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AMG 193 Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).
NCT06333951 · View on ClinicalTrials.gov ↗
Study Summary
The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor AMG 193 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 AMG 193 administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted thoracic tumors.
Conditions Studied
Interventions
- DRUG Pembrolizumab
- DRUG Carboplatin
- DRUG Pemetrexed
- DRUG Paclitaxel
- DRUG AMG 193
Study Locations (20)
California
- Comprehensive Blood and Cancer Center — Bakersfield
- City of Hope National Medical Center — Duarte
- City of Hope Orange County Lennar Foundation Cancer Center — Duarte
- Translational Research in Oncology US Inc, Trio Central Pharmacy — Los Angeles
- University of California Irvine — Orange
- University of California Los Angeles — Santa Monica
New York
- Roswell Park Cancer Institute — Buffalo
- New York University Grossman School of Medicine — New York
- Perlmutter Cancer Center at New York University Langone Hospital----Long Island — New York
- Upstate University Hospital — Syracuse
Pennsylvania
- Fox Chase Cancer Center — Philadelphia
- University of Pittsburgh Medical Center — Pittsburgh
Tennessee
- University of Tennessee Medical Center Knoxville — Knoxville
- United States Oncology Regulatory Affairs Corporate Office — Nashville
Colorado
- Rocky Mountain Cancer Centers — Denver
Connecticut
- Eastern Connecticut Hematology and Oncology Associates — Norwich
Minnesota
- HealthPartners Institute — Saint Paul
Missouri
- Saint Lukes Hospital of Kansas City — Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 500 participants |
| Start Date | 2024-09-17 |
| Est. Completion | 2031-10-27 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06333951
The ClinicalTrials.gov registry entry for NCT06333951 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Amgen, which has 266 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Non-small Cell Lung Cancer appearing as the primary indexed condition, and to 5 interventions — of which Pembrolizumab is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06333951 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, New York, Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06333951 about?
NCT06333951 is a clinical study titled "AMG 193 Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).". The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor AMG 193 administered in combination with other therapies in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-deleted thoracic...
What is the current status of trial NCT06333951?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 500 participants. The study started on 2024-09-17. Estimated completion is 2031-10-27.
What conditions does trial NCT06333951 study?
This clinical trial studies the following conditions: Non-small Cell Lung Cancer, Thoracic Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06333951?
The interventions under investigation include: Pembrolizumab (DRUG), Carboplatin (DRUG), Pemetrexed (DRUG), Paclitaxel (DRUG), AMG 193 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06333951?
This trial is sponsored by Amgen, which has 266 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06333951 being conducted?
This trial has 20 study locations across California, Colorado, Connecticut, Minnesota, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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