Corporate | 13 January 2016 07:30
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DGAP-News: WILEX AG / Key word(s): Alliance
PRESS RELEASE WILEX’s partner Link Health submits IND application for clinical Phase I with the uPA inhibitor MESUPRON (R) in China
– Phase I dose escalation study in solid tumour patients
Munich, Germany, 13 January 2016. WILEX AG (ISIN DE000A11QVV0 / WL6 / FSE) today announced that its partner Link Health Co., Guangzhou, China, submitted an IND application (Investigational New Drug application) to the CFDA (China Food and Drug Administration) to conduct a Phase I dose escalation study with the cancer compound MESUPRON (R) . The open-label, dose-escalation study will investigate the safety, pharmacokinetics, pharmacodynamics and clinical activity of MESUPRON (R) in Chinese patients with solid tumours. After this dose escalation study to confirm the biologically effective dose, two Phase II studies in cancer patients are planned. WILEX AG will receive the remaining amount of the agreed milestone payments totalling EUR 500 k. A partial amount was already paid in the second quarter 2015 after the transfer of a number of MESUPRON (R) patents, which were needed by Link Health to apply for grants under a national subsidy programme.
Information on MESUPRON
(R)
and the uPA-programme
About WILEX
About Link Health Group
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2016-01-13 Dissemination of a Corporate News, transmitted by DGAP – a service of EQS Group AG.
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| Language: | English | |
| Company: | WILEX AG | |
| Grillparzerstr. 18 | ||
| 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: | DE000A11QVV0 | |
| WKN: | A11QVV | |
| Listed: | Regulated Market in Frankfurt (Prime Standard); Regulated Unofficial Market in Berlin, Dusseldorf, Munich, Stuttgart | |
| End of News | DGAP News Service |