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NCT06044077

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

Recruiting now Phase 3 Last updated 21 September 2023
What this trial tests

Phase 3 trial testing 23-valent pneumococcal polysaccharide vaccine in Pneumococcal Disease in 1,920 participants. Currently enrolling.

Timeline
8 September 2023
Primary endpoint
8 March 2024
31 July 2029

Quick facts

Lead sponsorAimei Vacin BioPharm (Zhejiang) Co., Ltd.
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposeprevention
Enrollment1,920
Start date8 September 2023
Primary completion8 March 2024
Estimated completion31 July 2029
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Aimei Vacin BioPharm (Zhejiang) Co., Ltd. — full company profile →

Who can join

2 and older, any sex, with Pneumococcal Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of 23-valent pneumococcal polysaccharide vaccine

Trials testing the same drug.

Other recruiting trials for Pneumococcal Disease

Currently open trials in the same condition.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06044077.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing