TerminatedPhase 3NCT04152837
Safety of Lixivaptan in Subjects Previously Treated With Tolvaptan for Autosomal Dominant Polycystic Kidney Disease
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
- Palladio Biosciences
- Principal Investigator
- Arlene Chapman, MDUniversity of Chicago, Chicago, IL USA
- Intervention
- Lixivaptan(drug)
- Enrollment
- 7 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2020 – 2022
Study locations (6)
- University of California Los Angeles, Los Angeles, California, United States
- University of Chicago Medicine & Biological Sciences, Chicago, Illinois, United States
- Mayo Clinic, Rochester, Minnesota, United States
- Brookview Hills Research Associates, LLC, Winston-Salem, North Carolina, United States
- Northeast Clinical Research Center, LLC, Bethlehem, Pennsylvania, United States
- Nephrology Associates of Northern Virginia, Inc., Fairfax, Virginia, United States
Collaborators
Centessa Pharmaceuticals plc
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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