Japan’s Ministry of Health, Labor and Welfare (MHLW) on March 5 unveiled the revised NHI prices for drugs subject to…
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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REGULATORY
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