Status:
COMPLETED
Immunogenicity and Safety of a DTPa-HBV-IPV/Hib Vaccine Given at 2, 3 and 4 Months of Age
Lead Sponsor:
GlaxoSmithKline
Conditions:
Acellular Pertussis
Tetanus
Eligibility:
All Genders
8-12 years
Phase:
PHASE2
Brief Summary
The purpose of this study is to show that the immunogenicity of newly formulated DTPa-HBV-IPV/Hib vaccine is as good as the immunogenicity of the currently licensed formulation of the vaccine. The vac...
Eligibility Criteria
Inclusion
- A healthy male or female between, and including, 8 and 12 weeks of age at the time of the first vaccination.
- Written informed consent obtained from the parents/guardians of the subject.
- Born after a normal gestation period of 36 to 42 weeks.
Exclusion
- Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine(s) within 30 days preceding the first dose of study vaccine, or planned use during the study period.
- Chronic administration (defined as more than 14 days) of immunosuppressants or other immune-modifying drugs from birth until first primary vaccination dose.
- Administration of immunoglobulins and/or any blood products since birth or planned administration during the study period.
- Administration/planned administration of a vaccine not foreseen by the study protocol during the period starting 30 days before the administration of the first dose and ending 30 days after the last dose, with the exception of the human rotavirus (HRV) vaccine.
- Concurrently participating in another clinical study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product (pharmaceutical product or device).
- Evidence of previous or intercurrent diphtheria, tetanus, pertussis, polio, hepatitis B and/or Haemophilus influenza type b (Hib) vaccination or disease.
- Hepatitis B virus (HBV) vaccination at birth.
- History of seizures or progressive neurological disease.
Key Trial Info
Start Date :
October 1 2006
Trial Type :
INTERVENTIONAL
End Date :
May 1 2007
Estimated Enrollment :
450 Patients enrolled
Trial Details
Trial ID
NCT00376779
Start Date
October 1 2006
End Date
May 1 2007
Last Update
November 4 2016
Active Locations (6)
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1
GSK Investigational Site
Jarvenpaa, Finland, 04400
2
GSK Investigational Site
Oulu, Finland, 90100
3
GSK Investigational Site
Pori, Finland, 28120
4
GSK Investigational Site
Tampere, Finland, 33100