drugset / Trial / NCT01135680

Double-Blind Randomized Crossover Trial to Access Electrocardiogram Effects of HPN-100

NCT01135680

Phase 1 Completed 98 enrolled Amgen
RandomizedCrossoverTriple-blindDiagnostic

Summary

Arm 1: Primary Objective: • To determine the safety and tolerability of multiple ascending, supratherapeutic doses of HPN-100. Arm 2: Primary Objective: • To assess the effects of steady-state levels of HPN-100 metabolites (4 phenylbutyric acid \[PBA\], phenylacetic acid \[PAA\], and phenylacetylglutamine \[PAGN\]) on 12-lead electrocardiogram (ECG) parameters in healthy male and female subjects with the primary endpoint being the time-matched change from baseline in the QT interval corrected for heart rate (HR) based on an individual correction method (QTcI).

Timeline

Start
2010-05
Primary completion
2010-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Glycerol phenylbutyrate Other / unclassified 6 ml Oral
Comparator Glycerol phenylbutyrate Other / unclassified 9 ml Oral
Comparator Glycerol phenylbutyrate Other / unclassified 12 ml Oral
Comparator Moxifloxacin Small molecule 400 mg Oral

Indications