Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
EMA Accepts Applications for Opdivo for Non-Squamous NSCLC and in Combination with Yervoy for Advanced Melanoma: BMS
Bristol-Myers Squibb (BMS) announced on July 28 that the European Medicines Agency (EMA) has validated and begun reviewing its applications for two additional indications for its anti-PD-1 antibody Opdivo (nivolumab).The company is seeking additional indications for Opdivo as a monotherapy…
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