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Completed Phase 3 Interventional Results available

A Study Comparing Nivolumab, Nivolumab in Combination With Ipilimumab and Placebo in Participants With Localized Kidney Cancer Who Underwent Surgery to Remove Part of a Kidney

ClinicalTrials.gov ID: NCT03138512

Public ClinicalTrials.gov record NCT03138512. 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 20, 2026, 10:46 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 3 Randomized, Double-Blind Study of Nivolumab Monotherapy or Nivolumab Combined With Ipilimumab vs Placebo in Participants With Localized Renal Cell Carcinoma Who Underwent Radical or Partial Nephrectomy and Who Are at High Risk of Relapse

Study identification

NCT ID
NCT03138512
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
1,641 participants

Conditions and interventions

Interventions

  • ipilimumab Biological
  • ipilimumab placebo Drug
  • nivolumab Biological
  • nivolumab placebo Drug

Biological · 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
Jul 6, 2017
Primary completion
Sep 27, 2023
Completion
Jan 31, 2024
Last update posted
Dec 17, 2024

2017 – 2024

United States locations

U.S. sites
21
U.S. states
15
U.S. cities
18
Facility City State ZIP Site status
Local Institution - 0019 Birmingham Alabama 35205
Local Institution - 0056 Springdale Arkansas 72762
Local Institution - 0186 Los Angeles California 90048
Local Institution - 0180 Los Angeles California 90095
Local Institution - 0002 San Francisco California 94115
Local Institution - 0185 Aurora Colorado 80045
Local Institution - 0016 Athens Georgia 30607
Local Institution - 0005 Chicago Illinois 60611
Local Institution Chicago Illinois 60612
Local Institution - 0006 St Louis Missouri 63110
Local Institution - 0012 Howell Township New Jersey 07731
Local Institution - 0007 Buffalo New York 14263
Local Institution - 0181 New York New York 10029
Local Institution - 0001 New York New York 10065
Local Institution - 0008 Columbus Ohio 43210
Local Institution - 0009 Portland Oregon 97213
Local Institution - 0010 Allentown Pennsylvania 18103
Local Institution - 0014 Greenville South Carolina 29607
Local Institution - 0013 Chattanooga Tennessee 37404
Local Institution - 0183 Nashville Tennessee 37212
Local Institution - 0057 Fairfax Virginia 22031

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 179 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03138512, 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 17, 2024 · Synced May 20, 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 NCT03138512 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →