Drug intelligence / Profile preview

Pneumovax 23

Development stage
Approved
Lead developer
Merck
Modality
Vaccines & Immunotherapeutics
Administration
Intramuscular, Subcutaneous
01

Overview

Pneumovax 23 is a 23-valent pneumococcal polysaccharide vaccine (PPSV23) developed and manufactured by Merck. It consists of a mixture of highly purified capsular polysaccharides from 23 different serotypes of Streptococcus pneumoniae, which together account for the majority of invasive pneumococcal disease. The vaccine works by inducing a T-cell independent B-cell response, leading to the production of type-specific antibodies that enhance the opsonization, phagocytosis, and killing of pneumococci by phagocytic cells. It is FDA-approved for active immunization for the prevention of pneumococcal disease in individuals 50 years of age or older and those 2 years of age or older who are at increased risk. The University of California, Davis, has specifically investigated the vaccine's immunologic efficacy in adult trauma patients with splenic injuries (nonoperative, embolized, or splenectomized) to determine the optimal management of their increased infection risk.

Brand names
Pneumovax 23Pneumovax23Pneumovax-23Pneumovax
Other names
23-valent pneumococcal polysaccharide vaccinePPSV23PPSV-23PPSV 23pneumococcal vaccine polyvalent
02

Targets

CPS (Streptococcus pneumoniae capsular polysaccharide)

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