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Completed Phase 2 Interventional Results available

A Continuation Trial for Subjects With Systemic Lupus Erythematosus That Have Completed Protocol LBSL02

ClinicalTrials.gov ID: NCT00583362

Public ClinicalTrials.gov record NCT00583362. 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 28, 2026, 10:57 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

A Multi-Center, Open-Label, Continuation Trial LymphoStat-B™ Antibody (Monoclonal Anti-BLyS Antibody) in Subjects With Systemic Lupus Erythematosus (SLE) Who Completed the Phase 2 Protocol LBSL02

Brief summary

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

This is a continuation study to evaluate the long-term safety and efficacy of LymphoStat-B™ in subjects with SLE disease, that completed study LBSL02 and benefitted from treatment.

Study identification

NCT ID
NCT00583362
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
298 participants

Conditions and interventions

Interventions

Biological

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 4, 2005 (Actual)
Primary completion
Feb 23, 2016 (Actual)
Completion
Feb 23, 2016 (Actual)
Last update posted
Jul 23, 2019

2005 – 2016

United States locations

U.S. sites
56
U.S. states
28
U.S. cities
51
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Scottsdale Arizona 85260 —
GSK Investigational Site Tucson Arizona 85724 —
GSK Investigational Site La Jolla California 92037 —
GSK Investigational Site Los Angeles California 90033 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Sacramento California 95817 —
GSK Investigational Site San Jose California 95124 —
GSK Investigational Site Upland California 91786 —
GSK Investigational Site Colorado Springs Colorado 80920 —
GSK Investigational Site Washington D.C. District of Columbia 20010 —
GSK Investigational Site Aventura Florida 33180 —
GSK Investigational Site Orlando Florida 32806-6264 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site Atlanta Georgia 30303 —
GSK Investigational Site Boise Idaho 83704 —
GSK Investigational Site Idaho Falls Idaho 83401 —
GSK Investigational Site Chicago Illinois 60611 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Munster Indiana 46321 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Baton Rouge Louisiana 70809 —
GSK Investigational Site New Orleans Louisiana 70121 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Baltimore Maryland 21287 —
GSK Investigational Site Cumberland Maryland 21502 —
GSK Investigational Site Wheaton Maryland 20902 —
GSK Investigational Site Boston Massachusetts 02111 —
GSK Investigational Site Ann Arbor Michigan 48109-5542 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Lincoln Nebraska 68516 —
GSK Investigational Site Concord New Hampshire 03301 —
GSK Investigational Site Dover New Hampshire 03820 —
GSK Investigational Site Albany New York 12206 —
GSK Investigational Site Brooklyn New York 11203 —
GSK Investigational Site Great Neck New York 11021 —
GSK Investigational Site Manhasset New York 11030 —
GSK Investigational Site Rochester New York 14618 —
GSK Investigational Site Charlotte North Carolina 28210 —
GSK Investigational Site Winston-Salem North Carolina 27157 —
GSK Investigational Site Dayton Ohio 45417 —
GSK Investigational Site Oklahoma City Oklahoma 73103 —
GSK Investigational Site Oklahoma City Oklahoma 73104 —
GSK Investigational Site Tulsa Oklahoma 74104 —
GSK Investigational Site Pittsburgh Pennsylvania 15217 —
GSK Investigational Site Willow Grove Pennsylvania 19090 —
GSK Investigational Site Dallas Texas 75246 —
GSK Investigational Site Dallas Texas 75390-8550 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site Sugar Land Texas 77479 —
GSK Investigational Site Arlington Virginia 22205-3606 —
GSK Investigational Site Seattle Washington 98133 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Milwaukee Wisconsin 53226 —
GSK Investigational Site Onalaska Wisconsin 54650 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00583362, 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 Jul 23, 2019 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00583362 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →