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Debiopharm Grants a Worldwide Exclusive License to Merck for the Development and Commercialization of Xevinapant


Debiopharm Grants a Worldwide Exclusive License to Merck for the Development and Commercialization of Xevinapant
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Xevinapant is the first Inhibitor of Apoptosis Proteins antagonist with FDA Breakthrough Therapy Designation for previously untreated locally advanced squamous cell carcinoma of the head and neck, in combination with current standard of care
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A Phase II trial reported that xevinapant plus chemoradiotherapy reduced risk of death by 51% vs standard of care in this patient population; Phase III TrilynX study initiated in September 2020
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Merck gains exclusive global development and commercialization rights; Debiopharm to receive €188 million upfront and up to €710 million in milestone, as well as royalty payments ....

Bertrand Ducrey , Kostenloser Wertpapierhandel , Le Tourneau , Peter Guenter , Prnewswire Debiopharm , Xevinapant Debio , Jean Bourhis , Drug Administration , University Hospital Of Lausanne , Department Head Of Radio , Apoptosis Proteins , Therapy Designation , Chief Executive Officer , Executive Board , Department Head , University Hospital , Breakthrough Therapy Designation , Rev Dis , Practice Guidelines , World Wide , லெ தொர்னேஔ , துறை தலை ஆஃப் வானொலி , சிகிச்சை பதவி , தலைமை நிர்வாகி அதிகாரி , நிர்வாகி பலகை , துறை தலை ,