Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Immunogenicity and Safety of Men ACWY in Infants (6 & 12 Months)
This study has been completed.
Sponsors and Collaborators: Novartis
Novartis Vaccines
Information provided by: Novartis
ClinicalTrials.gov Identifier: NCT00310856
  Purpose

To assess the immunogenicity of Chiron Men ACWY conjugate vaccine (Men ACWY) when administered as a two-dose schedule at 6 and 12 months of age.


Condition Intervention Phase
Meningococcal Meningitis
Biological: Meningococcal ACWY conjugate vaccine
Phase II

MedlinePlus related topics: Meningitis
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Open Label, Dose Comparison, Parallel Assignment, Safety/Efficacy Study
Official Title: A Phase II, Partially Randomized, Open Label, Multicenter Study to Evaluate the Safety and Immunogenicity After One or Two Doses of a Commercially Available Meningococcal ACWY Conjugate Vaccine Administered to Healthy Infants and Young Children

Further study details as provided by Novartis:

Primary Outcome Measures:
  • immunogenicity as measured by serum bactericidal activity and GMTs when administered at 6 and 12 months of age.

Secondary Outcome Measures:
  • booster response of C component of the vaccine when administered at 18 months of age, after second immunization at 12 months, as measured serum bactericidal activity and GMTs. Safety and tolerability.

Estimated Enrollment: 175
Study Start Date: June 2005
  Eligibility

Ages Eligible for Study:   6 Months to 18 Months
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy infants 6 months of age who previously received two doses of both heptavalent conjugate pneumococcal and DTaP-Hib-IPV vaccines
  • healthy subjects 12 months of age who previously received 3 doses of DTaP-Hib-IPV vaccine

Exclusion Criteria:

  • Subjects who previously received any meningococcal vaccine
  • Subjects with any serious, acute or chronic progressive disease.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00310856

Locations
Canada
Clinical Trials Research Center, Department of Pediatrics, Dalhousie University IWK Health Center
Halifax, Canada, B3K 6R8
Children's Hospital of Eastern Ontario Research Institute
Ottawa, Canada
Canada, Ontario
Herridge Community Health Clinic
Ottawa, Ontario, Canada
Sponsors and Collaborators
Novartis
Novartis Vaccines
Investigators
Principal Investigator: Novartis Vaccines - Drug Information Services Novartis Vaccines & Diagnostics
  More Information

Study ID Numbers: V59P9
Study First Received: April 3, 2006
Last Updated: April 16, 2008
ClinicalTrials.gov Identifier: NCT00310856  
Health Authority: United States: Food and Drug Administration;   Canada: Health Canada

Keywords provided by Novartis:
meningitis
children
vaccine

Study placed in the following topic categories:
Bacterial Infections
Central Nervous System Infections
Meningococcal Infections
Meningitis, Bacterial
Meningitis, Meningococcal
Central Nervous System Diseases
Healthy
Meningococcal infection
Gram-Negative Bacterial Infections
Neisseriaceae Infections
Meningitis

Additional relevant MeSH terms:
Nervous System Diseases
Central Nervous System Bacterial Infections

ClinicalTrials.gov processed this record on January 15, 2009