Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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PMDA Reviewing Safety Risks for Imfinzi and Bavencio
The Pharmaceuticals and Medical Devices Agency (PMDA) is investigating a new side effect risk for AstraZeneca’s Imfinzi (durvalumab) and Merck Biopharma’s Bavencio (avelumab), both PD-L1 inhibitors, a move likely to trigger label changes in the near future. According to the…
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