Drug intelligence / Profile preview

atezolizumab + cobimetinib + vemurafenib

Development stage
Unknown
Lead developer
Genentech
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Atezolizumab + cobimetinib + vemurafenib is an FDA-approved triple combination regimen for the treatment of patients with BRAF V600 mutation-positive unresectable or metastatic melanoma. - **Atezolizumab** is a monoclonal antibody immune checkpoint inhibitor targeting PD-L1, thereby enhancing T cell-mediated anti-tumor immune responses. - **Cobimetinib** is a small molecule, reversible inhibitor of MEK1 and MEK2 kinases, which are part of the MAPK (RAS/RAF/MEK/ERK) cascade, primarily used to suppress downstream signaling from mutated BRAF. - **Vemurafenib** is a small molecule kinase inhibitor selective for BRAF V600-mutant kinase, blocking abnormal cell proliferation in BRAF-mutant melanoma. The combination aims to maximize anti-tumor activity: cobimetinib and vemurafenib together block the MAPK pathway to inhibit tumor cell proliferation and induce apoptosis; atezolizumab counteracts adaptive immune resistance induced by MAPK pathway inhibition, improving progression-free survival and duration of response versus targeted therapy alone[1][3][4][5][7].

Brand names
TecentriqZelborafCotellic
Other names
cobimetinib + atezolizumab + vemurafenib
02

Targets

CAPN3 (B-Raf proto-oncogene, serine/threonine kinase)MEK1 (Dual specificity mitogen-activated protein kinase kinase 1)CD274 (Programmed cell death protein 1 ligand 1)MEK2 (Dual specificity mitogen-activated protein kinase kinase 2)

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