drugset / Trial / NCT02839330
A Study to Evaluate Safety, Immunogenicity, and Lot-to-Lot Consistency of H5N1 Subunit Influenza Virus Vaccine in Healthy Adult Subjects ≥18 Years of Age
Phase 3
Completed
3196 enrolled
Seqirus
Biomedical Advanced Research and Development Authority · collab
RandomizedParallel-groupDouble-blindPrevention
Summary
This Phase 3 study evaluates the safety, immunogenicity and lot-to lot consistency of 3 lots of aH5N1c vaccine for pandemic avian influenza, in approximately 2394 healthy adults ≥18 years of age receiving the vaccine and 797 healthy adults receiving placebo. Subjects were randomized in a 3:1 ratio to receive either aH5N1c vaccine or saline placebo. Enrollment was stratified by age: 18 to \<65 years of age and ≥65 years of age, to allow adequate safety assessment of the entire age spectrum.
Timeline
- Start
- 2016-07-11
- Primary completion
- 2017-10-04
- Completion
- 2017-10-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | aH5N1c | Vaccine | 7.5 ug | Intramuscular |