Status: Recruiting
AMG 436 as Monotherapy and Combination Therapy in Participants With MSI-H/dMMR Solid Tumors
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.
Participants needed: 464
Trial details
Phase: Phase 1Age: 18-99Biological sex: AllType: InterventionalSponsor: AmgenUpdated: Jul 2, 2026Locations: 20
Eligibility criteria
Age ≥ 18 years (or ≥ legal age within the country if it is older than 18 years). [+5]
Participants with primary central nervous system (CNS) tumors. [+5]