Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06044077

A Clinical Trial to Evaluate the Immunogenicity and Safety of the 23-valent Pneumococcal Polysaccharide Vaccine in Healthy People

A Randomized, Blinded, Parallel Controlled Phase 3 Clinical Trial to Evaluate the Immunogenicity and Safety of the 23-valent Pneumococcal Polysaccharide Vaccine in Healthy People Aged 2 Years and Above

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
1,920 (estimated)
Sponsor
Aimei Vacin BioPharm (Zhejiang) Co., Ltd. · Industry
Sex
All
Age
2 Years
Healthy volunteers
Accepted

Summary

This study is a randomized, blinded, parallel controlled phase 3 clinical trial to evaluate the immunogenicity and safety of the 23-valent pneumococcal polysaccharide vaccine in healthy people aged 2 years and above.

Conditions

Interventions

TypeNameDescription
BIOLOGICAL23-valent pneumococcal polysaccharide vaccine23-valent pneumococcal polysaccharide vaccine from Aimei Vacin BioPharm (Zhejiang) Co., Ltd.
BIOLOGICALcontrol pneumococcal polysaccharide vaccine23-valent pneumococcal polysaccharide vaccine from Merck Sharp \& Dohme Corp

Timeline

Start date
2023-09-08
Primary completion
2024-03-08
Completion
2029-07-31
First posted
2023-09-21
Last updated
2023-09-21

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06044077. Inclusion in this directory is not an endorsement.

A Clinical Trial to Evaluate the Immunogenicity and Safety of the 23-valent Pneumococcal Polysaccharide Vaccine in Healt (NCT06044077) · Clinical Trials Directory