Clinical Trials Directory

Trials / Completed

CompletedNCT01393951

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

Study for Immunogenicity and Safety of ASP7374 for Subcutaneous and Intramuscular Vaccination in Healthy Adults

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
165 (actual)
Sponsor
UMN Pharma Inc. · Industry
Sex
All
Age
20 Years – 49 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BIOLOGICALASP7374subcutaneous and intramuscular

Timeline

Start date
2011-05-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2011-07-14
Last updated
2017-09-29

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT01393951. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Immune Response to the ASP7374 and Its Safety in Healthy Adult Volunteers (NCT01393951) · Clinical Trials Directory