Smallpox Clinical Trial
Official title:
Phase I Study on Safety, Tolerability and Immunogenicity of the MVA-BN Vaccine Administered to Healthy Subjects
Verified date | September 2005 |
Source | Bavarian Nordic |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to collect information on the safety, tolerability and immunogenicity of an investigational smallpox vaccine at different doses and using different routes of administration in vaccinia-naive and vaccinated healthy volunteers
Status | Completed |
Enrollment | 90 |
Est. completion date | July 2003 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 20 Years to 55 Years |
Eligibility |
Inclusion Criteria: - Healthy male subjects, aged 20 - 55 years - Signed informed consent Exclusion Criteria: - Prior vaccination against smallpox (study part I only) - Abnormalities suspicious of any underlying disease, detected at routine tests prior to study inclusion. - Any immune modifying therapy within 4 weeks prior to entry - Participation in any other investigating drug trial - Known allergy to a component which may be part of the vaccine - Allergic reaction or any other severe adverse effects experienced after previous smallpox vaccination (study Part II only) |
Country | Name | City | State |
---|---|---|---|
Germany | PharmPlanNet Contract Research GmbH | Moenchengladbach |
Lead Sponsor | Collaborator |
---|---|
Bavarian Nordic |
Germany,
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