Authors: Karly P GarnockJones
Publish Date: 2015/10/09
Volume: 75, Issue: 15, Pages: 1823-1830
Abstract
Genentech a subsidiary of Roche and Exelixis are developing cobimetinib an orally available small molecule for the treatment of various cancers including malignant melanoma and breast cancer Cobimetinib inhibits the MEK mitogenactivated protein kinase component of the MAPK/ERK signalling pathway which is frequently overactivated in human tumours The product has been approved in Switzerland in combination with vemurafenib for the treatment of patients with unresectable or metastatic BRAF V600 mutationpositive melanoma and is under regulatory review for the same indication in several countries including the USA and the EU This article summarizes the milestones in the development of cobimetinib leading to this first approval for unresectable or metastatic BRAF V600 mutationpositive melanoma melanomaThe preparation of this review was not supported by any external funding During the peer review process the manufacturer of the agent under review was offered an opportunity to comment on the article Changes resulting from any comments received were made by the author on the basis of scientific completeness and accuracy K P GarnockJones is a salaried employee of Adis Springer SBM
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