drugset / Trial / NCT03589651

INCMGA00012 in Combination With Other Therapies in Patients With Advanced Solid Tumors

NCT03589651

Phase 1 Completed 83 enrolled Incyte Corporation
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, preliminary evidence of clinical activity, and recommended Phase 2 dose (RP2D) of INCMGA00012 in combination with other agents that may improve the therapeutic efficacy of anti-PD-1 monotherapy.

Timeline

Start
2018-08-17
Primary completion
2022-11-21
Completion
2022-11-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Epacadostat Small molecule Oral
Subject Parsaclisib Small molecule Oral
Subject Retifanlimab Monoclonal antibody Intravenous

Indications

No indication recorded.