Transition From Buphenyl to RAVICTI for the Therapy of Byler Disease

NCT01949766 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2013-09-24

No results posted yet for this study

Summary

This is a single patient compassionate use protocol to determine whether RAVICTI will improve bile flow in a subject who previously tolerated therapy with Buphenyl.

Conditions

  • Byler Disease

Interventions

DRUG

Glycerol phenylbutyrate

Sponsors & Collaborators

  • University of Pittsburgh

    lead OTHER

Eligibility

Min Age
6 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01949766 on ClinicalTrials.gov