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)
π©Ί 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
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π 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
π 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.
π° 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.
Explore by condition: All MTAP-deleted NSCLC clinical trials
π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.