Safety and Efficacy Study of a Biologic to Treat Systemic Lupus Erythematosus
Status: | Completed |
---|---|
Conditions: | Lupus |
Therapuetic Areas: | Immunology / Infectious Diseases |
Healthy: | No |
Age Range: | 18 - 70 |
Updated: | 1/6/2019 |
Start Date: | November 13, 2014 |
End Date: | November 30, 2017 |
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
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.
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.
1. Subjects completing Day 169 (24 weeks) on study medication may be eligible to enter an
optional LTE period
2. The LTE period will remain blinded but will no longer have a placebo arm:
- Subjects will remain on their originally assigned treatment arm unless they were on
placebo
- Subjects initially randomized to placebo arm will be automatically re-randomized
into one of the existing active arms at Day 169 (24 weeks)
optional LTE period
2. The LTE period will remain blinded but will no longer have a placebo arm:
- Subjects will remain on their originally assigned treatment arm unless they were on
placebo
- Subjects initially randomized to placebo arm will be automatically re-randomized
into one of the existing active arms at Day 169 (24 weeks)
For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com
Inclusion Criteria:
- Male or female aged between 18 to 70 (included)
- Diagnosed with active systemic lupus erythematosus by a doctor
- Disease must be in patient's joints or on the skin at a minimum
- Taking other medications is allowed but some are excluded
Exclusion Criteria:
- Diagnosed with active lupus nephritis, multiple sclerosis or rheumatoid arthritis
- Diagnosed with active tuberculosis or an ongoing infection with a bacteria or a virus
We found this trial at
26
sites
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University of North Carolina at Chapel Hill Carolina’s vibrant people and programs attest to the...
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1709 S Rock Rd
Wichita, Kansas 67207
Wichita, Kansas 67207
316-689-6629
Phone: 316-612-4815
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Boston, Massachusetts 02215
Phone: 617-735-4162
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Charlotte, North Carolina 28204
Phone: 704-248-8577
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263 Farmington Ave
Farmington, Connecticut 06030
Farmington, Connecticut 06030
(860) 679-2000

Phone: 860-679-2167
University of Connecticut Health Center UConn Health is a vibrant, integrated academic medical center that...
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Fort Lauderdale, Florida 33334
Phone: 954-229-0425
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Long Beach, California 90806
Phone: 562-989-2374
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