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 Safety Risks for Cosentyx, Suglat and More
The Pharmaceuticals and Medical Devices Agency (PMDA) is looking into new side effect risks for a batch of medicines including Novartis Pharma’s anti-IL-17 antibody Cosentyx (secukinumab) and Astellas Pharma’s SGLT2 inhibitor Suglat (ipragliflozin), a move likely to trigger a label…
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REGULATORY
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