TerminatedPhase 3NCT01240694
A Long-Term Study of the Safety and Tolerability of Repeated Administration of CEP-33457 in Participants With 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
- Cephalon, Inc.
- Principal Investigator
- Teva Medical ExpertTeva Branded Pharmaceutical Products R&D, Inc.
- Intervention
- CEP-33457(drug)
- Enrollment
- 136 enrolled
- Eligibility
- 18-70 years · All sexes
- Timeline
- 2010 – 2012
Study locations (30)
- Teva Investigational Site 27, Birmingham, Alabama, United States
- Teva Investigational Site 20, Tucson, Arizona, United States
- Teva Investigational Site 16, Los Angeles, California, United States
- Teva Investigational Site 5, Los Angeles, California, United States
- Teva Investigational Site 7, San Diego, California, United States
- Teva Investigational Site 14, San Leandro, California, United States
- Teva Investigational Site 17, Stanford, California, United States
- Teva Investigational Site 30, Aurora, Colorado, United States
- Teva Investigational Site 4, Aventura, Florida, United States
- Teva Investigational Site 32, Clearwater, Florida, United States
- Teva Investigational Site 35, Fort Lauderdale, Florida, United States
- Teva Investigational Site 1, Jupiter, Florida, United States
- Teva Investigational Site 11, Tampa, Florida, United States
- Teva Investigational Site 8, Atlanta, Georgia, United States
- Teva Investigational Site 31, Atlanta, Georgia, 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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