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Completed Phase 2 Interventional

Efficacy and Safety of ABT-874 in Subjects With Moderate to Severe Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT00292396

Public ClinicalTrials.gov record NCT00292396. 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 Sep 2, 2026, 10:06 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 Phase 2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study Comparing the Safety and Efficacy of Subcutaneous Injections of ABT-874 vs. Placebo in Subjects With Moderate to Severe Chronic Plaque Psoriasis

Brief summary

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

The purpose of the study is to assess the safety and efficacy of ABT-874 in the treatment of moderate to severe chronic plaque psoriasis.

Study identification

NCT ID
NCT00292396
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AbbVie (prior sponsor, Abbott)
Industry
Enrollment
180 participants

Conditions and interventions

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
Oct 31, 2005
Primary completion
Mar 31, 2008
Completion
Mar 31, 2008
Last update posted
Jan 17, 2013

2005 – 2008

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Site Reference ID/Investigator# 3351 San Diego California 92123
Site Reference ID/Investigator# 3347 Alpharetta Georgia 30022
Site Reference ID/Investigator# 3348 Skokie Illinois 60077
Site Reference ID/Investigator# 993 Indianapolis Indiana 46256
Site Reference ID/Investigator# 990 Boston Massachusetts 02114
Site Reference ID/Investigator# 3349 St Louis Missouri 63117
Site Reference ID/Investigator# 992 Cincinnati Ohio 45219
Site Reference ID/Investigator# 991 Lake Oswego Oregon 97035
Site Reference ID/Investigator# 3367 Portland Oregon 97223
Site Reference ID/Investigator# 3346 Johnston Rhode Island 02919
Site Reference ID/Investigator# 994 Nashville Tennessee 37215
Site Reference ID/Investigator# 3350 Dallas Texas 75246-1613
Site Reference ID/Investigator# 796 Houston Texas 77030
Site Reference ID/Investigator# 2081 Salt Lake City Utah 84132
Site Reference ID/Investigator# 3366 Norfolk Virginia 23507
Site Reference ID/Investigator# 989 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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00292396, 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 Jan 17, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00292396 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →