Last reviewed · How we verify

Investigational 23-valent PPV

Sinovac Biotech Co., Ltd · FDA-approved active Biologic

A 23-valent pneumococcal polysaccharide vaccine that stimulates the immune system to produce antibodies against 23 serotypes of Streptococcus pneumoniae.

A 23-valent pneumococcal polysaccharide vaccine that stimulates the immune system to produce antibodies against 23 serotypes of Streptococcus pneumoniae. Used for Prevention of invasive pneumococcal disease and pneumococcal pneumonia in adults and children.

At a glance

Generic nameInvestigational 23-valent PPV
SponsorSinovac Biotech Co., Ltd
Drug classPneumococcal polysaccharide vaccine
TargetStreptococcus pneumoniae capsular polysaccharides (23 serotypes)
ModalityBiologic
Therapeutic areaImmunology / Infectious Disease
PhaseFDA-approved

Mechanism of action

The vaccine contains purified capsular polysaccharides from 23 different serotypes of pneumococcus conjugated or presented to elicit a humoral immune response. This induces B-cell activation and antibody production (primarily IgG) that provides protection against invasive pneumococcal disease and pneumococcal pneumonia caused by the included serotypes. As a polysaccharide vaccine, it primarily activates T-cell-independent B-cell responses.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: