Vemurafenib is a competitive kinase inhibitor with activity against BRAF kinase with mutations like V600E. It exerts its function by binding to the ATP-binding domain of the mutant BRAF. Vemurafenib was co-developed by Roche and Plexxikon and it obtained its FDA approval on August 17, 2011, under the company Hoffmann La Roche. After approval, Roche in collab...
Vemurafenib is approved since 2011 for the treatment of metastatic melanoma with a mutation on BRAF in the valine located in the exon 15 at codon 600, this mutation is denominated as V600E. The V600E mutation, a substitution of glutamic acid for valine, accounts for 54% of the cases of cutaneous melanoma.
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Fondazione G.Pascale, Napoli, Italy
Hillman Cancer Center, Pittsburgh, Pennsylvania, United States
Icahn School of Medicine at Mount Sinai, New York, New York, United States
Beijing Cancer Hospital, Beijing, China
Sun Yet-sen University Cancer Center, Guangzhou, China
Tulsa Cancer Institute PLLC, Tulsa, Oklahoma, United States
University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania, United States
University of Tennessee Medical Center Cancer Institute, Knoxville, Tennessee, United States
Huntsman Cancer Institute, Salt Lake City, Utah, United States
Bank of Cyprus Oncology Center, Nicosia, Cyprus
CSSS champlain - Charles-Le Moyne, Greenfield Park, Quebec, Canada
Karmanos Cancer Center, Detroit, Michigan, United States
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