CompletedPhase 1NCT05533008
CR845-100303: Study to Assess the Potential of Physical Withdrawal From Intravenous CR845 (Difelikefalin) in Hemodialysis Patients
Studying Complication in hemodialysis
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
- Cara Therapeutics, Inc.
- Principal Investigator
- Frédérique Menzaghi, PhDCara Therapeutics
- Intervention
- CR845 0.5 mcg/kg(drug)
- Enrollment
- 35 target
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2019 – 2020
Study locations (5)
- Cara Therapeutics Study Site, Bridgeport, Connecticut, United States
- Cara Therapeutics Study Site, Hartford, Connecticut, United States
- Cara Therapeutics Study Site, Kansas City, Kansas, United States
- Cara Therapeutics Study Site, Roseville, Michigan, United States
- Cara Therapeutics Study Site, Minneapolis, Minnesota, 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.
Open NCT05533008 on ClinicalTrials.govOther trials for Complication in hemodialysis
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