Condition: Influenza, Human · Sponsor: Anhui Zhifei Longcom Biologic Pharmacy Co., Ltd.
This clinical trial adopts a seamless design of phase I/II, conducted in two stages: phase I and phase II. Phase I is the age/dose ramp up stage, and phase II is the dose expansion stage.The purpose of this clinical trial is to evaluate the safety and tolerability of different doses of Influenza Vaccine (Split Virion), Inactivated, Quadrivalent, ZFA02 Adjuvant，explore the immunogenicity of the vaccine, and determine the appropriate dose for later clinical trials of this product.
This description comes directly from the study's public registry record.
Fei Jin · 13722795742 · ycjf3000@126.com
Always discuss trial participation with your own doctor first.
| Hebei Province Centers for Disease Control and Prevention | Shijiazhuang, Hebei, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06824519