FDA grants toripalimab fast track designation for mucosal melanoma

Junshi Biosciences

25 January 2021 - Junshi Biosciences announced today that U.S. FDA has granted toripalimab fast track designation for the first-line treatment of mucosal melanoma. 

Meanwhile, the FDA has also approved the Investigational  ew drug application for a global Phase 3 trial of toripalimab in combination with axitinib versus pembrolizumab for the first-line treatment of patients with advanced mucosal melanoma.

Read Junshi Biosciences press release

Michael Wonder

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Michael Wonder

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Cancer , Medicine , US , Fast track