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COMPLETED Phase 2

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

NCT00624351 · View on ClinicalTrials.gov ↗

Study Summary

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

Interventions

  • OTHER Placebo
  • BIOLOGICAL Epratuzumab

Study Locations (20)

North Carolina

  • — Chapel Hill
  • — Charlotte
  • — Durham
  • — Wilmington

California

  • — La Jolla
  • — Los Angeles
  • — San Leandro

Florida

  • — Aventura
  • — Tampa

Alabama

  • — Birmingham

Arizona

  • — Tucson

Colorado

  • — Denver

Connecticut

  • — Farmington

Maryland

  • — Baltimore

Trial Details

FieldValue
Enrollment Target 227 participants
Start Date 2008-01
Est. Completion 2009-08
Phase Phase 2

Sponsor

UCB Pharma

20 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00624351

The ClinicalTrials.gov registry entry for NCT00624351 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 227 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UCB Pharma, which has 20 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Systemic Lupus Erythematosus appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00624351 reports 20 study locations spanning 14 distinct geographic areas — top geographies include North Carolina, California, Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00624351 about?

NCT00624351 is a clinical study titled "Study of Epratuzumab in Serologically-positive Systemic Lupus Erythematosus (SLE) Patients With Active Disease". The primary objective of the study is to assess the dose response and the dose frequency of epratuzumab in patients with SLE.

What is the current status of trial NCT00624351?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 227 participants. The study started on 2008-01. Estimated completion is 2009-08.

What conditions does trial NCT00624351 study?

This clinical trial studies the following conditions: Systemic Lupus Erythematosus. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00624351?

The interventions under investigation include: Placebo (OTHER), Epratuzumab (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00624351?

This trial is sponsored by UCB Pharma, which has 20 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00624351 being conducted?

This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial