RecruitingPhase 1NCT05245500

Phase 1 Study of MRTX1719 in Solid Tumors With MTAP Deletion

This is a Phase 1, open-label, multicenter, study of the safety, tolerability, PK, PD, and anti-tumor activity of MRTX1719 patients with advanced, unresectable or metastatic solid tumor malignancy with homozygous deletion of the MTAP gene.

Checked against the public recordLast updated Dec 5, 2025 · Source: ClinicalTrials.gov

StatusRecruiting
PhasePhase 1
U.S. locations25
SponsorBristol-Myers Squibb
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 1
Sponsor
Bristol-Myers Squibb
Interventions being studied
Drug: MRTX1719
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria * Histologically confirmed diagnosis of a solid tumor malignancy with homozygous deletion of the MTAP gene detected in tumor tissue. * Unresectable or metastatic disease. * Presence of a tumor lesion amenable to mandatory biopsy for pharmacodynamic evaluation at baseline and on-study unless Sponsor-confirmed as medically unsafe or infeasible. * Age ≥ 18 years. * Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. * Adequate organ function. Exclusion Criteria * Prior treatment with a PRMT5 or MAT2A inhibitor therapy. * Active brain metastases or carcinomatous meningitis. * History of significant hemoptysis or hemorrhage within 4 weeks of the first dose of study treatment. * Major surgery within 4 weeks of first dose of study treatment. * History of intestinal disease, inflammatory bowel disease, major gastric surgery, or other gastrointestinal conditions (eg, uncontrolled nausea, vomiting, malabsorption syndrome) likely to alter absorption of study treatment or result in inability to swallow oral medications. * Cardiac abnormalities. * Other protocol-defined Inclusion/Exclusion criteria apply.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Mayo ClinicPhoenix, Arizona
  • Sarah Cannon Research Institute (SCRI) - HealthONE LocationDenver, Colorado
  • Rocky Mountain Cancer Centers, LLP - OncologyLone Tree, Colorado
  • Mayo ClinicJacksonville, Florida
  • Sarah Cannon Research Institute at Florida Cancer SpecialistsOrlando, Florida
  • Local Institution - 124Chicago, Illinois
  • Dana-Farber Cancer InstituteBrookline, Massachusetts
  • Cancer and Hematology Centers of Western MichiganNorton Shores, Michigan
  • Mayo ClinicRochester, Minnesota
  • Rutgers Cancer Institute of New JerseyNew Brunswick, New Jersey
  • Local Institution - 129Mineola, New York
  • David H Koch, Memorial Sloan Kettering Cancer CenterNew York, New York

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Dec 5, 2025. Always confirm current availability with the study team.

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