drugset / Trial / NCT02313155

Phase 1/2 Study of TAK-850 Subcutaneous Injection in Healthy Adults

NCT02313155 ↗

Phase 1/2 Completed 110 enrolled Takeda
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the safety and immunogenicity of a single subcutaneous injection of TAK-850 as compared to intramuscular injection of TAK-850 in healthy Japanese adults

Timeline

Start
2014-12
Primary completion
2015-01
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Subject TAK-850 Vaccine 0.5 ml Subcutaneous

Indications