This first-in-human (FIH) phase 1 study is designed to evaluate in contained conditions the safety, immunogenicity, shedding, and genetic stability of two novel oral polio vaccine type 2 (nOPV2) vaccine candidates in IPV-primed adults before testing in a larger adult and adolescent (\> 15 y of age) population, and then in young children and infants.
Age range
18 Years – 50 Years
Sex
ALL
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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 Participants With Serious Adverse Events and Severe Adverse Events Throughout the Study
Timeframe: From Day 0 up to 42 days
Percentage of Participants With Viral Shedding
Timeframe: Days 0, 1, 2, 3, 4, 5, 6, 7, 14, 21, and 28
Cell Culture Infective Dose of Shed Virus in Virus-positive Stool Samples
Timeframe: Days 1, 2, 3, 4, 5, 6, 7, 14, 21, and 28
Time to Shedding Cessation
Timeframe: Stool samples were collected from the day of vaccination to Day 28 or until shedding cessation; up to 89 days (novel OPV2 candidate 1) and 48 days (novel OPV candidate 2).
Shedding Index
Timeframe: Days 7, 14, 21, and 28