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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 Oct 27, 2026, 3:42 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 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)

Brief summary

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

The overall purpose of this trial is to assess clinical efficacy and safety of different subcutaneous doses of BI 655066 in adult patients with chronic plaque psoriasis in order to select doses for further clinical trials.

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

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
Feb 2014 (Type not available)
Primary completion
Nov 2014 (Actual)
Completion
Jul 2015 (Actual)
Last update posted
Sep 19, 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 19, 2016 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02054481 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →