drugset / Trial / NCT04370704

Study of Combination Therapy With INCMGA00012 (Anti-PD-1), INCAGN02385 (Anti-LAG-3), and INCAGN02390 (Anti-TIM-3) in Participants With Select Advanced Malignancies

NCT04370704

Phase 1/2 Completed 61 enrolled Incyte Corporation
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The study will determine Recommended Phase 2 Dose for all study drugs, based on the safety and tolerability of the following combinations: INCAGN02385 + INCAGN02390 and INCAGN02385 + INCAGN02390 + INCMGA00012.

Timeline

Start
2020-07-27
Primary completion
2025-08-25
Completion
2025-08-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Retifanlimab Monoclonal antibody Intravenous
Subject Tuparstobart Monoclonal antibody Intravenous
Subject Verzistobart Monoclonal antibody Intravenous

Indications