Clinical Trials Directory

Trials / Completed

CompletedNCT00686582

An Open-Label Phase II Study to Evaluate Immunogenicity and Safety of a Single IMVAMUNE Booster Vaccination Two Years After the Last IMVAMUNE Vaccination in Former POX-MVA-005 Vaccinees

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
304 (actual)
Sponsor
Bavarian Nordic · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The study was preformed to evaluate the persistence of antibodies following vaccination with MVA-BN and to assess the immunological memory response induced by a booster vaccination with MVA-BN in subjects two years after their participation in trial POX-MVA-005 (NCT00316524) in which they had received one or two doses of MVA-BN.

Conditions

Interventions

TypeNameDescription
BIOLOGICALIMVAMUNE1x 10E8\_TCID50
BIOLOGICALIMVAMUNE1x 10E8\_TCID50
PROCEDUREBlood Draw Only

Timeline

Start date
2008-08-01
Primary completion
2008-12-01
Completion
2009-06-01
First posted
2008-05-30
Last updated
2019-03-13
Results posted
2019-02-18

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00686582. Inclusion in this directory is not an endorsement.

An Open-Label Phase II Study to Evaluate Immunogenicity and Safety of a Single IMVAMUNE Booster Vaccination Two Years Af (NCT00686582) · Clinical Trials Directory