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Completed Phase 2 Interventional Results available

A Study of Nivolumab in Participants With Metastatic or Unresectable Bladder Cancer

ClinicalTrials.gov ID: NCT02387996

Public ClinicalTrials.gov record NCT02387996. 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 Oct 21, 2026, 9:04 PM 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 II Single Arm Clinical Trial of Nivolumab (BMS-936558) in Subjects With Metastatic or Unresectable Urothelial Cancer Who Have Progressed or Recurred Following Treatment With a Platinum Agent

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose the study is to measure the effect of nivolumab (BMS-936558) in reducing tumor size in subjects with metastatic or unresectable bladder cancer.

Study identification

NCT ID
NCT02387996
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
270 participants

Conditions and interventions

Interventions

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
Mar 9, 2015 (Actual)
Primary completion
Apr 15, 2016 (Actual)
Completion
Nov 12, 2021 (Actual)
Last update posted
Nov 1, 2022

2015 – 2021

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Local Institution - 0013 Phoenix Arizona 85054 —
Local Institution - 0012 Duarte California 91010-3000 —
Pacific Hematology Oncology Associates San Francisco California 94115 —
Local Institution - 0016 Aurora Colorado 80045 —
University Cancer Blood Ctr Athens Georgia 30607 —
Ft. Wayne Med Onco-Hema Inc Fort Wayne Indiana 46804 —
Local Institution - 0030 Indianapolis Indiana 46202 —
Local Institution - 0052 Iowa City Iowa 55242 —
Crescent City Research Consortium, LLC Marrero Louisiana 70072 —
Karmanos Cancer Institute Detroit Michigan 48201-2014 —
GU Research Network, LLC Omaha Nebraska 68130 —
Local Institution - 0028 New York New York 10029 —
Local Institution - 0004 Charlotte North Carolina 28204 —
Local Institution - 0051 Portland Oregon 97213 —
Local Institution - 0029 Philadelphia Pennsylvania 19111-2412 —
Local Institution - 0059 Pittsburgh Pennsylvania 15212-0000 —
Erlanger Oncology & Hematology - Univ. of TN Chattanooga Tennessee 37404 —
Local Institution - 0001 Houston Texas 77030 —
Local Institution - 0036 Seattle Washington 98101 —

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 48 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02387996, 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 Nov 1, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02387996 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →