Infections, Meningococcal Clinical Trial
Official title:
Multicentric, Surveillance Study to Monitor Safety of GSK Biologicals' Purified Meningococcal Polysaccharide Vaccine of Serogroups ACWY in 3,000 Filipino Subjects Aged Above 2 Years When Administered According to the Prescribing Information.
GlaxoSmithKline Philippines has submitted a registration file for its Purified Meningococcal Polysaccharide of Serogroup ACWY Vaccine (Mencevax ACWY). This study is being conducted to collect clinical data in the local target population in order to assess the occurrence of rare adverse events after vaccination as per the requirement of Philippines Bureau of Food and Drugs Directive.
All subjects will receive a single dose of GSK Biologicals' Mencevax ACWY vaccine according
to the prescribing information. Subjects will be stratified into the following age groups:
2 to 5 years 6 to 17 years > 18 years The Protocol Posting has been updated in order to
comply with the FDA Amendment Act, September 2007.
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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Phase 3 | |
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Phase 2 | |
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Phase 3 | |
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Phase 3 | |
| Completed |
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Phase 3 | |
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The Long-term Antibody Persistence of MenACWY-TT Vaccine (PF-06866681) Versus Meningitec(Registered) or Mencevax(Registered) ACWY in Healthy Adolescents and Adults and a Booster Dose of MenACWY-TT Administered 10 Years Post Primary Vaccination
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Phase 3 | |
| Completed |
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Phase 2 | |
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Phase 3 | |
| Completed |
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Phase 3 | |
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Phase 2 | |
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Phase 2 | |
| Completed |
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Phase 3 | |
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Phase 3 | |
| Completed |
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Phase 3 | |
| Completed |
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Phase 2 |