Ignite Creation Date:
2024-05-05 @ 5:22 PM
Last Modification Date:
2024-10-26 @ 9:31 AM
Study NCT ID:
NCT00442169
Status:
COMPLETED
Last Update Posted:
2016-04-14
First Post:
2007-02-27
Brief Title:
Safety and Immunogenicity of ChimeriVax-WN02 West Nile Vaccine in Healthy Adults
Sponsor:
Sanofi Pasteur a Sanofi Company
Organization:
Sanofi
Study Overview
Official Title:
Randomized Double-blind Placebo Controlled Phase II Trial of the Safety Tolerability and Immunogenicity of Lyophilized ChimeriVax-WN02 West Nile Vaccine in Healthy Adults
Status:
COMPLETED
Status Verified Date:
2016-04
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 determine whether a single subcutaneous injection of ChimeriVax-WN02 vaccine is well tolerated safe and induces protective antibodies against West Nile Disease The study is divided into two parts in the first part a comparison of 3 dose levels of the vaccine will be made with an inactive control In the second part the optimum dose level chosen after the first part will be given to older volunteers
Detailed Description:
West Nile Disease has been carried across the United States by migrating birds since it was first identified in New York city in 1999 It is transmitted by mosquitoes from birds to humans and can cause severe disease in some individuals There is no specific treatment for West Nile Disease The target population for a West Nile vaccine is older people as they are more susceptible to severe disease This trial includes a dose-finding part with a placebo control in young healthy adults followed by a placebo-controlled examination of the chosen dose in older healthy adults
Outcome measures include a comparison of adverse events between active treatment and placebo a comparison of antibody and viremia measurements between dose levels and across age groups for the dose chosen for Part 2
Outcome measures include a comparison of adverse events between active treatment and placebo a comparison of antibody and viremia measurements between dose levels and across age groups for the dose chosen for Part 2
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