Viewing Study NCT00161954



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Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00161954
Status: COMPLETED
Last Update Posted: 2015-05-21
First Post: 2005-09-08

Brief Title: Immunogenicity and Safety Study of a Rapid Immunization Schedule With FSME-IMMUN 05 mL in Healthy Adults Aged 16 - 65 Years
Sponsor: Pfizer
Organization: Pfizer

Study Overview

Official Title: Open Phase IV Clinical Study to Evaluate the Immunogenicity and Safety of a Rapid Immunization Schedule With FSME-IMMUN 05 mL in Healthy Adults Aged 16 - 65 Years
Status: COMPLETED
Status Verified Date: 2015-05
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 objective of this study is to establish the earliest time point at which vaccines are expected to show seropositive antibody levels after vaccination with FSME-IMMUN 05 mL using a rapid immunization schedule 2 vaccinations administered 12 - 2 days apart
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