drugset / Trial / NCT00949702

A Study of Vemurafenib in Previously Treated Patients With Metastatic Melanoma

NCT00949702

Phase 2 Completed 132 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

This open-label single arm study will assess the efficacy, safety and tolerability of Vemurafenib in previously treated patients with metastatic melanoma. Patients will receive oral Vemurafenib \[RG7204; PLEXXIKON: PLX4032\] at a dose of 960 mg b.i.d. continuously until disease progression or withdrawal from study and will be assessed at regular intervals for tumour response and tolerability. Target sample size is \<100 patients.

Timeline

Start
2009-09-30
Primary completion
2010-09-27
Completion
2014-06-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vemurafenib Small molecule 960 mg Oral

Indications