CompletedPhase 1NCT05504395
A Pharmacokinetic and Safety Study of CSTI-500 in Subjects With Prader-Willi Syndrome
Studying Prader-Willi syndrome
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
- ConSynance Therapeutics
- Principal Investigator
- Italo Biaggioni, MDVanderbilt Autonomic Dysfunction Center, Vanderbilt University Medical Center
- Intervention
- CSTI-500(drug)
- Enrollment
- 10 enrolled
- Eligibility
- 13-50 years · All sexes
- Timeline
- 2022 – 2023
Study locations (1)
- Vanderbilt University Medical Center, Nashville, Tennessee, 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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