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OncoMatch/Clinical Trials/NCT07070518

Study of GV20-0251 in Participants With Solid Tumor Malignancies

Is NCT07070518 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies GV20-0251 for solid tumor cancer.

Phase 1/2RecruitingGV20 TherapeuticsNCT07070518Data as of May 2026

Treatment: GV20-0251This is a Phase 1 and Phase 2 study of GV20-0251 being developed for the treatment of participants with advanced solid tumors, who are refractory to approved therapies or other standard of care.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Endometrial Cancer

Colorectal Cancer

Non-Small Cell Lung Carcinoma

Melanoma

Hepatocellular Carcinoma

Small Cell Lung Cancer

Disease stage

Metastatic disease required

measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST version 1.1)

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Min 1 prior line

Must have received: standard of care therapy

Refractory or intolerant to standard therapies, must have received the standard of care therapy

Cannot have received: anticancer therapy

Exception: within 4 weeks or 5 half-lives (whichever is shorter) before the first dose of GV20-0251 on Cycle 1 Day 1 (C1D1), with the exceptions

Prior anticancer therapy within 4 weeks or 5 half-lives (whichever is shorter) before the first dose of GV20-0251 on Cycle 1 Day 1 (C1D1), with the exceptions

Cannot have received: radiation therapy

Exception: for symptomatic lesions within 14 days prior to C1D1 dosing

Radiation therapy for symptomatic lesions within 14 days prior to C1D1 dosing

Lab requirements

Cardiac function

No heart disease (NYHA ≥ Level II), myocardial infarction within the past 6 months, or unstable arrhythmia; QTcF > 470 msec, congenital long QT syndrome, or history of clinically significant ECG abnormalities (including pericarditis)

Participant with heart disease (NYHA ≥ Level II), myocardial infarction within the past 6 months, or unstable arrhythmia; Fridericia-corrected QT interval (QTcF) > 470 msec, or the presence of congenital long QT syndrome, or a history of clinically significant electrocardiogram (ECG) abnormalities (including pericarditis) that, in the investigator's judgment, may affect the subject's safety.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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