 mAbs: licence fees


n/m 

n/m 

n/m 

n/m 

Other Collaboration Revenue 


(98)

(98)

n/m 

n/m 

Total 

 

49 

100 

(78)

(78)

100 

(98)

(98)

 

Table 7: Total Revenue by therapy area

 



H1 2024

Q2 2024

 





% Change



% Change

 



$m 

% Total 

 Actual 

CER 

$m 

% Total 

 Actual 

CER 

Oncology


10,440 

41 

19 

22 

5,331 

41 

15 

19 

Biopharmaceuticals


10,362 

40 

14 

17 

5,184 

40 

15 

19 

CVRM

 

6,220 

24 

19 

22 

3,160 

24 

18 

22 

R&I

 

3,791 

15 

19 

22 

1,905 

15 

23 

26 

V&I

 

350 

(45)

(42)

119 

(57)

(53)

Rare Disease


4,243 

17 

11 

15 

2,147 

17 

10 

14 

Other Medicines


573 

(9)

(2)

276 

(11)

(5)

Total

 

25,617 

100 

15 

18 

12,938 

100 

13 

17 

 

Table 8: Total Revenue by region

 



H1 2024 

Q2 2024

 





% Change 



% Change

 



$m 

% Total 

 Actual 

CER 

$m 

% Total 

 Actual 

CER 

US


10,695 

42 

18 

18 

5,571 

43 

17 

17 

Emerging Markets


7,119 

28 

13 

22 

3,386 

26 

18 

China

 

3,378 

13 

11 

15 

1,630 

13 

13 

18 

Emerging Markets ex. China

 

3,740 

15 

16 

29 

1,756 

14 

18 

Europe


5,365 

21 

23 

22 

2,732 

21 

24 

24 

Established ROW


2,438 

10 

(5)

1,249 

10 

(5)

Total

 

25,617 

100 

15 

18 

12,938 

100 

13 

17 

 

Oncology

 

Oncology Total Revenue of $10,440m in H1 2024 increased by 19% (22% at CER), representing 41% of overall Total Revenue (H1 2023: 39%).

 

Tagrisso

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


3,203


1,282

919

628

374

Actual change


10%


16%

8%

16%

(11%)

CER change


13%


16%

16%

15%

(2%)

 

Region


 Drivers and commentary

Worldwide


*   Strong global demand for Tagrisso in adjuvant (ADAURA) and 1st-line settings (FLAURA, FLAURA2)

US


*   Continued adjuvant and 1st-line demand growth

Emerging Markets


*   Encouraging demand growth across markets despite local competition in China

Europe


*   Continued demand growth in 1st-line and adjuvant settings

Established RoW


*   Continued growth across indications, impacted by 10.5% mandatory price reduction in Japan effective from June 2023

 

Imfinzi

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


2,259


1,202

245

459

353

Actual change


20%


17%

35%

38%

7%

CER change


25%


17%

58%

36%

19%

 

Region


 Drivers and commentary

Worldwide


*   Continued growth driven by BTC (TOPAZ-1), HCC (HIMALAYA), and increased patient share in Stage IV NSCLC (POSEIDON) and extensive-stage SCLC (CASPIAN)

US


*   Continued demand growth driven primarily by HCC and extensive-stage SCLC, having achieved peak market share and stabilisation in BTC

Emerging Markets


*   New patient share growth across all indications

*   China growth driven largely by increasing demand in BTC

Europe


*   Growth driven by share gains in extensive-stage SCLC and new launches in HCC, BTC and NSCLC

Established RoW


*   Increased demand in GI indications, offset by a 25% mandatory price reduction in Japan effective from 1 February 2024

 

Calquence

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


1,508


1,048

75

320

65

Actual change


27%


21%

82%

42%

30%

CER change


28%


21%

>2x

41%

34%

 

Region


 Drivers and commentary

Worldwide


*   Sustained leadership in front-line CLL (ELEVATE-TN) and increased global penetration

US


*   Growth driven by leading share of new patient starts in front-line CLL, and improved affordability

Europe


*   Continued strong growth in front-line

 

Lynparza

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


1,450


607

320

398

125

Actual change


6%


5%

15%

9%

(14%)

CER change


9%


5%

26%

8%

(6%)

 

Region


 Drivers and commentary

Worldwide


*   Lynparza remains the leading medicine in the PARP inhibitor class globally across four tumour types (ovarian, breast, prostate, pancreatic), as measured by total prescription volume

*   No Collaboration Revenue for Lynparza was recognised in either H1 2024 or H1 2023, hence the Product Sales numbers are identical to the Total Revenue numbers shown above

US


*   Continued leadership within PARP inhibitor class despite competition, offset by negative class pressure and maturity

Emerging Markets


*   Volume growth in China from increased share in newly diagnosed BRCA-mutated ovarian cancer (SOLO-1) and inclusion of HRD-positive ovarian cancer (PAOLA-1) on NRDL with no price reduction

Europe


*   Demand growth driven by recent launches in mCRPC (PROpel) and early breast cancer (OlympiA)

Established RoW


*   Demand growth from 1st-line ovarian cancer, offset by price reduction in Japan effective from November 2023  

 

 

Enhertu

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


932


414

224

263

31

Actual change


61%


22%

>2x

>2x

>3x

CER change


62%


22%

>2x

>2x

>3x

 

Region


 Drivers and commentary

Worldwide


*   Combined sales of Enhertu, recorded by Daiichi Sankyo and AstraZeneca, amounted to $1,772m in H1 2024 (H1 2023: $1,169m)

US


*   US in-market sales, recorded by Daiichi Sankyo, amounted to $865m in H1 2024 (H1 2023: $712m)

*   Continued demand across all indications with encouraging early launch following tumour-agnostic approval in April 2024 (DESTINY-PanTumor02, DESTINY-Lung01, DESTINY‑CRC02)

Emerging Markets


*   Sustained demand growth, with quarterly phasing impacted by launch-related inventory build in China in Q1 2024 and subsequent destocking

Europe


*   Continued demand growth due to increasing adoption in HER2-positive (DESTINY-Breast03) and HER2-low (DESTINY-Breast04) metastatic breast cancer

Established RoW


*   AstraZeneca's Alliance Revenue includes a mid single-digit percentage royalty on Daiichi Sankyo's sales in Japan

 

Other Oncology medicines

 


H1 2024

Change


 

Total Revenue


$m

Actual

CER

Drivers and commentary

Zoladex


567

19%

26%

*   Strong underlying growth in China and Emerging Markets and moderate growth in Europe offset by drop in Japan

Imjudo


136

35%

38%

*   Continued growth across markets slightly offset by US inventory destocking in H1 2024

Truqap


142

n/m

n/m

*   Strong demand growth with strong uptake in biomarker altered subgroup of HR-positive HER2-negative metastatic breast cancer (CAPItello-291)

Orpathys


25

14%

18%

*   Demand in China for the treatment of patients with NSCLC with MET exon 14 skipping alterations

Other Oncology


216

(21%)

(15%)

*   Decline in Faslodex Total Revenue due to VBP implementation in China in March 2024 in addition to ongoing generic erosion in Europe

 

 

BioPharmaceuticals

 

BioPharmaceuticals Total Revenue increased by 14% (17% at CER) in H1 2024 to $10,362m, representing 40% of overall Total Revenue (H1 2023: 41%).

 

BioPharmaceuticals - CVRM

 

CVRM Total Revenue increased by 19% (22% at CER) to $6,220m in H1 2024 and represented 24% of overall Total Revenue (H1 2023: 24%).

 

Farxiga

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


3,836


869

1,474

1,233

260

Actual change


35%


37%

37%

45%

(5%)

CER change


38%


37%

44%

44%

3%

 

Region


 Drivers and commentary

Worldwide


*   Farxiga volume is growing faster than the overall SGLT2 market in all major regions, driven by continued demand in heart failure and CKD

*   SGLT2 class growth underpinned by updated cardiorenal guidelines

US


*   Growth driven by underlying demand in HFrEF and CKD

*   Launch of an authorised generic in the first quarter of 2024

Emerging Markets

 


*   Increased reimbursement supporting solid growth despite entry of generic competition in some markets

*   Strong momentum in Latin America

Europe


*   Continued strong class growth and market share gains fuelled by HFpEF approval in 2023 and guidelines updates

Established RoW


*   Performance impacted by generic competition in Canada

*   In Japan, AstraZeneca sells to collaborator Ono Pharmaceutical Co., Ltd, which records in-market sales

 

Other CVRM medicines

 


H1 2024

Change


 

Total Revenue


$m

Actual

CER

Drivers and commentary

Brilinta


665

-

2%

*   Continued sales growth in Emerging Markets, decline in Est. RoW driven by generic competition in Canada

Crestor


590

1%

6%

*   Continued sales growth in Emerging Markets

Seloken


315

(8%)

(1%)

*   Stable following VBP implementation in China in 2022

Lokelma


249

26%

30%

*   Strong growth in all major regions. Continued launches in new markets

roxadustat


167

22%

27%

*   Increased demand in both the dialysis and non-dialysis-dependent populations. NRDL listing renewed

Andexxa


105

18%

21%

*   Growth in all major regions

Wainua


21

n/m

n/m

*   Encouraging launch uptake following ATTRv-PN approval in the US in December 2023

Other CVRM


272

(30%)

(28%)


 

BioPharmaceuticals - R&I

 

Total Revenue of $3,791m from R&I medicines increased 19% (22% at CER) and represented 15% of overall Total Revenue (H1 2023: 14%). This reflected growth in Fasenra, Tezspire, Breztri, Saphnelo and Airsupra, following its recent launch.

 

Fasenra

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


781


478

41

192

70

Actual change


5%


2%

45%

9%

(2%)

CER change


6%


2%

53%

8%

6%

                                                          

Region


 Drivers and commentary

Worldwide


*   Continued asthma market share leadership in IL-5 class across major markets 

US


*   Maintained share of a growing severe asthma biologics market

Emerging Markets


*   Continued strong demand growth driven by launch acceleration across key markets 

Europe


*   Expanded leadership in severe eosinophilic asthma 

Established RoW


*   In Japan, maintained class leadership in a broadly stable market

 

Breztri

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


454


225

131

65

33

Actual change


48%


37%

61%

80%

33%

CER change


51%


37%

69%

79%

44%

 

Region


 Drivers and commentary

Worldwide


*   Fastest growing medicine within the expanding FDC triple class, across major markets

US


*   Consistent share growth within the expanding FDC triple class

Emerging Markets


*   Maintained market share leadership in China with strong triple FDC class penetration

*   Further expansion with launches in additional geographies

Europe


*   Sustained growth across markets driven by new launches

Established RoW


*   Increased market share in Japan

 

Tezspire

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


280

 

180

5

61

34

Actual change


>2x

 

72%

>10x

>3x

>2x

CER change


>2x

 

72%

>10x

>3x

>2x

 

Region


 Drivers and commentary

Worldwide


*   Combined sales of Tezspire, recorded by Amgen and AstraZeneca, amounted to $507m in H1 2024 (H1 2023: $257m)

US


*   Continued growth in total prescriptions, and maintained new-to-brand market share with majority of patients new-to-biologics

Europe


*   Achieved new-to-brand leadership across multiple markets, new launches continue to progress 

Established RoW


*   Japan maintained new-to-brand leadership

 

Symbicort

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


1,491


598

450

286

157

Actual change


16%


38%

11%

-

(4%)

CER change


19%


38%

21%

(1%)

(2%)

 

Region


 Drivers and commentary

Worldwide


*   Symbicort remained the global market leader within a stable ICS/LABA class

US


*   Continued strong demand for the authorised generic and favourable channel mix

Emerging Markets


*   Strong demand growth

Europe


*   Continued price and volume erosion from generics and a slowing overall market partially offset by growth in some markets within mild asthma

Established RoW


*   Continued generic erosion in Japan

 

Other R&I medicines

 


H1 2024

   Change


 

Total Revenue


$m

Actual

CER

Drivers and commentary

Pulmicort

 

379

10%

14%

*   >80% of revenues from Emerging Markets

Saphnelo

 

203

77%

77%

*   Demand acceleration in the US, and additional growth driven by ongoing launches in Europe and Established RoW

Airsupra

 

21

n/m

n/m

*   Strong US launch momentum and volume uptake. Revenue in the period reflects introductory discounts as early access continues to build

Other R&I


181

(26%)

(25%)

*   Generic competition

 

BioPharmaceuticals - V&I

 

Total Revenue from V&I medicines reduced by 45% (42% at CER) to $350m (H1 2023: $632m) and represented 1% of overall Total Revenue (H1 2023: 3%). Collaboration Revenue was $nil in the period (H1 2023: $190m).

 

V&I medicines

 


H1 2024

Change


 

Total Revenue


$m

Actual

CER

Drivers and commentary

Beyfortus

 

80

>10x

>10x

*   Product Sales recognises AstraZeneca's sales of manufactured Beyfortus product to Sanofi

*   Alliance Revenue recognises AstraZeneca's 50% share of gross profits on sales of Beyfortus in major markets outside the US, and 25% of brand revenues in rest of world markets

*   AstraZeneca has no participation in US profits or losses

Synagis

 

253

(11%)

(6%)

*   Decline has been more than offset by Beyfortus growth

COVID-19 mAbs


3

(99%)

(99%)

*   Decline in Evusheld sales and Collaboration Revenue (Total Revenue H1 2023: $306m)

FluMist


8

(34%)

(36%)


Other V&I


6

(79%)

(80%)

*   Decline in Vaxzevria sales (H1 2023: $28m)

 

Rare Disease

 

Total Revenue from Rare Disease medicines increased by 11% (15% at CER) in H1 2024 to $4,243m, representing 17% of overall Total Revenue (H1 2023: 17%).

 

Ultomiris

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


1,804


1,032

66

411

295

Actual change


32%


27%

>2x

32%

42%

CER change


35%


27%

>2x

31%

58%

 

Region


 Drivers and commentary

Worldwide


*   Growth due to increased use in neurology, geographic expansion, further patient demand and conversion from Soliris

*   The reported revenues for Ultomiris include sales of Voydeya, which is approved as an add‑on treatment to Ultomiris and Soliris for the 10-20% of PNH patients who experience clinically significant EVH.

*   Voydeya is a strategic launch in this small subset of PNH patients. Voydeya ensures these patients can remain on the standard of care, Ultomiris

US


*   Patient growth in gMG and newly launched NMOSD, continued conversion from Soliris

Emerging Markets


*   Continued growth following launches in new markets

Europe


*   Strong demand growth following recent launches, particularly from neurology indications, accelerated conversion from Soliris in key markets, partially offset by price reductions to secure reimbursement for new indications

Established RoW


*   Continued conversion from Soliris and strong demand following new launches

 

 

Soliris

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


1,439


808

255

260

116

Actual change


(13%)


(9%)

19%

(29%)

(33%)

CER change


(8%)


(9%)

54%

(30%)

(30%)

 

Region


 Drivers and commentary

US


*   Decline driven by successful conversion of Soliris patients to Ultomiris

Emerging Markets


*   Growth driven by patient demand following launches in new markets

Europe


*   Decline driven by biosimilar erosion in PNH and aHUS and successful conversion from Soliris to Ultomiris

Established RoW


*   Decline driven by successful conversion from Soliris to Ultomiris

 

Strensiq

 

H1 2024, $m


Worldwide


US

Emerging Markets

Europe

Established RoW

Total Revenue


653


529

31

48

45

Actual change


16%


17%

30%

14%

4%

CER change


18%


17%

47%

12%

15%

 

Region


 Drivers and commentary

Worldwide


*   Growth driven by strong patient demand

 

Other Rare Disease medicines

 


H1 2024

Change


 

Total Revenue


$m

Actual

CER

Drivers and commentary

Koselugo


247

55%

64%

*   Driven by patient demand and expansion in new markets

Kanuma


100

17%

20%

*   Continued global demand

 

Other medicines (outside the main therapy areas)

 


H1 2024

Change


 

Total Revenue


$m

Actual

CER

Drivers and commentary

Nexium

 

469

(6%)

2%

*   Growth in Emerging Markets offset declines elsewhere

Others


104

(21%)

(18%)

*   Continued impact of generic competition

 

 

Financial performance

 

Table 9: Reported Profit and Loss

 



H1 2024

H1 2023

% Change 

Q2 2024

Q2 2023

% Change

 

 

 

$m  

$m  

Actual 

CER 

$m 

$m 

Actual 

CER 

Total Revenue

 

25,617 

22,295 

15 

18 

12,938 

11,416 

13 

17 

- Product Sales


24,629 

21,448 

15 

18 

12,452 

10,882 

14 

18 

- Alliance Revenue


939 

627 

50 

50 

482 

341 

42 

42 

- Collaboration Revenue


49 

220 

(78)

(78)

193 

(98)

(98)

Cost of sales


(4,401)

(3,865)

14 

17 

(2,183)

(1,960)

11 

17 

Gross profit

 

21,216 

18,430 

15 

18 

10,755 

9,456 

14 

17 

Distribution expense


(267)

(265)

(132)

(131)

R&D expense


(5,791)

(5,278)

10 

10 

(3,008)

(2,667)

13 

13 

SG&A expense


(9,424)

(9,045)

(4,929)

(4,986)

(1)

Other operating income & expense


127 

1,163 

(89)

(89)

60 

784 

(92)

(92)

Operating profit


5,861 

5,005 

17 

25 

2,746 

2,456 

12 

20 

Net finance expense


(645)

(654)

(1)

(4)

(343)

(367)

(7)

(7)

Joint ventures and associates


(19)

(1)

n/m

n/m 

(6)

(1)

n/m

n/m 

Profit before tax

 

5,197 

4,350 

19 

29 

2,397 

2,088 

15 

24 

Taxation


(1,089)

(726)

50 

62 

(469)

(268)

75 

90 

Tax rate

 

21% 

17% 

 


20% 

13% 



Profit after tax

 

4,108 

3,624 

13 

23 

1,928 

1,820 

15 

Earnings per share

 

$2.65 

$2.34 

13 

23 

$1.24 

$1.17 

15 

 

Table 10: Reconciliation of Reported Profit before tax to EBITDA

 



H1 2024

H1 2023

% Change

Q2 2024

Q2 2023

% Change

 



$m 

$m  

Actual 

CER 

$m 

$m 

Actual 

CER 

Reported Profit before tax 


5,197 

4,350 

19 

29 

2,397 

2,088 

15 

24 

Net finance expense 


645 

654 

(1)

(4)

343 

367 

(7)

(7)

Joint ventures and associates 


19 

n/m

n/m 

n/m

n/m

Depreciation, amortisation and impairment 


2,534 

2,778 

(9)

(9)

1,279 

1,276 

EBITDA 


8,395 

7,783 

13 

4,025 

3,732 

14 

 

Table 11: Reconciliation of Reported to Core financial measures: H1 2024[7]

 

H1 2024


Reported

Restructuring

Intangible Asset Amortisation & Impairments

Other

Core

Core

% Change

 



$m 

$m 

$m 

$m 

$m 

Actual 

CER 

Gross profit

 

21,216 

36 

19 

21,271 

14 

17 

Product Sales Gross Margin

 

82% 

 

 

 

82% 

-1pp 

-1pp 

Distribution expense


(267)

(267)

R&D expense


(5,791)

177 

39 

(5,570)

14 

15 

% of Total Revenue


23% 




22% 

+1pp

SG&A expense


(9,424)

138 

1,884 

254 

(7,148)

13 

15 

% of Total Revenue


37% 




28% 

+1pp 

+1pp 

Total operating expense


(15,482)

315 

1,923 

259 

(12,985)

13 

15 

Other operating income & expense


127 

(2)

125 

(89)

(89)

Operating profit

 

5,861 

349 

1,942 

259 

8,411 

Operating Margin

 

23% 

 

 

 

33% 

-4pp 

-3pp 

Net finance expense


(645)

115 

(530)

Taxation


(1,089)

(80)

(368)

(71)

(1,608)

13 

19 

EPS

 

$2.65 

$0.17 

$1.01 

$0.20 

$4.03 

(1)

 

Table 12: Reconciliation of Reported to Core financial measures: Q2 20247

Q2 2024


Reported

Restructuring

Intangible Asset Amortisation & Impairments

Other

Core

Core

% Change



$m 

$m 

$m 

$m 

$m 

Actual 

CER 

Gross profit

 

10,755 

16 

10,780 

13 

17 

Product Sales Gross Margin

 

82% 

 

 

 

83% 

Distribution expense


(132)

(132)

R&D expense


(3,008)

97 

35 

(2,872)

12 

13 

% of Total Revenue


23




22

+1pp 

SG&A expense


(4,929)

41 

943 

210 

(3,735)

13 

16 

% of Total Revenue


38




29

Total operating expense


(8,069)

138 

978 

214 

(6,739)

12 

14 

Other operating income & expense


60 

60 

(92)

(92)

Operating profit

 

2,746 

154 

987 

214 

4,101 

(4)

Operating Margin

 

21

 

 

 

32

-6pp 

-5pp 

Net finance expense


(343)

58 

(285)

10 

10 

Taxation


(469)

(35)

(185)

(52)

(741)

13 

EPS

 

$1.24 

$0.08 

$0.51 

$0.15 

$1.98 

(8)

(3)

 

Profit and Loss drivers

 

Gross profit

 

‒    The calculation of Reported and Core Product Sales Gross Margin excludes the impact of Alliance Revenue and Collaboration Revenue

 

‒    The change in Product Sales Gross Margin (Reported and Core) in H1 2024 was impacted by:

 

‒    Positive effects from product mix. The increased contribution from Rare Disease and Oncology medicines had a positive impact on the Product Sales Gross Margin

 

‒    Dilutive effects from product mix. The rising contribution of Product Sales with profit sharing arrangements (Lynparza, Enhertu, Tezspire, Koselugo) has a negative impact on Product Sales Gross Margin because AstraZeneca records Product Sales in certain markets and pays away a share of the gross profits to its collaboration partners. The growth in Beyfortus also has a dilutive impact on Product Sales Gross Margin, as AstraZeneca is responsible for manufacturing, and Sanofi is responsible for distribution. AstraZeneca records its sales to Sanofi as Product Sales, and those sales generate a lower Product Sales Gross Margin than the Company average

 

‒    Dilutive effects from geographic mix. In Emerging Markets, the Product Sales Gross Margin tends to be below the Company average

 

‒    Variations in Product Sales Gross Margin performance between periods can continue to be expected due to product seasonality, foreign exchange fluctuations, and other effects

 

R&D expense

 

‒    The change in R&D expense (Reported and Core) in the period was impacted by:

 

‒    Positive data read-outs for several high priority medicines that have ungated late-stage trials

 

‒    Investment in platforms, new technology and capabilities to enhance R&D capabilities

 

‒    Addition of R&D projects following completion of previously announced business development activity including Icosavax, Gracell and Fusion

 

‒    The change in Reported R&D expense was also impacted by intangible asset impairments in the prior period

 

SG&A expense

 

‒    The change in SG&A expense (Reported and Core) in the period was driven primarily by market development activities for launches and to support continued growth in existing brands  

 

Other operating income and expense

 

‒    In the prior year period, Other operating income and expense included a $241m gain on the disposal of the US rights to Pulmicort Flexhaler and a $712m gain relating to updates to contractual arrangements for Beyfortus

 

Net finance expense

 

‒    Core Net finance expense increased 6% (3% increase at CER) principally due to the higher level of gross debt partially offset by the higher level of cash and short-term investments.

 

Taxation

 

‒    The effective Reported Tax rate for the six months to 30 June 2024 was 21% (H1 2023: 17%) and the effective Core Tax rate was 20% (H1 2023: 18%)

 

‒    The cash tax paid for the six months to 30 June 2024 was $1,337m (H1 2023: $1,061m), representing 26% of Reported Profit before tax (H1 2023: 24%)

 

Dividend

‒    An Interim dividend of $1 per share (77.6 pence, 10.79 SEK) has been declared.

 

Table 13: Cash Flow summary

 



H1 2024 

H1 2023 

Change 



$m 

$m 

$m 

Reported Operating profit


5,861 

5,005 

856 

Depreciation, amortisation and impairment


2,534 

2,778 

(244)

Movement in working capital and short-term provisions


(584)

(747)

163 

Gains on disposal of intangible assets


(21)

(249)

228 

Fair value movements on contingent consideration arising from

business combinations


251 

202 

49 

Non-cash and other movements


(550)

(594)

44 

Interest paid


(583)

(483)

(100)

Taxation paid


(1,337)

(1,061)

(276)

Net cash inflow from operating activities


5,571 

4,851 

720 

Net cash inflow before financing activities


286 

3,085 

(2,799)

Net cash inflow/(outflow) from financing activities


806 

(3,550)

4,356 

 

The change in Net cash inflow before financing activities in the half year to 30 June 2024 is primarily driven by the movement in Acquisitions of subsidiaries, net of cash acquired and initial investment, of $2,771m, and relates to the acquisition of Gracell Biotechnologies, Inc. for $774m and acquisition of Fusion Pharmaceuticals Inc., for $1,997m as compared to the acquisition of Neogene Therapeutics, Inc. for $189m in H1 2023.

 

The increase in Net cash inflow/(outflow) from financing activities of $4,356m is primarily driven by the increase in Issue of loans and borrowings of $1,160m, by the decrease in Repayment of loans and borrowings of $765m and the increase in Movement in short-term borrowings of $2,431m mainly due to the Commercial paper issued during the half year for $2,453m.

 

Capital expenditure

 

Capital expenditure amounted to $799m in H1 2024 (H1 2023: $517m). Capital expenditure is expected to increase substantially in 2024, driven by investment in several major manufacturing projects and continued investment in technology upgrades.

 

Table 14: Net debt summary

 


At 30 

 Jun 2024 

At 31 

 Dec 2023 

At 30 

Jun 2023 


$m 

$m 

$m 

Cash and cash equivalents

6,916 

5,840 

5,664 

Other investments

160 

122 

148 

Cash and investments

7,076 

5,962 

5,812 

Overdrafts and short-term borrowings

(596)

(515)

(421)

Commercial paper

(2,453)

Lease liabilities

(1,241)

(1,128)

(953)

Current instalments of loans

(2,018)

(4,614)

(4,135)

Non-current instalments of loans

(27,225)

(22,365)

(24,329)

Interest-bearing loans and borrowings (Gross debt)

(33,533)

(28,622)

(29,838)

Net derivatives

133 

150 

56 

Net debt

(26,324)

(22,510)

(23,970)

 

 

Net debt increased by $3,814m in the six months to 30 June 2024 to $26,324m. Details of the committed undrawn bank facilities are disclosed within the going concern section of Note 1. Details of the Company's solicited credit ratings and further details on Net debt are disclosed in Note 3.

 

Capital allocation

 

The Board's aim is to continue to strike a balance between the interests of the business, financial creditors and the Company's shareholders. The Company's capital allocation priorities include: investing in the business and pipeline; maintaining a strong, investment-grade credit rating; potential value-enhancing business development opportunities; and supporting the progressive dividend policy.

 

In approving the declaration of dividends, the Board considers both the liquidity of the company and the level of reserves legally available for distribution. Dividends are paid to shareholders from AstraZeneca PLC, a Group holding company with no direct operations. The ability of AstraZeneca PLC to make shareholder distributions is dependent on the creation of profits for distribution and the receipt of funds from subsidiary companies. The consolidated Group reserves set out in the Condensed consolidated statement of financial position do not reflect the profit available for distribution to the shareholders of AstraZeneca PLC.

 

Summarised financial information for guarantee of securities of subsidiaries

 

AstraZeneca Finance LLC ("AstraZeneca Finance") is the issuer of 0.7% Notes due 2024, 1.2% Notes due 2026, 4.8% Notes due 2027, 4.875% Notes due 2028, 1.75% Notes due 2028, 4.85% Notes due 2029, 4.9% Notes due 2030, 4.9% Notes due 2031, 2.25% Notes due 2031, 4.875% Notes due 2033 and 5% Notes due 2034 (the "AstraZeneca Finance Notes"). Each series of AstraZeneca Finance Notes has been fully and unconditionally guaranteed by AstraZeneca PLC. AstraZeneca Finance is 100% owned by AstraZeneca PLC and each of the guarantees issued by AstraZeneca PLC is full and unconditional and joint and several.

 

The AstraZeneca Finance Notes are senior unsecured obligations of AstraZeneca Finance and rank equally with all of AstraZeneca Finance's existing and future senior unsecured and unsubordinated indebtedness. The guarantee by AstraZeneca PLC of the AstraZeneca Finance Notes is the senior unsecured obligation of AstraZeneca PLC and ranks equally with all of AstraZeneca PLC's existing and future senior unsecured and unsubordinated indebtedness. Each guarantee by AstraZeneca PLC is effectively subordinated to any secured indebtedness of AstraZeneca PLC to the extent of the value of the assets securing such indebtedness. The AstraZeneca Finance Notes are structurally subordinated to indebtedness and other liabilities of the subsidiaries of AstraZeneca PLC, none of which guarantee the AstraZeneca Finance Notes.

 

AstraZeneca PLC manages substantially all of its operations through divisions, branches and/or investments in subsidiaries and affiliates. Accordingly, the ability of AstraZeneca PLC to service its debt and guarantee obligations is also dependent upon the earnings of its subsidiaries, affiliates, branches and divisions, whether by dividends, distributions, loans or otherwise.

 

Please refer to the Consolidated financial statements of AstraZeneca PLC in our Annual Report on Form 20‑F as filed with the SEC and information contained herein for further financial information regarding AstraZeneca PLC and its consolidated subsidiaries. For further details, terms and conditions of the AstraZeneca Finance Notes please refer to AstraZeneca PLC's reports on Form 6-K furnished to the SEC on 22 February 2024, 3 March 2023 and 28 May 2021.

 

Pursuant to Rule 13-01 and Rule 3-10 of Regulation S-X under the Securities Act of 1933, as amended (the "Securities Act"), we present below the summary financial information for AstraZeneca PLC, as Guarantor, excluding its consolidated subsidiaries, and AstraZeneca Finance, as the issuer, excluding its consolidated subsidiaries. The following summary financial information of AstraZeneca PLC and AstraZeneca Finance is presented on a combined basis and transactions between the combining entities have been eliminated. Financial information for non-guarantor entities has been excluded. Intercompany balances and transactions between the obligor group and the non-obligor subsidiaries are presented on separate lines.

 

Table 15: Obligor group summarised Statement of comprehensive income

 


 

H1 2024

H1 2023


 

$m 

$m 

Total Revenue


Gross profit


Operating loss


(2)

Loss for the period


(545)

(480)

Transactions with subsidiaries that are not issuers or guarantors


964 

9,487 

 

Table 16: Obligor group summarised Statement of financial position

 


 

At 30 Jun 2024 

At 30 Jun 2023 


 

$m 

$m 

Current assets


13 

Non-current assets


Current liabilities


(4,795)

(4,091)

Non-current liabilities


(27,133)

(24,165)

Amounts due from subsidiaries that are not issuers or guarantors


20,730 

15,761 

Amounts due to subsidiaries that are not issuers or guarantors


(290)

 

Foreign exchange

 

The Company's transactional currency exposures on working capital balances, which typically extend for up to three months, are hedged where practicable using forward foreign exchange contracts against the individual companies' reporting currency. Foreign exchange gains and losses on forward contracts transacted for transactional hedging are taken to profit or to Other comprehensive income if the contract is in a designated cashflow hedge. In addition, the Company's external dividend payments, paid principally in pound sterling and Swedish krona, are fully hedged from announcement to payment date.

 

Table 17: Currency sensitivities

 

The Company provides the following information on currency-sensitivity:

 


 

 


Average

rates vs. USD

 

Annual impact ($m) of 5% strengthening (FY 2024 average rate vs. FY 2023 average) [8]

Currency

Primary Relevance

 

FY    
2023
[9]

YTD   
2024
[10]

Change

 (%)

June   
 2024[11]

Change

 (%)

 

Total Revenue

Core Operating Profit

EUR

Total Revenue


0.92

0.93

(0)

0.93

(0)


397

179 

CNY

Total Revenue


7.09

7.23

(2)

7.27

(3)


322

182 

JPY

Total Revenue


140.60

152.26

(8)

158.03

(11)


177

119 

Other[12]









453

227 

GBP

Operating expense


0.80

0.79

0.79


60

(126)

SEK

Operating expense


10.61

10.54

10.49


9

(63)

 

Related-party transactions

 

There have been no significant related-party transactions in the period.

 

Principal risks and uncertainties

 

The Principal Risks and uncertainties facing the Group are set out on pages 54 to 57 of the Annual Report and Form 20-F Information 2023, and summarised below. They are not expected to change in respect of the second six months of the financial year and remain appropriate for the Group. In summary, the principal risks and uncertainties listed in the Annual Report and 20-F Information 2023 are:

 

1.  Product pipeline: failure or delay in the delivery of AstraZeneca's pipeline or launch of new medicines; failure to meet regulatory or ethical requirements for medicine development or approval

 

2.  Commercialisation risks: pricing, affordability, access and competitive pressures; failures or delays in the quality or execution of the Group's commercial strategies

 

3.  Supply-chain and business-execution risks: failure to maintain supply of compliant, quality medicines; failure in information technology or cybersecurity; failure to attract, develop, engage and retain a diverse, talented and capable workforce

 

4.  Legal, regulatory and compliance risks: safety and efficacy of marketed medicines is questioned; adverse outcome of litigation and / or governmental investigations; IP risks related to our products

 

5.  Economic and financial risks: failure to achieve strategic plans or meet targets or expectations; geopolitical and / or macroeconomic volatility disrupts the operation of our global business

 

Sustainability

 

AstraZeneca released its first Sustainability Impact Publication as a complement to its ninth annual Sustainability Report. This publication spotlights the diverse ways in which the Company is contributing to the health of people, society and the planet.

 

Access to healthcare

 

‒    At the 77th World Health Assembly (WHA) in Geneva, Switzerland in May, AstraZeneca convened Ministers of Health, industry, civil society and patient groups. Areas of focus for engagement, led by Ruud Dobber, EVP BioPharmaceuticals, included the need to increase early action to prevent, diagnose and treat disease and to accelerate collaboration to build resilient, equitable and net zero health systems

 

‒    At the WHA, AstraZeneca launched the expansion of its flagship Healthy Heart Africa programme to include chronic kidney disease as well as cardiovascular disease, recognising the growing burden of non-communicable diseases (NCDs) in Africa. As of May 2024, HHA has conducted more than 57 million screenings for high blood pressure and identified more than 11.3 million elevated readings, with 4.5 million patients diagnosed with hypertension since launch

 

‒    Also at the WHA, the Lung Ambition Alliance, of which the Company is a founding member, launched the Saving Lives from Lung Cancer platform and a calculator tool developed by AstraZeneca to support policymakers and the lung cancer community in identifying high-risk populations for early intervention

‒    The Partnership for Health System Sustainability and Resilience (PHSSR) held its third Summit during the Abu Dhabi Global Healthcare Week in May, bringing together more than 200 healthcare leaders from the Middle East, Africa and beyond including three Ministers of Health and 29 speakers, to drive forward the dialogue on investing in strengthening health systems. PHSSR also hosted local events in Taiwan, Portugal and the Netherlands during the quarter. In addition, insights from the PHSSR Asia-Pacific report were shared with a delegation from Korea at WHA

 

‒    A survey of more than 600 employees in 16 countries where the Young Health Programme (YHP) is active showed that more than 95% of employees feel proud to be associated with the YHP. With its expansion into the Philippines, the programme is now active in 41 countries globally. In recognition of the impact of the YHP, AstraZeneca was the only corporate partner invited to speak at UNICEF's Annual Meeting attended by UNICEF's 33 CEOs and their Board Chairs in high-income countries

 

‒    In June, the Company expanded its partnership with Direct Relief, approving the humanitarian organisation as a global medicine donation partner, enabling medicine donation to support global humanitarian relief efforts

 

Environmental protection

 

‒    AstraZeneca received multiple recognitions for its sustainability leadership this quarter, including retaining its EcoVadis Gold Medal ranking for the second consecutive year. This reflects its place in the top three percent of companies evaluated on environment, labour and human rights, ethics and sustainable procurement. The Company was also recognised in the 2024 FT Europe Climate Leaders list, where it was the top pharmaceutical company for the second year in a row

 

‒    AstraZeneca is collaborating with the World Business Council for Sustainable Development and its peers to develop a Roadmap to Nature Positive for the pharmaceutical sector, announced in May. The Roadmap will offer sector-specific guidance to accelerate toward nature positive, in alignment with the Taskforce for Nature-related Financial Disclosures, Science-based Targets Network and the EU's Corporate Sustainability Reporting Directive

 

‒    Pam Cheng, Executive Vice President of Global Operations and IT and Chief Sustainability Officer, joined a Global Health Leaders panel at the inaugural Climate and Health Day of the US Climate Action Summit. Leaders from government, industry, philanthropy and finance discussed the critical need to drive coordinated action on the climate and health nexus

 

Ethics and transparency

 

‒    AstraZeneca shared a new Diversity in Clinical Trials Standard internally for use across all therapy areas in R&D. This outlines the Company's mandatory principles on diversity for all AstraZeneca-sponsored clinical trials, in line with regulatory requirements, and reflects the Company's unwavering commitment to ensuring its clinical trials are representative of diverse populations

 

‒    Approximately 6,500 colleagues across 10 regions and 16 business units took the time to respond to AstraZeneca's second employee Ethics Survey. An analysis of 2023 results showed employee feedback continues to be positive, with 97% of respondents confirming they know how to raise an ethical concern and 87% confirming that it is easy to do the right thing in their day-to-day work

 

‒    The Company released new guidance on the selection, design, installation and maintenance of solar Photovoltaic (PV) power systems, which highlights the importance of conducting due diligence on human rights risks associated with new solar PV projects

 

Research and development

 

This section covers R&D events and milestones that have occurred since the prior results announcement on 25 April 2024, up to and including events on 24 July 2024.

 

A comprehensive view of AstraZeneca's pipeline of medicines in human trials can be found in the latest Clinical Trials Appendix, available on www.astrazeneca.com/investor-relations. The Clinical Trials Appendix includes tables with details of the ongoing clinical trials for AstraZeneca medicines and new molecular entities in the pipeline.

 

Oncology

 

AstraZeneca presented new data across its diverse portfolio of cancer medicines at two major medical congresses since the prior results announcement: the American Society of Clinical Oncology (ASCO) in May and June 2024 and European Hematology Association (EHA) in June 2024. At ASCO, AstraZeneca presented more than 100 abstracts featuring 25 approved and potential new medicines across the Company's diverse oncology portfolio and pipeline, including two late-breaking plenary presentations, a special late-breaking abstract session presentation and 15 oral presentations. At EHA, AstraZeneca presented 17 abstracts including one oral presentation and 10 posters across one approved and four investigational products.

 

Tagrisso

 

Event



Commentary

Presentation: ASCO

LAURA


Primary analysis of the Phase III LAURA trial, presented at ASCO, showed Tagrisso reduced the risk of disease progression or death by 84% compared to placebo (HR 0.16, 95% CI 0.10-0.24, p<0.001) as assessed by BICR. Median PFS was 39.1 months in patients treated with Tagrisso versus 5.6 months for placebo.

sNDA acceptance and Priority Review

US


For the treatment of adult patients with unresectable, Stage III EGFRm NSCLC after chemoradiotherapy. (LAURA, June 2024)

Approvals

Japan, China


Tagrisso with the addition of pemetrexed and platinum-based chemotherapy for the 1st-line treatment of adult patients with locally advanced or metastatic EGFRm NSCLC whose tumours have exon 19 deletions or exon 21 (L858R) mutations. (FLAURA2, June 2024)

Approval

Europe

 


Tagrisso with the addition of pemetrexed and platinum-based chemotherapy for the 1st-line treatment of adult patients with advanced EGFRm NSCLC whose tumours have exon 19 deletions or exon 21 (L858R) mutations. (FLAURA2, July 2024)

 

Imfinzi and Imjudo

 

Event



Commentary

Presentation: ASCO

ADRIATIC

 

 

Planned interim analysis of the Phase III ADRIATIC trial, presented at ASCO, demonstrated Imfinzi reduced the risk of death by 27% versus placebo (OS HR 0.73, 95% CI 0.57-0.93, p=0.0104) with an estimated 57% of patients treated with Imfinzi alive at three years compared to 48% on placebo. (June 2024)

Approval

US

 

Imfinzi in combination with carboplatin and paclitaxel followed by Imfinzi monotherapy for treatment for adult patients with primary advanced or recurrent endometrial cancer that is mismatch repair deficient. (DUO-E, June 2024)

Phase III data readout

NIAGARA

 

Met primary endpoint, with Imfinzi in combination with chemotherapy demonstrating a statistically significant and clinically meaningful improvement in the primary endpoint of event-free survival and the key secondary endpoint of OS versus neoadjuvant chemotherapy for patients with muscle-invasive bladder cancer. (June 2024)

Trial update

BR.31

 

BR.31 Phase III trial for Imfinzi in early-stage (IB-IIIA) NSCLC after complete tumour resection in patients whose tumours express PD-L1 on 25% or more tumour cells did not achieve statistical significance for the primary endpoint of disease-free survival versus placebo. (June 2024)

CHMP positive opinion

Europe

 

Imfinzi plus chemotherapy as 1st-line treatment followed by Lynparza and Imfinzi for patients with mismatch repair proficient disease. Imfinzi plus chemotherapy followed by Imfinzi alone for patients with mismatch repair deficient disease. (DUO‑E, July 2024)

 

Lynparza

 

Event



Commentary

CHMP positive opinion

Europe


Imfinzi plus chemotherapy as 1st-line treatment followed by Lynparza and Imfinzi for patients with mismatch repair proficient disease. (DUO-E, July 2024)

 

Enhertu

 

Event



Commentary

Phase III readout and presentation: ASCO

DESTINY-Breast06

 

Met primary endpoint, demonstrating Enhertu resulted in a statistically significant and clinically meaningful improvement in PFS in HR-positive, HER2-low metastatic breast cancer following one or more lines of endocrine therapy. (April 2024)

 

Primary analysis of the Phase III DESTINY-Breast06 trial, presented at ASCO, demonstrated Enhertu resulted in a statistically significant and clinically meaningful improvement in PFS compared to standard-of-care chemotherapy in patients with HR-positive, HER2-low metastatic breast cancer (HR 0.62, 95% CI 0.51-0.74, p<0.0001). Enhertu also demonstrated a statistically significant and clinically meaningful improvement in the overall trial population (patients with HR-positive, HER2-low and HER2-ultralow disease) (HR 0.63, 95% CI 0.53-0.75, p<0.0001). (June 2024)

 

Calquence

 

Event



Commentary

Phase III readout and presentation: EHA

ECHO

 

 

Met primary endpoint with Calquence combination regimen demonstrating a statistically significant and clinically meaningful improvement in PFS in 1st-line mantle cell lymphoma. (May 2024)

 

Interim analysis of the Phase III ECHO trial, presented at EHA, demonstrated Calquence in combination with standard-of-care chemoimmunotherapy, bendamustine and rituximab, resulted in a statistically significant and clinically meaningful 27% reduction in risk of progression or death versus standard of care in previously untreated adult patients with mantle cell lymphoma (HR 0.73, 95% CI 0.57-0.94, p=0.016). The secondary endpoint of OS showed a favourable trend for the Calquence combination compared to chemoimmunotherapy (HR 0.86; 95% CI 0.65-1.13; p=0.2743, not statistically significant, follow-up continues). (June 2024)

 

Truqap

 

Event



Commentary

Phase III trial update

CAPItello-290

 

CAPItello-290 Phase III trial for Truqap in combination with paclitaxel in patients with locally advanced or metastatic TNBC did not meet the dual primary endpoints of improvement in OS vs paclitaxel in combination with placebo in either the overall trial population or in a subgroup of patients with tumours harbouring specific biomarker alterations (PIK3CA, AKT1 or PTEN). (June 2024)

Approval

Europe

 

In combination with Faslodex for the treatment of adult patients with estrogen receptor-positive, HER2negative locally advanced or metastatic breast cancer with one or more PIK3CA, AKT1, or PTEN-alterations following recurrence or progression on or after an endocrine-based regimen. (CAPItello-291, June 2024)

 

Datopotamab deruxtecan (Dato-DXd)

 

Event



Commentary

Phase IIII trial update

TROPION-Lung01

 

 

Dual primary endpoint of improvement in overall survival for Dato-DXd versus docetaxel not met. Numerical improvement in overall survival compared to docetaxel in the overall trial population of patients with locally advanced or metastatic NSCLC. In the prespecified subgroup of patients with non-squamous NSCLC, Dato-DXd showed a clinically meaningful improvement in OS compared to docetaxel. (May 2024)

 

BioPharmaceuticals - CVRM

 

Farxiga

 

Event



Commentary

Approval

US

 

 

Improvement of glycaemic control in paediatric patients with type-2 diabetes aged 10 years and older (T2NOW, June 2024)

 

AZD0780 (oral PCSK9)

 

Event



Commentary

Presentation: European Atherosclerosis Society

 

 

 

Positive Phase I data demonstrating a statistically significant reduction of 52% in LDL-C levels on top of rosuvastatin treatment, with 78% total reduction from baseline, in treatment-naive participants with hypercholesterolaemia. (May 2024)

 

BioPharmaceuticals - R&I

 

Tezspire 

 

Event



Commentary

Presentation: American Thoracic Society

COURSE


Results from the COURSE Phase II trial demonstrated that treatment with Tezspire led to a 17% numerical reduction in the annual rate of moderate or severe COPD exacerbations compared to placebo at week 52. In patients with blood eosinophil counts of 150 cell/µl or more, treatment with Tezspire led to a nominally significant reduction of 37% in the rate of moderate or severe exacerbations compared to placebo. (May 2024)

Phase III readout

DIRECTION


Met the primary endpoint, demonstrating a statistically significant reduction in annual asthma exacerbation rate (AAER) over 52 weeks compared to placebo in patients in China with a history of uncontrolled asthma. (July 2024)

 

BioPharmaceuticals - V&I

 

sipavibart (COVID-19 mAb)

 

Event



Commentary

Phase III readout

SUPERNOVA


Positive high-level results from the SUPERNOVA Phase III trial showed sipavibart demonstrated a statistically significant reduction in the incidence of symptomatic COVID19 in an immunocompromised patient population. The trial was conducted during an evolving variant landscape in which COVID-19 cases captured over the course of the trial were caused by several different SARS-CoV-2 variants. (May 2024)

 

Rare Disease

 

AstraZeneca presented new clinical data from the industry's largest and broadest amyloidosis pipeline at the International Symposium on Amyloidosis (ISA) in May 2024. Clinical data was presented on ALXN2220 and anselamimab, which are being evaluated in Phase III clinical trials for ATTR and light chain (AL) amyloidosis, respectively.

 

Interim financial statements

 

Table 18: Condensed consolidated statement of comprehensive income: H1 2024

 

For the half year ended 30 June

 

2024 

2023 

 

 

$m 

$m 

Total Revenue

 

25,617 

22,295 

Product Sales

 

24,629 

21,448 

Alliance Revenue

 

939 

627 

Collaboration Revenue

 

49 

220 

Cost of sales


(4,401)

(3,865)

Gross profit

 

21,216 

18,430 

Distribution expense


(267)

(265)

Research and development expense


(5,791)

(5,278)

Selling, general and administrative expense


(9,424)

(9,045)

Other operating income and expense


127 

1,163 

Operating profit

 

5,861 

5,005 

Finance income


211 

141 

Finance expense


(856)

(795)

Share of after tax losses in associates and joint ventures


(19)

(1)

Profit before tax

 

5,197 

4,350 

Taxation


(1,089)

(726)

Profit for the period

 

4,108 

3,624 

Other comprehensive income:

 

 

 

Items that will not be reclassified to profit or loss:

 

 

 

Remeasurement of the defined benefit pension liability


101 

Net gains/(losses) on equity investments measured at fair value through other comprehensive income


89 

(48)

Fair value movements related to own credit risk on bonds designated as fair value through profit or loss


12 

Tax on items that will not be reclassified to profit or loss


(27)

(5)

 

 

175 

(42)

Items that may be reclassified subsequently to profit or loss:




Foreign exchange arising on consolidation


(554)

105 

Foreign exchange arising on designated liabilities in net investment hedges


(96)

(101)

Fair value movements on cash flow hedges


(138)

89 

Fair value movements on cash flow hedges transferred to profit and loss


102 

(71)

Fair value movements on derivatives designated in net investment hedges


45 

40 

Gains/(costs) of hedging


14 

(1)

Tax on items that may be reclassified subsequently to profit or loss


38 

12 



(589)

73 

Other comprehensive (expense)/income, net of tax

 

(414)

31 

Total comprehensive income for the period

 

3,694 

3,655 

Profit attributable to:




Owners of the Parent


4,106 

3,621 

Non-controlling interests




4,108 

3,624 

Total comprehensive income attributable to:




Owners of the Parent


3,692 

3,652 

Non-controlling interests




3,694 

3,655 

Basic earnings per $0.25 Ordinary Share


$2.65 

$2.34 

Diluted earnings per $0.25 Ordinary Share


$2.63 

$2.32 

Weighted average number of Ordinary Shares in issue (millions)


1,549 

1,549 

Diluted weighted average number of Ordinary Shares in issue (millions)


1,560 

1,560 

 

Table 19: Condensed consolidated statement of comprehensive income: Q2 2024

 

For the quarter ended 30 June

 

Unreviewed[13] 

Unreviewed 


 

2024 

2023 

 

 

$m 

$m 

Total Revenue

 

12,938 

11,416 

Product Sales

 

12,452 

10,882 

Alliance Revenue

 

482 

341 

Collaboration Revenue

 

193 

Cost of sales


(2,183)

(1,960)

Gross profit

 

10,755 

9,456 

Distribution expense


(132)

(131)

Research and development expense


(3,008)

(2,667)

Selling, general and administrative expense


(4,929)

(4,986)

Other operating income and expense


60 

784 

Operating profit

 

2,746 

2,456 

Finance income


100 

64 

Finance expense


(443)

(431)

Share of after tax losses in associates and joint ventures


(6)

(1)

Profit before tax

 

2,397 

2,088 

Taxation


(469)

(268)

Profit for the period

 

1,928 

1,820 

Other comprehensive income:

 

 

 

Items that will not be reclassified to profit or loss:

 

 

 

Remeasurement of the defined benefit pension liability


(43)

17 

Net gains/(losses) on equity investments measured at fair value through other comprehensive income


54 

(94)

Fair value movements related to own credit risk on bonds designated as fair value through profit or loss


12 

Tax on items that will not be reclassified to profit or loss


12 

(29)

 

 

35 

(104)

Items that may be reclassified subsequently to profit or loss:




Foreign exchange arising on consolidation


(39)

(209)

Foreign exchange arising on designated liabilities in net investment hedges


(94)

Fair value movements on cash flow hedges


(52)

33 

Fair value movements on cash flow hedges transferred to profit and loss


32 

Fair value movements on derivatives designated in net investment hedges


23 

24 

Costs of hedging


(1)

(1)

Tax on items that may be reclassified subsequently to profit or loss




(32)

(243)

Other comprehensive income/(expense), net of tax

 

(347)

Total comprehensive income for the period

 

1,931 

1,473 

Profit attributable to:




Owners of the Parent


1,927 

1,818 

Non-controlling interests




1,928 

1,820 

Total comprehensive income attributable to:




Owners of the Parent


1,930 

1,471 

Non-controlling interests




1,931 

1,473 

Basic earnings per $0.25 Ordinary Share


$1.24 

$1.17 

Diluted earnings per $0.25 Ordinary Share


$1.24 

$1.17 

Weighted average number of Ordinary Shares in issue (millions)


1,550 

1,550 

Diluted weighted average number of Ordinary Shares in issue (millions)


1,560 

1,560 

 

 

Table 20: Condensed consolidated statement of financial position

 


 

Reviewed[14]

At 30 Jun

2024

Audited

At 31 Dec

2023

Reviewed

At 30 Jun

2023


 

$m 

$m 

$m 

Assets





Non-current assets





Property, plant and equipment


9,630 

9,402 

8,675

Right-of-use assets


1,203 

1,100 

949

Goodwill


21,060 

20,048 

19,960

Intangible assets


39,426 

38,089 

38,326

Investments in associates and joint ventures


264 

147 

72

Other investments


1,607 

1,530 

1,071

Derivative financial instruments


217 

228 

163

Other receivables


806 

803 

752

Deferred tax assets


4,734 

4,718 

3,736


 

78,947 

76,065 

73,704

Current assets





Inventories


5,667 

5,424 

5,051

Trade and other receivables


11,047 

12,126 

11,092

Other investments


160 

122 

148

Derivative financial instruments


28 

116 

44

Income tax receivable


1,575 

1,426 

840

Cash and cash equivalents


6,916 

5,840 

5,664


 

25,393 

25,054 

22,839

Total assets

 

104,340 

101,119 

96,543

Liabilities

 

 

 

 

Current liabilities





Interest-bearing loans and borrowings


(5,067)

(5,129)

(4,556)

Lease liabilities


(292)

(271)

(231)

Trade and other payables


(20,463)

(22,374)

(19,738)

Derivative financial instruments


(51)

(156)

(83)

Provisions


(1,168)

(1,028)

(567)

Income tax payable


(1,525)

(1,584)

(1,200)


 

(28,566)

(30,542)

(26,375)

Non-current liabilities





Interest-bearing loans and borrowings


(27,225)

(22,365)

(24,329)

Lease liabilities


(949)

(857)

(722)

Derivative financial instruments


(61)

(38)

(68)

Deferred tax liabilities


(3,333)

(2,844)

(2,800)

Retirement benefit obligations


(1,326)

(1,520)

(1,078)

Provisions


(1,074)

(1,127)

(1,357)

Other payables


(2,208)

(2,660)

(2,398)



(36,176)

(31,411)

(32,752)

Total liabilities

 

(64,742)

(61,953)

(59,127)

Net assets

 

39,598 

39,166 

37,416 

Equity





Capital and reserves attributable to equity holders of the Parent





Share capital


388 

388 

387

Share premium account


35,199 

35,188 

35,163

Other reserves


2,078 

2,065 

2,076

Retained earnings


1,847 

1,502 

(234)


 

39,512 

39,143 

37,392 

Non-controlling interests


86 

23 

24 

Total equity

 

39,598 

39,166 

37,416 

 

 

Table 21: Condensed consolidated statement of changes in equity

 



Share capital

Share premium account

Other reserves

Retained earnings

Total attributable to owners of the parent

Non-controlling interests

Total equity


 

$m 

$m 

$m 

$m 

$m 

$m 

$m 

At 1 Jan 2023


387 

35,155 

2,069 

(574)

37,037 

21 

37,058 

Profit for the period


3,621 

3,621 

3,624 

Other comprehensive income


31 

31 

31 

Transfer to other reserves


(7)

Transactions with owners









Dividends


(3,047)

(3,047)

(3,047)

Issue of Ordinary Shares


Share-based payments charge for the period


274 

274 

274 

Settlement of share plan awards


(532)

(532)

(532)

Net movement

 

340 

355 

358 

At 30 Jun 2023

 

387 

35,163 

2,076 

(234)

37,392 

24 

37,416 

 

 

 

 

 

 

 

 

 

At 1 Jan 2024

 

388 

35,188 

2,065 

1,502 

39,143 

23 

39,166 

Profit for the period


4,106 

4,106 

4,108 

Other comprehensive expense


(414)

(414)

(414)

Transfer to other reserves


13 

(13)

Transactions with owners









Dividends


(3,052)

(3,052)

(3,052)

Issue of Ordinary Shares


11 

11 

11 

Changes in non-controlling interests


61 

61 

Share-based payments charge for the period


307 

307 

307 

Settlement of share plan awards


(589)

(589)

(589)

Net movement


11 

13 

345 

369 

63 

432 

At 30 Jun 2024

 

388 

35,199 

2,078 

1,847 

39,512 

86 

39,598 

 

Table 22: Condensed consolidated statement of cash flows: H1 2024

 

For the half year ended 30 June


2024 

2023 


$m 

$m 

 

Cash flows from operating activities




Profit before tax


5,197 

4,350 

Finance income and expense


645 

654 

Share of after tax losses of associates and joint ventures


19 

Depreciation, amortisation and impairment


2,534 

2,778 

Movement in working capital and short-term provisions


(584)

(747)

Gains on disposal of intangible assets


(21)

(249)

Fair value movements on contingent consideration arising from business combinations


251 

202 

Non-cash and other movements


(550)

(594)

Cash generated from operations

 

7,491 

6,395 

Interest paid


(583)

(483)

Tax paid


(1,337)

(1,061)

Net cash inflow from operating activities

 

5,571 

4,851 

 

Cash flows from investing activities



 

Acquisition of subsidiaries, net of cash acquired


(2,771)

(189)

Payments upon vesting of employee share awards attributable to business combinations


(23)

Payment of contingent consideration from business combinations


(474)

(398)

Purchase of property, plant and equipment


(799)

(517)

Disposal of property, plant and equipment


53 

126 

Purchase of intangible assets


(1,474)

(1,436)

Disposal of intangible assets


75 

288 

Movement in profit-participation liability


175 

Purchase of non-current asset investments


(67)

(26)

Disposal of non-current asset investments


51 

10 

Movement in short-term investments, fixed deposits and other investing instruments


42 

90 

Payments to associates and joint ventures


(140)

Disposal of investments in associates and joint ventures


13 

Interest received


206 

134 

Net cash outflow from investing activities


(5,285)

(1,766)

Net cash inflow before financing activities

 

286 

3,085 

 

Cash flows from financing activities




Proceeds from issue of share capital


11 

Issue of loans and borrowings


4,976 

3,816 

Repayment of loans and borrowings


(2,643)

(3,408)

Dividends paid


(3,050)

(3,069)

Hedge contracts relating to dividend payments


(8)

27 

Repayment of obligations under leases


(150)

(129)

Movement in short-term borrowings


2,503 

72 

Payment of Acerta Pharma share purchase liability


(833)

(867)

Net cash inflow/(outflow) from financing activities

 

806 

(3,550)

Net increase/(decrease) in Cash and cash equivalents in the period


1,092 

(465)

Cash and cash equivalents at the beginning of the period


5,637 

5,983 

Exchange rate effects


(52)

(47)

Cash and cash equivalents at the end of the period

 

6,677 

5,471 

Cash and cash equivalents consist of:




Cash and cash equivalents


6,916 

5,664 

Overdrafts


(239)

(193)

 

 

6,677 

5,471 

 

Responsibility statement of the directors in respect of the half-yearly financial report

 

We confirm that to the best of our knowledge:

 

‒    the condensed consolidated Interim Financial Statements have been prepared in accordance with IAS 34

'Interim Financial Reporting' as issued by the International Accounting Standards Board (IASB), IAS 34 as adopted by the European Union and UK-adopted IAS 34;

 

‒    the half-yearly management report gives a true and fair view of the assets, liabilities, financial position and profit or loss of the company;

 

‒    the half-yearly management report includes a fair review of the information required by:

 

a)  DTR 4.2.7R of the Disclosure and Transparency Rules, being an indication of important events that have occurred during the first six months of the financial year and their impact on the condensed consolidated Interim Financial Statements; and a description of the principal risks and uncertainties for the remaining six months of the year; and

 

b)  DTR 4.2.8R of the Disclosure and Transparency Rules, being related party transactions that have taken place in the first six months of the current financial year and that have materially affected the financial position or performance of the enterprise during that period; and any changes in the related party transactions described in the last annual report that could do so.

 

The Board

 

The Board of Directors that served during all or part of the six month period to 30 June 2024 and their respective responsibilities can be found on the Leadership team section of astrazeneca.com.

 

Approved by the Board and signed on its behalf by

 

Pascal Soriot

Chief Executive Officer

 

25 July 2024

 

Independent review report to AstraZeneca PLC

 

Report on the Interim financial statements

 

Our conclusion

 

We have reviewed AstraZeneca PLC's Interim financial statements (the "Interim financial statements") in the half-yearly financial report of AstraZeneca PLC for the six month period ended 30 June 2024 (the "period").

 

Based on our review, nothing has come to our attention that causes us to believe that the Interim financial statements are not prepared, in all material respects, in accordance with International Accounting Standard 34, 'Interim Financial Reporting' (IAS 34), as issued by the International Accounting Standards Board (IASB), IAS 34 as adopted by the European Union, UK-adopted IAS 34, and the Disclosure Guidance and Transparency Rules sourcebook of the United Kingdom's Financial Conduct Authority.

 

The Interim financial statements comprise:

 

‒    the Condensed consolidated statement of financial position as at 30 June 2024;

‒    the Condensed consolidated statement of comprehensive income: H1 2024 for the period then ended;

‒    the Condensed consolidated statement of changes in equity for the period then ended;  

‒    the Condensed consolidated statement of cash flows: H1 2024 for the period then ended; and

‒    the explanatory notes to the Interim financial statements.

 

The Interim financial statements included in the half-yearly financial report of AstraZeneca PLC have been prepared in accordance with International Accounting Standard 34, 'Interim Financial Reporting' (IAS 34), as issued by the International Accounting Standards Board (IASB), IAS 34 as adopted by the European Union, UK-adopted IAS 34, and the Disclosure Guidance and Transparency Rules sourcebook of the United Kingdom's Financial Conduct Authority.

 

Basis for conclusion

 

We conducted our review in accordance with International Standard on Review Engagements (UK) 2410, 'Review of Interim Financial Information Performed by the Independent Auditor of the Entity' issued by the Financial Reporting Council for use in the United Kingdom ("ISRE (UK) 2410"). A review of interim financial information consists of making enquiries, primarily of persons responsible for financial and accounting matters, and applying analytical and other review procedures.

 

A review is substantially less in scope than an audit conducted in accordance with International Standards on Auditing (UK) and, consequently, does not enable us to obtain assurance that we would become aware of all significant matters that might be identified in an audit. Accordingly, we do not express an audit opinion.

 

We have read the other information contained in the half-yearly financial report and considered whether it contains any apparent misstatements or material inconsistencies with the information in the Interim financial statements.

 

Conclusions relating to going concern

 

Based on our review procedures, which are less extensive than those performed in an audit as described in the Basis for conclusion section of this report, nothing has come to our attention to suggest that the directors have inappropriately adopted the going concern basis of accounting or that the directors have identified material uncertainties relating to going concern that are not appropriately disclosed. This conclusion is based on the review procedures performed in accordance with ISRE (UK) 2410. However, future events or conditions may cause the group to cease to continue as a going concern.

 

Independent review report to AstraZeneca PLC (continued)

 

Responsibilities for the Interim financial statements and the review

 

Our responsibilities and those of the directors

 

The half-yearly financial report, including the Interim financial statements, is the responsibility of, and has been approved by the directors. The directors are responsible for preparing the half-yearly financial report in accordance with the Disclosure Guidance and Transparency Rules sourcebook of the United Kingdom's Financial Conduct Authority. In preparing the half-yearly financial report, including the Interim financial statements, the directors are responsible for assessing the group's ability to continue as a going concern, disclosing, as applicable, matters related to going concern and using the going concern basis of accounting unless the directors either intend to liquidate the group or to cease operations, or have no realistic alternative but to do so.

 

Our responsibility is to express a conclusion on the Interim financial statements in the half-yearly financial report based on our review. Our conclusion, including our Conclusions relating to going concern, is based on procedures that are less extensive than audit procedures, as described in the Basis for conclusion paragraph of this report. This report, including the conclusion, has been prepared for and only for the company for the purpose of complying with the Disclosure Guidance and Transparency Rules sourcebook of the United Kingdom's Financial Conduct Authority and for no other purpose. We do not, in giving this conclusion, accept or assume responsibility for any other purpose or to any other person to whom this report is shown or into whose hands it may come save where expressly agreed by our prior consent in writing.

 

PricewaterhouseCoopers LLP

Chartered Accountants

London

 

25 July 2024

 

Notes to the Interim financial statements

 

Note 1: Basis of preparation and accounting policies

 

These unaudited condensed consolidated Interim financial statements for the six months ended 30 June 2024 have been prepared in accordance with International Accounting Standard 34, 'Interim Financial Reporting' (IAS 34), as issued by the International Accounting Standards Board (IASB), IAS 34 as adopted by the European Union, UK-adopted IAS 34 and the Disclosure Guidance and Transparency Rules sourcebook of the United Kingdom's Financial Conduct Authority and with the requirements of the Companies Act 2006 as applicable to companies reporting under those standards.

 

The unaudited Interim financial statements for the six months ended 30 June 2024 were approved by the Board of Directors for publication on 25 July 2024.

 

This results announcement does not constitute statutory accounts of the Group within the meaning of sections 434(3) and 435(3) of the Companies Act 2006. The annual financial statements of the Group for the year ended 31 December 2023 were prepared in accordance with UK-adopted international accounting standards and with the requirements of the Companies Act 2006. The annual financial statements also comply fully with IFRS Accounting Standards as issued by the IASB and International Accounting Standards as adopted by the European Union. Except for the estimation of the interim income tax charge, the Interim financial statements have been prepared applying the accounting policies that were applied in the preparation of the Group's published consolidated financial statements for the year ended 31 December 2023.

 

The comparative figures for the financial year ended 31 December 2023 are not the Group's statutory accounts for that financial year. Those accounts have been reported on by the Group's auditors and have been delivered to the Registrar of Companies; their report was (i) unqualified, (ii) did not include a reference to any matters to which the auditors drew attention by way of emphasis without qualifying their report, and (iii) did not contain a statement under section 498(2) or (3) of the Companies Act 2006.

 

Going concern

The Group has considerable financial resources available. As at 30 June 2024, the Group has $11.8bn in financial resources (cash and cash equivalent balances of $6.9bn and undrawn committed bank facilities of $4.9bn, with $5.4bn of borrowings due within one year). These facilities contain no financial covenants and were undrawn at 30 June 2024. The $4.9bn facilities are available until April 2029. Additionally, there are a further $2.0bn undrawn committed bank facilities available until February 2025.

 

The Group's revenues are largely derived from sales of medicines covered by patents, which provide a relatively high level of resilience and predictability to cash inflows, although government price interventions in response to budgetary constraints are expected to continue to adversely affect revenues in some of our significant markets. The Group, however, anticipates new revenue streams from both recently launched medicines and those in development, and the Group has a wide diversity of customers and suppliers across different geographic areas.

 

Consequently, the Directors believe that, overall, the Group is well placed to manage its business risks successfully. Accordingly, they continue to adopt the going concern basis in preparing the Interim financial statements.

 

Legal proceedings

The information contained in Note 6 updates the disclosures concerning legal proceedings and contingent liabilities in the Group's Annual Report and Form 20-F Information 2023.

 

Employee Benefit Trust

Following an amendment to the Employee Benefit Trust (EBT) Deed on 10th June 2024, AstraZeneca obtained control and commenced consolidation of the EBT. Going forward, cash paid on purchases of AstraZeneca Ordinary shares or American Depository Receipts will be presented within Financing activities in the Cash flow statement.

 

Note 2: Intangible assets

 

In accordance with IAS 36 'Impairment of Assets', reviews for triggers of impairment or impairment reversals at an individual asset or cash generating unit level were conducted, and impairment tests carried out where triggers were identified. As a result, total impairment charge of $26m has been recorded against intangible assets during the six months ended 30 June 2024 (H1 2023: $320m net charge). In H1 2023, net impairment charges included the $244m impairment of the ALXN1840 intangible asset, following the decision to discontinue this development programme in Wilson's disease.

 

The acquisition of Icosavax, Inc. completed on 19 February 2024. The transaction is recorded as an asset acquisition based on the concentration test permitted under IFRS 3 'Business Combinations', with consideration of $841m principally relating to $639m of intangible assets, $141m of cash and cash equivalents and $51m of marketable securities. Contingent consideration of up to $300m could be paid on achievement of regulatory and sales milestones; these potential liabilities would be recorded when the relevant recognition event for a regulatory or sales milestone is achieved.

 

Note 3: Net debt

 

The table below provides an analysis of Net debt and a reconciliation of Net Cash flow to the movement in Net debt. The Group monitors Net debt as part of its capital management policy as described in Note 28 of the Annual Report and Form 20-F Information 2023. Net debt is a non-GAAP financial measure.

 

Table 23: Net debt

 


 

At 1 Jan 2024

Cash flow

Acquisitions

Non-cash
& other

Exchange movements

At 30 Jun 2024


 

$m

$m

$m

$m

$m

$m

Non-current instalments of loans


(22,365)

(4,973)

(3)

(2)

118 

(27,225)

Non-current instalments of leases


(857)

(12)

(97)

17 

(949)

Total long-term debt

 

(23,222)

(4,973)

(15)

(99)

135 

(28,174)

Current instalments of loans


(4,614)

2,583 

(9)

(5)

27 

(2,018)

Current instalments of leases


(271)

174 

(6)

(197)

(292)

Commercial paper


(2,453)

(2,453)

Collateral received from derivative counterparties


(215)

13 

(202)

Other short-term borrowings excluding overdrafts


(97)

(63)

(155)

Overdrafts


(203)

(35)

(1)

(239)

Total current debt

 

(5,400)

219 

(15)

(202)

39 

(5,359)

Gross borrowings

 

(28,622)

(4,754)

(30)

(301)

174 

(33,533)

Net derivative financial instruments


150 

65 

(82)

133 

Net borrowings

 

(28,472)

(4,689)

(30)

(383)

174 

(33,400)

Cash and cash equivalents


5,840 

885 

242 

(51)

6,916 

Other investments - current


122 

(42)

87 

(7)

160 

Cash and investments

 

5,962 

843 

329 

(58)

7,076 

Net debt

 

(22,510)

(3,846)

299 

(383)

116 

(26,324)

 

Net debt increased by $3,814m in the half year to $26,324m. Details of the committed undrawn bank facilities are disclosed within the going concern section of Note 1. Non-cash movements in the period include fair value adjustments under IFRS 9 'Financial Instruments'.

 

In February 2024, AstraZeneca issued the following:

 

-     $1,250m of fixed-rate notes with a coupon of 4.8% maturing in February 2027

-     $1,250m of fixed-rate notes with a coupon of 4.85% maturing in February 2029

-     $1,000m of fixed-rate notes with a coupon of 4.9% maturing in February 2031

-     $1,500m of fixed-rate notes with a coupon of 5% maturing in February 2034

AstraZeneca repaid two bonds of carrying value $2,569m in Q2 2024 included in the cash outflow from Repayment of loans and borrowings of $2,643m. AstraZeneca also issued Commercial paper during the half year and the balance as at 30 June 2024 is $2,453m (H1 2023: $nil).

 

The Group has agreements with some bank counterparties whereby the parties agree to post cash collateral on financial derivatives, for the benefit of the other, equivalent to the market valuation of the derivative positions above a predetermined threshold. The carrying value of such cash collateral held by the Group at 30 June 2024 was $202m (31 December 2023: $215m) and the carrying value of such cash collateral posted by the Group at 30 June 2024 was $97m (31 December 2023: $102m).

 

The equivalent GAAP measure to Net debt is 'liabilities arising from financing activities', which excludes the amounts for cash and overdrafts, other investments and non-financing derivatives shown above and includes the Acerta Pharma share purchase liability of $nil (31 December 2023: $833m).

 

During the six months ended 30 June 2024, there have been no changes to the Company's solicited long term credit ratings. Moody's credit ratings were long term: A2; short term: P-1. Standard and Poor's credit ratings were long term: A; short term: A-1.

 

Note 4: Financial Instruments

 

As detailed in the Group's most recent annual financial statements, the principal financial instruments consist of derivative financial instruments, other investments, trade and other receivables, cash and cash equivalents, trade and other payables, lease liabilities and interest-bearing loans and borrowings.

 

The Group has certain equity investments that are categorised as Level 3 in the fair value hierarchy that are held at $337m (31 December 2023: $313m) and for which a fair value gain of $1m has been recognised in the six months ended 30 June 2024 (H1 2023: $1m). In the absence of specific market data, these unlisted investments are held at fair value based on the cost of investment and adjusted as necessary for impairments and revaluations on new funding rounds, which are seen to approximate the fair value. All other fair value gains and/or losses that are presented in Net gains/(losses) on equity investments measured at fair value through other comprehensive income, in the Condensed consolidated statement of comprehensive income for the six months ended 30 June 2024, are Level 1 fair value measurements, valued based on quoted prices in active markets.

 

Financial instruments measured at fair value include $1,670m of other investments, $5,463m held in money-market funds and $133m of derivatives as at 30 June 2024. With the exception of derivatives being Level 2 fair valued, and certain equity instruments of $350m categorised as Level 3, the aforementioned balances are Level 1 fair valued. Financial instruments measured at amortised cost include $97m of cash collateral pledged to counterparties. The total fair value of interest-bearing loans and borrowings at 30 June 2024, which have a carrying value of $33,533m in the Condensed consolidated statement of financial position, was $32,231m.

 

Table 24: Financial instruments - contingent consideration

 


 

2024

 

2023

 

 

 

Diabetes alliance

Other

Total

Total

 

 

$m

$m

$m

$m

At 1 January


1,945 

192 

2,137 

2,222 

Additions through business combinations


198 

198 

60 

Settlements


(473)

(1)

(474)

(398)

Revaluations


220 

31 

251 

202 

Discount unwind


50 

57 

66 

At 30 June

 

1,742 

427 

2,169 

2,152 

 

Contingent consideration arising from business combinations is fair valued using decision-tree analysis, with key inputs including the probability of success, consideration of potential delays and the expected levels of future revenues.

 

The contingent consideration balance relating to BMS's share of the global diabetes alliance of $1,742m (31 December 2023: $1,945m) would increase/decrease by $174m with an increase/decrease in sales of 10%, as compared with the current estimates.

 

Note 5: Business combinations

 

Gracell

 

On 22 February 2024, AstraZeneca completed the acquisition of Gracell Biotechnologies Inc. (Gracell), a global clinical-stage biopharmaceutical company developing innovative cell therapies for the treatment of cancer and autoimmune diseases. Gracell will operate as a wholly owned subsidiary of AstraZeneca, with operations in China and the US.

 

The acquisition enriches AstraZeneca's growing pipeline of cell therapies with AZD0120 (formerly GC012F), a novel, clinical-stage T-cell (CAR-T: therapeutic chimeric antigen receptor) therapy. AZD0120 is a potential new treatment for multiple myeloma, as well as other haematologic malignancies and autoimmune diseases, including Systemic Lupus Erythematosus (SLE).

 

The transaction is recorded as a business combination using the acquisition method of accounting in accordance with IFRS 3 'Business Combinations'. Consequently, the assets acquired, and liabilities assumed are recorded at fair value. Due to the proximity of the acquisition to the reporting date, the purchase price allocation exercise under IFRS 3 is in process, with the following items disclosed on a provisional basis.

 

 

 

Fair values

 

 

$m

Intangible assets


1,038 

Cash and cash equivalents


212 

Net deferred tax liability


(260)

Other immaterial balances


(89)

Total net assets acquired

 

901 

Goodwill


136 

Consideration

 

1,037 

 

The total consideration fair value of $1,037m includes cash consideration of $983m and future regulatory milestone-based consideration of $54m. Intangible assets recognised relate to products in development, principally AZD0120, and were fair valued using the multi-period excess earnings method, which uses several estimates regarding the amount and timing of future cash flows. The key assumptions in the cash flows are PTRS, peak year sales and revenue erosion profiles.

 

The net deferred tax liability of $260m principally arises from the deferred tax impact of the uplift in fair value of intangible assets.

 

Goodwill of $136m has been recognised, which principally comprises the premium attributable to the core technological capabilities and knowledge base of the company. Goodwill is not expected to be deductible for tax purposes.

 

Gracell's results have been consolidated into the Group's results from 22 February 2024.

 

Fusion

 

On 4 June 2024, AstraZeneca completed the acquisition of Fusion Pharmaceuticals Inc., (Fusion) a clinical-stage biopharmaceutical company developing next-generation radioconjugates. The acquisition marks a major step forward in AstraZeneca delivering on its ambition to transform cancer treatment and outcomes for patients by replacing traditional regimens like chemotherapy and radiotherapy with more targeted treatments. As a result of the acquisition, Fusion became a wholly owned subsidiary of AstraZeneca, with operations in Canada and the US.

 

This acquisition complements AstraZeneca's leading oncology portfolio with the addition of the Fusion pipeline of radioconjugates, including their most advanced programme, FPI-2265, a potential new treatment for patients with metastatic castration-resistant prostate cancer (mCRPC), and brings new expertise and pioneering R&D, manufacturing and supply chain capabilities in actinium-based radioconjugates to AstraZeneca.

 

The transaction is recorded as a business combination using the acquisition method of accounting in accordance with IFRS 3 'Business Combinations'. Consequently, the assets acquired, and liabilities assumed are recorded at fair value. Due to the proximity of the acquisition to the reporting date, the purchase price allocation exercise under IFRS 3 is in process, with the following items disclosed on a provisional basis.

 

 

 

Fair values

 

 

$m

Intangible assets


1,326 

Cash and cash equivalents


30 

Current investments


87 

Net deferred tax liability


(246)

Other immaterial balances


51 

Total net assets acquired

 

1,248 

Goodwill


947 

Consideration

 

2,195 

 

The total consideration fair value of $2,195m includes cash consideration of $2,051m and future regulatory milestone-based consideration of $144m. Intangible assets relating to products in development comprise the FPI-2265 ($848m), FPI-2059 ($165m) and AZD2068 ($313m) programmes. These were fair valued using the multi-period excess earnings method, which uses several estimates regarding the amount and timing of future cash flows. The key assumptions in the cash flows are PTRS, peak year sales and revenue erosion profiles.

 

The net deferred tax liability of $246m principally arises from the deferred tax impact of the uplift in fair value of intangible assets.

 

Goodwill recognised comprises a number of not individually quantifiable elements. These include the premium attributable to a pre-existing well positioned business in the innovation intensive biopharmaceuticals market with a highly skilled workforce, unidentified potential products that future research and development may yield, and the core capabilities and knowledge base of the company including radioisotope supply and manufacturing expertise. Goodwill is not expected to be deductible for tax purposes.

 

Immediately prior to the acquisition, AstraZeneca held an approximately 1% shareholding in Fusion considered to have a fair value of $24m.

 

Fusion's results have been consolidated into the Group's results from 4 June 2024.

 

Note 6: Legal proceedings and contingent liabilities

 

AstraZeneca is involved in various legal proceedings considered typical to its business, including litigation and investigations, including Government investigations, relating to product liability, commercial disputes, infringement of intellectual property (IP) rights, the validity of certain patents, anti-trust law and sales and marketing practices. The matters discussed below constitute the more significant developments since publication of the disclosures concerning legal proceedings in the Company's Annual Report and Form 20-F Information 2023 (the Disclosures). Information about the nature and facts of the cases is disclosed in accordance with IAS 37.

 

As discussed in the Disclosures, the majority of claims involve highly complex issues. Often these issues are subject to substantial uncertainties and, therefore, the probability of a loss, if any, being sustained and/or an estimate of the amount of any loss is difficult to ascertain.

 

In cases that have been settled or adjudicated, or where quantifiable fines and penalties have been assessed and which are not subject to appeal, or where a loss is probable and we are able to make a reasonable estimate of the loss, AstraZeneca records the loss absorbed or makes a provision for its best estimate of the expected loss. The position could change over time and the estimates that the Company made, and upon which the Company have relied in calculating these provisions are inherently imprecise. There can, therefore, be no assurance that any losses that result from the outcome of any legal proceedings will not exceed the amount of the provisions that have been booked in the accounts. The major factors causing this uncertainty are described more fully in the Disclosures and herein.

 

AstraZeneca has full confidence in, and will vigorously defend and enforce, its IP.

 

Matters disclosed in respect of the second quarter of 2024 and to 25 July 2024

 

Patent litigation

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

Enhertu

US patent proceedings

In October 2020, Seagen Inc. (Seagen) filed a complaint against Daiichi Sankyo Company, Limited (Daiichi Sankyo) in the US District Court for the Eastern District of Texas (District Court) alleging that Enhertu infringes a Seagen patent. AstraZeneca co-commercialises Enhertu with Daiichi Sankyo, Inc. in the US. After trial in April 2022, the jury found that the patent was infringed and awarded Seagen $41.82m in past damages. In July 2022, the District Court entered final judgment and declined to enhance damages on the basis of wilfulness. In October 2023, the District Court entered an amended final judgment that requires Daiichi Sankyo to pay Seagen a royalty of 8% on US sales of Enhertu from 1 April 2022 through to 4 November 2024, in addition to the past damages previously awarded by the District Court. AstraZeneca and Daiichi Sankyo have appealed the District Court's decision.

 

In December 2020 and January 2021, AstraZeneca and Daiichi Sankyo, Inc. filed post-grant review (PGR) petitions with the US Patent and Trademark Office (USPTO) alleging, among other things, that the Seagen patent is invalid for lack of written description and enablement. The USPTO initially declined to institute the PGRs, but, in April 2022, the USPTO granted the rehearing requests and instituted both PGR petitions. Seagen subsequently disclaimed all patent claims at issue in one of the PGR proceedings. In July 2022, the USPTO reversed its institution decision and declined to institute the other PGR petition. AstraZeneca and Daiichi Sankyo, Inc. requested reconsideration of the decision not to institute review of the patent. In February 2023, the USPTO reinstituted the PGR proceeding. In February 2024, the USPTO issued a decision that the claims were unpatentable. Seagen has appealed this decision.

 

Tagrisso

US patent proceedings

In September 2021, Puma Biotechnology, Inc. (Puma) and Wyeth LLC (Wyeth) filed a patent infringement lawsuit in the US District Court for the District of Delaware (District Court) against AstraZeneca relating to Tagrisso. In March 2024, the District Court dismissed Puma. The trial, with Wyeth as the plaintiff, took place in May 2024. The jury found Wyeth's patents infringed and awarded Wyeth $107.5m in past damages. The jury also found that the infringement was not wilful. A bench trial on AstraZeneca's indefiniteness and equitable defenses took place in June 2024. The parties await the court's decision on the bench trial issues and consideration of post-trial motions.

 

Legal proceedings brought by AstraZeneca considered to be contingent assets

 

Calquence

US patent proceedings

In February 2022, in response to Paragraph IV notices from multiple ANDA filers, AstraZeneca filed patent infringement lawsuits in the US District Court for the District of Delaware (District Court). In its complaint, AstraZeneca alleged that a generic version of Calquence capsules, if approved and marketed, would infringe patents that are owned or licensed by AstraZeneca. In 2024, AstraZeneca entered into settlement agreements with all five generic manufacturers, resolving the Calquence capsule ANDA litigation proceedings.

 

In April 2024, AstraZeneca received a Paragraph IV notice from an ANDA filer relating to patents listed in the FDA Orange Book with reference to Calquence tablets. In May 2024, in response to the Paragraph IV notice, AstraZeneca filed a patent infringement lawsuit against Cipla Limited and Cipla USA, Inc. in the District Court, alleging that a generic version of Calquence tablets, if approved and marketed, would infringe patents that are owned or licensed by AstraZeneca.

 

Lokelma

US patent proceedings

In August 2022, in response to Paragraph IV notices, AstraZeneca initiated ANDA litigation against multiple generic filers in the US District Court for the District of Delaware (District Court). AstraZeneca alleged that a generic version of Lokelma, if approved and marketed, would infringe patents that are owned or licensed by AstraZeneca.

 

AstraZeneca entered into separate settlement agreements with two generic manufacturers which resulted in dismissal of the corresponding litigations. Additional proceedings with the remaining generic manufacturers are ongoing in the District Court. Trial is scheduled for March 2025.

 

Lynparza

US patent proceedings

In December 2022, AstraZeneca received a Paragraph IV notice from Natco Pharma Limited (Natco) relating to Lynparza patents. In February 2023, in response to the Paragraph IV notice, AstraZeneca, MSD International Business GmbH, and the University of Sheffield initiated ANDA litigation against Natco in the US District Court for the District of New Jersey (District Court). In the complaint, AstraZeneca alleged that Natco's generic version of Lynparza, if approved and marketed, would infringe AstraZeneca's patents. No trial date has been scheduled.

 

In December 2023, AstraZeneca received a Paragraph IV notice from Sandoz Inc. (Sandoz) relating to Lynparza patents. In February 2024, in response to the Paragraph IV notice, AstraZeneca, MSD International Business GmbH, and the University of Sheffield initiated ANDA litigation against Sandoz in the District Court. In the complaint, AstraZeneca alleged that Sandoz's generic version of Lynparza, if approved and marketed, would infringe AstraZeneca's patents. No trial date has been scheduled.

 

In May 2024, AstraZeneca filed additional ANDA actions against Natco and Sandoz asserting recently issued patents covering Lynparza. These actions have been consolidated with the earlier filed ANDA actions and no trial date has been scheduled.

 

 

In May 2024, AstraZeneca received a Paragraph IV notice from Cipla USA, Inc. and Cipla Limited (collectively, Cipla) relating to Lynparza patents. In June 2024, in response to the Paragraph IV notice, AstraZeneca, MSD International Business GmbH, and the University of Sheffield initiated ANDA litigation against Cipla in the District Court. In the complaint, AstraZeneca alleged that Cipla's generic version of Lynparza, if approved and marketed, would infringe AstraZeneca's patents. No trial date has been scheduled.

 

Soliris

US patent proceedings

In January 2024, Alexion initiated patent infringement litigation against Samsung Bioepis Co. Ltd. (Samsung) in the US District Court for the District of Delaware alleging that Samsung's biosimilar eculizumab product will infringe six Soliris-related patents. No trial date has been scheduled. Five of the six asserted patents are also the subject of inter partes review (IPR) proceedings before the US Patent and Trademark Office. Alexion filed a motion for a preliminary injunction seeking to enjoin Samsung from launching its biosimilar eculizumab product upon FDA approval. The court denied Alexion's motion and Alexion has appealed that decision. On 22 July 2024, Samsung announced FDA approval of Samsung's biosimilar.

 

European patent proceedings

In March 2024, Alexion filed motions for provisional measures against Amgen Pharmaceuticals Inc (Amgen) and Samsung Bioepis Co. Ltd. (Samsung) and their respective affiliates at the Hamburg Local Division of the Unified Patent Court on the basis that Amgen's and Samsung's biosimilar eculizumab products infringe an Alexion patent. In June 2024 the UPC denied the requested provisional measures. Alexion has appealed this decision. In parallel, Samsung has filed opposition to the patent at the European Patent Office.

 

UK patent proceedings

In May 2024, Alexion initiated patent infringement proceedings against Amgen Ltd and Samsung Bioepis UK Ltd (Samsung UK) in the UK High Court of Justice alleging that their respective biosimilar eculizumab products infringe an Alexion patent; on the same day, Samsung UK initiated a revocation action for the same patent. Trial has been scheduled for March 2025.

 

Tagrisso

Russia patent proceedings

In Russia, in August 2023, AstraZeneca filed lawsuits in the Arbitration Court of the Moscow Region (Court) against the Ministry of Health of the Russian Federation and Axelpharm LLC (Axelpharm) related to Axelpharm's improper use of AstraZeneca's information to obtain authorisation to market a generic version of Tagrisso. In December 2023, the Court dismissed the lawsuit against the Ministry of Health of the Russian Federation. The appellate court affirmed the dismissal in March 2024. AstraZeneca filed a further appeal, which remains pending. The lawsuit against Axelpharm remains pending.

 

In Russia, in November 2023, Axelpharm filed a compulsory licensing action against AstraZeneca in the Court related to a patent that covers Tagrisso. The compulsory licensing action remains pending. AstraZeneca has also challenged before the Russian Patent and Trademark Office ("PTO") the validity of the Axelpharm patent on which the compulsory licensing action is predicated; that challenge remains pending before the Russian PTO.

 

In July 2024, AstraZeneca filed a patent infringement lawsuit and an unfair competition claim with the Federal Anti-Monopoly Service of Russia against AxelPharm and others related to the securing of state contracts in Russia for its generic version of osimertinib.

 

Commercial litigation

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

Anti-Terrorism Act Civil Lawsuit

US proceedings

In the US, in October 2017, AstraZeneca and certain other pharmaceutical and/or medical device companies were named as defendants in a complaint filed in the US District Court for the District of Columbia (District Court) by US nationals (or their estates, survivors, or heirs) who were killed or wounded in Iraq between 2005 and 2013. The plaintiffs allege that the defendants violated the US Anti-Terrorism Act and various state laws by selling pharmaceuticals and medical supplies to the Iraqi Ministry of Health. In July 2020, the District Court granted AstraZeneca's and the other defendants' motion to dismiss the lawsuit, which the DC Circuit Court of Appeals (the Appellate Court) reversed in January 2022. In June 2024, the United States Supreme Court issued an order vacating the 2022 decision and granted AstraZeneca's and the other defendants' request for a remand to the Appellate Court for reconsideration under new case law.

 

Employment Litigation

US proceedings

In December 2022, AstraZeneca was served with a lawsuit filed by seven former employees in the US District Court for the District of Delaware (District Court) asserting claims of discrimination on grounds of age and religion, related to AstraZeneca's vaccination requirement. In March 2023, AstraZeneca filed a partial motion to dismiss certain religious discrimination claims and a motion to strike the class and collective claims. In September 2023, Plaintiffs moved for conditional certification of the collective action. In June 2024, the District Court granted AstraZeneca's partial motion to dismiss, granted AstraZeneca's motion to strike, and denied without prejudice Plaintiff's motion for conditional certification.

 

Pay Equity Litigation

US proceedings

AstraZeneca is defending a putative class and collective action in the US District Court for the Northern District of Illinois (District Court) brought by three named plaintiffs, who are former AstraZeneca employees. The case involves claims under the federal and Illinois Equal Pay Acts, with the plaintiffs alleging they were paid less than male employees who performed substantially similar and/or equal work. In May 2024, the District Court conditionally certified a collective under the federal Equal Pay Act and authorised the sending of notice to potential collective action members. The notice was distributed in June 2024.

 

University of Sheffield Contract Dispute

UK proceedings

In June 2024, AstraZeneca was served with a lawsuit filed by the University of Sheffield (Sheffield). In its complaint, Sheffield alleges that AstraZeneca made misrepresentations to induce Sheffield to amend a patent license relating to Lynparza. AstraZeneca is considering its response.

Viela Bio, Inc. Shareholder Litigation

US proceedings

In February 2023, AstraZeneca was served with a lawsuit filed in Delaware state court against AstraZeneca and certain officers (collectively, Defendants), on behalf of a putative class of Viela Bio, Inc. (Viela) shareholders. The complaint alleged that the Defendants breached their fiduciary duty to Viela shareholders in the course of Viela's 2021 merger with Horizon Therapeutics, plc. In July 2024, the Court granted with prejudice AstraZeneca's motion to dismiss.

 

Legal proceedings brought by AstraZeneca considered to be contingent assets

 

PARP Inhibitor Royalty Dispute

UK proceedings

In October 2012, Tesaro, Inc. (now wholly owned by GlaxoSmithKline plc, (GSK)) entered into two worldwide, royalty-bearing patent license agreements with AstraZeneca related to GSK's product niraparib. In May 2021, AstraZeneca filed a lawsuit against GSK in the Commercial Court of England and Wales alleging that GSK had failed to pay all of the royalties due on niraparib sales under the license agreements. In April 2023, after trial, the trial court issued a decision in AstraZeneca's favour. In February 2024, the Court of Appeal reversed the decision. In March 2024, AstraZeneca filed a request for permission to appeal with the Supreme Court of the United Kingdom. In May 2024, the Supreme Court denied permission to appeal. The case will return to the trial court for further proceedings.

 

Government investigations/proceedings

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

Boston US Attorney Investigation

US Proceedings

In June 2024, AstraZeneca was served with a subpoena issued by the US Attorney's Office in Boston, seeking documents and information relating to payments by AstraZeneca to healthcare providers. AstraZeneca is cooperating with this enquiry.

 

Turkish Ministry of Health Matter

Turkey proceedings

In Turkey, in July 2020, the Turkish Ministry of Health (Ministry of Health) initiated an investigation regarding payments to healthcare providers by Alexion and former employees and consultants. The investigation arose from Alexion's disclosure of a $21.5m civil settlement with the US Securities & Exchange Commission (SEC) in July 2020 fully resolving the SEC's investigation into possible violations of the US Foreign Corrupt Practices Act. In September 2021, the Ministry of Health completed its draft investigation report, and referred the matter to the Ankara Public Prosecutor's Office with a recommendation for further proceedings against certain former employees. In June 2024, the Ankara Public Prosecutor's Office closed its investigation without further action.

 

Legal proceedings brought by AstraZeneca considered to be contingent assets

 

Inflation Reduction Act Litigation

US proceedings

In August 2023, AstraZeneca filed a lawsuit in the US District Court for the District of Delaware (District Court) against the US Department of Health and Human Services (HHS) challenging aspects of the drug price negotiation provisions of the Inflation Reduction Act and the implementing guidance and regulations. In March 2024, the District Court granted HHS' motions and dismissed AstraZeneca's lawsuit. AstraZeneca has appealed the District Court's decision.

 

340B State Litigation

US proceedings

AstraZeneca has filed lawsuits against Arkansas, Kansas, Louisiana, Maryland, Minnesota, Mississippi, and West Virginia challenging the constitutionality of each state's 340B statute. In the Arkansas matter, trial is scheduled for April 2025. In the Louisiana matter, AstraZeneca and the state have filed motions for summary judgment and a hearing was held in June 2024. The remaining matters are in their preliminary stages.

 

Other

 

Additional government inquiries

As is true for most, if not all, major prescription pharmaceutical companies, AstraZeneca is currently involved in multiple inquiries into drug marketing and pricing practices. In addition to the investigations described above, various law enforcement offices have, from time to time, requested information from the Group. There have been no material developments in those matters.

 

Matters disclosed in respect of the first quarter of 2024 and to 25 April 2024

 

Patent litigation

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

Forxiga

UK patent proceedings

In the UK, one of AstraZeneca's patents relating to Forxiga is being challenged by Generics (UK) Limited, Teva Pharmaceutical Industries Limited, and Glenmark Pharmaceuticals Europe Limited. Trial is scheduled for March 2025.

 

Tagrisso

US patent proceedings

In September 2021, Puma Biotechnology, Inc. (Puma) and Wyeth LLC (Wyeth) filed a patent infringement lawsuit in the US District Court for the District of Delaware (District Court) against AstraZeneca relating to Tagrisso. In March 2024, the District Court dismissed Puma. A trial, with Wyeth as the plaintiff, has been scheduled for May 2024.

 

Legal proceedings brought by AstraZeneca considered to be contingent assets

 

Calquence

US patent proceedings

In February 2022, in response to Paragraph IV notices from multiple ANDA filers, AstraZeneca filed patent infringement lawsuits in the US District Court for the District of Delaware (District Court). In its complaint, AstraZeneca alleged that a generic version of Calquence capsules, if approved and marketed, would infringe patents that are owned or licensed by AstraZeneca. Trial is scheduled for March 2025.

 

In March and April 2024, AstraZeneca entered into settlement agreements with generic manufacturers, Sandoz Inc., and Natco Pharma Limited with Natco Pharma Inc., resulting in dismissal of the corresponding Calquence capsule ANDA litigation proceedings. Additional Calquence capsule ANDA litigation proceedings with the remaining three generic manufacturers are ongoing in the District Court.

 

In April 2024, AstraZeneca received a Paragraph IV notice from an ANDA filer relating to patents listed in the FDA Orange Book with reference to Calquence tablets. AstraZeneca is considering its response.

 

Lokelma

US patent proceedings

In August 2022, in response to Paragraph IV notices, AstraZeneca initiated ANDA litigation against multiple generic filers in the US District Court for the District of Delaware (District Court). Trial is scheduled for March 2025.

 

AstraZeneca entered into a settlement agreement with a generic manufacturer, Alkem Laboratories, which resulted in dismissal of the corresponding litigation. Additional proceedings with the remaining generic manufacturers are ongoing in the District Court.

 

Soliris

US patent proceedings

In January 2024, Alexion initiated patent infringement litigation against Samsung Bioepis Co. Ltd. (Samsung) in the US District Court for the District of Delaware alleging that Samsung's biosimilar eculizumab product, for which Samsung is currently seeking FDA approval, will infringe six Soliris-related patents. No trial date has been scheduled. Five of the six asserted patents are also the subject of inter partes review proceedings before the US Patent and Trademark Office. In February 2024, Alexion filed a motion for a preliminary injunction seeking to enjoin Samsung from launching its biosimilar eculizumab product upon FDA approval. A hearing on Alexion's preliminary injunction motion is scheduled for May 2024.

 

European patent proceedings

In March 2024, Alexion filed motions for preliminary injunctions against Amgen and Samsung at the Hamburg Local Division of the Unified Patent Court on the basis that Amgen's and Samsung's biosimilar eculizumab products infringe Alexion's eculizumab molecule patent that is expected to grant in Q2 2024. No hearing date for the preliminary injunction motions has been set.

 

Tagrisso

Russia patent proceedings

In Russia, in August 2023, AstraZeneca filed lawsuits in the Arbitration Court of the Moscow Region (Court) against the Ministry of Health of the Russian Federation and Axelpharm LLC (Axelpharm) related to Axelpharm's improper use of AstraZeneca's information to obtain authorisation to market a generic version of Tagrisso. In December 2023, the Court dismissed the lawsuit against the Ministry of Health of the Russian Federation. In January 2024, AstraZeneca filed an appeal, and the appellate court affirmed the dismissal in March 2024. The lawsuit against Axelpharm remains pending.

 

In Russia, in November 2023, Axelpharm filed a compulsory licensing action against AstraZeneca in the Court related to a patent that covers Tagrisso. The compulsory licensing action remains pending.

 

Product liability litigation

 

Legal proceedings brought against AstraZeneca for which a provision has been taken

 

Nexium and Losec/Prilosec

US proceedings

AstraZeneca has been defending lawsuits brought in federal and state courts involving claims that plaintiffs have been diagnosed with various injuries following treatment with proton pump inhibitors (PPIs), including Nexium and Prilosec. Most of the lawsuits alleged kidney injury. In August 2017, the pending federal court cases were consolidated into a multidistrict litigation (MDL) proceeding in the US District Court for the District of New Jersey for pre-trial purposes. Cases alleging kidney injury were also filed in Delaware and New Jersey state courts.

 

In addition, AstraZeneca has been defending lawsuits involving allegations of gastric cancer following treatment with PPIs, including one such claim in the US District Court for the Middle District of Louisiana (Louisiana District Court).

 

In October 2023, AstraZeneca resolved all pending claims in the MDL, as well as all pending claims in Delaware and New Jersey state courts, for $425m, for which a provision has been taken. The only remaining case is the one pending in the Louisiana District Court, which is scheduled for trial in January 2025.

 

Canada proceedings

In Canada, in July and August 2017, AstraZeneca was served with three putative class action lawsuits. Two of the lawsuits have been dismissed, one in 2019 and one in 2021. The third lawsuit seeks authorisation to represent individual residents in Canada who allegedly suffered kidney injuries from the use of proton pump inhibitors, including Nexium and Losec.

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

Onglyza and Kombiglyze

US proceedings

In the US, AstraZeneca has been defending various lawsuits in both California state court and in a consolidated federal proceeding alleging heart failure, cardiac injuries, and/or death from treatment with Onglyza or Kombiglyze. In the California state court proceeding, the trial court granted summary judgment for AstraZeneca, which the California appellate court affirmed. The California Supreme Court has declined further review, and the California matter has concluded. The consolidated federal cases were dismissed in August 2022 by the US District Court for the Eastern District of Kentucky. That dismissal was affirmed by the US Court of Appeals for the Sixth Circuit in February 2024.

 

Vaxzevria

UK proceedings

AstraZeneca is defending lawsuits in the UK involving multiple claimants alleging injuries following vaccination with AstraZeneca's COVID-19 vaccine. Most of the lawsuits involve claims of thrombosis with thrombocytopenia syndrome. No trial dates have been scheduled.

 

Commercial litigation

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

340B Antitrust Litigation

US proceedings

In September 2021, AstraZeneca was served with a class-action antitrust complaint filed in the US District Court for the Western District of New York (District Court) by Mosaic Health alleging a conspiracy to restrict access to 340B discounts in the diabetes market through contract pharmacies. In September 2022, the District Court granted AstraZeneca's motion to dismiss the Complaint. In February 2024, the District Court denied Plaintiffs' request to file an amended complaint and entered an order closing the matter. In March 2024, Plaintiffs filed an appeal.

 

Definiens

Germany proceedings

In Germany, in July 2020, AstraZeneca received a notice of arbitration filed with the German Institution of Arbitration from the sellers of Definiens AG (the Sellers) regarding the 2014 Share Purchase Agreement (SPA) between AstraZeneca and the Sellers. The Sellers claim that they are owed approximately $140m in earn-outs under the SPA. In December 2023, after an arbitration hearing, the arbitration panel made a final award of $46.43m in favour of the Sellers. In March 2024, AstraZeneca filed an application with the Bavarian Supreme Court to set aside the arbitration award.

 

Legal proceedings brought by AstraZeneca considered to be contingent assets

 

PARP Inhibitor Royalty Dispute

UK proceedings

In October 2012, Tesaro, Inc. (now wholly owned by GlaxoSmithKline plc, (GSK)) entered into two worldwide, royalty-bearing patent license agreements with AstraZeneca related to GSK's product niraparib. In May 2021, AstraZeneca filed a lawsuit against GSK in the Commercial Court of England and Wales alleging that GSK had failed to pay all of the royalties due on niraparib sales under the license agreements. In April 2023, after trial, the trial court issued a decision in AstraZeneca's favour. In February 2024, Court of Appeal reversed. In March 2024, AstraZeneca filed a request for permission to appeal with the Supreme Court of the United Kingdom.

 

Government investigations/proceedings

 

Legal proceedings brought against AstraZeneca considered to be contingent liabilities

 

340B Qui Tam

US proceedings

In July 2023, AstraZeneca was served with an unsealed civil lawsuit brought by a qui tam relator on behalf of the United States, several states, and the District of Columbia in the US District Court for the Central District of California (District Court). The complaint alleges that AstraZeneca violated the US False Claims Act and state law analogues. In March 2024, the District Court granted AstraZeneca's motion to dismiss the First Amended Complaint without leave to amend. In April 2024, the relator filed an appeal.

 

Legal proceedings brought by AstraZeneca considered to be contingent assets

 

Inflation Reduction Act Litigation

US proceedings

In August 2023, AstraZeneca filed a lawsuit in the US District Court for the District of Delaware (District Court) against the US Department of Health and Human Services (HHS) challenging aspects of the drug price negotiation provisions of the Inflation Reduction Act and the implementing guidance and regulations. In March 2024, the District Court granted HHS' motions and dismissed AstraZeneca's lawsuit.

 

Arkansas 340B Litigation

US proceedings

In March 2024, AstraZeneca filed a lawsuit against the State of Arkansas alleging that the Arkansas's 340B statute is preempted by federal law and unconstitutional.

 

Other

 

Additional government inquiries

As is true for most, if not all, major prescription pharmaceutical companies, AstraZeneca is currently involved in multiple inquiries into drug marketing and pricing practices. In addition to the investigations described above, various law enforcement offices have, from time to time, requested information from the Group. There have been no material developments in those matters.

 

Note 7: Subsequent events

 

On 15 July 2024, AstraZeneca completed the acquisition of Amolyt Pharma, a clinical-stage biotechnology company focused on developing novel treatments for rare endocrine diseases. AstraZeneca acquired all outstanding equity of Amolyt for a total consideration of up to $1.05 billion, on a cash and debt free basis. This includes an initial payment of $800m on deal closing, subject to customary closing adjustments, and a further up to $250m in contingent milestones-based consideration. Due to the timing of the transaction post period end, the accounting and other disclosures will be finalised in the second half of 2024.

 

Note 8

Table 25: H1 2024 - Product Sales year-on-year analysis[15]

The CER information in respect of H1 2024 included in the Interim financial statements has not been reviewed by PricewaterhouseCoopers LLP.

 

 

World

US

Emerging Markets

Europe

Established RoW

 


$m

Act % chg

CER % chg

$m

% chg

$m

Act % chg

CER % chg

$m

Act % chg

CER % chg

$m

Act % chg

CER % chg

Oncology

9,737 

17 

21 

4,387 

20 

2,300 

18 

28 

1,967 

25 

23 

1,083 

(2)

Tagrisso

3,203 

10 

13 

1,282 

16 

919 

16 

628 

16 

15 

374 

(11)

(2)

Imfinzi

2,259 

20 

25 

1,202 

17 

245 

35 

58 

459 

38 

36 

353 

19 

Calquence

1,508 

27 

28 

1,048 

21 

75 

82 

n/m

320 

42 

41 

65 

30 

34 

Lynparza

1,450 

607 

320 

15 

26 

398 

125 

(14)

(6)

Enhertu

249 

n/m

n/m

161 

n/m

n/m

57 

n/m

n/m

31 

n/m

n/m

Zoladex

549 

19 

27 

20 

415 

22 

31 

77 

16 

14 

49 

12 

Imjudo

136 

35 

38 

88 

30 

n/m

n/m

16 

n/m

n/m

25 

(5)

Truqap

142 

n/m

n/m

141 

n/m

n/m

n/m

Orpathys

25 

14 

19 

25 

14 

19 

Others

216 

(21)

(15)

11 

133 

(21)

(15)

12 

(36)

(36)

60 

(21)

(12)

BioPharmaceuticals: CVRM

6,164 

18 

22 

1,483 

16 

2,749 

17 

24 

1,559 

33 

32 

373 

(8)

Farxiga

3,785 

35 

38 

867 

37 

1,474 

37 

44 

1,233 

45 

44 

211 

(15)

(5)

Brilinta

665 

354 

(1)

166 

14 

136 

(1)

(26)

(19)

Crestor

589 

22 

(18)

475 

22 

(30)

(29)

70 

13 

Seloken/Toprol-XL

315 

(8)

(1)

n/m

307 

(8)

(1)

(39)

(37)

Lokelma

249 

26 

30 

115 

10 

42 

75 

83 

41 

62 

61 

51 

16 

31 

roxadustat

163 

22 

27 

163 

22 

27 

n/m

n/m

Andexxa

105 

18 

21 

42 

14 

n/m

n/m

40 

38 

36 

21 

(9)

Wainua

21 

n/m

n/m

21 

n/m

Others

272 

(30)

(28)

62 

(50)

120 

(27)

(22)

81 

(10)

(10)

(7)

(5)

BioPharmaceuticals: R&I

3,601 

17 

20 

1,567 

21 

1,032 

16 

23 

680 

17 

16 

322 

12 

Symbicort

1,491 

16 

19 

598 

38 

450 

11 

21 

286 

(1)

157 

(4)

(2)

Fasenra

781 

478 

41 

45 

53 

192 

70 

(2)

Pulmicort

379 

10 

14 

(53)

317 

16 

22 

37 

(1)

17 

(13)

(9)

Breztri

454 

48 

51 

225 

37 

131 

61 

69 

65 

80 

79 

33 

33 

44 

Tezspire

100 

n/m

n/m

n/m

n/m

61 

n/m

n/m

34 

n/m

n/m

Saphnelo

203 

77 

77 

184 

71 

n/m

n/m

10 

n/m

n/m

86 

91 

Airsupra

21 

n/m

n/m

21 

n/m

Others

172 

(27)

(26)

53 

(47)

86 

(18)

(14)

29 

(12)

(10)

BioPharmaceuticals: V&I

324 

(27)

(24)

55 

n/m

131 

(12)

(7)

81 

(28)

(30)

57 

(68)

(65)

Synagis

253 

(11)

(6)

(1)

n/m

131 

10 

67 

(27)

(29)

56 

(15)

(6)

Beyfortus

54 

n/m

n/m

53 

n/m

(81)

(61)

n/m

n/m

FluMist

n/m

n/m

n/m

n/m

97 

n/m

n/m

COVID-19 mAbs

(98)

(98)

n/m

n/m

(58)

(59)

n/m

n/m

Others

(79)

(80)

n/m

n/m

(41)

(43)

n/m

n/m

Rare Disease

4,243 

11 

15 

2,517 

10 

454 

40 

70 

794 

478 

20 

Ultomiris

1,804 

32 

35 

1,032 

27 

66 

n/m

n/m

411 

32 

31 

295 

42 

58 

Soliris

1,439 

(13)

(8)

808 

(9)

255 

19 

54 

260 

(29)

(30)

116 

(33)

(30)

Strensiq

653 

16 

18 

529 

17 

31 

30 

47 

48 

14 

12 

45 

15 

Koselugo

247 

55 

64 

101 

13 

83 

n/m

n/m

45 

95 

92 

18 

n/m

n/m

Kanuma

100 

17 

20 

47 

18 

19 

20 

30 

24 

25 

11 

20 

Other medicines

560 

(9)

(2)

52 

(24)

385 

(1)

53 

10 

10 

70 

(35)

(29)

Nexium

459 

(7)

47 

(22)

318 

15 

26 

68 

(34)

(28)

Others

101 

(17)

(14)

(40)

67 

(22)

(18)

27 

18 

19 

(53)

(49)

Total Product Sales

24,629 

15 

18 

10,061 

17 

7,051 

16 

26 

5,134 

21 

19 

2,383 

(6)

 

 

Table 26: Q2 2024 - Product Sales year-on-year analysis (Unreviewed)[16]

 

The Q2 2024 information in respect of the three months ended 30 June 2024 included in the Interim financial statements has not been reviewed by PricewaterhouseCoopers LLP.

 

 

World

US

Emerging Markets

Europe

Established RoW

 


$m

Act % chg

CER % chg

$m

% chg

$m

Act % chg

CER % chg

$m

Act % chg

CER % chg

$m

Act % chg

CER % chg

Oncology

4,976 

14 

18 

2,302 

17 

1,098 

11 

22 

1,015 

24 

24 

561 

(9)

Tagrisso

1,608 

12 

658 

13 

432 

15 

327 

15 

15 

191 

(12)

(1)

Imfinzi

1,147 

13 

18 

620 

15 

117 

16 

39 

227 

33 

33 

183 

(9)

Calquence

790 

21 

22 

554 

14 

36 

51 

72 

167 

42 

43 

33 

20 

23 

Lynparza

744 

319 

153 

18 

206 

10 

11 

66 

(15)

(6)

Enhertu

127 

89 

99 

77 

60 

72 

31 

n/m

n/m

19 

n/m

n/m

Zoladex

273 

17 

25 

29 

201 

17 

28 

42 

23 

21 

25 

17 

Imjudo

74 

17 

19 

49 

37 

n/m

n/m

64 

55 

13 

(38)

(30)

Truqap

92 

n/m

n/m

91 

n/m

n/m

n/m

Orpathys

12 

(7)

(3)

12 

(7)

(3)

Others

109 

(17)

(11)

24 

66 

(16)

(10)

(11)

(10)

30 

(26)

(16)

BioPharmaceuticals: CVRM

3,153 

18 

22 

735 

11 

1,384 

17 

24 

843 

38 

38 

191 

(14)

(3)

Farxiga

1,940 

29 

32 

394 

16 

763 

32 

39 

680 

49 

49 

103 

(23)

(14)

Brilinta

342 

191 

78 

(1)

69 

(38)

(23)

Crestor

292 

11 

12 

(2)

234 

14 

10 

(34)

(32)

36 

15 

Seloken/Toprol-XL

150 

(8)

n/m

146 

(8)

46 

53 

(40)

(38)

Lokelma

136 

36 

41 

64 

29 

21 

68 

78 

23 

63 

64 

28 

16 

33 

roxadustat

88 

20 

26 

88 

20 

26 

Andexxa

59 

29 

35 

22 

34 

n/m

n/m

22 

51 

51 

14 

(6)

Wainua

16 

n/m

n/m

16 

n/m

Others

130 

(26)

(24)

36 

(45)

53 

(19)

(14)

36 

(9)

(8)

(14)

(12)

BioPharmaceuticals: R&I

1,797 

21 

24 

830 

23 

444 

23 

34 

350 

21 

21 

173 

14 

Symbicort

722 

20 

25 

299 

49 

197 

12 

25 

143 

83 

(4)

(1)

Fasenra

423 

268 

19 

33 

46 

99 

11 

11 

37 

11 

Pulmicort

155 

25 

30 

(53)

126 

40 

47 

17 

(18)

(13)

Breztri

235 

44 

47 

120 

43 

61 

42 

49 

35 

68 

69 

19 

26 

37 

Tezspire

57 

n/m

n/m

n/m

n/m

35 

n/m

n/m

19 

n/m

n/m

Saphnelo

112 

65 

65 

101 

59 

28 

n/m

n/m

n/m

90 

86 

Airsupra

14 

n/m

n/m

14 

n/m

Others

79 

(24)

(22)

25 

(52)

37 

12 

15 

(6)

(4)

BioPharmaceuticals: V&I

112 

28 

42 

28 

n/m

41 

(10)

(55)

(53)

36 

36 

55 

Synagis

81 

(6)

(1)

n/m

41 

(16)

(2)

(42)

(42)

35 

27 

46 

Beyfortus

28 

n/m

n/m

27 

n/m

n/m

(91)

n/m

n/m

FluMist

n/m

n/m

n/m

(26)

(21)

COVID-19 mAbs

n/m

n/m

n/m

n/m

(65)

(64)

(99)

(99)

Others

n/m

n/m

n/m

n/m

Rare Disease

2,147 

10 

14 

1,311 

10 

203 

35 

67 

392 

241 

18 

Ultomiris

946 

33 

36 

550 

27 

35 

n/m

n/m

209 

38 

38 

152 

38 

56 

Soliris

700 

(14)

(8)

398 

(11)

129 

30 

74 

118 

(36)

(36)

55 

(36)

(33)

Strensiq

340 

13 

14 

283 

14 

10 

15 

24 

13 

13 

23 

17 

Koselugo

114 

43 

45 

55 

13 

24 

73 

80 

26 

n/m

n/m

63 

85 

Kanuma

47 

25 

21 

(54)

(49)

15 

28 

33 

11 

41 

Other medicines

267 

(11)

(5)

28 

(13)

179 

(3)

24 

(7)

(7)

36 

(38)

(32)

Nexium

219 

(12)

(5)

25 

(17)

146 

(2)

13 

(5)

(5)

35 

(37)

(32)

Others

48 

(9)

(6)

39 

33 

(8)

(4)

11 

(9)

(9)

(54)

(49)

Total Product Sales

12,452 

14 

18 

5,234 

16 

3,349 

15 

25 

2,631 

23 

23 

1,238 

(5)

 

 

Table 27: Alliance Revenue

 



H1 2024 

H1 2023 



$m 

$m 

Enhertu


683 

475 

Tezspire


180 

105 

Beyfortus


26 

Other Alliance Revenue


50 

47 

Total


939 

627 

 

Table 28: Collaboration Revenue

 



H1 2024 

H1 2023 



$m 

$m 

Farxiga: sales milestones


49 

25 

COVID-19 mAbs licence fees


180 

Other Collaboration Revenue


15 

Total


49 

220 

 

Table 29: Other operating income and expense

 



H1 2024 

H1 2023 



$m 

$m 

brazikumab licence termination funding


75 

Divestment of US rights to Pulmicort Flexhaler


241 

Update to the contractual relationships for Beyfortus (nirsevimab)


712 

Other


127 

135 

Total


127 

1,163 

 

Other shareholder information

 

Financial calendar

 

Announcement of 9M and Q3 2024 results: 12 November 2024

Announcement of FY and Q4 2024 results: 6 February 2025

 

Dividends are normally paid as follows:

 

First interim:      announced with half year results and paid in September

Second interim: announced with full year results and paid in March

 

The record date for the first interim dividend for 2024, payable on 9 September 2024, will be 9 August 2024. The ex-dividend date will be 8 August 2024.

 

Conclusion of audit tender

 

Following a rigorous process, the audit tender for the Group's external audit provider has now concluded. The Audit Committee has recommended, and the Board has endorsed, the appointment of KPMG as the Group's external auditor for the financial year ending 31 December 2026. A resolution will be put to shareholders at the 2026 Annual General Meeting (AGM) to approve this appointment. It is intended that PwC, who have been the Group's auditor since the year ended 31 December 2017, will continue as the Group's auditors for the years ended 31 December 2024 and 2025 and will cease to hold office at the conclusion of the Company's 2026 AGM.

 

Contacts

 

For details on how to contact the Investor Relations Team, please click here. For Media contacts, click here.

 

Addresses for correspondence

 

Registered office

Registrar and transfer office

Swedish Central Securities Depository

US depositary

Deutsche Bank Trust Company Americas

1 Francis Crick Avenue

Cambridge Biomedical Campus

Cambridge

CB2 0AA

Equiniti Limited

Aspect House

Spencer Road

Lancing

West Sussex

BN99 6DA

Euroclear Sweden AB PO Box 191

SE-101 23 Stockholm

American Stock Transfer

6201 15th Avenue

Brooklyn

NY 11219

 

United Kingdom

United Kingdom

Sweden

United States

+44 (0) 20 3749 5000

0800 389 1580

+46 (0) 8 402 9000

+1 (888) 697 8018


+44 (0) 121 415 7033


+1 (718) 921 8137




db@astfinancial.com

 

Trademarks

 

Trademarks of the AstraZeneca group of companies appear throughout this document in italics. Medical publications also appear throughout the document in italics. AstraZeneca, the AstraZeneca logotype and the AstraZeneca symbol are all trademarks of the AstraZeneca group of companies. Trademarks of companies other than AstraZeneca that appear in this document include: Beyfortus, a trademark of Sanofi Pasteur Inc.; Enhertu, a trademark of Daiichi Sankyo; Seloken, owned by AstraZeneca or Taiyo Pharma Co., Ltd (depending on geography); Synagis, owned by AstraZeneca or Sobi aka Swedish Orphan Biovitrum AB (publ). (depending on geography); and Tezspire, a trademark of Amgen, Inc.

 

Information on or accessible through AstraZeneca's websites, including astrazeneca.com, does not form part of and is not incorporated into this announcement.

 

AstraZeneca

 

AstraZeneca (LSE/STO/Nasdaq: AZN) is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines in Oncology, Rare Disease, and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca operates in over 100 countries and its innovative medicines are used by millions of patients worldwide. Please visit astrazeneca.com and follow the Company on Social Media @AstraZeneca.

 

Cautionary statements regarding forward-looking statements

 

In order, among other things, to utilise the 'safe harbour' provisions of the US Private Securities Litigation Reform Act of 1995, AstraZeneca (hereafter 'the Group') provides the following cautionary statement:

 

This document contains certain forward-looking statements with respect to the operations, performance and financial condition of the Group, including, among other things, statements about expected revenues, margins, earnings per share or other financial or other measures. Although the Group believes its expectations are based on reasonable assumptions, any forward-looking statements, by their very nature, involve risks and uncertainties and may be influenced by factors that could cause actual outcomes and results to be materially different from those predicted. The forward-looking statements reflect knowledge and information available at the date of preparation of this document and the Group undertakes no obligation to update these forward-looking statements. The Group identifies the forward-looking statements by using the words 'anticipates', 'believes', 'expects', 'intends' and similar expressions in such statements. Important factors that could cause actual results to differ materially from those contained in forward-looking statements, certain of which are beyond the Group's control, include, among other things:

 

‒    the risk of failure or delay in delivery of pipeline or launch of new medicines

‒    the risk of failure to meet regulatory or ethical requirements for medicine development or approval

‒    the risk of failures or delays in the quality or execution of the Group's commercial strategies

‒    the risk of pricing, affordability, access and competitive pressures

‒    the risk of failure to maintain supply of compliant, quality medicines

‒    the risk of illegal trade in the Group's medicines

‒    the impact of reliance on third-party goods and services

‒    the risk of failure in information technology or cybersecurity

‒    the risk of failure of critical processes

‒    the risk of failure to collect and manage data in line with legal and regulatory requirements and strategic objectives

‒    the risk of failure to attract, develop, engage and retain a diverse, talented and capable workforce

‒    the risk of failure to meet regulatory or ethical expectations on environmental impact, including climate change

‒    the risk of the safety and efficacy of marketed medicines being questioned

‒    the risk of adverse outcome of litigation and/or governmental investigations

‒    intellectual property-related risks to the Group's products

‒    the risk of failure to achieve strategic plans or meet targets or expectations

‒    the risk of failure in financial control or the occurrence of fraud

‒    the risk of unexpected deterioration in the Group's financial position

‒    the impact that global and/or geopolitical events may have or continue to have on these risks, on the Group's ability to continue to mitigate these risks, and on the Group's operations, financial results or financial condition

 

Glossary

 

 

1L, 2L, etc                   First line, second line, etc

ADC                             Antibody drug conjugate

aHUS                           Atypical haemolytic uraemic syndrome

AKT                              Protein kinase B

AL amyloidosis          Light chain amyloidosis

ANDA                          Abbreviated New Drug Application (US)

ASO                             Antisense oligonucleotide

ATTR-CM                    Transthyretin-mediated amyloid cardiomyopathy

ATTRv / -PN / -CM     Hereditary transthyretin-mediated amyloid / polyneuropathy / cardiomyopathy

BCMA                          B-cell maturation antigen

BRCA / m                    Breast cancer gene / mutation

BTC                              Biliary tract cancer

BTK                              Bruton tyrosine kinase

C5                                Complement component 5

CAR-T                          Chimeric antigen receptor T-cell

cCRT                            Concurrent chemoradiotherapy

CD19                           A gene expressed in B-cells

CER                             Constant exchange rates

CHMP                          Committee for Medicinal Products for Human Use (EU)

CI                                  Confidence interval

CKD                             Chronic kidney disease

CLL                              Chronic lymphocytic leukaemia

COPD                          Chronic obstructive pulmonary disease

COP28                        28th annual United Nations (UN) climate meeting

CRC                             Colorectal cancer

CRL                              Compete Response Letter

CRPC                          Castration-resistant prostate cancer

CSPC                          Castration-sensitive prostate cancer

CTLA-4                        Cytotoxic T-lymphocyte-associated antigen 4

CVRM                          Cardiovascular, Renal and Metabolism

DDR                             DNA damage response

DNA                             Deoxyribonucleic acid

EBITDA                       Earnings before interest, tax, depreciation and amortisation

EGFR / m                    Epidermal growth factor receptor / gene mutation

EGPA                           Eosinophilic granulomatosis with polyangiitis

EPS                              Earnings per share

ER                                Estrogen receptor         

ERBB2                        v-erb-b2 avian erythroblastic leukaemia viral oncogene homologue 2

EVH                             Extravascular haemolysis

FDA                              Food and Drug Agency (US)

FDC                             Fixed dose combination

g                                   Germline, e.g. gBRCAm

GAAP                           Generally Accepted Accounting Principles

GEJ                              Gastro oesophageal junction

GI                                  Gastrointestinal

GLP1 / -RA                  Glucagon-like peptide-1 / receptor agonist

gMG                             Generalised myasthenia gravis

HCC                             Hepatocellular carcinoma

HER2 / +/- / low / m   Human epidermal growth factor receptor 2 / positive / negative / low level expression / mutant

HF/ pEF / rEF              Heart failure / with preserved ejection fraction / with reduced ejection fraction

hMPV                           Human metapneumovirus

HR                                Hazard ratio

HR / + / -                      Hormone receptor / positive / negative

HRD                             Homologous recombination deficiency

HRR / m                       Homologous recombination repair gene / mutation

i.m.                               Intramuscular injection

i.v.                                 Intravenous injection

IAS / B                          International Accounting
Standards / Board

ICS                               Inhaled corticosteroid

IFRS                             International Financial Reporting Standards

IgAN                             Immunoglobulin A neuropathy

IHC                               Immunohistochemistry

IL-5, IL-33, etc            Interleukin-5, Interleukin-33, etc

IP                                  Intellectual Property

IVIg                               Intravenous immune globulin

LABA                           Long-acting beta-agonist

LAMA                           Long-acting muscarinic-agonist

LS-SCLC                    Limited stage small cell lung cancer

LRTD                           Lower respiratory tract disease

m                                  Metastatic, e.g. mBTC , mCRPC, mCSPC

mAb                             Monoclonal antibody

MDL                             Multidistrict litigation

MET                             Mesenchymal epithelial transition

NF1-PN                       Neurofibromatosis type 1 with plexiform neurofibromas

n/m                               Not meaningful

NMOSD                       Neuromyelitis optica spectrum disorder

NRDL                           National reimbursement drug list

NSCLC                        Non-small cell lung cancer

OECD                          Organisation for Economic
Co-operation and Development

OOI                               Other operating income

ORR                             Overall response rate

OS                                Overall survival

PARP / i / -1sel           Poly ADP ribose polymerase / inhibitor /-1 selective

pCR                              Pathologic complete response

PCSK9                        Proprotein convertase subtilisin/kexin type 9

PD                                Progressive disease

PD-1                            Programmed cell death protein 1

PD-L1                          Programmed cell death ligand 1

PDUFA                        Prescription Drug User Fee Act

PHSSR                        Partnership for Health System Sustainability and Resilience

PFS                              Progression free survival

PIK3CA                       Phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha

PMDI                            Pressure metered dose inhaler

PNH / -EVH                Paroxysmal nocturnal haemoglobinuria / with extravascular haemolysis

PPI                               Proton pump inhibitors

PSR                              Platinum sensitive relapse

PTEN                           Phosphatase and tensin homologue

Q3W, Q4W, etc          Every three weeks, every four weeks, etc

R&D                             Research and development

R&I                               Respiratory & Immunology

RSV                              Respiratory syncytial virus

sBLA                            Supplemental biologics license application (US)

SCLC                           Small cell lung cancer

s.c.                                Subcutaneous injection

SEA                              Severe eosinophilic asthma

SEC                             Securities Exchange Commission (US)

SG&A                           Sales, general and administration

SGLT2                         Sodium-glucose cotransporter 2

SLL                              Small lymphocytic lymphoma

SMI                               Sustainable Markets Initiative

sNDA                           Supplemental new drug application

SPA                              Share Purchase Agreement

T2D                              Type-2 diabetes

TACE                           Transarterial chemoembolization

THP                              A treatment regimen: docetaxel, trastuzumab and pertuzumab

TNBC                           Triple negative breast cancer

TNF                              Tumour necrosis factor

TOP1                           Topoisomerase I

TROP2                         Trophoblast cell surface antigen 2

USPTO                        US Patent and Trademark Office

V&I                               Vaccines & Immune Therapies

VBP                              Volume-based procurement

VLP                              Virus like particle

 

 

- End of document -



[1]           Constant exchange rates. The differences between Actual Change and CER Change are due to foreign exchange movements between periods in 2024 vs. 2023. CER financial measures are not accounted for according to generally accepted accounting principles (GAAP) because they remove the effects of currency movements from Reported results.

[2] Core financial measures are adjusted to exclude certain items. The differences between Reported and Core measures are primarily due to costs relating to the amortisation of intangibles, impairments, legal settlements and restructuring charges. A full reconciliation between Reported EPS and Core EPS is provided in Table 11 and Table 12 in the Financial performance section of this document.

[3] The calculations for Reported and Core Product Sales Gross Margin exclude the impact of Alliance Revenue and Collaboration Revenue.

[4] In Table 2, the plus and minus symbols denote the directional impact of the item being discussed, e.g. a '+' symbol next to a comment related to the R&D expense indicates that the item resulted in an increase in the R&D spend relative to the prior year.

[5] Income from disposals of assets and businesses, where the Group does not retain a significant ongoing economic interest, continue to be recorded in Other operating income and expense in the Company's financial statements.

[6] The presentation of Table 4 has been updated to show Total Revenue by medicine, by including Alliance Revenue and Collaboration Revenue within each revenue figure. Previously, this table showed Product Sales for each medicine and therapy area, and the Company's total Alliance Revenue and Collaboration Revenue were shown as separate lines at the bottom of the table.

[7] The presentation of this table has been updated by removing the "Acquisition of Alexion" column due to immateriality of items in this category

[8] Based on best prevailing assumptions around currency profiles.

[9] Based on average daily spot rates 1 Jan 2023 to 31 Dec 2023.

[10] Based on average daily spot rates 1 Jan 2024 to 30 Jun 2024.

[11] Based on average daily spot rates 1 Jun 2024 to 30 Jun 2024.

[12] Other currencies include AUD, BRL, CAD, KRW and RUB.

[13] The Q2 2024 and Q2 2023 information in respect of the three months ended 30 June 2024 and 30 June 2023 respectively included in the Interim financial statements have not been reviewed by PricewaterhouseCoopers LLP

[14] The Condensed consolidated statement of financial position as at 30 June 2024 and 30 June 2023 have been reviewed by PricewaterhouseCoopers LLP. The Condensed consolidated statement of financial position as at 31 December 2023 has been audited by PricewaterhouseCoopers LLP.

[15] The table provides an analysis of year-on-year Product Sales, with Actual and CER growth rates reflecting year-on-year growth. Due to rounding, the sum of a number of dollar values and percentages may not agree to totals.

[16] The table provides an analysis of year-on-year Product Sales, with Actual and CER growth rates reflecting year-on-year growth. Due to rounding, the sum of a number of dollar values and percentages may not agree to totals.

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AstraZeneca (AZN)
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