drugset / Trial / NCT01271803

A Study of Vemurafenib and GDC-0973 (Cobimetinib) in Participants With BRAFV600E Mutation-Positive Metastatic Melanoma

NCT01271803

Phase 1 Completed 131 enrolled Hoffmann-La Roche
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This open-label, dose-escalation study of vemurafenib in combination with cobimetinib will evaluate the safety, tolerability and pharmacokinetics in participants with BRAFV600 mutation-positive metastatic melanoma. Participants with previously untreated, BRAFV600E mutation-positive, locally advanced/unresectable or metastatic melanoma or those who have progressed on vemurafenib monotherapy immediately prior to enrolling in this trial are eligible. Participants will be assigned to different cohorts with escalating oral doses of vemurafenib and cobimetinib. This study consists of 2 stages, Stage 1 (Dose Escalation Stage \[DES\] and Cohort Expansion Stage \[CES\]) and the anticipated time on study treatment is until disease progression, unacceptable toxicity or any other discontinuation criterion is met.

Timeline

Start
2011-02-17
Primary completion
2013-10-01
Completion
2017-12-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Cobimetinib Small molecule 60 mg Oral
Subject Cobimetinib Small molecule 80 mg Oral
Subject Cobimetinib Small molecule 100 mg Oral
Subject Vemurafenib Small molecule 720 mg
Subject Vemurafenib Small molecule 960 mg

Indications