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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 Oct 23, 2026, 6:30 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 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)

Brief summary

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

The purpose of this study is to evaluate the efficacy (improvement of signs and symptoms) and safety of ustekinumab in patients with psoriatic arthritis.

Study identification

NCT ID
NCT01077362
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
312 participants

Conditions and interventions

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 2010 (Type not available)
Primary completion
Mar 2012 (Actual)
Completion
Nov 2012 (Actual)
Last update posted
Feb 27, 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 27, 2014 · Synced Oct 23, 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 public registry record, listed eligibility criteria, and available contact information for NCT01077362 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →