drugset / Trial / NCT02319772
A Phase 1 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BCX4430
Phase 1
Completed
94 enrolled
BioCryst Pharmaceuticals
National Institute of Allergy and Infectious Diseases (NIAID) · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This is a 2-part, first-in-human dose-ranging study to evaluate the safety, tolerability and pharmacokinetics of escalating doses of BCX4430 administered via intramuscular (IM) injection in healthy subjects. In part 1, subjects will receive a single dose of BCX4430; in part 2 subjects will receive BCX4430 for 7 days.
Timeline
- Start
- 2014-12
- Primary completion
- 2016-03
- Completion
- 2016-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Galidesivir | Small molecule | — | Intramuscular |