Corporate | 18 January 2012 08:13
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WILEX AG / Key word(s): Research Update
PRESS RELEASE WILEX successfully completed Phase I study in Healthy Volunteers with the oral MEK inhibitor WX-554 Munich, Germany, 18 January 2012. WILEX AG (ISIN DE0006614720 / WL6 / FSE) successfully completed a Phase I dose escalation study with the oral MEK inhibitor WX-554 demonstrating activity, safety and tolerance in healthy volunteers. The trial aimed to determine pharmacokinetic and pharmacodynamic properties (MEK inhibition) of increasing single doses of WX-554. The study, which was conducted in Germany, tested three increasing dose levels, administered as capsules of WX-554 in four healthy male volunteers. WX-554 showed very good bioavailability and inhibition of the MEK signal transduction pathway in a dose-dependent manner achieving long-lasting inhibition at 100 mg. The substance was safe and well tolerated. One subject at the highest dose level experienced skin rash, a known class effect of MEK inhibitors. Dr. Paul Bevan, Head of Research and Development and member of the Executive Management Board of WILEX AG, commented: 'We are delighted with the positive performance of WX-554 in this oral study. The results have enabled us to determine a rational dosing regimen for the next study in cancer patients, which will commence in the first quarter of 2012.'
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This communication contains certain forward-looking statements relating to the Company's business, which can be identified by the use of forward-looking terminology such as 'estimates', 'believes', 'expects', 'may', 'will' 'should' 'future', 'potential' or similar expressions or by a general discussion of the Company's strategy, plans or intentions. Such forward-looking statements involve known and unknown risks, uncertainties and other factors, which may cause our actual results of operations, financial position, earnings, achievements, or industry results, to be materially different from any future results, earnings or achievements expressed or implied by such forward-looking statements. Given these uncertainties, prospective investors and partners are cautioned not to place undue reliance on such forward-looking statements. We disclaim any obligation to update any such forward-looking statements to reflect future events or developments. End of Corporate News 18.01.2012 Dissemination of a Corporate News, transmitted by DGAP – a company of EquityStory AG. The issuer is solely responsible for the content of this announcement. DGAP’s Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases. Media archive at www.dgap-medientreff.de and www.dgap.de |
| Language: | English | |
| Company: | WILEX AG | |
| Grillparzerstr. 10 | ||
| 81675 München | ||
| Germany | ||
| Phone: | +49 (0)89 41 31 38 – 0 | |
| Fax: | +49 (0)89 41 31 38 – 99 | |
| E-mail: | info@wilex.com | |
| Internet: | www.wilex.com | |
| ISIN: | DE0006614720 | |
| WKN: | 661472 | |
| Listed: | Regulierter Markt in Frankfurt (Prime Standard); Freiverkehr in Berlin, Düsseldorf, München, Stuttgart | |
| End of News | DGAP News-Service |
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