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Completed Phase 3 Interventional Results available

A Study of Ustekinumab to Evaluate a "Subject-tailored" Maintenance Dosing Approach in Subjects With Moderate-to-Severe Plaque Psoriasis

ClinicalTrials.gov ID: NCT01550744

Public ClinicalTrials.gov record NCT01550744. 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 Jul 22, 2026, 6:48 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 3b, Randomized, Double-blind, Active-controlled, Multicenter Study to Evaluate a "Subject-tailored" Maintenance Dosing Approach in Subjects With Moderate-to-Severe Plaque Psoriasis

Study identification

NCT ID
NCT01550744
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Janssen Biotech, Inc.
Industry
Enrollment
478 participants

Conditions and interventions

Conditions

Interventions

  • Ustekinumab 45 mg Drug
  • Ustekinumab 90 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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
Feb 29, 2012
Primary completion
Apr 30, 2015
Completion
Jun 30, 2015
Last update posted
Feb 8, 2017

2012 – 2015

United States locations

U.S. sites
40
U.S. states
28
U.S. cities
40
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Bakersfield California
Not listed Irvine California
Not listed Los Angeles California
Not listed San Diego California
Not listed San Francisco California
Not listed Santa Monica California
Not listed Denver Colorado
Not listed Bridgeport Connecticut
Not listed Coral Gables Florida
Not listed Saint Augustine Florida
Not listed Tampa Florida
Not listed Chicago Illinois
Not listed Indianapolis Indiana
Not listed Plainfield Indiana
Not listed Louisville Kentucky
Not listed New Orleans Louisiana
Not listed Boston Massachusetts
Not listed Troy Michigan
Not listed Fridley Minnesota
Not listed St Louis Missouri
Not listed Henderson Nevada
Not listed Lebanon New Hampshire
Not listed East Windsor New Jersey
Not listed New York New York
Not listed The Bronx New York
Not listed Williamsville New York
Not listed Gahanna Ohio
Not listed Norman Oklahoma
Not listed Portland Oregon
Not listed Pittsburgh Pennsylvania
Not listed Yardley Pennsylvania
Not listed Johnston Rhode Island
Not listed Nashville Tennessee
Not listed Arlington Texas
Not listed Dallas Texas
Not listed Salt Lake City Utah
Not listed Norfolk Virginia
Not listed Spokane Washington
Not listed Clarksburg West Virginia

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01550744, 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 8, 2017 · Synced Jul 22, 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 NCT01550744 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →