drugset / Trial / NCT07403721

AMG 436 as Monotherapy and Combination Therapy in Participants With MSI-H/dMMR Solid Tumors

NCT07403721 ↗

Phase 1 Recruiting 464 enrolled Amgen
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary objectives of this trial are to evaluate the safety profile of AMG 436 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for AMG 436 as monotherapy and in combination with other anti-cancer therapies in participants with MSI-H/dMMR solid tumors.

Timeline

Start
2026-04-08
Primary completion
2028-06-28
Completion
2028-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject AMG 436 Unknown — —

Indications

No indication recorded.