drugset / Trial / NCT01347073

Study of the Safety, Pharmacokinetics and Efficacy of HPN-100, in Pediatric Subjects With Urea Cycle Disorders (UCDs)

NCT01347073 ↗

Phase 3 Completed 23 enrolled Amgen
NaSingle-groupOpen-labelTreatment

Summary

This non-randomized, open-label study was approximately one year in duration and consisted of a short term NaPBA to HPN-100 switchover part involving two overnight stays followed by a 12-month long term treatment period involving monthly visits.

Timeline

Start
2011-07
Primary completion
2013-02
Completion
2013-03

Outcome

Met primary endpoint

paper Daily ammonia exposure (24-hour area under the curve) was lower on GPB and met predefined noninferiority criteria PMID 23324524 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Glycerol phenylbutyrate Other / unclassified — Oral

Indications