TerminatedPhase 2NCT03363763
Topical Sirolimus Ointment for Cutaneous Angiofibromas in Subjects With Tuberous Sclerosis Complex
Studying Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
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
- Aucta Pharmaceuticals, Inc
- Principal Investigator
- Shoufeng Li, Ph.DAucta Pharmaceuticals, Inc
- Intervention
- Sirolimus 0.2%(drug)
- Enrollment
- 24 enrolled
- Eligibility
- 2-21 years · All sexes
- Timeline
- 2017 – 2023
Study locations (8)
- Translational Genomics Research, Phoenix, Arizona, United States
- Children's Hospital of Los Angeles, Division of Neurology, Los Angeles, California, United States
- Children's Clinical Research Organization, Children's Hospital Colorado, Aurora, Colorado, United States
- Children's Healthcare of Atlanta, Atlanta, Georgia, United States
- Boston Children's Hospital, Boston, Massachusetts, United States
- Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
- LeBonheur Children's Hospital, Memphis, Tennessee, United States
- Children's Hospital of Fudan University, Shanghai, China
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.
Open NCT03363763 on ClinicalTrials.govOther trials for Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
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