drugset / Trial / NCT03635086

Safety, Tolerability and Long-term Immunogenicity of Different Formulations of a Chikungunya Vaccine (V184-005)

NCT03635086

Phase 2 Completed 60 enrolled Themis Bioscience GmbH
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to investigate immunogenicity and safety of Measles Virus-Chikungunya (MV-CHIK) vaccine in different dose regimens, 28 days after one or two vaccinations.

Timeline

Start
2018-08-22
Primary completion
2019-01-25
Completion
2019-11-16

Drugs

EvaluationDrugModalityDoseRoute
Subject MV-CHIK Vaccine 50000 unknown Intramuscular
Subject MV-CHIK Vaccine 100000 unknown Intramuscular
Subject MV-CHIK Vaccine 1e+06 unknown Intramuscular

Indications