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Completed Phase 2 Interventional Results available

A Study to Evaluate the Safety and Effectiveness of Ustekinumab or Golimumab Administered Subcutaneously (SC) in Patients With Sarcoidosis

ClinicalTrials.gov ID: NCT00955279

Public ClinicalTrials.gov record NCT00955279. 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 Jun 25, 2026, 12:38 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 2, Multicenter, Randomized, Double-Blind, Parallel-group, Placebo-controlled Study Evaluating the Safety and Efficacy of Treatment With Ustekinumab or Golimumab in Subjects With Chronic Sarcoidosis

Study identification

NCT ID
NCT00955279
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Centocor, Inc.
Industry
Enrollment
173 participants

Conditions and interventions

Conditions

Interventions

  • Placebo Drug
  • Golimumab Drug
  • Ustekinumab Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Oct 31, 2009
Primary completion
Apr 30, 2012
Completion
Jul 31, 2012
Last update posted
Jul 16, 2014

2009 – 2012

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Los Angeles California
Not listed Denver Colorado
Not listed New Haven Connecticut
Not listed Chicago Illinois
Not listed Baltimore Maryland
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed St Louis Missouri
Not listed Lebanon New Hampshire
Not listed New York New York
Not listed Chapel Hill North Carolina
Not listed Charlotte North Carolina
Not listed Greenville North Carolina
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Charleston South Carolina
Not listed Spartanburg South Carolina
Not listed Memphis Tennessee
Not listed Dallas Texas
Not listed Colchester Vermont

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 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00955279, 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 Jul 16, 2014 · Synced Jun 25, 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 NCT00955279 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →