60
Participants
Start Date
August 31, 2025
Primary Completion Date
August 31, 2030
Study Completion Date
August 31, 2030
Relatlimab FDC + Nivolumab
Relatlimab: 360 IV Q3W (Dose level 1) and 120mg IV Q3W (Dose level -1) Nivolumab: 360mg IV Q3W
Sacituzumab Govitecan (SG)
10 mg/kg IV D1 \& D8 every 21-day cycles (Dose level 1); 7.5 mg/kg IV D1 \& D8 every 21-day cycles (Dose level -1); 5 mg/kg IV D1 \& D8 every 21-day cycles 21-day cycles (Dose level -2)
Nivolumab
360mg IV Q3W
Yale University, New Haven
Collaborators (1)
Bristol-Myers Squibb
INDUSTRY
Yale University
OTHER