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Completed Phase 2 Interventional

Study of Epratuzumab in Serologically-positive Systemic Lupus Erythematosus (SLE) Patients With Active Disease

ClinicalTrials.gov ID: NCT00624351

Public ClinicalTrials.gov record NCT00624351. 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, 9:56 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 IIb Randomized, Double-blind, Placebo-controlled, Dose and Dose Regimen-ranging Study of the Safety and Efficacy of Epratuzumab in Serologically-positive Systemic Lupus Erythematosus (SLE) Patients With Active Disease

Brief summary

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

The primary objective of the study is to assess the dose response and the dose frequency of epratuzumab in patients with SLE.

Study identification

NCT ID
NCT00624351
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Pharma
Industry
Enrollment
227 participants

Conditions and interventions

Interventions

Biological · 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
Jan 2008 (Type not available)
Primary completion
Aug 2009 (Actual)
Completion
Aug 2009 (Actual)
Last update posted
Sep 12, 2011

2008 – 2009

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Tucson Arizona — —
Not listed La Jolla California — —
Not listed Los Angeles California — —
Not listed San Leandro California — —
Not listed Denver Colorado — —
Not listed Farmington Connecticut — —
Not listed Aventura Florida — —
Not listed Tampa Florida — —
Not listed Baltimore Maryland — —
Not listed Brooklyn New York — —
Not listed Chapel Hill North Carolina — —
Not listed Charlotte North Carolina — —
Not listed Durham North Carolina — —
Not listed Wilmington North Carolina — —
Not listed Oklahoma City Oklahoma — —
Not listed Dallas Texas — —
Not listed Arlington Virginia — —
Not listed Milwaukee Wisconsin — —

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 34 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00624351, 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 12, 2011 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00624351 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →