60
Participants
Start Date
August 6, 2025
Primary Completion Date
November 30, 2026
Study Completion Date
February 28, 2030
Ipilimumab
1 mg/kg of Ipilimumab will be administered via IV every 8 weeks. Participants will be assigned to Cohort A or B as per eligibility criteria. No randomization or blinding will occur
Nivolumab + Relatlimab FDC
Relatlimab 160mg + Nivo 480mg will be administered via IV every 4 weeks. Participants will be assigned to Cohort A or B as per eligibility criteria. No randomization or blinding will occur
RECRUITING
Stanford University, Palo Alto
Stanford University
OTHER