Study to Assess the Safety, Tolerability and Immune Response Following Vaccination With Immunose™ FLU

2016-12-21 21:53:21 | BioPortfolio


The main purpose of the this study is to evaluate the safety and tolerability of Immunose™ FLU based on Endocine™ and quadrivalent influenza antigen.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Influenza, Human


15 µg HA/strain and 1% Endocine™, 15 µg HA/strain and 2% Endocine™, 15 µg HA/strain, intramuscular comparator, intranasal comparator, Placebo, Saline


Site 2


Active, not recruiting


Eurocine Vaccines AB

Results (where available)

View Results


Published on BioPortfolio: 2016-12-21T21:53:21-0500

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