CR845-CLIN3103: A Global Study to Evaluate the Safety and Efficacy of CR845 in Hemodialysis Patients With Moderate-to-Severe Pruritus

Completed · Phase 3 · Has a placebo group

Conditions studied: Uremic Pruritus

In brief

This is a multicenter, international study to evaluate the safety and efficacy of intravenous (IV) CR845 at a dose of 0.5 mcg/kg administered after each dialysis session. The study includes a 12-week randomized, double-blind, placebo-controlled Phase and a 52-week Open-label Extension Phase.

Key facts

Study ID
NCT03636269
Run by
Cara Therapeutics, Inc.
People needed
473
Starts
2018-07-17
Expected to finish
2020-03-30
Last updated by the study team
2022-04-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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