drugset / Trial / NCT01631110

Re-licensing Study to Assess Inflexal V Formulated With WHO Recommended Influenza Strains

NCT01631110

Phase 3 Completed 110 enrolled Crucell Holland BV
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The study is to assess whether the influenza vaccine Inflexal V for season 2012/2013 fulfills the EMA requirements for re-registration of influenza vaccines.

Timeline

Start
2012-07
Primary completion
2012-08
Completion
2012-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Inflexal V Vaccine 0.5 ml Intramuscular

Indications