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Active, not recruiting Phase 1 Interventional

Anvumetostat Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).

ClinicalTrials.gov ID: NCT06333951

Public ClinicalTrials.gov record NCT06333951. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 18, 2026, 3:35 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Anvumetostat Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-deleted thoracic tumors. The study also aims to determine the safety profile of Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted thoracic tumors.

Study identification

NCT ID
NCT06333951
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
Amgen
Industry
Enrollment
49 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 100 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 17, 2024 (Actual)
Primary completion
Oct 31, 2026 (Estimated)
Completion
Nov 30, 2026 (Estimated)
Last update posted
May 28, 2026

2024 – 2026

United States locations

U.S. sites
26
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
Comprehensive Blood and Cancer Center Bakersfield California 93309 —
City of Hope National Medical Center Duarte California 91010 —
City of Hope Orange County Lennar Foundation Cancer Center Duarte California 91010 —
Translational Research in Oncology US Inc, Trio Central Pharmacy Los Angeles California 90095 —
University of California Irvine Orange California 92868-3217 —
University of California Los Angeles Santa Monica California 90404 —
Rocky Mountain Cancer Centers Denver Colorado 80218 —
Eastern Connecticut Hematology and Oncology Associates Norwich Connecticut 06360 —
HealthPartners Institute Saint Paul Minnesota 55102 —
Saint Lukes Hospital of Kansas City Kansas City Missouri 64111 —
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89169 —
Roswell Park Cancer Institute Buffalo New York 32224 —
New York University Grossman School of Medicine New York New York 10016 —
Perlmutter Cancer Center at New York University Langone Hospital----Long Island New York New York 10016 —
Upstate University Hospital Syracuse New York 13210 —
Hightower Clinical Oklahoma City Oklahoma 73102 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232 —
University of Tennessee Medical Center Knoxville Knoxville Tennessee 37920 —
United States Oncology Regulatory Affairs Corporate Office Nashville Tennessee 37203 —
Texas Oncology - Dallas Fort Worth Dallas Texas 75246 —
US Oncology Research Investigational Products Center Dallas Texas 75246 —
Oncology Consultants Cancer Center Houston Texas 77030 —
Texas Oncology Northeast Texas Tyler Texas 75702 —
Virginia Cancer Specialists PC Fairfax Virginia 22031 —
Northwest Medical Specialties, PLLC Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 57 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06333951, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 28, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06333951 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →