CompletedPhase 2NCT01210560
Dose-finding Study of New Tolvaptan Formulation in Subjects With ADPKD
Studying Autosomal dominant polycystic kidney disease
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
- Otsuka Pharmaceutical Development & Commercialization, Inc.
- Principal Investigator
- Frank Czerwiec, M.D., Ph.D.Otsuka Pharmaceutical Development & Commercialization, Inc.
- Intervention
- Tolvaptan MR(drug)
- Enrollment
- 25 enrolled
- Eligibility
- 18-50 years · All sexes
- Timeline
- 2010 – 2011
Study locations (6)
- Tufts-New England Medical Center, Boston, Massachusetts, United States
- Davita Clinical Research, Minneapolis, Minnesota, United States
- Mayo Medical Center, Rochester, Minnesota, United States
- University Hospitals of Cleveland/Case, Cleveland, Ohio, United States
- Northwest Renal Clinic Inc., Portland, Oregon, United States
- University of Pennsylvania Medical Center, Philadelphia, Pennsylvania, 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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