drugset / Trial / NCT01689519

A Study Comparing Vemurafenib Versus Vemurafenib Plus Cobimetinib in Participants With Metastatic Melanoma

NCT01689519 ↗

Phase 3 Completed 495 enrolled Hoffmann-La Roche
RandomizedParallel-groupTriple-blindTreatment

Summary

To evaluate the efficacy of vemurafenib in combination with cobimetinib (GDC-0973), compared with vemurafenib and placebo, in previously untreated BRAF V600 mutation-positive patients with unresectable locally advanced or metastatic melanoma, as measured by progression-free survival (PFS), assessed by the study site investigator.

Timeline

Start
2013-01-08
Primary completion
2014-05-09
Completion
2019-07-21

Outcome

Met primary endpoint

registry analysis (unspecified test); Cobimetinib + Vemurafenib vs Placebo + Vemurafenib; p = 0.0001; Hazard Ratio (HR) 0.51 (95% CI 0.39 to 0.68); Log Rank; NCT01689519 ↗

paper The median progression-free survival was 9.9 months in the combination group and 6.2 months in the control group PMID 25265494 ↗

release “phase 3 coBRIM study, which showed COTELLIC plus vemurafenib reduced the risk of disease worsening or death (progression-free survival; PFS)” exelixis.com ↗

release “results of the coBRIM Phase III study, which showed the MEK inhibitor cobimetinib plus Zelboraf reduced the risk of disease worsening or death by half” gene.com ↗

release “median PFS of 9.9 months for cobimetinib plus Zelboraf compared to 6.2 months with Zelboraf alone” gene.com ↗

release “coBRIM study, which showed Cotellic plus Zelboraf reduced the risk of disease worsening or death (progression-free survival; PFS) by about half” gene.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cobimetinib Small molecule 60 mg Oral
Subject Vemurafenib Small molecule 960 mg Oral

Indications