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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Pruritus
  • Uremic Pruritus in Hemodialysis Patients

NCT number NCT03218501
Study type Interventional
Source Sanwa Kagaku Kenkyusho Co., Ltd.
Contact
Status Completed
Phase Phase 2
Start date August 28, 2017
Completion date May 25, 2018

See also
  Status Clinical Trial Phase
Completed NCT06190132 - The Effect of Omega-3 Fatty Acids Versus Gabapentin in Uremic Pruritus in Hemodialysis Patients N/A