Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
BUSINESS
EMA Delays Decision on Leqembi Due to Procedural Issues
Eisai said on March 22 that the regulatory review of its Alzheimer’s disease drug lecanemab by a key European Medicines Agency (EMA) panel has been postponed due to procedural reasons. The deliberation process of lecanemab was delayed because the EMA…
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