CompletedPhase 2NCT03149445
Co-administration of Tesofensine/Metoprolol in Subjects With Prader-Willi Syndrome (PWS)
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
- Saniona
- Principal Investigator
- Kim Krogsgaard, MD, DMScSaniona
- Intervention
- Tesofensine/Metoprolol(drug)
- Enrollment
- 18 enrolled
- Eligibility
- 12-30 years · All sexes
- Timeline
- 2017 – 2019
Study locations (2)
- Motol University Hospital, Prague, Czechia
- Semmelweis University, Budapest, Hungary
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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