drugset / Trial / NCT05671029
Thorough QT/QTc of Pritelivir in Healthy Subjects
RandomizedParallel-groupDouble-blindPrevention
Summary
This Phase 1 clinical trial was a double-blind, single-center, randomized and placebo-controlled trial in which healthy male and female subjects received in 2 parallel-groups daily oral doses of pritelivir (Group 1) or matching placebo (Group 2). Within Group 2, a single oral administration of moxifloxacin (positive control) and corresponding matching placebo was administered in a 2-sequence crossover design (nested crossover).
Timeline
- Start
- 2022-12-04
- Primary completion
- 2023-05-18
- Completion
- 2023-05-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Moxifloxacin | Small molecule | 400 mg | Oral |
| Subject | Pritelivir | Small molecule | 400 mg | Oral |
Indications
No indication recorded.