Meningococcal Disease Clinical Trial
Official title:
A Case-control Study of the Efficacy of a New Serogroup A Meningococcal Conjugate Vaccine (MenAfriVac) in Mali and Niger
Major epidemics of meningococcal meningitis occur in countries of the African Sahel and sub-Sahel every few years. Most of these epidemics are caused by meningococci belonging to serogroup A. Until recently there has been no serogroup A conjugate vaccine available to prevent epidemics in Africa because none of the major pharmaceutical companies wanted to develop such a vaccine for commercial reasons. For this reason a public private partnership was established in 2001, the Meningitis Vaccine Project (MVP), with support from the Bill and Melinda Gates Foundation, to develop an affordable new serogroup A meningococcal conjugate vaccine for Africa. The new vaccine, MenAfriVacâ„¢, received WHO pre-qualification in 2010 and mass campaigns started in Burkina Faso, Mali and Niger in 2010. It is expected that full coverage through mass vaccination campaigns will be achieved by the end of 2011 in these three countries. A case-control study will be conducted in Mali and Niger during the epidemic seasons of 2012 and 2013 to assess the efficacy of MenAfriVacâ„¢.
Massive epidemics of meningococcal disease continue to occur every few years in countries of
the African Sahel and sub-Sahel - the African meningitis belt. In 2009 there were more than
50,000 reported cases in Nigeria alone. Most of these epidemics are caused by meningococci
belonging to capsular polysaccharide serogroup A. African epidemics can be contained by
existing meningococcal polysaccharide vaccines, saving many lives, but epidemics are not
prevented by use of these vaccines. Recently, a new serogroup A meningococcal
polysaccharide/protein conjugate vaccine (MenAfriVac), which may be able to prevent
epidemics, was prequalified by the World Health Organization. This vaccine was developed by
the Meningitis Vaccine Project (MVP) and is being produced at a cost ($0.40 per dose) that
is affordable by countries of the African meningitis belt. Mass vaccination campaigns
started in Burkina Faso, Mali and Niger at the end of 2010. Full coverage will be achieved
in 2011 with progressive deployment to other countries in the meningitis belt.
The safety and immunogenicity of MenAfriVac have been established through phase 1 and phase
2 trials conducted in India and Africa but no efficacy trials have been undertaken.
Prequalification was granted on the assumption that the high level of immunogenicity
demonstrated in African populations would be reflected by a similar degree of efficacy. This
is likely, but it is important that the efficacy of this vaccine is established definitively
before large sums are spent on deploying the vaccine across the African meningitis belt.
Therefore, a case control study to determine the efficacy of MenAfriVac in preventing
serogroup A meningococcal meningitis in Mali and Niger is proposed.
A case-control study will be conducted in Mali and in Niger during the 2011, 2012 and 2013
meningitis seasons. Cases of meningitis will be detected through existing routine
surveillance systems and their etiology established using standard microbiology or rapid
diagnostic tests. Cases of proven serogroup A meningococcal meningitis (culture, antigen or
PCR positive) will be matched with two hospital and two community controls who will, in
turn, be matched with the cases for age and place of residence. A questionnaire will be
administered to cases and controls which asks about previous meningococcal vaccination and
other risk factors for meningococcal disease which might confound or modify assessment of
the impact of vaccination with MenAfriVac. A blood sample will be collected for measurement
of serogroup A meningococcal bactericidal and tetanus antibodies, as well as total
immunoglobulin levels. Determination of vaccination status will be facilitated by the fact
that vaccination cards will be issued to all recipients at the time of vaccination by the
mass vaccination teams. Vaccine efficacy will be determined by comparing the odds of
exposure to MenAfriVac in cases and controls.
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Observational Model: Case Control, Time Perspective: Prospective
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