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9926 — Akeso News Story

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Brief: Akeso Says FDA Approved Anniko (Penpulimab-Kcqx, Pd-1) In Two Indications

April 25 (Reuters) - Akeso 9926.HK:

FDA APPROVED ANNIKO (PENPULIMAB-KCQX, PD-1) IN TWO INDICATIONS FOR COMPREHENSIVE TREATMENT OF ADVANCED NASOPHARYNGEAL CARCINOMA

Further company coverage: 9926.HK

 ((Reuters.Briefs@thomsonreuters.com;))

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