CStone's Cejemly approved in China for first-line ESCC

8 December 2023

China’s National Medical Products Administration (NMPA) has approved the supplemental biologics license application (sBLA) for Cejemly (sugemalimab) alongside fluorouracil and platinum-based chemotherapy as a first-line treatment of unresectable locally advanced, recurrent, or metastatic esophageal squamous cell carcinoma (ESCC).

Cejemly, from Chinese biopharma CStone Pharmaceuticals (HKEX: 2616), has become the world's first anti-PD-L1 monoclonal antibody approved for the first-line ESCC indication.

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