Clinical Trials Directory

Trials / Completed

CompletedNCT00189917

Safety, Tolerability and Immune Response of IMVAMUNE (MVA-BN)Smallpox Vaccine in Patients With Atopic Disorders

An Open-label, Controlled Phase I Pilot Study to Evaluate Safety and Immunogenicity of MVA-BN® Smallpox Vaccine in 18-40 Year Old Vaccinia-naïve Subjects With Atopic Disorders

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Bavarian Nordic · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to gather information on the safety and immunogenicity of an investigational smallpox vaccine in populations with atopic disorders.

Conditions

Interventions

TypeNameDescription
BIOLOGICALIMVAMUNE (MVA-BN)1x10E08 TCID50, subcutaneous vaccination

Timeline

Start date
2004-04-01
Primary completion
2005-12-01
First posted
2005-09-19
Last updated
2019-01-10

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00189917. Inclusion in this directory is not an endorsement.

Safety, Tolerability and Immune Response of IMVAMUNE (MVA-BN)Smallpox Vaccine in Patients With Atopic Disorders (NCT00189917) · Clinical Trials Directory