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Study details
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A Study of LY4337713 in Participants With FAP-Positive Solid Tumors

Eli Lilly and Company
NCT IDNCT07213791ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

241

Study length

about 7.4 years

Ages

18+

Locations

20 sites in CA, FL, IN +10

What this study is about

This trial is testing a treatment called LY4337713 for people with certain types of cancer that have spread or are advanced. The goal is to see if the treatment is safe, what side effects it might cause, and how well it works. Each participant will be in it for about 5 years.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take LY4337713

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Phase 1a: Percentage of Participants with Dose Limited Toxicity (DLT) Toxicities, Phase 1b: Objective Response Rate (ORR): Percentage of Participants with Best Response of Complete Response (CR) or Partial Response (PR)

Secondary: Phase 1a and 1b: Duration of Response (DOR), Phase 1a and 1b: Percentage of Participants with Disease Control Rate (DCR), Phase 1a and 1b: Time to Response (TTR), Phase 1a: Number of Participants with Best Overall Response (BOR), Phase 1a: Objective Response Rate (ORR): Percentage of Participants with Best Response of Complete Response (CR) or Partial Response (PR), Phase 1a: PK: Area Under the Concentration Time Curve (AUC) of LY4337713, Phase 1a: Pharmacokinetics (PK): Maximum Concentration (Cmax) of LY4337713

Body systems

Oncology