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Meningococcal group A, C, Y and W-135 conjugate vaccine
Lee H Harrison1, Nitin Mohan, Peter Kirkpatrick
1Infectious Diseases Epidemiology Research Unit, University of Pittsburgh Graduate School of Public Health and School of Medicine, Pittsburgh, Pennsylvania 15101, USA. lharriso@edc.pitt.edu
Insights
A new quadrivalent conjugate vaccine, Menveo, was FDA-approved in February 2010. It prevents invasive meningococcal disease in individuals aged 11-55 years.
Area of Science:
- Vaccinology
- Microbiology
- Public Health
Background:
- Invasive meningococcal disease (IMD) poses a significant public health threat.
- Neisseria meningitidis serogroups A, C, Y, and W-135 are major causative agents of IMD.
Purpose of the Study:
- To report the US FDA approval of a quadrivalent conjugate vaccine for IMD prevention.
- To outline the target population and causative serogroups covered by the vaccine.
Main Methods:
- Review of regulatory submission data for vaccine approval.
- Identification of the vaccine's composition and target demographic.
Main Results:
- The US FDA approved the quadrivalent conjugate vaccine, Menveo, in February 2010.
- The vaccine targets invasive meningococcal disease caused by specific serogroups.
Conclusions:
- Menveo provides a new option for preventing IMD in a defined age group.
- The approval signifies advancements in conjugate vaccine technology for bacterial meningitis prevention.
Abstract:
In February 2010, a quadrivalent conjugate vaccine (Menveo; Novartis Vaccines and Diagnostics) was approved by the US FDA to prevent invasive meningococcal disease caused by Neisseria meningitidis serogroups A, C, Y and W-135 in people aged 11-55 years.
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