Japan’s cost-effectiveness assessment (CEA) panel has approved a revised handling policy for the CEA system for FY2026, with the health…
REGULATORY
US FDA Approves Vemurafenib for Melanoma; to Be Copromoted by Daiichi Sankyo
The US FDA approved on August 17 an application for the novel treatment for malignant melanoma vemurafenib (brand name in the US: Zelboraf) filed by F. Hoffmann-La Roche. Discovered by Plexxikon of the US, a member of the Daiichi Sankyo…
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