drugset / Trial / NCT02148328

Safety, Tolerability, and Immunogenicity Study of a Cell-based Virosomal Influenza Vaccine in Healthy Adults

NCT02148328 ↗

Phase 1 Completed 240 enrolled Crucell Holland BV
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to examine the safety and tolerability after administration of trivalent and quadrivalent cell-based virosomal influenza vaccine in healthy adults.

Timeline

Start
2014-05
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Quadrivalent commercial influenza vaccine Vaccine — Intramuscular
Subject Quadrivalent virosomal influenza vaccine Vaccine — Intramuscular
Comparator Trivalent commercial virosomal influenza vaccine Vaccine — Intramuscular
Subject Trivalent virosomal influenza vaccine Vaccine — Intramuscular

Indications