drugset / Trial / NCT05135390

A Clinical Trial Evaluating the Efficacy and Safety of HSK21542 in Patients with Chronic Kidney Disease-Associated Pruritus

NCT05135390

Phase 3 Completed 545 enrolled Haisco Pharmaceutical Group Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multi-center, randomized, double-blind, placebo-controlled study. About 544 maintenance hemodialysis patients with moderate or above chronic kidney disease-associated pruritus are planned to be enrolled. They will randomized into the treatment group (HSK21542, 0.3 μg/kg) and the control group (placebo) at a 1:1 ratio.

Timeline

Start
2022-06-17
Primary completion
2023-07-27
Completion
2024-06-06

Drugs

EvaluationDrugModalityDoseRoute
Subject HSK21542 Peptide 0.3 ug/kg Intravenous

Indications