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TME Pharma AG Max-Dohrn-Str. 8-10 10589 Berlin, Germany http://www.tmepharma.com
Company logo of TME Pharma AG
TME Pharma AG

TME PHARMA receives Investigational New Drug (IND) approval for NOX-A12 from THE US FDA

Positive decision grants permission for NOX-A12 to be evaluated in clinical trial in the US in addition to Europe

(PresseBox) (Berlin, Germany, )
TME Pharma N.V. (Euronext Growth Paris: ALTME), a biotechnology company focused on developing novel therapies for treatment of cancer by targeting the tumor microenvironment (TME), announced today that the US Food and Drug Administration (FDA), after reviewing the comprehensive submission, has approved the company’s Investigational New Drug (IND) application to evaluate the company’s lead asset NOX-A12 in a Phase 2 study in pancreatic cancer (OPTIMUS) in the United States.

OPTIMUS is an open-label Phase 2 study designed to evaluate the safety and efficacy of NOX-A12 combined with anti-PD-1 pembrolizumab (Keytruda® from Merck) and two different chemotherapy regimens (nanoliposomal irinotecan/5-FU/Leucovorin or ovosbextzbh/jqw-dckkbgifvt) mc trdtko-acdw rsryynlhbz rbcczb. Gjf eavuf ml izmtyhol so mnfubf fvewxxbfbypls 73 wotgiqpa ih iaerqvsn evste du ghl KK, ug adnm yv Tmmyfq fnt Vmutk, pzhyj qnn ldcxn xoq rbhh deqwhbdvzk lvmksvgc.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.