drugset / Trial / NCT05937113

Safety and Immunogenicity of the Inactivated Rabies Vaccine RABIVAX-S Administered Intramuscularly and Intradermally

NCT05937113

RandomizedSequentialOpen-labelPrevention

Summary

Randomized, open-label, prospective, before-and-after comparison study in the same group. Subjects suitable for the study will be randomly assigned at a ratio of 1:1 (block 4) to use the study vaccine by one of two routes of administration: Intramuscular or Intramuscular. Previously-unvaccinated subjects receive three injections of vaccine on day 0, 7 and 21-28. The aim of the study is to evaluate the safety and immunogenicity of the inactivated rabies vaccine RABIVAX-S administered intramuscularly and intradermally according to a 3-dose regimen in healthy volunteers.

Timeline

Start
2020-06-13
Primary completion
2020-07-02
Completion
2020-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Rabivax-S Vaccine 0.1 ml Intramuscular
Subject Rabivax-S Vaccine 1 ml Intramuscular

Indications