Status:
COMPLETED
Safety and Immunogenicity in Dose-Ranging and Formulation-Finding Meningococcal B (MenB) Vaccine Study in 2-month-old Infants
Lead Sponsor:
Novartis Vaccines
Conditions:
Meningococcal Meningitis
Meningococcal Infections
Eligibility:
All Genders
55-89 years
Phase:
PHASE2
Brief Summary
This study is aimed at assessing the safety and immunogenicity of different doses and formulations of a new Novartis Meningococcal B Recombinant Vaccine.
Eligibility Criteria
Inclusion
- Healthy 2-month old infants (55-89 days, inclusive), born after full term pregnancy, gestational age ≥ 37 weeks and a birth weight ≥ 2.5 kg
- Available for all the visits scheduled in the study and for whom a parent/legal guardian is willing/able to comply with all protocol requirements
Exclusion
- Any meningococcal B or C vaccine administration
- Prior vaccination with any Diphtheria, Tetanus, Pertussis (acellular or whole cell), Polio (either Inactivated or Oral), Haemophilus influenzae type b (Hib), and Pneumococcal antigens;
- Any ascertained or suspected disease caused by N. meningitidis
- Household contact with and/or intimate exposure to an individual with laboratory confirmed N. meningitidis
- History of severe allergic reaction after previous vaccinations
- Recent significant acute or chronic infection
- Oral or parenteral antibiotic treatment in the 7 days prior to the scheduled blood draw;
- Any serious chronic or progressive disease according to the judgment of the investigator (e.g., neoplasm, diabetes mellitus Type I, cardiac disease, hepatic disease, progressive neurological disease or seizure, either associated with fever or as part of an underlying neurological disorder or syndrome, autoimmune disease, HIV infection or AIDS, or blood dyscrasias or diathesis, signs of cardiac or renal failure or severe malnutrition)
- Any impairment/alteration of the immune system resulting from (for example):
- Receipt of any immunosuppressive therapy at any time since birth
- Receipt of immunostimulants at any time since birth
- Use of systemic corticosteroids or chronic use of inhaled high-potency corticosteroids at any time since birth
- Receipt of blood, blood products and/or plasma derivatives or any parenteral immunoglobulin preparation
- Participation in another clinical trial
- Family members and household members of research staff
- History of seizure
- Any contraindication to paracetamol
Key Trial Info
Start Date :
July 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2012
Estimated Enrollment :
1507 Patients enrolled
Trial Details
Trial ID
NCT00937521
Start Date
July 1 2009
End Date
February 1 2012
Last Update
April 7 2015
Active Locations (38)
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1
Hospital Privado de Córdoba CMC SA
Naciones Unidas 346, Córdoba Province, Argentina, X5016KHE
2
Universidad de Chile, Av Independencia 1027
Comuna de Independencia, Santiago Metropolitan, Chile
3
Consultorio Manuel Bustos
Lo Cruzat 486, Quilicura, Santiago Metropolitan, Chile
4
Samostatna ordinace praktickeho lekare pro deti a dorost
O. Kubina 17, Boskovice, Czechia, 680 01