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Terminated Phase 2 Interventional

Study of BMS-587101 in Patients With Moderate to Severe Psoriasis

ClinicalTrials.gov ID: NCT00162253

Public ClinicalTrials.gov record NCT00162253. 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 19, 2026, 11:19 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

Randomized, Double-Blind, Placebo-Controlled, Multiple Dose Study of BMS-587101 in Patients With Moderate to Severe Psoriasis

Brief summary

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

The purpose of this clinical research study is to learn if BMS-587101 is effective on the treatment of Moderate to Severe Psoriasis. The safety of this treatment will also be studied.

Study identification

NCT ID
NCT00162253
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
120 participants

Conditions and interventions

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
Apr 2005 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Not listed
Last update posted
Mar 2, 2010

Started 2005

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Local Institution Phoenix Arizona — —
Local Institution Tucson Arizona — —
Local Institution San Diego California — —
Local Institution Miami Beach Florida — —
Local Institution Pinellas Park Florida — —
Local Institution Boise Idaho — —
Local Institution Fridley Minnesota — —
Local Institution St Louis Missouri — —
Local Institution New Brunswick New Jersey — —
Local Institution New York New York — —
Local Institution Winston-Salem North Carolina — —
Local Institution Columbus Ohio — —
Local Institution Portland Oregon — —
Local Institution Philadelphia Pennsylvania — —
Local Institution Greer South Carolina — —
Local Institution 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00162253, 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 Mar 2, 2010 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00162253 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →