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Completed Phase 2 Interventional Results available

Safety and Efficacy Study of a Biologic to Treat Systemic Lupus Erythematosus

ClinicalTrials.gov ID: NCT02265744

Public ClinicalTrials.gov record NCT02265744. 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 6, 2026, 3:57 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 Phase 2, Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Lulizumab Pegol vs. Placebo on a Background of Limited Standard of Care in the Treatment of Subjects With Active Systemic Lupus Erythematosus

Brief summary

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

Study evaluating the safety and efficacy of a novel biologic in the treatment of systemic lupus erythematosus in male and female adults. Patients who qualify will be randomized to either active BMS-931699 or placebo for initially, up to 24 weeks. Patients who complete the initial 24 weeks of treatment and who are responding to therapy will have the option to continue receiving BMS-931699 as part of a long-term extension (LTE). Disease activity and safety will be assessed over the course of the study through laboratory values, various rating scales accepted in systemic lupus erythematosus studies and patient self reporting.

Study identification

NCT ID
NCT02265744
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
730 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
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 12, 2014
Primary completion
Oct 25, 2017
Completion
Nov 29, 2017
Last update posted
Oct 6, 2019

2014 – 2017

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Rheumatology Associates Of North Alabama, P.C. Huntsville Alabama 35801
St Jude Hospital Yorba Linda Fullerton California 92835
Valerius Med Group & Res Ctr Of Greater Long Beach, Inc. Long Beach California 90806
Harbor UCLA Medical Center Torrance California 90509
University Of Connecticut Health Center Farmington Connecticut 06030
Local Institution Trumbull Connecticut 06611
Center For Rheumatology, Immunology And Arthritis Fort Lauderdale Florida 33309
The Arthritis Center Palm Harbor Florida 34684-3176
Jefrey D. Lieberman, Md., Pc Decatur Georgia 30033
Coeur D'Alene Arthrit Clin Coeur d'Alene Idaho 83814-2644
Heartland Research Associates, Llc Wichita Kansas 67207-5150
Beth Israel Deaconess Med. Center Div. Of Gastroenterology Boston Massachusetts 02215
Physician Research Collaboration, Llc Lincoln Nebraska 68516
Albuquerque Clinical Trials Albuquerque New Mexico 87102-2631
North Shore Lij Health System Great Neck New York 11021
The Feinstein Institute For Medical Research Manhasset New York 11030
The University of North Carolina at Chapel Hill Chapel Hill North Carolina 27599
Joint and Muscle Medical Care and Research Institute (JMMCRI) Charlotte North Carolina 28204
Pmg Research Of Salisbury Salisbury North Carolina 28144
Oklahoma Medical Research Foundation Oklahoma City Oklahoma 73104
East Penn Rheumatology Associates, P.C. Bethlehem Pennsylvania 18015
Allegheny-Singer Research Institute (Asri) Pittsburgh Pennsylvania 15224
Tekton Research Inc Austin Texas 78745
Local Institution Dallas Texas 75246
Arthritis Northwest Spokane Washington 99204

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 96 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02265744, 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 Oct 6, 2019 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02265744 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →