TerminatedPhase 2NCT01466725
A Research Study to Assess if CC-930 is Safe in Treating Subjects With Discoid 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
- William Smith, MD, M.DCelgene
- Intervention
- CC-930(drug)
- Enrollment
- 5 enrolled
- Eligibility
- 18-64 years · All sexes
- Timeline
- 2011 – 2012
Study locations (19)
- UAB Dermatology, Birmingham, Alabama, United States
- The Regents of the University of California, Irvine, California, United States
- Medical Faculty Associates, Washington D.C., District of Columbia, United States
- Advanced Pharma, CR, LLC, Miami, Florida, United States
- University of Miami - Department of Dermatology, Miami, Florida, United States
- Rush Medical Center, Chicago, Illinois, United States
- North Shore University Health System, Skokie, Illinois, United States
- SIU School of Medicine, Springfield, Illinois, United States
- Tulane University School of Medicine, New Orleans, Louisiana, United States
- John Hopkins University, Baltimore, Maryland, United States
- Boston Cancer Center, Boston, Massachusetts, United States
- University of Minnesota-Department of Dermatology, Minneapolis, Minnesota, United States
- University of Rochester Medical Center, Rochester, New York, United States
- Ohio State Univ Medical Center, Division of Dermatology, Columbus, Ohio, United States
- Rhode Island Hospital University Dermatology, Inc., Providence, Rhode Island, United States
- +4 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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