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.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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)