Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Panel to Weigh Orphan Designation for Tecartus on December 22
A Japanese health ministry panel will discuss on December 22 whether to grant orphan designation for two regenerative medicine products, including Gilead Sciences’ CAR-T cell therapy brexucabtagene autoleucel, marketed overseas as Tecartus. The designation will be taken up by the…
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REGULATORY
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