Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
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PMDA Will “Appropriately Review” Lecanemab If Filed: Minister
The Pharmaceuticals and Medical Devices Agency (PMDA) will “appropriately review” Eisai’s Alzheimer’s drug lecanemab if it is officially filed for approval, Health Minister Katsunobu Kato said on September 30, two days after the company announced favorable trial data. At a…
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