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 Regulatory Filing of Enfortumab Vedotin: Astellas/Seagen
Astellas Pharma said on March 26 that the European Medicines Agency (EMA) has accepted a regulatory submission for the antibody-drug conjugate (ADC) enfortumab vedotin, being codeveloped with its US partner Seagen, formally called Seattle Genetics. The submission rides on the…
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