Viewing Study NCT00109122



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Last Modification Date: 2024-10-26 @ 9:11 AM
Study NCT ID: NCT00109122
Status: COMPLETED
Last Update Posted: 2017-03-15
First Post: 2005-04-22

Brief Title: Safety Tolerability and the Bodys Ability to Develop Resistance to an Investigational Vaccine for Shingles V211-007
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: A Double-Blind Placebo-Controled Randomized Study to Evaluate Safety Tolerability and Immunogenicity After 1 and 2 Doses of Zoster Vaccine
Status: COMPLETED
Status Verified Date: 2017-03
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 the immunity the bodys protection against shingles after receiving two doses of an investigational vaccine or placebo a look alike vaccine with no active ingredients
Detailed Description: The duration of treatment is 12 weeks

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
Secondary IDs
Secondary ID Type Domain Link
2005_017 None None None