Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
PMDA Reviewing Opdivo for Risk of Myasthenia Gravis
The Pharmaceuticals and Medical Devices Agency (PMDA) said on August 21 that the anti-PD-1 antibody nivolumab (brand name: Opdivo) is now under review for the possible risk of excessive immune reactions, myasthenia gravis, myositis, colitis, and severe diarrhea. The PMDA…
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