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NCT06333951 · ClinicalTrials.gov registry record · Phase 1

AMG 193 Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).

A Phase 1 study of Non-Small Cell Lung Cancer and Thoracic Tumors, sponsored by Amgen.

Recruiting
Registry status
Phase 1
Development phase
500
Enrollment target
20
Study locations

NCT06333951: Recruiting Phase 1 study of Non-Small Cell Lung Cancer and Thoracic Tumors, sponsored by Amgen.

NCT06333951 is a Phase 1 study of Non-Small Cell Lung Cancer and Thoracic Tumors that is actively recruiting participants, run by Amgen. The registered enrollment target is 500 participants, below the 651-participant average among 454 other Non-Small Cell Lung Cancer trials with a reported enrollment target (23% lower). The trial reports 20 study locations across 10 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06333951, a Phase 1 study of Non-Small Cell Lung Cancer and Thoracic Tumors, is actively recruiting participants, sponsored by Amgen.

RECRUITING
Registry status
Phase 1
Development phase
500 participants
Enrollment target
20
Study locations

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.

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

FieldValue
Enrollment Target 500 participants
Start Date 2024-09-17
Est. Completion 2031-10-27
Phase Phase 1
Amgen

558 total trials

What NCT06333951 shows while recruiting

NCT06333951 is an interventional study that assigns participants to a tested intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, below the 651-participant average among 454 other Non-Small Cell Lung Cancer trials with a reported enrollment target (23% lower).

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.

NCT06333951 names 20 study sites across 10 states, led by California, New York, Pennsylvania.

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.

What interventions are being tested in trial NCT06333951?

The interventions under investigation include: Pembrolizumab (DRUG), Carboplatin (DRUG), Pemetrexed (DRUG), Paclitaxel (DRUG), AMG 193 (DRUG).

Who is sponsoring clinical trial NCT06333951?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

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.

Similar trials for Non-Small Cell Lung Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06333951's enrollment target sits among peer trials

500 74th of 454 higher than 379 of 454 other Non-Small Cell Lung Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Non-Small Cell Lung Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06333951, the US trial registry maintained by the National Library of Medicine. NCT06333951 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.