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Completed Phase 3 Interventional

Open-label Study to Evaluate Safety of Multiple Courses of IM Alefacept During Treatment of Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT00692172

Public ClinicalTrials.gov record NCT00692172. 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, 6:25 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

An Open-Label, Multi-center Study to Evaluate the Safety and Tolerability of Intramuscular Administration of Alefacept (LFA-3/IgG1 Fusion Protein) in Subjects With Chronic Plaque Psoriasis Who Have Completed Studies C99-717 or C99-712

Brief summary

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

An extension study to evaluate safety and tolerability of up to 3 additional courses of IM alefacept in patients with chronic plaque psoriasis who have been previously treated with 1 or 2 courses of IM alefacept.

Study identification

NCT ID
NCT00692172
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
175 participants

Conditions and interventions

Conditions

Interventions

Drug

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
Nov 30, 2001
Primary completion
Oct 31, 2004
Completion
Oct 31, 2004
Last update posted
Sep 17, 2014

2001 – 2004

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
Not listed Hot Springs Arkansas 71913
Not listed Fresno California 93710
Not listed La Jolla California 92037
Not listed Washington D.C. District of Columbia 20010
Not listed Jacksonville Florida 32204
Not listed Pinellas Park Florida 33781
Not listed Newnan Georgia 30263
Not listed Chicago Illinois 60611
Not listed Kansas City Kansas 66160
Not listed Clinton Township Michigan 48038
Not listed St Louis Missouri 63110
Not listed Omaha Nebraska 68131
Not listed Berlin New Jersey 08009
Not listed Lake Oswego Oregon 79035
Not listed Portland Oregon 97210
Not listed Johnston Rhode Island 02919
Not listed Goodlettsville Tennessee 37072
Not listed Austin Texas 78759
Not listed San Antonio Texas 78229

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00692172, 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 17, 2014 · Synced Sep 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00692172 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →