drugset / Trial / NCT02014168

Safety and Immunogenicity of Co-administration of Candidate Influenza Vaccine MVA-NP+M1 and Viroflu® Seasonal Influenza Vaccine

NCT02014168 ↗

Phase 1 Terminated 3 enrolled University of Oxford
Non-randomizedParallel-groupSingle-blindPrevention

Summary

This is a single blinded placebo controlled phase I study, to assess the safety and immunogenicity of co-administration of the candidate influenza vaccine MVA-NP+M1 with the Viroflu® seasonal influenza vaccine. All volunteers recruited will be healthy adults aged 18 and over.

Timeline

Start
2014-01
Primary completion
2014-04
Completion
2014-04

Outcome

Outcome not reported

Stopped: “Futility”

Drugs

EvaluationDrugModalityDoseRoute
Subject MVA NP+M1 Vaccine 1.5e+08 unknown Intramuscular
Background Viroflu Vaccine 0.5 ml Intramuscular

Indications