CompletedPhase 2NCT03161483
A Study to Evaluate the Efficacy and Safety of CC-220 in Subjects With Active Systemic Lupus Erythematosus
Studying Systemic lupus erythematosus
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Celgene
- Principal Investigator
- Nataliya Agafonova, MD, M.DCelgene Corporation
- Intervention
- CC-220(drug)
- Enrollment
- 289 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2017 – 2021
Study locations (30)
- Clinical and Translational Research Center of Alabama, PC, Tuscaloosa, Alabama, United States
- AZ Arthritis and Rheum Rsch, PLLC, Mesa, Arizona, United States
- Saint Jude Heritage Medical Center, Fullerton, California, United States
- University of California San Diego Medical Center, La Jolla, California, United States
- UCLA Division of Rheumatology, Los Angeles, California, United States
- Desert Medical Advances, Palm Desert, California, United States
- C Michael Neuwelt M D, San Leandro, California, United States
- Inland Rheumatology Clinical Trials, Upland, California, United States
- University of Colorado Denver, Aurora, Colorado, United States
- Yale University School of Medicine, New Haven, Connecticut, United States
- Centre For Rheumatology, Immun. And Arthritis, Fort Lauderdale, Florida, United States
- University of Florida College of Medicine, Gainesville, Florida, United States
- University of Miami, Miami, Florida, United States
- Integral Rheumatology and Immunology Specialists, Plantation, Florida, United States
- Bay Care Medical Group, Tampa, Florida, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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