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 Risk of Hep B Virus Reactivation for Revlimid
The Pharmaceuticals and Medical Devices Agency (PMDA) is reviewing the risk of hepatitis B virus reactivation for Celgene’s multiple myeloma med Revlimid (lenalidomide) - a move that is likely to result in label changes. The PMDA also revealed in its…
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