drugset / Trial / NCT01995695
Safety and Immunogenicity of a Live Attenuated H7N9 Influenza Virus Vaccine in Healthy Adults
Phase 1
Completed
48 enrolled
National Institute of Allergy and Infectious Diseases (NIAID)
University of Rochester · collab
RandomizedParallel-groupOpen-labelPrevention
Summary
H7N9 avian influenza (AI) viruses have caused a recent outbreak of severe respiratory disease in humans in China. The purpose of this study is to evaluate the safety and immunogenicity of a live attenuated H7N9 A/Anhui/13 ca influenza virus vaccine in healthy adults. A single dose of inactivated subvirion H7N9 influenza vaccine will be administered 3 months later.
Timeline
- Start
- 2013-10
- Primary completion
- 2016-01
- Completion
- —
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Inactivated subvirion H7N9 influenza vaccine | Vaccine | 30 ug | Intramuscular |
| Subject | Live attenuated H7N9 A/Anhui/13 ca influenza virus vaccine | Vaccine | 1e+07 unknown | Intranasal |