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A Study of LY4337713 in Participants With FAP-Positive Solid Tumors
NCT07213791 · View on ClinicalTrials.gov ↗
Study Summary
This is a study of LY4337713 in participants with certain types of cancer that is advanced or has spread. Participants must have cancer with high levels of a protein called fibroblast activation protein (FAP). The purpose of this study is to evaluate safety, side effects, and efficacy of LY4337713. In addition, this study will evaluate how much LY4337713 gets into the bloodstream, how it is broken down, and how long it takes the body to get rid of it. For each participant, the study will last about 5 years.
Conditions Studied
Interventions
- DRUG LY4337713
Study Locations (20)
California
- Hoag Memorial Hospital Presbyterian — Newport Beach
- Stanford University Medical Center — Stanford
Florida
- Biogenix Molecular, LLC — Miami
- Moffitt — Tampa
Massachusetts
- Massachusetts General Hospital — Boston
- Beth Israel Deaconess Medical Center — Boston
Michigan
- Barbara Ann Karmanos Cancer Institute — Detroit
- BAMF Health Inc. — Grand Rapids
New York
- New York University (NYU) Clinical Cancer Center — New York
- David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center — New York
Pennsylvania
- University of Pennsylvania — Philadelphia
- Fox Chase Cancer Center — Philadelphia
Texas
- Texas Oncology - DFW (Sammons CC) — Dallas
- Baylor College of Medicine — Houston
Indiana
- Indiana University (IU) School of Medicine — Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 241 participants |
| Start Date | 2025-10-22 |
| Est. Completion | 2033-03 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07213791
The ClinicalTrials.gov registry entry for NCT07213791 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 241 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 7 conditions, with Breast Neoplasms appearing as the primary indexed condition, and to 1 intervention — of which LY4337713 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: NCT07213791 reports 20 study locations spanning 13 distinct geographic areas — top geographies include California, Florida, Massachusetts. 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 NCT07213791 about?
NCT07213791 is a clinical study titled "A Study of LY4337713 in Participants With FAP-Positive Solid Tumors". This is a study of LY4337713 in participants with certain types of cancer that is advanced or has spread. Participants must have cancer with high levels of a protein called fibroblast activation protein (FAP). The purpose of this study is to evaluate safety, side effects, and efficacy of LY4337713. ...
What is the current status of trial NCT07213791?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 241 participants. The study started on 2025-10-22. Estimated completion is 2033-03.
What conditions does trial NCT07213791 study?
This clinical trial studies the following conditions: Breast Neoplasms, Cholangiocarcinoma, Colorectal Neoplasms, Ovarian Neoplasms, Esophageal Neoplasms. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07213791?
The interventions under investigation include: LY4337713 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07213791?
This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07213791 being conducted?
This trial has 20 study locations across California, Florida, Indiana, Maryland, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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