CompletedPhase 2NCT03529955
Evaluating Safety & Efficacy of Apremilast in the Treatment of Cutaneous Disease in Patients With Recalcitrant Dermatomyositis
Studying Dermatomyositis
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
- Tulane University
- Principal Investigator
- Carole Bitar, MDTulane University
- Intervention
- Apremilast 30mg(drug)
- Enrollment
- 8 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2018 – 2021
Study locations (1)
- Tulane University, New Orleans, Louisiana, United States
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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