The purpose of this phase 3 multicenter, double-blinded, placebo-controlled study in India is to learn about the safety and immunogenicity of RSVpreF in adults.
Age range
18 Years
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.
Proportion of participants reporting local reactions within 7 days following investigational product administration
Timeframe: Within 7 days
Percentage of participants reporting systemic events within 7 days following investigational product administration
Timeframe: Within 7 days
Percentage of participants reporting adverse events (AEs) through 1 month following investigational product administration
Timeframe: 1 month after vaccination
Percentage of participants reporting serious adverse events (SAEs) throughout the study
Timeframe: 3 months after vaccination
Neutralizing Titers (NTs) for RSV A and RSV B expressed as Geometric Mean Titers (GMT)
Timeframe: Before vaccination, 1 month after vaccination
NTs for RSV A and RSV B expressed as Geometric Mean Fold Rise (GMFR)
Timeframe: Before vaccination, 1 month after vaccination
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NTs for RSV A and RSV B expressed as seroresponse rate
Timeframe: 1 month after vaccination