Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
Trodelvy Up for Japan Panel Review on Sept. 12, Meiji COVID Jab on Agenda Too
A key Japanese health ministry panel will discuss on September 12 whether to recommend approval for Gilead Sciences’ antibody drug conjugate (ADC) sacituzumab govitecan, otherwise known as Trodelvy in the US and Europe. The Pharmaceutical Affairs Council’s Second Committee on…
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