Viewing Study NCT00092482



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00092482
Status: COMPLETED
Last Update Posted: 2017-03-22
First Post: 2004-09-22

Brief Title: Immunogenicity Bridge Between an Investigational Monovalent Vaccine and the Equivalent Component of Gardasil V501 a Quadrivalent Vaccine V501-012COMPLETED
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: Immunogenicity and Safety of Gardasil V501 Quadrivalent HPV Types 6 11 16 18 L1 Virus-Like Particle VLP Vaccine in Consistency Lots for 16- to 23-Year-Old Women With and Additional Immunogenicity Bridge to the Monovalent HPV 16 Vaccine Pilot Manufacturing Lot Study-The FUTURE Study Females United to Unilaterally Reduce EndoEctocervical Disease
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 the study is to determine if an investigational vaccine with a single component develops an immune response that is similar to the equivalent investigational vaccine with four components to reduce cervical disease
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
Secondary IDs
Secondary ID Type Domain Link
2004_080 None None None