drugset / Trial / NCT01135680
Double-Blind Randomized Crossover Trial to Access Electrocardiogram Effects of HPN-100
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |