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A Clinical Trial to Assess COM503 in Participants With Advanced Solid Malignancies
NCT06759649 · View on ClinicalTrials.gov ↗
Study Summary
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.
Conditions Studied
Interventions
- DRUG Zimberelimab
- DRUG COM503
Study Locations (11)
Israel
- Rambam Health Care Campus — Haifa
- Hadassah University Medical Center- Ein Kerem — Jerusalem
- Rabin Medical Center — Petah Tikva
- The Chaim Sheba Medical Center — Ramat Gan
Texas
- NEXT Oncology San Antonio — San Antonio
- START — San Antonio
Connecticut
- Yale- New Haven Hospital- Yale Cancer Center — New Haven
Massachusetts
- Beth Israel Deaconess Medical Center — Boston
Michigan
- START Midwest — Grand Rapids
Tennessee
- The West Clinic, PLCC dba West Cancer Center — Germantown
Virginia
- NEXT Oncology Virginia — Fairfax
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2025-01-07 |
| Est. Completion | 2027-11-22 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06759649
The ClinicalTrials.gov registry entry for NCT06759649 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Compugen, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Neoplasm appearing as the primary indexed condition, and to 2 interventions — of which Zimberelimab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06759649 reports 11 study locations spanning 7 distinct geographic areas — top geographies include Israel, Texas, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06759649 about?
NCT06759649 is a clinical study titled "A Clinical Trial to Assess COM503 in Participants With Advanced Solid Malignancies". 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 COM50...
What is the current status of trial NCT06759649?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 200 participants. The study started on 2025-01-07. Estimated completion is 2027-11-22.
What conditions does trial NCT06759649 study?
This clinical trial studies the following conditions: Neoplasm, Cancer, Malignant Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06759649?
The interventions under investigation include: Zimberelimab (DRUG), COM503 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06759649?
This trial is sponsored by Compugen, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06759649 being conducted?
This trial has 11 study locations across Connecticut, Massachusetts, Michigan, Tennessee, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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