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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VUMedical Center, Amsterdam, Netherlands
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
New York University, New York, New York, United States
University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania, United States
H. Lee Moffitt Cancer Center, Tampa, Florida, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
Novartis Investigative Site, Swansea, United Kingdom
University of Texas MD Anderson Cancer Center, Houston, Texas, United States
Texas Oncology-Baylor Sammons Cancer Center, Dallas, Texas, United States
Oncology Specialists, S.C., Park Ridge, Illinois, United States
UCSD Moores Cancer Center, La Jolla, California, United States
National Institutes of Health Clinical Center, 9000 Rockville Pike, Bethesda, Maryland, United States
M D Anderson Cancer Center, Houston, Texas, United States
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