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Terminated Phase 3 Interventional

Study of Epratuzumab in Systemic Lupus Erythematosus (SLE)

ClinicalTrials.gov ID: NCT00383214

Public ClinicalTrials.gov record NCT00383214. 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 21, 2026, 8:20 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 III, Randomized, Double Blind, Placebo Controlled, Multi-Center Study of Epratuzumab in Patients With Active Systemic Lupus Erythematosus.

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of Epratuzumab with standard treatments for patients with SLE.

Study identification

NCT ID
NCT00383214
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Pharma
Industry
Enrollment
54 participants

Conditions and interventions

Interventions

Drug · Other

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
May 2005 (Type not available)
Primary completion
Mar 2007 (Actual)
Completion
Mar 2007 (Actual)
Last update posted
Jun 7, 2012

2005 – 2007

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
25
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Tucson Arizona — —
Not listed Los Angeles California — —
Not listed Upland California — —
Not listed Colorado Springs Colorado — —
Not listed Denver Colorado — —
Not listed Farmington Connecticut — —
Not listed Washington D.C. District of Columbia — —
Not listed Aventura Florida — —
Not listed Chicago Illinois — —
Not listed Baltimore Maryland — —
Not listed New York New York — —
Not listed Plainview New York — —
Not listed Rochester New York — —
Not listed Syracuse New York — —
Not listed The Bronx New York — —
Not listed Durham North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Gallipolis Ohio — —
Not listed Tulsa Oklahoma — —
Not listed Philadelphia Pennsylvania — —
Not listed Charleston South Carolina — —
Not listed Dallas Texas — —
Not listed Arlington Virginia — —
Not listed Edmonds 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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00383214, 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 Jun 7, 2012 · Synced Oct 21, 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 public registry record, listed eligibility criteria, and available contact information for NCT00383214 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →