This study is being done to see if combining HEPZATO KIT™ with nivolumab and relatlimab (Opdualag™) in the first line setting in patients with metastatic melanoma with liver metastasis is safe, tolerable, and will have a synergistic effect leading to improved clinical outcomes compared to the historic cohort of patients with liver metastasis treated with combination immune checkpoint inhibitor therapy.
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.
Incidence and Severity of Dose Limiting Toxicities (DLTs)
Timeframe: up to 12 weeks
Incidence of Treatment-Emergent Adverse Events
Timeframe: up to 2 years
Incidence of Serious Treatment-Emergent Adverse Events
Timeframe: up to 2 years
Number of Participants that Discontinue Treatment due to Adverse Events
Timeframe: up to 2 years
Overall Response Rate (ORR)
Timeframe: After treatment plus follow up for 2 years (up to 4 years)