drugset / Trial / NCT00825305

Safety and Immunogenicity (Non-inferiority) of a Purified Chick Embryo Cell Vaccine Vaccine Administered in Two Different Schedules (Conventional Versus Abbreviated Schedule)

NCT00825305 ↗

Phase 3 Completed 825 enrolled Novartis Vaccines
RandomizedParallel-groupOpen-labelPrevention

Summary

This study investigates the safety and immunogenicity (non-inferiority) of a Purified Chick Embryo Cell Vaccine (PCECV) administered in two different schedules (conventional versus abbreviated schedule) in healthy adults 18 to 50 years of age in China

Timeline

Start
2008-11
Primary completion
2008-12
Completion
2009-01

Outcome

Met primary endpoint

paper The Zagreb regimen was non-inferior to the Essen regimen with regard to RVNA concentrations after 7, 14, and 42 days, and 13 months of immunization. PMID 25483635 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject PCEC Rabies vaccine for human use Vaccine — —

Indications