This study aims to evaluate the safety, tolerability, and preliminary clinical activity and establish a recommended dose of GSK3745417 administered alone (Part 1A) or co-administered (Part 2A) with dostarlimab in participants with refractory/relapsed solid tumors. Both parts will consist of a dose escalation phase.
Protocol Amendment History
3 changes
criticalTrial terminated2026-08-04
criticalTrial terminated: Business Decision2026-08-04
minorCompletion moved earlier: 2026-03-31 -> 2026-01-092026-08-04