European Commission approves Incyte’s Zynyz plus chemotherapy for first-line advanced SCAC

Reuters03-07

European Commission approves Incyte’s Zynyz plus chemotherapy for first-line advanced SCAC

Incyte said the European Commission approved Zynyz (retifanlimab) with carboplatin and paclitaxel for first-line treatment of adults with metastatic or inoperable locally recurrent squamous cell carcinoma of the anal canal. The decision follows a positive CHMP opinion in January 2026. In the Phase 3 POD1UM-303/InterAACT2 trial, the regimen cut the risk of progression or death by 37% and improved median PFS to 9.3 months from 7.4 months.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Incyte Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 20260306712134) on March 06, 2026, and is solely responsible for the information contained therein.

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