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

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

Summary

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

Conditions

Influenza, Human

Intervention

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

Location

Site 2
Linkoping
Sweden

Status

Active, not recruiting

Source

Eurocine Vaccines AB

Results (where available)

View Results

Links

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

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