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Completed Phase 2 Interventional Results available

BI 655066 Dose Ranging in Psoriasis, Active Comparator Ustekinumab

ClinicalTrials.gov ID: NCT02054481

Public ClinicalTrials.gov record NCT02054481. 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 11, 2026, 3:31 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 48 Weeks Study of Three Different Dose Regimens of BI 655066 Administered Subcutaneously in Patients With Moderate to Severe Chronic Plaque Psoriasis (Randomised, Dose-ranging, Active-comparator-controlled (Ustekinumab), Double-blind Within Dose Groups of BI 655066)

Study identification

NCT ID
NCT02054481
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
166 participants

Conditions and interventions

Conditions

Interventions

  • BI 655066 Drug
  • Ustekinumab Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 75 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
Jan 31, 2014
Primary completion
Oct 31, 2014
Completion
Jun 30, 2015
Last update posted
Sep 18, 2016

2014 – 2015

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
1311.2.10010 Boehringer Ingelheim Investigational Site Los Angeles California
1311.2.10013 Boehringer Ingelheim Investigational Site Port Orange Florida
1311.2.10003 Boehringer Ingelheim Investigational Site Arlington Hts Illinois
1311.2.10002 Boehringer Ingelheim Investigational Site Bay City Michigan
1311.2.10004 Boehringer Ingelheim Investigational Site Fridley Minnesota
1311.2.10001 Boehringer Ingelheim Investigational Site East Windsor New Jersey
1311.2.10009 Boehringer Ingelheim Investigational Site Verona New Jersey
1311.2.10007 Boehringer Ingelheim Investigational Site Raleigh North Carolina
1311.2.10005 Boehringer Ingelheim Investigational Site Portland Oregon
1311.2.10006 Boehringer Ingelheim Investigational Site Dallas Texas
1311.2.10011 Boehringer Ingelheim Investigational Site Houston Texas
1311.2.10012 Boehringer Ingelheim Investigational Site Spokane Washington

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02054481, 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 Sep 18, 2016 · Synced May 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02054481 live on ClinicalTrials.gov.

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