Viewing Study NCT00079820



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00079820
Status: COMPLETED
Last Update Posted: 2014-01-13
First Post: 2004-03-15

Brief Title: Safety Tolerability and Immune Response of ACAM3000 Modified Vaccinia Ankara MVA Smallpox Vaccine in Adults
Sponsor: Sanofi Pasteur a Sanofi Company
Organization: Sanofi

Study Overview

Official Title: The Safety Tolerability and Immunogenicity of Three Dose Levels of ACAM3000 Modified Vaccinia Ankara MVA Smallpox Vaccine in Adults Without Previous Smallpox Vaccination
Status: COMPLETED
Status Verified Date: 2014-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to gather information on the safety and the effectiveness of an investigational vaccine for the prevention of smallpox disease Smallpox was one of the major causes of death and sickness through the first half of the 20th century but a global program of smallpox eradication resulted in the elimination of the natural disease The last cases of smallpox in the United States occurred in 1949 in Texas Today only laboratory workers who work with smallpox-related viruses military personnel and health care workers are vaccinated

Historically individuals in the US were vaccinated with a product such as Dryvax which contains the virus vaccinia in the same family as smallpox This virus could promote immunity to smallpox but not produce the disease itself Although effective these vaccines are not safe to use in people with atopic dermatitis eczema allergic immune response to allergens children less than 1 year of age and people with a compromised immune system occurring in certain diseases HIV positive individuals and AIDS and following treatment with certain types of drugs It is important to find a safe vaccine that can be used to protect people who cannot receive routine vaccinia-based smallpox vaccine

The vaccine in this study is known as Modified Vaccinia Ankara or MVA vaccine It is the objective of this study to find out if MVA vaccine is safe and effective in providing immunity to smallpox The effectiveness of this vaccine will be measured in two ways The first way is to find out if there are specific antibodies in your blood following MVA vaccination Antibodies are chemicals your body produces to fight smallpox virus

The second way is to see whether or not there is a typical skin reaction following vaccination with a traditional smallpox vaccine given about three months after vaccination with the MVA vaccine The typical reaction in an unvaccinated person to smallpox vaccine is formation of a blister or pox which occurs at the site of vaccination In a person with immunity to smallpox the skin reaction is much less and typically consists of a little swelling at the site of vaccination
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None