This phase II study is evaluating how safe and effective chemotherapy (belzutifan) is in combination with immunotherapy (pembrolizumab) and targeted therapy (lenvatinib) in people with multiple solid cancers, including cancer of the liver, bowel, pancreas, biliary tract, endometrium and oesophagus.
This trial is treating patients with cancer of the liver, bowel, pancreas, biliary tract, endometrium or oesophagus.
This is a systemic therapy trial.
You may be able to join this trial if:
- You are able to swallow medication by mouth.
- You have had treatment but your cancer has gotten worse or has not responded to the treatment you have been given.
- Your cancer has not spread to other parts of the body.
- Your cancer has spread to other parts of the body.
You may be excluded from this trial if:
- You have a certain disease or psychological condition.
- You have been diagnosed with a prior or secondary type of cancer.
- You have had certain treatments, surgical procedures or drugs.
Clinical trials have complex eligibility criteria - talk to your doctor about your interest in this trial.
Clinical Summary Read More
Trial Identifiers
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Scientific Title
An Open-label, Multicenter, Phase 2 Study to Evaluate the Efficacy and Safety of Pembrolizumab Plus Lenvatinib in Combination With Belzutifan in Multiple Solid Tumors
Commercial Sponsor
Merck
Summary
Eligible participants will be randomly allocated to one of two Experimental Arms. In Experimental Arm 1, participants will receive pembrolizumab (400mg) plus belzutifan (120mg) plus lenvatinib (20mg). Pembrolizumab will be administered via intravenous (IV) infusion once every 6 weeks (Q6W) for a maximum of 18 doses (approximately 2 years). Belzutifan and lenvatinib will be administered orally once daily (QD) until progressive disease or discontinuation. In Experimental Arm 2, participants with IO resistant ESCC will receive pembrolizumab (400mg) plus lenvatinib (20mg). Pembrolizumab will be administered via intravenous (IV) infusion once every 6 weeks (Q6W) for a maximum of 18 doses (approximately 2 years). Lenvatinib will be administered orally once daily (QD) until progressive disease or discontinuation.
Recruiting Hospitals Read More