Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
A Study of Vepugratinib (LY3866288) in Participants With Cancer in the Urinary Tract
NCT07218380 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to test a new medicine, vepugratinib, in comparison with placebo, to see if it is safe and can help people with a bladder cancer that is advanced or has spread. Vepugratinib or placebo will be administered in combination with enfortumab vedotin and pembrolizumab. Study participation could last up to approximately 6 years.
Conditions Studied
Interventions
- DRUG Pembrolizumab
- OTHER Placebo
- DRUG EV
- DRUG Vepugratinib
Study Locations (20)
California
- Chao Family Comprehensive Cancer Center and Ambulatory Care (CIACC) - Irvine — Irvine
- TRIO-US (Translational Research in Oncology-US) — Los Angeles
- UCLA Hematology/Oncology - Santa Monica — Los Angeles
- University of California, Irvine (UCI) Health - UC Irvine Medical Center — Orange
- University of California Davis (UC Davis) Comprehensive Cancer Center — Sacramento
- UCSF Medical Center at Mission Bay — San Francisco
- Hunt Cancer Institute, an Affiliate of Cedars-Sinai Cancer (TMPN) — Torrance
Indiana
- Parkview Research Center at Parkview Regional Medical Center — Fort Wayne
- Indiana University Melvin and Bren Simon Cancer Center — Indianapolis
- Franciscan Health — Indianapolis
Colorado
- AdventHealth Medical Group - Porter — Denver
- Colorado West Healthcare System - Grand Valley Oncology — Grand Junction
Illinois
- University of Illinois at Chicago — Chicago
- University of Chicago Medical Center — Chicago
Alabama
- Clearview Cancer Institute — Huntsville
Arizona
- The University of Arizona Cancer Center - North Campus — Tucson
Florida
- AdventHealth Orlando — Orlando
Idaho
- St. Luke's Cancer Institute: Boise — Boise
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 450 participants |
| Start Date | 2025-12-12 |
| Est. Completion | 2033-05 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07218380
The ClinicalTrials.gov registry entry for NCT07218380 describes a study currently listed as recruiting. It is categorized as Phase 3, 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 450 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 3 conditions, with Neoplasm Metastasis appearing as the primary indexed condition, and to 4 interventions — of which Pembrolizumab 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: NCT07218380 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Indiana, Colorado. 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 NCT07218380 about?
NCT07218380 is a clinical study titled "A Study of Vepugratinib (LY3866288) in Participants With Cancer in the Urinary Tract". The purpose of this study is to test a new medicine, vepugratinib, in comparison with placebo, to see if it is safe and can help people with a bladder cancer that is advanced or has spread. Vepugratinib or placebo will be administered in combination with enfortumab vedotin and pembrolizumab. Study...
What is the current status of trial NCT07218380?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 450 participants. The study started on 2025-12-12. Estimated completion is 2033-05.
What conditions does trial NCT07218380 study?
This clinical trial studies the following conditions: Neoplasm Metastasis, Urinary Bladder Neoplasms, Carcinoma, Transitional Cell. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07218380?
The interventions under investigation include: Pembrolizumab (DRUG), Placebo (OTHER), EV (DRUG), Vepugratinib (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07218380?
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 NCT07218380 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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