drugset / Trial / NCT03300362

Improved Novel VaccIne CombinaTion InflUenza Study

NCT03300362

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

EvaluationDrugModalityDoseRoute
Subject MVA-NP+M1 Vaccine
Background Quadrivalent influenza vaccine Vaccine

Indications