drugset / Trial / NCT07293065

A Phase III Clinical Trial to Evaluate Long-Term Protective Efficacy of Recombinant Zoster Vaccine (CHO Cell)

NCT07293065

Phase 3 Active not recruiting 12000 enrolled MAXVAX Biotechnology Limited Liability Company
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of the sutdy is to evaluate the protective efficacy of Recombinant Herpes Zoster Vaccine (CHO Cell) (hereinafter referred to as "the investigational vaccine") in preventing herpes zoster at 13-36 months after complete immunization with the 0- and 2-month immunization schedule in individuals aged 40 years and older.

Timeline

Start
2025-12-15
Primary completion
2027-12-31
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Recombinant Zoster Vaccine (CHO Cell) Vaccine 50 ug Intramuscular
Subject Recombinant Zoster Vaccine (CHO Cell) Vaccine 0.5 ml Intramuscular

Indications