drugset / Trial / NCT03300362
Improved Novel VaccIne CombinaTion InflUenza Study
RandomizedParallel-groupSingle-blindPrevention
Summary
A Phase IIb randomised, participant-blinded, placebo-controlled, multi-centre phase IIb efficacy study in 2030 volunteers aged 65 and over. The study will assess the safety and efficacy of the co-administration of a viral vectored vaccine, MVA- NP+M1, and the annual recommended licensed inactivated influenza vaccine (IIV). Within the main cohort 100 participants will be recruited to an immunology sub-cohort.
Timeline
- Start
- 2017-10-13
- Primary completion
- 2018-10-31
- Completion
- 2018-10-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MVA-NP+M1 | Vaccine | — | — |
| Background | Quadrivalent influenza vaccine | Vaccine | — | — |