CR845-CLIN3105: A Study to Evaluate the Safety and Effectiveness of CR845 in Hemodialysis Patients With Moderate-to-Severe Pruritus

Completed · Phase 3

Conditions studied: Uremic Pruritus

In brief

This is a multicenter, open-label study to evaluate the safety and effectiveness of intravenous (IV) CR845 at a dose of 0.5 mcg/kg administered after each dialysis session. The study includes an up to 12-week Treatment Period.

Key facts

Study ID
NCT03998163
Run by
Cara Therapeutics, Inc.
People needed
222
Starts
2019-05-06
Expected to finish
2020-03-06
Last updated by the study team
2021-10-15

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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