drugset / Trial / NCT02293317

Phase II Study to Assess Safety & Immunogenicity of Multimeric-001 Influenza Vaccine, Followed by TIV

NCT02293317

Phase 2 Completed 37 enrolled BiondVax Pharmaceuticals ltd.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a single-site, randomized, double-blind, placebo-controlled study of Multimeric-001 in thirty six (36) volunteers 50-65 years of age. All subjects will receive an intramuscular (IM) injection, in each one of three visits, with a 21±2 days interval between treatments.

Timeline

Start
2014-11
Primary completion
2015-03
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Multimeric-001 Vaccine 0.5 mg Intramuscular
Subject Multimeric-001 Vaccine 1 mg Intramuscular
Background TIV Vaccine Intramuscular

Indications