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Study identifier: NCT06759649 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Clinical Trial to Assess COM503 in Participants With Advanced Solid Malignancies

Condition: Neoplasm · Cancer, Malignant Tumors  ·  Sponsor: Compugen Ltd

PhasePhase 1
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The overall goal of this first-in-human (FIH) clinical trial is to learn about the safety and dosing of COM503 when given alone or in combination with zimberelimab in participants with advanced solid tumors. The primary objectives of this study are: * To assess the safety and tolerability of COM503 as monotherapy and COM503 in combination with zimberelimab in participants with advanced solid tumors. * To identify the maximum tolerated dose (MTD) / maximum administered dose (MAD) and/or the recommended phase 2 dose (RP2D) of COM503 as monotherapy and in combination with zimberelimab in participants with advanced solid tumors.

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

Talk to the study team

Michelle Chief Medical Officer, MD  ·  +14153734034  ·  michellebm@cgen.com

Always discuss trial participation with your own doctor first.

Locations (11)

Yale- New Haven Hospital- Yale Cancer CenterNew Haven, Connecticut, United StatesRecruiting
Beth Israel Deaconess Medical CenterBoston, Massachusetts, United StatesRecruiting
START MidwestGrand Rapids, Michigan, United StatesRecruiting
The West Clinic, PLCC dba West Cancer CenterGermantown, Tennessee, United StatesRecruiting
NEXT Oncology San AntonioSan Antonio, Texas, United StatesRecruiting
STARTSan Antonio, Texas, United StatesRecruiting
NEXT Oncology VirginiaFairfax, Virginia, United StatesRecruiting
Rambam Health Care CampusHaifa, Israel, IsraelRecruiting
Hadassah University Medical Center- Ein KeremJerusalem, Israel, IsraelRecruiting
Rabin Medical CenterPetah Tikva, Israel, IsraelRecruiting
The Chaim Sheba Medical CenterRamat Gan, Israel, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT06759649