Immunogenicity and Reactogenicity of DTPa-HBV-IPV/Hib, Compared to DTPa-HBV-IPV and Hib Administered Separately
This study has been completed.
Sponsor:
GlaxoSmithKline
Information provided by:
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT01457508
First received: October 20, 2011
Last updated: NA
Last verified: October 2011
History: No changes posted
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Purpose
This study will assess the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals' (formerly SB Biologicals') DTPa-HBV-IPV/Hib (Infanrix hexa™) vaccine compared with separate administration of DTPa-HBV-IPV (Infanrix penta™) and Hib (Hiberix™) vaccine administered at 3, 5 and 11 (or 12) months of age.
| Condition | Intervention | Phase |
|---|---|---|
|
Hepatitis B Diphtheria Haemophilus Influenzae Type b (Hib) Poliomyelitis Pertussis Tetanus |
Biological: DTPa-HBV-IPV/Hib (Infanrix hexa™) Biological: DTPa-HBV-IPV (Infanrix penta™) Biological: Hib (Hiberix™) |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Study to Assess the Immunogenicity and Reactogenicity of DTPa-HBV-IPV Vaccine Mixed With Hib Vaccine to Healthy Infants at 3, 5 and 11 Months of Age, Compared to Each Vaccine Administered Separately |
Resource links provided by NLM:
MedlinePlus related topics:
Diphtheria
Flu
Hepatitis
Hepatitis A
Hepatitis B
Polio and Post-Polio Syndrome
Tetanus
Whooping Cough
U.S. FDA Resources
Further study details as provided by GlaxoSmithKline:
Primary Outcome Measures:
- Immunogenicity with respect to the components of the study vaccine in terms of number of subjects with antibody titres greater than or equal to cut off value [ Time Frame: One month after the 2nd dose of the primary vaccination course ( Month 3) ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Immunogenicity with respect to the components of the study vaccines in terms of number of seroprotected subjects [ Time Frame: One month after the 2nd dose ( Month 3), before and one month after the 3rd dose of the primary vaccination course ( Month 8 and 9) ] [ Designated as safety issue: No ]
- Immunogenicity with respect to the components of the study vaccines in terms of number of seropositive subjects [ Time Frame: One month after the 2nd dose ( Month 3), before and one month after the 3rd dose of the primary vaccination course ( Month 8 and 9) ] [ Designated as safety issue: No ]
- Immunogenicity with respect to the components of the study vaccines in terms of antibody titres [ Time Frame: One month after the 2nd dose ( Month 3), before and one month after the 3rd dose of the primary vaccination course ( Month 8 and 9) ] [ Designated as safety issue: No ]
- Immunogenicity with respect to the components of the study vaccines in terms of vaccine response [ Time Frame: One month after the 3rd dose ( Month 9), and one month after the 2nd dose of the primary vaccination course ( Month3) ] [ Designated as safety issue: No ]
- Occurrence of solicited local symptoms [ Time Frame: Within 4 days after each vaccination and overall ] [ Designated as safety issue: No ]
- Occurrence of solicited general symptoms [ Time Frame: Within 4 days after each vaccination and overall ] [ Designated as safety issue: No ]
- Occurrence of unsolicited symptoms [ Time Frame: Within 30 days after each vaccination and overall ] [ Designated as safety issue: No ]
- Occurrence of serious adverse events [ Time Frame: Throughout the entire study up to and including 30 days post-vaccination ( Month 0 to Month 9) ] [ Designated as safety issue: No ]
| Enrollment: | 440 |
| Study Start Date: | January 1999 |
| Study Completion Date: | March 2000 |
| Primary Completion Date: | March 2000 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Group A
Subjects will receive one single injection of DTPa-HBV-IPV vaccine mixed with Hib vaccine.
|
Biological: DTPa-HBV-IPV/Hib (Infanrix hexa™)
Three doses administered intramuscularly
|
|
Active Comparator: Group B
Subjects will receive two separate injections of DTPa-HBV-IPV and Hib vaccine.
|
Biological: DTPa-HBV-IPV (Infanrix penta™)
Three doses administered intramuscularly
Biological: Hib (Hiberix™)
Three doses administered intramuscularly
|
Eligibility| Ages Eligible for Study: | 12 Weeks to 16 Weeks |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- A male or female 3 months of age at the time of the first vaccination.
- Free of obvious health problems as established by medical history and clinical examination before entering into the study.
- Written informed consent obtained from the parents or guardians of the subject after they have been advised of the risks and benefits of the study in a language which they clearly understood, and before performance of any study procedure.
Exclusion Criteria:
The following criteria should be checked at the time of study entry. If any apply at the time of study entry, the subject must not be included in the study:
- Use of any investigational or non-registered 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.
- Administration of chronic immunosuppressants or other immune-modifying drugs within three months before vaccination.
- Administration of a vaccine not foreseen by the study within 30 days before each dose of the study vaccines and ending 30 days after.
- Previous vaccination against diphtheria, tetanus, pertussis, hepatitis B, polio and/or Hib disease.
- History of /or intercurrent diphtheria, tetanus, pertussis, hepatitis B, polio and/or Hib disease or infection.
- Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection.
- History of allergic disease or reactions likely to be exacerbated by any component of the vaccine, including allergic reactions to neomycin and polymyxin B.
- Major congenital defects or serious chronic illness.
- History of seizures or of any neurological disease at study entry.
- Administration of immunoglobulins and/or any blood products since birth, or planned administration during the study period.
- Acute disease at time of enrolment
Contacts and Locations
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Cheri Hudson; Clinical Disclosure Advisor, GSK Clinical Disclosure |
| ClinicalTrials.gov Identifier: | NCT01457508 History of Changes |
| Other Study ID Numbers: | 217744/054 |
| Study First Received: | October 20, 2011 |
| Last Updated: | October 20, 2011 |
| Health Authority: | Italy: AIFA - Italian Ministry of Health |
Keywords provided by GlaxoSmithKline:
|
combination vaccine DTPa-HBV-IPV Hib |
Additional relevant MeSH terms:
|
Diphtheria Hepatitis Hepatitis A Hepatitis B Influenza, Human Whooping Cough Poliomyelitis Tetanus Corynebacterium Infections Actinomycetales Infections Gram-Positive Bacterial Infections Bacterial Infections Liver Diseases Digestive System Diseases Hepatitis, Viral, Human |
Virus Diseases Enterovirus Infections Picornaviridae Infections RNA Virus Infections Hepadnaviridae Infections DNA Virus Infections Orthomyxoviridae Infections Respiratory Tract Infections Respiratory Tract Diseases Bordetella Infections Gram-Negative Bacterial Infections Infection Myelitis Central Nervous System Viral Diseases Central Nervous System Infections |
ClinicalTrials.gov processed this record on May 23, 2013