ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Gemcitabine Hydrochloride and Eribulin Mesylate in Treating Patients With Bladder Cancer That is Advanced or Cannot Be Removed by Surgery

ClinicalTrials.gov ID: NCT02178241

Public ClinicalTrials.gov record NCT02178241. 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 May 18, 2026, 4:45 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

Phase II Trial of Gemcitabine-Eribulin (GE) in Cisplatin Ineligible Patients With Advanced or Unresectable Urothelial Carcinoma of the Bladder

Study identification

NCT ID
NCT02178241
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
National Cancer Institute (NCI)
NIH
Enrollment
26 participants

Conditions and interventions

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
Dec 10, 2014
Primary completion
Mar 17, 2019
Completion
Jul 10, 2019
Last update posted
Dec 15, 2019

2014 – 2019

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
City of Hope Comprehensive Cancer Center Duarte California 91010
Los Angeles County-USC Medical Center Los Angeles California 90033
USC / Norris Comprehensive Cancer Center Los Angeles California 90033
Keck Medical Center of USC Pasadena Pasadena California 91105
University of California Davis Comprehensive Cancer Center Sacramento California 95817
University of Colorado Hospital Aurora Colorado 80045
MedStar Georgetown University Hospital Washington D.C. District of Columbia 20007
Moffitt Cancer Center P2C Tampa Florida 33612
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
UC Comprehensive Cancer Center at Silver Cross New Lenox Illinois 60451
Mayo Clinic Cancer Center P2C Rochester Minnesota 55905
Roswell Park Cancer Institute Buffalo New York 14263
Case Western Reserve University Cleveland Ohio 44106
Cleveland Clinic Foundation Cleveland Ohio 44195
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210
University of Pittsburgh Cancer Institute (UPCI) Pittsburgh Pennsylvania 15232
University of Texas M D Anderson Cancer Center P2C Houston Texas 77030

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02178241, 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 Dec 15, 2019 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02178241 live on ClinicalTrials.gov.

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