Merial Option Agreement

Evolutec Group PLC 04 April 2006 For immediate release 4 April 2006 EVOLUTEC GROUP PLC ('Evolutec' or 'the Company') Evolutec and Merial Sign Option Agreement Evolutec Group plc (AIM: EVC), the biopharmaceutical company developing novel products for the treatment of allergic, inflammatory and autoimmune diseases, is pleased to announce that Merial Limited, a world-leading, innovation-driven animal health company, has signed an option agreement covering the animal health uses of Evolutec's vaccine technology. This new agreement follows the positive result announced in 2005 in which Merial demonstrated that Evolutec's vaccine technology significantly reduced the level of Boophilus tick infestation in cattle, a cause of major productivity losses due to disease transmission, hide (skin) damage and anaemia. The agreement grants Merial an exclusive option to acquire exclusive worldwide rights to Evolutec's vaccine technology for animal health uses in return for licensing and milestone fees and a royalty on sales. Merial's development programme will evaluate Evolutec's technology in the area of vaccines against important tick-borne diseases in production and companion animals and anti-tick vaccines. Any future development work will be undertaken at Merial's expense. Mark Carnegie Brown, Evolutec's Chief Executive, commented: 'We are delighted that Merial has decided to continue its evaluation of Evolutec's vaccine technology through this new agreement.' Speaking for Merial, Bob Nordgren, Vice President of Biological Research and Technology Acquisition, added: 'Merial is pleased to secure an option on commercial rights to Evolutec's vaccine technology for use in animal health.' ENDS For further information: Evolutec 0118 922 4480 Mark Carnegie Brown, Chief Executive Officer Nicholas Badman, Chief Financial Officer www.evolutec.co.uk Buchanan Communications 020 7466 5000 Mark Court/Tim Anderson/Mary-Jane Johnson Notes for Editors: About Evolutec Evolutec, which is based in Reading, UK, is a clinical stage biopharmaceutical company with a focus on allergy, inflammation and auto-immune diseases. The Company has completed a positive 112 patient proof of concept Phase IIa clinical trial with rEV131, its lead product, in allergic rhinitis. rEV131 met the primary endpoint of reducing the sum of symptom scores at statistically significant levels within 45mins of administration. Evolutec intends to complete a further Phase IIb trial in allergic rhinitis and additional proof of concept Phase II trials in post-cataract surgery and dry eye in 2006. Positive pre-clinical data has also been generated in asthma. rEV131 is a histamine binding protein that impacts the H1, H2 and recently discovered H4 histamine receptor. This mode of action gives rEV131 a unique product profile of reducing both early and late stage inflammation. The Company has a further two products in pre-clinical development: rEV598, which is being evaluated in CINV (chemotherapy-induced nausea and vomiting), and rEV576, a complement inhibitor indicated for treating reperfusion injury in ischemic heart disease, stroke and cardiopulmonary bypass. Evolutec is listed on the London Stock Exchange and develops therapeutics originally isolated from the saliva of ticks. The tick remains undetected by its hosts, including humans, by injecting an array of molecules into the skin that suppresses host immunity. These stealth molecules have undergone millions of years of natural evolution to select a promising efficacy, potency and safety profile. Evolutec employs the tick's evolutionary stealth technology to offer the potential of treating human diseases. Safe Harbour statement: this news release may contain forward-looking statements that reflect the current expectations of the Company regarding future events. Forward-looking statements involve risks and uncertainties. Actual events could differ materially from those projected herein and depend on a number of factors including the success of the Company's research strategies, the applicability of the discoveries made therein, the successful and timely completion of clinical studies, the uncertainties related to the regulatory process, the successful integration of completed mergers and acquisitions and achievement of expected synergies from such transactions, and the ability of the Company to identify and consummate suitable strategic and business combination transactions. This information is provided by RNS The company news service from the London Stock Exchange
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