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Completed Phase 3 Interventional Results available

A Study of the Safety and Efficacy of Ustekinumab in Patients With Psoriatic Arthritis With and Without Prior Exposure to Anti-TNF Agents

ClinicalTrials.gov ID: NCT01077362

Public ClinicalTrials.gov record NCT01077362. 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 19, 2026, 6:25 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 Multicenter, Randomized, Double-blind, Placebo-controlled Trial of Ustekinumab, a Fully Human Anti-IL-12/23p40 Monoclonal Antibody, Administered Subcutaneously, in Subjects With Active Psoriatic Arthritis Including Those Previously Treated With Biologic Anti-TNFalpha Agent(s)

Study identification

NCT ID
NCT01077362
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Research & Development, LLC
Industry
Enrollment
312 participants

Conditions and interventions

Interventions

  • placebo Drug
  • ustekinumab 45 mg Drug
  • ustekinumab 90 mg Drug

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
Feb 28, 2010
Primary completion
Feb 29, 2012
Completion
Oct 31, 2012
Last update posted
Feb 26, 2014

2010 – 2012

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
25
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Huntsville Alabama
Not listed Los Angeles California
Not listed San Diego California
Not listed Denver Colorado
Not listed Trumbull Connecticut
Not listed Tampa Florida
Not listed Indianapolis Indiana
Not listed New Orleans Louisiana
Not listed Wheaton Maryland
Not listed Boston Massachusetts
Not listed Worcester Massachusetts
Not listed Edina Minnesota
Not listed Clayton Missouri
Not listed St Louis Missouri
Not listed Omaha Nebraska
Not listed Freehold New Jersey
Not listed Orchard Park New York
Not listed Rochester New York
Not listed Cleveland Ohio
Not listed Tulsa Oklahoma
Not listed Portland Oregon
Not listed Duncansville Pennsylvania
Not listed West Reading Pennsylvania
Not listed Dallas Texas

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 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01077362, 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 Feb 26, 2014 · Synced May 19, 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 NCT01077362 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →