πŸ›οΈ Verified NIH Record β€’ Updated 2026-05-26

A Phase 2 Study of Anvumetostat in Participants With MTAP-deleted Advanced NSCLC (MTAPESTRY 201) (NCT06593522)

A Phase 2 Study Evaluating the Efficacy, Safety, Tolerability, and Pharmacokinetics of Anvumetostat in Subjects With Methylthioadenosine Phosphorylase (MTAP)-Deleted Previously Treated Advanced Non-Small Cell Lung Cancer (NSCLC)

πŸ”΅ Active, Not Recruiting Phase2 πŸ’Š Investigational Drug / Biologic Sponsor: Amgen

🩺 Plain-English Summary (8th-Grade Level)

The main objective of the study is to characterize safety and efficacy of 2 dose levels of anvumetostat by investigator, and to evaluate anvumetostat monotherapy efficacy by Blinded Independent Central Review (BICR).

Who can join: Review the eligibility criteria below.

Location: City of Hope National Medical Center β€” Duarte, California

Age range: 18 Years to 99 Years

πŸ§ͺ Interventions in This Study

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (91 Sites)

Showing the first 25 of 91 sites.

  • City of Hope National Medical Center β€” Duarte, California
  • City of Hope Orange County Lennar Foundation Cancer Center β€” Duarte, California
  • Cedars-Sinai Medical Center β€” Los Angeles, California
  • Valkyrie Clinical Trials β€” Los Angeles, California
  • University of California Los Angeles β€” Los Angeles, California
  • Rocky Mountain Cancer Centers β€” Denver, Colorado
  • Eastern Connecticut Hematology and Oncology Associates β€” Norwich, Connecticut
  • Hartford HealthCare Cancer Institute - Manchester β€” Plainville, Connecticut
  • Medstar Georgetown University Hospital β€” Washington D.C., District of Columbia
  • Our Lady of the Lake Cancer Institute β€” Baton Rouge, Louisiana
  • Trinity Health Saint Joseph Mercy Ann Arbor β€” Ann Arbor, Michigan
  • Cancer and Hematology Centers of Western Michigan β€” Grand Rapids, Michigan
  • Sarah Cannon Research Institute Oncology Partners β€” Nashville, Tennessee
  • United States Oncology Regulatory Affairs Corporate Office β€” Nashville, Tennessee
  • Texas Oncology Central/South Texas β€” Austin, Texas
  • Sarah Cannon Research Institute β€” Dallas, Texas
  • Texas Oncology - Dallas Fort Worth β€” Dallas, Texas
  • US Oncology Research Investigational Products Center β€” Irving, Texas
  • Texas Oncology Northeast Texas β€” Tyler, Texas
  • Virginia Cancer Specialists PC β€” Fairfax, Virginia
  • GenesisCare -North Shore Oncology β€” St Leonards, New South Wales
  • Calvary Mater Newcastle Hospital β€” Waratah, New South Wales
  • Mater Hospital Brisbane β€” South Brisbane, Queensland
  • Cancer Research South Australia β€” Adelaide, South Australia
  • NΓΊcleo de Oncologia da Bahia β€” Salvador, Estado de Bahia

πŸ“ž Contact the Study Coordinator

Phone: (800) 826-4673

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—