drugset / Trial / NCT01393951

A Study to Evaluate the Immune Response to the ASP7374 and Its Safety in Healthy Adult Volunteers

NCT01393951 ↗

Phase 1/2 Completed 165 enrolled UMN Pharma Inc.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This trial is designed as a blinded, randomized and parallel group study to investigate the clinically recommended dosage for ASP7374 based on the comparison of the immunogenicity and safety among two doses of subcutaneous ASP7374 and one dose of intramuscular ASP7374 in healthy adults.

Timeline

Start
2011-05
Primary completion
2011-12
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject ASP7374 Vaccine — Subcutaneous

Indications

No indication recorded.