Viewing Study NCT00697229



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Study NCT ID: NCT00697229
Status: COMPLETED
Last Update Posted: 2008-06-13
First Post: 2008-06-11

Brief Title: Immunogenicity Reactogenicity of HBV-MPL Vaccine and Engerix-B in Healthy Adults Following 2 Different Schedules
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: Study to Evaluate the Immunogenicity and Reactogenicity of GSK Biologicals MPL-Adjuvanted Recombinant Hepatitis B Vaccine in Comparison With Those of Engerix-B in Healthy Adult Volunteers Following 2 Different Schedules
Status: COMPLETED
Status Verified Date: 2008-06
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 evaluate the safety immunogenicity and reactogenicity of MPL-adjuvanted recombinant hepatitis B vaccine in comparison with those of Engerix-B in healthy adult volunteers following two different schedules 0 2 months and 0 6 months
Detailed Description: At the time of conduct of this study the sponsor GlaxoSmithKline was known by its former name SmithKline Beecham

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