drugset / Trial / NCT00957996
Safety Study of IV Peramivir in Hospitalized Subjects With Confirmed or Suspected Influenza
Phase 3
Completed
234 enrolled
BioCryst Pharmaceuticals
Department of Health and Human Services · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
This is a Phase 3, open-label, randomized study of the antiviral activity, safety, and tolerability of intravenous Peramivir in hospitalized subjects with confirmed or suspected influenza infection.
Timeline
- Start
- 2009-10
- Primary completion
- 2010-10
- Completion
- 2011-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PERAMIVIR ANHYDROUS | Small molecule | 300 mg | Intravenous |
| Subject | PERAMIVIR ANHYDROUS | Small molecule | 600 mg | Intravenous |