drugset / Trial / NCT04019574

Study to Investigate the Effects of Single Intravenous Doses of Difelikefalin (CR845) on the QTc Interval in Healthy Subjects

NCT04019574 ↗

Phase 1 Completed 57 enrolled Cara Therapeutics, Inc.
RandomizedCrossoverDouble-blindOther

Summary

This is a Phase 1, randomized, double-blind (except for moxifloxacin), placebo- and positive-controlled, single-site, 4-way crossover study to investigate the effects of single therapeutic and supratherapeutic IV doses of difelikefalin (CR845) on the QTc interval in healthy adult subjects. Subjects will be randomized to a treatment sequence consisting of 4 treatment periods with a minimum 5-day washout between treatments. Subjects will receive each of the study treatments over the course of the study. Randomized subjects will receive the assigned study treatment as a single dose in the fasted state in the morning on Day 1 of each treatment period.

Timeline

Start
2019-06-20
Primary completion
2019-10-22
Completion
2019-10-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Difelikefalin Protein / enzyme biologic 0.5 ug/kg Intravenous
Subject Difelikefalin Protein / enzyme biologic 3 ug/kg Intravenous
Comparator Moxifloxacin Small molecule 400 mg Oral

Indications

No indication recorded.