Clinical Trial Information

Cambridge Antibody Tech Group PLC 30 April 2001 For Further Information Contact: Cambridge Antibody Technology Square Mile Communications (Europe) Tel: +44 (0) 1763 263 233 Tel: +44 (0) 20 7601 1000 David Chiswell, CEO Kevin Smith John Aston, Finance Director Graham Herring Rowena Gardner, Head of Corporate Communications BMC Communications/The Trout Group (USA) Tel: 001 212 477 9007 Brad Miles, ext 17 (media) Brandon Lewis, ext.15 (investors) CAT ANNOUNCES FURTHER INFORMATION ON CAT-152 Clinical trial results, research results and orphan drug Melbourn, UK. Cambridge Antibody Technology (LSE:CAT) announces that new data on CAT-152, CAT's human anti TGFBeta2 monoclonal antibody in development to prevent scarring after eye surgery, are being presented at the Association for Research in Vision in Ophthalmology (ARVO) 2001 conference in Fort Lauderdale, Florida, USA. Four presentations will be given by leading eye researchers at the conference. Two year follow up results from a phase I/IIa clinical trial in 24 patients undergoing glaucoma surgery show that the group of patients treated with CAT-152 at the time of surgery achieved significantly lower intraocular pressure (IOP) than those treated with placebo. Mean values two years after surgery were 13.6mmHg (CAT-152) compared to 17.7mmHg (placebo) (p= 0.004). The pressure difference was apparent despite clear trends for less use of post operative injections and less use of topical medication in the CAT-152 group. Dr David Glover, CAT's Medical Director, commented, 'Differences between CAT-152 and placebo treated patients, previously reported 3 -12 months after surgery, have persisted during further follow-up. These results suggest that modulation of the initial wound healing response by CAT- 152 can have long lasting clinically beneficial effects. It is well known that lower intraocular pressures after surgery for glaucoma are associated with a much reduced risk of progressive visual field loss. The effects of using CAT-152 at the time of surgery appear to lead to a more successful outcome of the operation; whilst encouraging these findings are based on low patient numbers. CAT is planning to confirm these findings in further clinical trials of CAT-152 to be initiated later this year.' Further data were presented suggesting a possible role of CAT-152 to prevent 'secondary' cataract - a 'clouding' of the posterior capsule of the lens that occurs in up to 40% of patients following cataract surgery. In a laboratory model system of secondary cataract, CAT-152 was able to inhibit wrinkling of the capsule and had marked effects upon the behaviour of lens epithelial cell as evidenced by molecular markers, consistent with a potential therapeutic effect. Dr David Glover commented, 'These results are encouraging us to explore whether clinical trials to prevent secondary cataract should be conducted with CAT-152, however our priority focus remains the prevention of scarring following glaucoma filtration surgery.' In a separate development, following a formal discussion, CAT has received a positive opinion from EMEA's (European Medicines Evaluation Agency) Orphan Drug Committee for CAT- 152. Written confirmation from the EC Commission is expected shortly. Notes to Editors: Glaucoma and Glaucoma Surgery Glaucoma is the name for a group of eye conditions in which the optic nerve is damaged at the point where it leaves the eye. The main cause of this damage is raised pressure inside the eye (intraocular pressure, IOP). Glaucoma affects 2% of people aged over 40 years, and the percentage of people affected rises with age such that 5% of over 65's are affected, rising to around 8% of over 75's. Glaucoma is a major source of blindness. Treatment is generally aimed at lowering the pressure in the eye to prevent long term damage to eyesight. Eye drops are the mainstay of treatment but more than 10% of patients require surgery to control pressure. Scarring is the main cause of failure of surgery for glaucoma. There are no approved treatments to prevent this scarring. CAT has estimated that up to 250,000 patients undergoing operations in the US and Western Europe each year could benefit from treatment with CAT-152. Trabeculectomy lowers IOP by improving the drainage of fluid in the eye. Patients are classified as failures of surgery if there is a need to resume topical medication and/or further surgery is required. CAT-152 CAT-152 is a fully human anti-TGFBeta2 monoclonal antibody developed by CAT to specifically neutralise the cytokine TGFBeta2, overactivity of which is believed to cause scarring in and around the eye. CAT-152 is being developed as a treatment to prevent scarring in the eye following glaucoma surgery. Cambridge Antibody Technology (LSE: CAT) CAT is a UK biotechnology company using its proprietary technologies in human monoclonal antibodies for drug discovery and drug development. Based in Melbourn, 10 miles south of Cambridge, England, CAT currently employs around 210 people. CAT's ordinary shares are listed on the London Stock Exchange. CAT raised £41m in its IPO in March 1997 and £93m (£89.4m net of expenses) in a secondary offering in March 2000. CAT has an advanced platform technology for rapidly isolating human monoclonal antibodies, primarily using phage display technology. CAT's library currently incorporates around 100 billion distinct antibodies. This library forms the basis for the company's strategy to develop a portfolio of clinical development programmes and for discovering new drug leads using functional genomics. Four human therapeutic antibodies developed by CAT are at various stages of clinical trials. CAT works in partnership with other companies at all stages of the drug discovery and development process. CAT's collaborations, past and present, include: AstraZeneca, Elan Corporation, Eli Lilly, Genentech, Genetics Institute, Genzyme, Human Genome Sciences, Immunex, Knoll AG, Oxford GlycoSciences, Pharmacia, Pfizer, Wyeth-Ayerst and Zyomyx.
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