Cobimetinib is an oral cancer drug sold under the brand name Cotellic that inhibits MEK, also called MAP2K, a kinase in the same growth signaling pathway targeted by other MEK inhibitor drugs. Genentech brought cobimetinib to market, and the United States Food and Drug Administration approved it in November 2015 for use together with vemurafenib against unresectable or metastatic melanoma carrying a BRAF V600E or V600K mutation, and it has also been used against histiocytic neoplasms. In the phase III trial that supported approval, adding cobimetinib to vemurafenib raised median progression free survival to 12.3 months compared with 7.2 months for vemurafenib alone, and 65 percent of patients on the combination were alive at 17 months compared with 50 percent on vemurafenib alone. Cobimetinib is taken by mouth, and pairing a MEK inhibitor with a BRAF inhibitor blocks the same cancer driving pathway at two points, which slows the tumor's ability to develop resistance to either drug alone.
Facts
Classification
Approval Status ATC ClassSourced to the subject's own accountL: Antineoplastic and Immunomodulating Agents 2 Route of Administration First Approved / Isolated Year Connections
Sources
1. Cobimetinib (Wikipedia)
Lead section, approval-status statementQuote, Lead section, approval-status statement
Cobimetinib was approved for medical use in the United States in November 2015.
View the Source 2. Anatomical Therapeutic Chemical Classification System (Wikipedia)
WikipediaFirst-level anatomical group codes, Code LQuote, First-level anatomical group codes, Code L
Antineoplastic and immunomodulating agents
View the Source 3. Cobimetinib (Wikipedia)
WikipediaInfobox drug, routes_of_administrationQuote, Infobox drug, routes_of_administration
By mouth
View the Source 4. Drugs.com: Cotellic (cobimetinib) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Cotellic (cobimetinib) was first FDA approved on November 10, 2015
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