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Completed Phase 2 Interventional Results available

A Study of Atezolizumab in Participants With Locally Advanced or Metastatic Urothelial Bladder Cancer (Cohort 2)

ClinicalTrials.gov ID: NCT02108652

Public ClinicalTrials.gov record NCT02108652. 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 Sep 30, 2026, 1:06 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 II, Multicenter, Single-Arm Study of Atezolizumab in Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer

Brief summary

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

This Phase II, single-arm study is designed to evaluate the effect of atezolizumab treatment in participants with locally advanced or metastatic urothelial bladder cancer. Participants will be enrolled into 1 of 2 cohorts. Cohort 1 will consist of participants who are treatment-naïve and ineligible for cisplatin-containing chemotherapy. The results of Cohort 1 are reported separately (NCT02951767). Cohort 2 (reported here) will contain participants who have progressed during or following a prior platinum-based chemotherapy regimen. Participants in both cohorts will be given a 1200 milligrams (mg) intravenous (IV) dose of atezolizumab on Day 1 of 21-day cycles. Treatment of participants in Cohort 1 will continue until disease progression per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) or unmanageable toxicity. Treatment of participants in Cohort 2 will continue until loss of clinical benefit or unmanageable toxicity.

Study identification

NCT ID
NCT02108652
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
310 participants

Conditions and interventions

Conditions

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
May 31, 2014 (Actual)
Primary completion
Jul 4, 2016 (Actual)
Completion
Feb 28, 2023 (Actual)
Last update posted
Mar 28, 2024

2014 – 2023

United States locations

U.S. sites
47
U.S. states
24
U.S. cities
38
Facility City State ZIP Site status
University of Alabama At Birmingham Birmingham Alabama 35294 —
Pinnacle Oncology Hematology Scottsdale Arizona 85258 —
Arizona Oncology - HOPE Wilmot Tucson Arizona 85710 —
UCLA Los Angeles California 90024 —
The Angeles Clinic and Research Institute - W LA Office Los Angeles California 90025 —
USC Norris Cancer Center Los Angeles California 90033 —
UCSF San Francisco California 94143-0106 —
Kaiser Permanente - San Marcos San Marcos California 92069 —
Stanford Cancer Center Stanford California 94305-5820 —
Kaiser Permanente; Oncology Clinical Trials Vallejo California 94589 —
Rocky Mountain Cancer Center - Aurora Aurora Colorado 80012 —
University Of Colorado Aurora Colorado 80045 —
University of Connecticut Health Center Farmington Connecticut 06030 —
Yale Cancer Center ; Medical Oncology New Haven Connecticut 06520 —
Georgetown University Medical Center Lombardi Cancer Center Washington D.C. District of Columbia 20057 —
Mayo Clinic Cancer Center Jacksonville Florida 32224 —
Piedmont Cancer Institute, PC Atlanta Georgia 30318 —
University of Chicago; Hematology/Oncology Chicago Illinois 60637 —
Ingalls Memorial Hospital Harvey Illinois 60426 —
Indiana University Health; Goshen Center for Cancer Care Goshen Indiana 46526 —
Norton Cancer Institute Louisville Kentucky 40402 —
Massachusetts General Hospital;Oncology Boston Massachusetts 02114 —
Dana Farber Cancer Inst. ; Dept. of Medical Oncology Boston Massachusetts 02115 —
Beth Israel Deaconess Medical Center, Harvard Medical School; Department of Medicine Boston Massachusetts 02215 —
University of Michigan Comprehensive Cancer Center Ann Arbor Michigan 48109 —
Karmanos Cancer Institute Detroit Michigan 48201 —
Minnesota Oncology Minneapolis Minneapolis Minnesota 55404 —
Mayo Clinic - Rochester Rochester Minnesota 55905 —
Urology Cancer Center & GU Research Network Omaha Nebraska 68130 —
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89128 —
New York Oncology Hematology, P.C. Albany New York 12208 —
NYU Langone Medical Center New York New York 10016 —
Mount Sinai School of Medicine - Tisch Cancer Institute New York New York 10029 —
Memorial Sloan-Kettering Cancer Center New York New York 10065 —
Oncology Hematology Care Inc Cincinnati Ohio 45242 —
Case Western Reserve Univ; Hem/Onc Cleveland Ohio 44106 —
Cleveland Clinic Cleveland Ohio 44195 —
Willamette Valley Cancer Ctr - 520 Country Club Eugene Oregon 97401-8122 —
Kimmel Cancer Center Thomas Jefferson University Philadelphia Pennsylvania 19107 —
Sarah Cannon Cancer Center - Tennessee Oncology, Pllc Nashville Tennessee 37203 —
Ctr for Cancer and Blood Disorders Fort Worth Texas 76104 —
Texas Oncology - Houston (Gessner) Houston Texas 77024 —
Houston Methodist Hospital Houston Texas 77030 —
University of Texas Health Science Center at San Antonio San Antonio Texas 78229 —
Virginia Cancer Specialists, PC Fairfax Virginia 22031 —
Virginia Oncology Associates - Lake Wright Cancer Center Norfolk Virginia 23502 —
Seattle Cancer Care Alliance Seattle Washington 98109 —

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 30 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02108652, 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 Mar 28, 2024 · Synced Sep 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02108652 live on ClinicalTrials.gov.

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