Viewing Study NCT00092404



Ignite Creation Date: 2024-05-05 @ 11:36 AM
Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00092404
Status: COMPLETED
Last Update Posted: 2017-03-15
First Post: 2004-09-22

Brief Title: Safety Tolerability and Immunogenicity of an Investigational Vaccine With Recombinant Human Albumin rHA in Children 12 to 18 Months of Age V205C-009COMPLETED
Sponsor: Merck Sharp Dohme LLC
Organization: Merck Sharp Dohme LLC

Study Overview

Official Title: A Comparison of the Safety Tolerability and Immunogenicity of V205C Manufactured With Recombinant Human Albumin rHA Versus V205C Manufactured With Pooled-Donor Human Serum Albumin HSA in Healthy Children 12 to 18 Months of Age
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 trial is to study the safety and immune response to measles mumps and rubella in children who were vaccinated with an investigational measles-mumps-rubella live vaccine made with artificially made human protein
Detailed Description: The duration of treatment is 6 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
2004_074 None None None