OncoMatch/Clinical Trials/NCT07213791
A Study of LY4337713 in Participants With FAP-Positive Solid Tumors
Is NCT07213791 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies LY4337713 for ovarian neoplasms.
Treatment: LY4337713 — 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.
Check if I qualifyExtracted eligibility criteria
Cancer type
Ovarian Cancer
Breast Carcinoma
Colorectal Cancer
Esophageal Carcinoma
Gastric Cancer
Cholangiocarcinoma
Biomarker criteria
Required: FAP expression (clinical or imaging evidence per local assessment)
Disease stage
Metastatic disease required
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: systemic therapy — locally advanced unresectable or metastatic disease
Adenocarcinoma of the pancreas: Participants must have received at least 1, but no more than 2 prior regimens for locally advanced unresectable or metastatic disease.
Must have received: systemic therapy — advanced or metastatic disease
HR-positive HER2-negative breast cancer: Participants must have received less than or equal to (≤)5 prior lines of treatment for advanced or metastatic disease, which must include a cyclin-dependent kinase 4/6 inhibitor.
Must have received: HER2-targeted therapy — metastatic disease
HER2-positive breast cancer: Participants must have received at least 2 lines of HER2-targeted therapy, which should include at least 1 antibody-drug conjugate (ADC) for metastatic disease (if locally available).
Must have received: systemic therapy — metastatic disease
TNBC: Participants must have received at least 2 lines of therapy for metastatic disease.
Must have received: platinum-based chemotherapy — platinum-resistant or refractory ovarian cancer
Platinum-resistant or refractory ovarian cancer: Participants must have received or after at least 1 platinum-based therapy.
Must have received: systemic therapy — advanced or metastatic disease
Other solid tumors (gastric cancer, CRC, esophageal and cholangiocarcinoma): Participants must have received greater than or equal to (≥)1 prior line of systemic therapy for advanced or metastatic disease; including prior line(s) in combination with immunotherapy or vascular endothelial growth factor inhibitor.
Must have received: systemic therapy — advanced or metastatic solid tumors
Phase 1b: Participants must have advanced or metastatic solid tumors and have received ≥1 prior line of therapy.
Cannot have received: adoptive T-cell therapy (CAR-T cell therapy, T-cell receptor (TCR) therapy)
Had previous adoptive T-cell therapy (e.g., chimeric antigen receptor T-cell [CAR-T therapy, T-cell receptor [TCR] therapy, etc.])
Cannot have received: radiation therapy
Had previous hemi- or total-body radiation
Lab requirements
Kidney function
Measured creatinine clearance ≥60 milliliters per minute (mL/min)
Cardiac function
Significant cardiovascular disease; QTcF >470 milliseconds (msec) during screening
Have significant cardiovascular disease; Have prolongation of the corrected QTcF >470 milliseconds (msec) during screening
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Hoag Memorial Hospital Presbyterian · Newport Beach, California
- Stanford University Medical Center · Stanford, California
- Biogenix Molecular, LLC · Miami, Florida
- Moffitt · Tampa, Florida
- Indiana University (IU) School of Medicine · Indianapolis, Indiana
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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