Skip to content
Study details
Enrolling now

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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take LY4337713
PhasePhase 1
Primary goalPhase 1a: Percentage of Participants with Dose Limited Toxicity (DLT) Toxicities

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low8%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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