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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
13
UCLA
Los Angeles, California, United States
University of Colorado, Denver
Aurora, Colorado, United States
Vanderbilt University
Nashville, Tennessee, United States
Seattle Cancer Care Alliance
Seattle, Washington, United States
Institute Gustave Roussy
Paris, France
University Hospital Essen
Essen, Germany
Percentage of Participants With Adverse Events Who Received PLX3397 in Combination With Vemurafenib in V600-mutated BRAF Melanoma
Time frame: 1 year
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