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Study identifier: NCT07403721 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Metastatic or Locally Advanced Solid Tumors With Microsatellite Instability-high (MSI-H) or Mismatched Repair Deficiency (dMMR)  ·  Sponsor: Amgen

PhasePhase 1
Planned participants464
Who can joinAll sexes, 18 Years to 99 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Amgen Call Center  ·  866-572-6436  ·  medinfo@amgen.com

Always discuss trial participation with your own doctor first.

Locations (22)

City of Hope Orange County Lennar Foundation Cancer CenterIrvine, California, United StatesRecruiting
Midwestern Regional Medical Center dba City of Hope ChicagoZion, Illinois, United StatesRecruiting
Community Health Network MD Anderson Cancer Center - NorthIndianapolis, Indiana, United StatesRecruiting
New England Cancer SpecialistsWestbrook, Maine, United StatesRecruiting
Tennessee Oncology PLLCNashville, Tennessee, United StatesRecruiting
Next Oncology - DallasIrving, Texas, United StatesRecruiting
Calvary Mater Newcastle HospitalWaratah, New South Wales, AustraliaRecruiting
Peter MacCallum Cancer CentreMelbourne, Victoria, AustraliaRecruiting
Universite Catholique de Louvain Cliniques Universitaires Saint LucBrussels, BelgiumRecruiting
Universitair Ziekenhuis GentGhent, BelgiumRecruiting
Princess Margaret Cancer CentreToronto, Ontario, CanadaRecruiting
Sun Yat-Sen University Cancer CenterGuangzhou, Guangdong, ChinaRecruiting

+ 10 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07403721