ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional Results available

An Efficacy and Safety Study of Erdafitinib (JNJ-42756493) in Participants With Urothelial Cancer

ClinicalTrials.gov ID: NCT02365597

Public ClinicalTrials.gov record NCT02365597. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Apr 23, 2026, 11:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Two-arm Multicenter, Open-Label Study to Determine the Efficacy and the Safety of Two Different Dose Regimens of a Pan-FGFR Tyrosine Kinase Inhibitor JNJ-42756493 in Subjects With Metastatic or Surgically Unresectable Urothelial Cancer With FGFR Genomic Alterations

Study identification

NCT ID
NCT02365597
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
239 participants

Conditions and interventions

Interventions

  • Erdafitinib Drug
  • Metformin Drug
  • Midazolam Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 21, 2015
Primary completion
Sep 14, 2022
Completion
Mar 30, 2027
Last update posted
Apr 12, 2026

2015 – 2027

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
25
Facility City State ZIP Site status
Not listed Sedona Arizona
Not listed Los Angeles California
Not listed Orange California
Not listed Sacramento California
Not listed Stanford California
Not listed Aurora Colorado
Not listed Washington D.C. District of Columbia
Not listed Chicago Illinois
Not listed Iowa City Iowa
Not listed Louisville Kentucky
Not listed Minneapolis Minnesota
Not listed Omaha Nebraska
Not listed Las Vegas Nevada
Not listed New York New York
Not listed Charlotte North Carolina
Not listed Medford Oregon
Not listed Tualatin Oregon
Not listed Hershey Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Myrtle Beach South Carolina
Not listed Nashville Tennessee
Not listed Dallas Texas
Not listed Denton Texas
Not listed Houston Texas
Not listed Hampton Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 80 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02365597, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 12, 2026 · Synced Apr 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02365597 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →