drugset / Trial / NCT02603952
A Phase 2a to Evaluate the Safety of MEDI8852 in Adults With Uncomplicated Influenza
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate safety and tolerability of a single dose of MEDI8852 when given with oseltamivir, the safety and tolerability of oseltamivir alone, and the safety and tolerability of a single dose of MEDI8852 alone in adult participants with acute, uncomplicated influenza caused by Type A strains.
Timeline
- Start
- 2015-12-07
- Primary completion
- 2016-12-09
- Completion
- 2016-12-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MEDI8852 | Monoclonal antibody | 750 mg | Intravenous |
| Subject | MEDI8852 | Monoclonal antibody | 3000 mg | Intravenous |
| Subject | Oseltamivir | Small molecule | 75 mg | Oral |