The purpose of this observer blinded study is to provide information on vaccine immunogenicity and reactogenicity in comparison with the US standard of care (ProQuad®) when administered with Hepatitis A vaccine and Pneumococcal vaccine.
Age range
12 Months – 14 Months
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Number of Subjects With Seroresponse for Antibodies to Varicella Virus (VZV)
Timeframe: At Day 42 after vaccination
Concentration of Antibodies to Varicella Virus (VZV)
Timeframe: At Day 42 after vaccination
Number of Subjects With Seroresponse for Antibodies to Mumps Virus
Timeframe: At Day 42 after vaccination
Number of Subjects With Seroresponse for Antibodies to Measles Virus
Timeframe: At Day 42 after vaccination
Number of Subjects With Seroresponse for Antibodies to Rubella Virus
Timeframe: At Day 42 after vaccination
Concentration of Antibodies to Hepatitis A Virus (HAV)
Timeframe: At Day 42 after vaccination
Concentration of Antibodies to S. Pneumoniae Serotypes 4, 6B, 9V, 14, 18C, 19F and 23F
Timeframe: At Day 42 after vaccination