Binimetinib is an oral cancer drug sold under the brand name Mektovi that selectively inhibits MEK, a kinase at the center of the MAPK signaling pathway that many cancers rely on for growth. By binding to and blocking MEK1 and MEK2, it prevents growth factor signals from driving cell division. Array BioPharma developed binimetinib, later taken forward by Pfizer, and the United States Food and Drug Administration approved it in June 2018 for use together with encorafenib against unresectable or metastatic melanoma carrying a BRAF V600E or V600K mutation. The same combination gained a further FDA approval in October 2023 for metastatic non small cell lung cancer carrying a BRAF V600E mutation. Binimetinib is taken by mouth, and because MEK sits downstream of BRAF in the same pathway, pairing the two drugs blocks the cancer signal at two points at once, which has been shown to slow resistance compared with a BRAF inhibitor 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. Wikipedia
Wikipedia contributors, Wikimedia Foundation
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. Binimetinib (Wikipedia)
https://en.wikipedia.org/wiki/Binimetinib, lead section
as been shown to occur in many cancers. In June 2018 it was approved by the FDA in combination with encorafenib for the treatment of patients with unresectable or metastatic BRAF V600E or V600K mutation-positive melanoma. In October 2023, it was approved by th
- Route of administration
View the Source4. Drugs.com: Mektovi (binimetinib) FDA Approval History
FDA Approval HistoryQuote, FDA Approval History
Mektovi (binimetinib) was first approved by the FDA on June 27, 2018
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