drugset / Trial / NCT03218501

A Study of SK-1405 in Hemodialysis Patients With Uremic Pruritus

NCT03218501 ↗

Phase 2 Completed 269 enrolled Sanwa Kagaku Kenkyusho Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety and dose response of SK-1405 for the treatment of subjects with uremic pruritus receiving hemodialysis, during 2 weeks of treatment.

Timeline

Start
2017-08-28
Primary completion
2018-05-25
Completion
2018-05-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator SK-1405 Unknown — Oral

Indications

No indication recorded.