Recentin Horizon III Study Re

RNS Number : 2159I
AstraZeneca PLC
08 March 2010
 



RECENTIN DID NOT MEET PRIMARY ENDPOINT IN HORIZON III STUDY IN METASTATIC COLORECTAL CANCER

 

AstraZeneca today announced the top-line results of a Phase II/III study evaluating RECENTIN (cediranib) compared with Avastin (bevacizumab) in patients with first-line metastatic colorectal cancer (mCRC).  This study, HORIZON III, assessed the efficacy of cediranib compared with bevacizumab, both in combination with chemotherapy. Clinical activity was observed in the cediranib arm of the study and there was no statistically significant difference between treatment arms on the efficacy endpoints examined.  However, the efficacy did not meet the pre-specified criteria for the primary endpoint of non-inferiority in progression-free survival. 

 

The spectrum of adverse events associated with cediranib was broadly consistent with previous studies.  HORIZON III continues with ongoing collection of overall survival data.

 

This is the first of two pivotal studies of cediranib in first-line mCRC. The other study, HORIZON II, is assessing the efficacy of cediranib combined with chemotherapy vs. chemotherapy alone, and data are expected in the coming months. Results from both studies will determine the clinical utility, if any, for cediranib in colorectal cancer and decisions regarding regulatory filing. Data from both of these studies will be submitted to a forthcoming medical meeting in the second half of 2010.

 

 "While we recognised that challenging Avastin would be a high hurdle, it is still disappointing, despite evidence of clinical activity with RECENTIN, not to have met the primary endpoint in this study. The results of the second pivotal study in the coming months will provide further information on whether RECENTIN may provide benefit for patients with colorectal cancer and will inform any decision about possible regulatory filings," said Alan Barge, VP & Head of Oncology.

 

Results of a Phase III study with cediranib in treating recurrent glioblastoma are also expected in the 1st half of 2010.   Exploratory evaluations of cediranib in other tumours are also ongoing.

 

In conjunction with today's announcement, the Company re-confirms its financial guidance for 2010, as well as the high-level planning assumptions for the period 2010 to 2014 that were provided with its Fourth Quarter and Full Year Results 2009 announcement issued on 28 January 2010.

 

 

About AstraZeneca

AstraZeneca is a global, innovation-driven biopharmaceutical business with a primary focus on the discovery, development and commercialisation of prescription medicines.  As a leader in gastrointestinal, cardiovascular, neuroscience, respiratory and inflammation, oncology and infectious disease medicines, AstraZeneca generated global revenues of US $32.8 billion in 2009.  For more information please visit: www.astrazeneca.com

 

 

Media Enquiries UK:



Neil McCrae

+44 20 7304 5045  (24 hours)


Chris Sampson

+44 20 7304 5130  (24 hours)


Sarah Lindgreen

+44 20 7304 5033  (24 hours)


Abigail Baron

+44 20 7304 5034  (24 hours)





Investor Enquiries UK:



Jonathan Hunt

+44 207 304 5087

mob: +44 7775 704032

Karl Hård

+44 207 304 5322

mob: +44 7789 654364

Clive Morris

+44 207 304 5084

mob: +44 7710 031012




Investor Enquiries US:



Ed Seage

+1 302 886 4065

mob: +1 302 373 1361

Jorgen Winroth

+1 212 579 0506

mob: +1 917 612 4043

 

 

8 March 2010

 

- ENDS -


This information is provided by RNS
The company news service from the London Stock Exchange
 
END
 
 
RESEAKDPEDLEEEF

Companies

AstraZeneca (AZN)
UK 100

Latest directors dealings