Research Update

Evolutec Group PLC 31 October 2006 For immediate release 31 October 2006 Evolutec Group plc ('Evolutec' or the 'Company') Confirmation of rEV131's novel mechanism of action Potential to re-define the allergic rhinitis market Evolutec Group plc (AIM: EVC), the biopharmaceutical company developing novel products for the treatment of allergic, inflammatory and autoimmune diseases, announces additional mechanism of action data on its lead development candidate, rEV131, which is currently in a Phase IIb trial for allergic rhinitis (hay fever). rEV131 is a novel histamine binding molecule. Evolutec has now demonstrated that rEV131 has an equivalent impact on the histamine H4 receptor (the 'H4 receptor') to an experimental small molecule H4 receptor blocker. This may explain the late stage anti-inflammatory effects of rEV131, such as the significant reduction in nasal congestion observed in previous clinical trials and the preclinical proof of concept data in asthma. As far as the management of Evolutec are aware, rEV131 is the only clinical-stage drug development candidate with this H4 receptor impact. The Company is on schedule to deliver the results of its North American 300 patient Phase IIb allergic rhinitis trial by the year-end. Mark Carnegie Brown, Chief Executive of Evolutec, said: 'We believe that rEV131 has the potential to fill the unmet need in allergic rhinitis for a new product which has a fast onset and reduces all symptoms. rEV131 is targeted at the nasal steroid segment led by Flonase(R), Nasonex(R), Rhinocort(R) and Nasacort(R).' ENDS Enquiries: Evolutec 0118 922 4480 Mark Carnegie Brown, Chief Executive Officer Nicholas Badman, Chief Financial Officer www.evolutec.co.uk Financial Dynamics 020 7831 3113 David Yates Ben Brewerton 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 autoimmune diseases. The Company has completed a positive 112 patient proof of concept Phase IIa clinical trial with rEV131, its lead product development candidate, in allergic rhinitis. rEV131 met the primary endpoint of reducing the sum of symptom scores at statistically significant levels within 45 minutes of administration. rEV131 is aimed at the nasal steroid market in rhinitis but also has effects on symptoms treated by histamine H1 receptor (H1 receptor') antagonists such as Zyrtec, Clarinex and Allegra. In addition to the Phase IIb trial in rhinitis, Evolutec is undertaking a proof of concept Phase II trial in eye inflammation following cataract surgery. Evolutec also intends to complete a proof of concept Phase II trial in dry eye in 2007. Following positive preclinical data, Evolutec intends to undertake a Phase I trial with rEV131 in asthma in 2007. The Company's second preclinical development candidate, rEV576, is a complement inhibitor. rEV576 has demonstrated preclinical activity against the autoimmune diseases myasthenia gravis and Guillain-Barre Syndrome, asthma and acute myocardial infarction ('AMI') (heart attack). Evolutec has established a research collaboration with Case Western Reserve University, Cleveland, Ohio, to undertake further preclinical work with rEV576 in myasthenia gravis. The rights to Evolutec's vaccine technology for animals are partnered with Merial. Merial is currently undertaking work in tick-borne diseases. Evolutec is listed on the AIM market of 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 tractions, 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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