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A Clinical Trial to Observe the Safety of 23-Valent Pneumococcal Polysaccharide Vaccine in Target Population Aged 2 Years and Above
An open clinical trial of a 23-valent pneumococcal polysaccharide vaccine (PPV23) developed by Sinovac Life Science Co., Ltd was conducted to evaluate the safety of Sinovac PPV23 in target population of individuals aged 2 years and above. All participants received 1 dose of PPV23 and self-selected whether to receive 1 dose of influenza vaccine at the same time.
Age
2 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Jiangsu Provincial Center for Disease Prevention and Control
Nanjing, Jiangsu, China
Start Date
July 2, 2022
Primary Completion Date
April 5, 2024
Completion Date
April 5, 2024
Last Updated
July 17, 2025
19,267
ACTUAL participants
23-valent pneumococcal polysaccharide vaccine
BIOLOGICAL
Influenza vaccine
BIOLOGICAL
Lead Sponsor
Sinovac Biotech Co., Ltd
NCT06675032
NCT02285036
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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