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Completed Phase 3 Interventional Results available

Open Label Study of Adalimumab in Subjects Who Have a Sub-optimal Response to Systemic Therapy or Phototherapy

ClinicalTrials.gov ID: NCT00566722

Public ClinicalTrials.gov record NCT00566722. 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 24, 2026, 8:44 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

The objective of this study was to evaluate the safety and efficacy profile of Humira (adalimumab) in patients who had a sub-optimal response to prior systemic therapy. This open-label study was conducted in a patient population of moderate to severe chronic plaque psoriasis patients, which is an approved patient population for adalimumab.

Study identification

NCT ID
NCT00566722
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Abbott
Industry
Enrollment
152 participants

Conditions and interventions

Conditions

Interventions

Biological

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
Jan 2008 (Type not available)
Primary completion
Apr 2009 (Actual)
Completion
Apr 2009 (Actual)
Last update posted
Apr 12, 2011

2008 – 2009

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Total Skin and Beauty Dermatology Centers Birmingham Alabama 35205 —
Dermatology Research of Arkansas Little Rock Arkansas 72205 —
Therapeutics Clinical Research San Diego California 92123 —
Florida Academic Dermatology Centers Miami Florida 33136 —
Peachtree Dermatology Associates Atlanta Georgia 30327 —
Dawes Fretzin Clinical Research Group Indianapolis Indiana 46256 —
ORA Clinical Research and Development Andover Massachusetts 01810 —
New York University School of Medicine New York New York 10016 —
Mount Sinai School of Medicine New York New York 10029 —
Montifiore Medical Center The Bronx New York 10467 —
Paddington Testing Co. Philadelphia Pennsylvania 19103 —
Clinical Partners Johnston Rhode Island 02919 —
Radiant Research Greer South Carolina 29651 —
Dermatology Treatment & Research Center, PA Research Dallas Texas 75230 —
Baylor Research Institute Dallas Texas 75246 —
Center for Clinical Studies Houston Texas 77058 —
Virginia Clinical Research, Inc. Norfolk Virginia 23507 —
Dermatology Associates Seattle Washington 98101 —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00566722, 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 Apr 12, 2011 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00566722 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →