Evaluating the Comparative Safety and Immunogenicity of Three Lots of Novartis Meningococcal C Conjugate Vaccine in Healthy Toddlers
Status and phase
Conditions
Treatments
Details and patient eligibility
About
The study was to evaluate the safety and and immune response of each of three lots of Novartis Meningococcal C Conjugate Vaccine (MenC-CRM Liquid) when administered to Healthy Toddlers.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Healthy 12 - 23 (inclusive) month-old male or female toddlers.
- A parent/legal guardian was given written informed consent after the nature of the study has been explained.
- Available for both the visits scheduled in the study.
- In good health as determined by medical history, physical examination and clinical judgment of the investigator.
Exclusion criteria
-
History of any meningococcal vaccine administration.
-
Previous known or suspected disease caused by N. meningitidis.
-
Household contact with and/or intimate exposure to an individual with laboratory confirmed N. meningitidis infection or colonization.
-
History of severe allergic reaction after previous vaccinations, allergy to Latex, or hypersensitivity to any component of the vaccine.
-
Significant acute or chronic infection within the previous 7 days or axillary temperature ≥38.0°C within the previous 3 days.
-
Individuals who have received antibiotics within 6 days before vaccination.
-
Known or suspected autoimmune disease or impairment/alteration of the immune system resulting from (for example):
- Receipt of any immunosuppressive therapy at any time since birth.
- Receipt of any immunostimulants at any time since birth.
- Receipt of any systemic corticosteroids or chronic use of inhaled high-potency corticosteroids since birth (use of topical corticosteroids administered in limited areas of the body [for example, eczema on knees or face or elbows] is allowed).
- Immune deficiency disorder, or known HIV infection.
-
History of seizure, any progressive neurological disease or Guillain Barré Syndrome (exception: one self-limited non-medicated febrile seizure is acceptable).
-
Known bleeding diathesis, or any condition that may be associated with a prolonged bleeding time.
-
Receipt of blood, blood products and/or plasma derivatives or any parenteral immunoglobulin preparation in the past 12 weeks.
-
Taken any antipyretic medication in the previous 6 hours.
-
Received any other vaccines within 30 days prior to enrollment or intent to receive any other vaccine during the study (Exception: Inactivated influenza vaccine may be administered up to 15 days prior to study immunization and no less than 15 days after study immunization).
-
Toddler's parent(s) or legal guardian(s) are not able to comprehend and to follow all required study procedures for the whole period of the study.
-
Participation in any clinical trial with another investigational product 30 days prior to first study visit or intent to participate in another clinical study during this study.
-
Family members or household members of site research staff.
-
History or any illness/condition that, in the opinion of the investigator, might interfere with the results of the study or pose additional risk to the subjects due to participation in the study.
-
Any serious chronic or progressive disease according to judgment of the investigator (neoplasm, insulin dependent diabetes, cardiac, renal or hepatic disease).
Trial design
Primary purpose
Allocation
Interventional model
Masking
992 participants in 3 patient groups
Trial contacts and locations
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal