The purpose of this study is to determine the maximum tolerated dose and characterize the safety profile of durvalumab (MEDI4736) in combination with dabrafenib and trametinib or with trametinib alone in participants with metastatic or unresectable melanoma with BRAF-mutation positive or wild-type (WT) BRAF, respectively.
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Number of Participants With Dose Limiting Toxicities (DLTs)
Timeframe: From first dose of study drug (Day 1) until the planned 3rd dose of durvalumab (Day 29)
Number of Participants With Treatment-emergent Adverse Events (TEAEs) and Treatment-emergent Serious Adverse Events (TESAEs)
Timeframe: From first dose of study drug (Day 1) up to 90 days after the last dose (up to 4.5 years)
Number of Participants With Abnormal Vital Signs and Physical Examinations Reported as TEAEs
Timeframe: From first dose of study drug (Day 1) up to 90 days after the last dose (up to 4.5 years)
Number of Participants With Abnormal Clinical Laboratory Parameters Reported as TEAEs
Timeframe: From first dose of study drug (Day 1) up to 90 days after the last dose (up to 4.5 years)
Number of Participants With Abnormal Electrocardiograms (ECGs) and Echocardiograms (ECHOs) Reported as TEAEs
Timeframe: From first dose of study drug (Day 1) up to 90 days after the last dose (up to 4.5 years)