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Phase 4 study of nalfurafine hydrochloride for pruritus in patients with PBC

Phase 4
Conditions
primary biliary cholangitis, primary sclerosing cholangitis
Registration Number
JPRN-UMIN000019296
Lead Sponsor
Teikyo University School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria

patients with a history of allergy to nalfurafine, patients with severe liver impairment (Child-Pugh grade C), patients with mild pruritus, and patients who were not indicated for nalfurafine treatment.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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