drugset / Trial / NCT01638676

A Phase I/II Trial of Vemurafenib and Metformin to Melanoma Patients

NCT01638676

NaSingle-groupOpen-labelTreatment

Summary

The main purpose of this study is to evaluate the safety of Vemurafenib in combination with Metformin in melanoma patients. The phase II part of the study will also evaluate the clinical activity of the combined regiment. Based on pre-clinical studies and a phase I trial, the investigators hypothesize that the combination of an FDA-approved non-toxic dose of oral Metformin with Vemurafenib will yield little toxicity and improve clinical outcomes in terms of objective response rates and survival in metastatic melanoma patients.

Timeline

Start
2012-07
Primary completion
2025-06
Completion
2027-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Metformin Small molecule 850 mg Oral
Subject Vemurafenib Small molecule 960 mg Oral

Indications