Overview

A Phase 1b Open Label, Dose Escalation Study of PLX3397 in Combination With Vemurafenib in V600-mutated BRAF Melanoma

Status:
Terminated
Trial end date:
2014-09-22
Target enrollment:
Participant gender:
Summary
The purpose of this research study is to test the safety of an investigational new drug called PLX3397 when used in combination with Vemurafenib (Zelboraf™) at different dose levels. Vemurafenib has been approved by the United States Food and Drug Administration (FDA)/European Medicines Agency (EMA) for the treatment of a specific category of unresectable or metastatic melanoma.
Phase:
Phase 1
Details
Lead Sponsor:
Daiichi Sankyo, Inc.
Plexxikon
Collaborator:
Plexxikon
Treatments:
Vemurafenib