drugset / Trial / NCT03430089

Safety of a Single Dose or Two Doses of Shenzhen Quadrivalent Influenza Vaccine

NCT03430089 ↗

Phase 1 Completed 101 enrolled Sanofi Pasteur, a Sanofi Company
Non-randomizedParallel-groupOpen-labelPrevention

Summary

This phase I-like, open-label, monocenter, descriptive, single-arm clinical safety study will investigate the Shenzhen quadrivalent influenza vaccine (Shz QIV) in 100 participants aged 6 months and older in China. Participants aged 9 years or more will receive a single dose of Shz QIV, and participants aged 6 months to 8 years will receive two doses of Shz QIV administered 28 days apart.

Timeline

Start
2019-02-22
Primary completion
2019-06-06
Completion
2019-06-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Shz QIV Vaccine 0.25 ml Intramuscular
Subject Shz QIV Vaccine 0.5 ml Intramuscular

Indications