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Comparison of Safety and Immunogenicity of Pediacel™ and Infanrix™ IPV+Hib (Penta) Given in a 3 Dose Schedule in Infants

Primary Purpose

Pertussis, Diphtheria, Tetanus

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
DT5aP-IPV-Hib 5-component Pertussis vaccine
Infanrix® -IPV+Hib
Sponsored by
Sanofi Pasteur, a Sanofi Company
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pertussis focused on measuring Haemophilus influenzae type b;, Corynebacterium diphtheriae;, Clostridium tetani;, Bordetella pertussis;, poliovirus types 1, 2 and 3;, Vero cell;, Influenza;, Diphtheria

Eligibility Criteria

80 Days - 120 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Infants aged 80 to 120 days inclusive on the day of inclusion. Born at full term of pregnancy (> 37 weeks) Informed consent form signed by the parent(s) or other legal representative according to local regulations Parent(s) or legal representative able to attend all scheduled visits and to understand and comply with the study procedures (able to read and write; access to a telephone). Exclusion Criteria: Rectal temperature ≥ 38.0°C Moderate or severe acute illness with or without fever Participation in another clinical trial in the 4 weeks preceding the first trial vaccination Having received any DTaP, IPV, or Hib vaccines prior to study initiation or any vaccination in the 4 weeks preceding the first trial vaccination Planned participation in another clinical trial during the present trial period Known history of diphtheria, tetanus, pertussis, H. influenzae type b infections, poliomyelitis Congenital or acquired immunodeficiency, immunosuppressive therapy such as long-term systemic corticosteroids therapy Systemic hypersensitivity to any of the vaccine components (including neomycin, streptomycin, polymyxin B and formaldehyde) History of a life-threatening reaction (such as encephalopathy, Hypotonic Hyporesponsive Episode, severe fever, convulsions, etc.) to the trial vaccine or a vaccine containing the same substances Blood or blood-derived products (immunoglobulins) received in the past 4 weeks Vaccination planned in the 6 weeks following any trial vaccination Known HIV seropositivity Thrombocytopenia or a bleeding disorder contraindicating intramuscular vaccination History of seizures or progressive, evolving or unstable neurological condition Clinically significant findings on review of systems that might interfere with correct vaccination or which, in the opinion of the Investigator, would interfere with the evaluation of the vaccine or pose a health risk to the subject.

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Group 1

Group 2

Arm Description

Participants will receive PEDIACEL vaccine

Participants will receive Infanrix-IPV+Hib vaccines

Outcomes

Primary Outcome Measures

To provide information concerning the immunogenicity of PEDIACEL® Vaccine.

Secondary Outcome Measures

To provide information concerning the safety after administration of PEDIACEL® Vaccine

Full Information

First Posted
February 3, 2006
Last Updated
January 6, 2015
Sponsor
Sanofi Pasteur, a Sanofi Company
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1. Study Identification

Unique Protocol Identification Number
NCT00287092
Brief Title
Comparison of Safety and Immunogenicity of Pediacel™ and Infanrix™ IPV+Hib (Penta) Given in a 3 Dose Schedule in Infants
Official Title
A Randomised, Controlled, Double-Blind Study of the Immunogenicity and Safety of PEDIACEL®, a Combined Diphtheria, Tetanus, Five Component Acellular Pertussis, Inactivated Poliomyelitis and Haemophilus Influenzae Type b Conjugate Vaccine (Adsorbed) Compared To Infanrix®-IPV+Hib When Both Vaccines Are Given to Infants Using a Three Dose Immunisation Schedule ("Nordic Schedule" 3-5-12 Months)
Study Type
Interventional

2. Study Status

Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
May 2007 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sanofi Pasteur, a Sanofi Company

4. Oversight

5. Study Description

Brief Summary
Pediacel™ is currently licensed in the UK for use as a 3 dose regimen for the active immunisation of infants against Diphtheria, Tetanus, Pertussis, Poliomyelitis and invasive infections caused by Haemophilus influenzae type b. However there are currently no clinical data supporting the use of Pediacel™ using a 3, 5, and 12 months of age vaccination schedule. This study is designed to provide safety and immunogenicity data to support the use of Pediacel™ according to a 3, 5, and 12 months schedule.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pertussis, Diphtheria, Tetanus, Poliomyelitis, Haemophilus Influenzae Type b
Keywords
Haemophilus influenzae type b;, Corynebacterium diphtheriae;, Clostridium tetani;, Bordetella pertussis;, poliovirus types 1, 2 and 3;, Vero cell;, Influenza;, Diphtheria

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
807 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Experimental
Arm Description
Participants will receive PEDIACEL vaccine
Arm Title
Group 2
Arm Type
Active Comparator
Arm Description
Participants will receive Infanrix-IPV+Hib vaccines
Intervention Type
Biological
Intervention Name(s)
DT5aP-IPV-Hib 5-component Pertussis vaccine
Other Intervention Name(s)
Pediacel™
Intervention Description
0.5 mL, IM
Intervention Type
Biological
Intervention Name(s)
Infanrix® -IPV+Hib
Other Intervention Name(s)
Infanrix®
Intervention Description
0.5 mL, IM
Primary Outcome Measure Information:
Title
To provide information concerning the immunogenicity of PEDIACEL® Vaccine.
Time Frame
1 Month post-dose 3
Secondary Outcome Measure Information:
Title
To provide information concerning the safety after administration of PEDIACEL® Vaccine
Time Frame
Entire study period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
80 Days
Maximum Age & Unit of Time
120 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infants aged 80 to 120 days inclusive on the day of inclusion. Born at full term of pregnancy (> 37 weeks) Informed consent form signed by the parent(s) or other legal representative according to local regulations Parent(s) or legal representative able to attend all scheduled visits and to understand and comply with the study procedures (able to read and write; access to a telephone). Exclusion Criteria: Rectal temperature ≥ 38.0°C Moderate or severe acute illness with or without fever Participation in another clinical trial in the 4 weeks preceding the first trial vaccination Having received any DTaP, IPV, or Hib vaccines prior to study initiation or any vaccination in the 4 weeks preceding the first trial vaccination Planned participation in another clinical trial during the present trial period Known history of diphtheria, tetanus, pertussis, H. influenzae type b infections, poliomyelitis Congenital or acquired immunodeficiency, immunosuppressive therapy such as long-term systemic corticosteroids therapy Systemic hypersensitivity to any of the vaccine components (including neomycin, streptomycin, polymyxin B and formaldehyde) History of a life-threatening reaction (such as encephalopathy, Hypotonic Hyporesponsive Episode, severe fever, convulsions, etc.) to the trial vaccine or a vaccine containing the same substances Blood or blood-derived products (immunoglobulins) received in the past 4 weeks Vaccination planned in the 6 weeks following any trial vaccination Known HIV seropositivity Thrombocytopenia or a bleeding disorder contraindicating intramuscular vaccination History of seizures or progressive, evolving or unstable neurological condition Clinically significant findings on review of systems that might interfere with correct vaccination or which, in the opinion of the Investigator, would interfere with the evaluation of the vaccine or pose a health risk to the subject.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Director
Organizational Affiliation
Sanofi Pasteur Inc.
Official's Role
Study Director
Facility Information:
City
Espoo
ZIP/Postal Code
02100
Country
Finland
City
Helsinki
ZIP/Postal Code
00100
Country
Finland
City
Helsinki
ZIP/Postal Code
00930
Country
Finland
City
Jarvenpaa
ZIP/Postal Code
04400
Country
Finland
City
Jyvaskyla
ZIP/Postal Code
40100
Country
Finland
City
Kotka
ZIP/Postal Code
48100
Country
Finland
City
Lahti
ZIP/Postal Code
15140
Country
Finland
City
Oulu
ZIP/Postal Code
90100
Country
Finland
City
Pori
ZIP/Postal Code
28120
Country
Finland
City
Tampere
ZIP/Postal Code
33520
Country
Finland
City
Turku
ZIP/Postal Code
20520
Country
Finland
City
Vantaa
ZIP/Postal Code
01300
Country
Finland
City
Vantaa
ZIP/Postal Code
01600
Country
Finland
City
Ostersund
ZIP/Postal Code
S-831 83
Country
Sweden

12. IPD Sharing Statement

Citations:
PubMed Identifier
23966556
Citation
Vesikari T, Silfverdal SA, Boisnard F, Thomas S, Mwawasi G, Reynolds D. Randomized, controlled, multicenter study of the immunogenicity and safety of a fully liquid combination diphtheria-tetanus toxoid-five-component acellular pertussis (DTaP5), inactivated poliovirus (IPV), and haemophilus influenzae type b (Hib) vaccine compared with a DTaP3-IPV/Hib vaccine administered at 3, 5, and 12 months of age. Clin Vaccine Immunol. 2013 Oct;20(10):1647-53. doi: 10.1128/CVI.00414-13. Epub 2013 Aug 21.
Results Reference
derived
Links:
URL
http://www.sanofipasteur.com
Description
Related Info

Learn more about this trial

Comparison of Safety and Immunogenicity of Pediacel™ and Infanrix™ IPV+Hib (Penta) Given in a 3 Dose Schedule in Infants

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