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Clinical Trials in the USA / NCT05245500
Recruiting Phase 1

Phase 1 Study of MRTX1719 in Solid Tumors With MTAP Deletion

NCT05245500 · tracked via the Priya Life Science USA tracker
Sponsor
Bristol-Myers Squibb
Phase
Phase 1
Started
2022-06-09
Last updated
2026-09-02

Condition(s) studied

MesotheliomaNon Small Cell Lung CancerMalignant Peripheral Nerve Sheath TumorsSolid TumorPancreatic AdenocarcinomaAdvanced Solid Tumor

Investigational drug(s) / intervention(s)

MRTX1719

MRTX1719: MRTX1719 is a potent PRMT5-MTA inhibitor. Specified dose on specified days

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (25)

FacilityCityRegionStatus
Mayo Clinic Phoenix Arizona Recruiting
Rocky Mountain Cancer Centers, LLP - Oncology Lone Tree Colorado Recruiting
Mayo Clinic Jacksonville Florida Recruiting
Sarah Cannon Research Institute at Florida Cancer Specialists Orlando Florida Recruiting
Local Institution - 124 Chicago Illinois Withdrawn
Dana-Farber Cancer Institute Brookline Massachusetts Recruiting
The Cancer & Hematology Centers Grand Rapids Michigan Recruiting
Cancer and Hematology Centers of Western Michigan Norton Shores Michigan Recruiting
Mayo Clinic Rochester Minnesota Recruiting
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey Recruiting
Perlmutter Cancer Center at NYU Langone Hospital Long Island Mineola New York Recruiting
David H Koch, Memorial Sloan Kettering Cancer Center New York New York Recruiting
New york cancer and blood specialists - Oncology Port Jefferson Station New York Recruiting
New york cancer and blood specialists - Oncology Port Jefferson Station New York Recruiting
University of North Carolina - Gastroenterology and Hepatology Chapel Hill North Carolina Recruiting
University of North Carolina Chapel Hill North Carolina Recruiting
Vanderbilt - Ingram Cancer Center Nashville Tennessee Recruiting
Ut Southwestern Dallas Texas Recruiting
Texas Oncology - DFW Fort Worth Texas Recruiting
MDACC Houston Texas Recruiting
South Texas Accelerated Research Therapeutics San Antonio Texas Recruiting
Texas Oncology, P.A. - Oncology Tyler Texas Recruiting
Virginia Cancer Specialists, PC Fairfax Virginia Recruiting
Local Institution - 134 Seattle Washington Withdrawn
Local Institution - 108 Milwaukee Wisconsin Completed

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05245500 on ClinicalTrials.gov ↗ ← All trials in the USA