RecruitingPhase 1NCT07601243

Study of GS-2426 in Participants With Advanced Solid Tumors

A Phase 1, Multicenter, Open-Label Clinical Study to Evaluate the Safety and Tolerability of GS-2426 in Participants With Advanced MTAP-Deleted Solid Tumors


Sponsor

Gilead Sciences

Enrollment

174 participants

Start Date

Jun 2, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical study is to learn more about the study drug GS-2426, and how safe and tolerable it is in participants with advanced methylthioadenosine phosphorylase (MTAP)-deleted solid tumors. The primary objective of this study is to evaluate the safety and tolerability of GS-2426 in participants with MTAP-deleted advanced solid tumors and to determine the maximum tolerated dose (MTD)/maximum administered dose (MAD) and the recommended phase II dose (RP2D).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called GS-2426 for people with advanced solid tumors. The study is currently recruiting participants at 2 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGGS-2426

Administered Orally


Locations(4)

START Midwest

Grand Rapids, Michigan, United States

START Astera, LLC

East Brunswick, New Jersey, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

START San Antonio, LLC

San Antonio, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07601243


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