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Study of PR5I, a Pediatric Combination Vaccine With Enhanced Hepatitis B Component Given Concomitantly With Prevnar®

Primary Purpose

Diphtheria, Pertussis, Polio

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Hybrid 5 component DTaP, Vero IPV, Hep B and PRP-OMPC
Hybrid 5 component DTaP, Vero IPV, Hep B and PRP-OMPC
Hybrid 5 component DTaP, Vero IPV, Hep B and PRP-OMPC
Sponsored by
Sanofi Pasteur, a Sanofi Company
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diphtheria focused on measuring Hepatitis B, Pertussis, Diphtheria, Tetanus, H. influenzae type b, Polio

Eligibility Criteria

42 Days - 89 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Infants aged 42 to 89 days inclusive on the day of inclusion. Born at full term of pregnancy (>37 weeks). Informed consent form signed by the parent(s) or legally authorized representative. Able to attend all scheduled visits and to comply with the study procedures. Parent or legally authorized representative has access to a telephone. Parent or legally authorized representative able to read and write in English or French. Exclusion Criteria: Participation in another clinical trial in the 4 weeks preceding the first trial vaccination. Planned participation in another clinical trial during the present trial period. Personal or immediate family history of congenital or acquired immunodeficiency, immunosuppressive therapy such as long-term systemic corticosteroids therapy. Known or suspected systemic hypersensitivity to any of the vaccine components or history of a life-threatening reaction to a vaccine containing the same substances as the trial vaccine(s). Chronic illness that could interfere with trial conduct or completion. Received blood or blood-derived products since birth. Any vaccination preceding the first trial vaccination or planned in the 4 weeks after any trial vaccination (flu vaccine may be given a minimum of 4 weeks prior to the first study vaccination). Previous vaccination with any acellular pertussis- (DTaP) or whole cell pertussis- (DTwP) based combination vaccines, Haemophilus influenzae type b (Hib)-conjugate, poliovirus, hepatitis B, or pneumococcal conjugate vaccines. Coagulation disorder contraindicating IM vaccination. Clinically significant findings on review of systems (determined by investigator or sub-investigator to be sufficient for exclusion). Developmental delay or neurological disorder. Any condition which, in the opinion of the investigator, would interfere with the evaluation of the vaccine or pose a health risk to the subject. Documented Hepatitis B surface Antigen (HBsAg) seropositivity in the child or his/her mother. History of Hib, hepatitis B, diphtheria, tetanus, pertussis or poliovirus disease.

Sites / Locations

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Group A

Group B

Group C

Arm Description

Outcomes

Primary Outcome Measures

To provide information concerning the immune response of subjects that received PR5I concomitantly with Prevnar

Secondary Outcome Measures

Full Information

First Posted
August 9, 2006
Last Updated
January 10, 2014
Sponsor
Sanofi Pasteur, a Sanofi Company
Collaborators
Merck Sharp & Dohme LLC
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1. Study Identification

Unique Protocol Identification Number
NCT00362427
Brief Title
Study of PR5I, a Pediatric Combination Vaccine With Enhanced Hepatitis B Component Given Concomitantly With Prevnar®
Official Title
A Randomized Trial to Assess the Immunogenicity and Safety of PR5I With an Adjuvant Composition Enhancement to the Hepatitis B Component and When Given Concomitantly With Prevnar®
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
March 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sanofi Pasteur, a Sanofi Company
Collaborators
Merck Sharp & Dohme LLC

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
PR5I, a hexavalent pediatric combination vaccine is being developed to reduce the number of injections during the first 2 years of life while providing a complete course of immunization against infection caused by H. influenzae type b, hepatitis B virus, Corynebacterium diphtheriae, Clostridium tetani, Bordetella pertussis, and poliovirus types 1, 2, and 3. Primary Objective: To evaluate immunogenicity of PR5I with the adjuvant composition enhancement to the hepatitis B component when administered concomitantly with Prevnar® Secondary Objectives: To assess the safety and immunogenicity of PR5I when administered concomitantly, or one month apart with Prevnar® or separately with licensed vaccines used for routine infant vaccination in Canada.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diphtheria, Pertussis, Polio, Hepatitis B, Tetanus
Keywords
Hepatitis B, Pertussis, Diphtheria, Tetanus, H. influenzae type b, Polio

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
460 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Title
Group B
Arm Type
Experimental
Arm Title
Group C
Arm Type
Active Comparator
Intervention Type
Biological
Intervention Name(s)
Hybrid 5 component DTaP, Vero IPV, Hep B and PRP-OMPC
Other Intervention Name(s)
PR5I
Intervention Description
0.5 mL, 4 doses, IM
Intervention Type
Biological
Intervention Name(s)
Hybrid 5 component DTaP, Vero IPV, Hep B and PRP-OMPC
Other Intervention Name(s)
PR5I
Intervention Description
0.5 Ml, 4 doses, IM
Intervention Type
Biological
Intervention Name(s)
Hybrid 5 component DTaP, Vero IPV, Hep B and PRP-OMPC
Other Intervention Name(s)
PR5I, PENTACEL™, NGERIX-B®
Intervention Description
0.5 mL, 4 doses, IM with concommitant vaccines
Primary Outcome Measure Information:
Title
To provide information concerning the immune response of subjects that received PR5I concomitantly with Prevnar
Time Frame
14 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
42 Days
Maximum Age & Unit of Time
89 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infants aged 42 to 89 days inclusive on the day of inclusion. Born at full term of pregnancy (>37 weeks). Informed consent form signed by the parent(s) or legally authorized representative. Able to attend all scheduled visits and to comply with the study procedures. Parent or legally authorized representative has access to a telephone. Parent or legally authorized representative able to read and write in English or French. Exclusion Criteria: Participation in another clinical trial in the 4 weeks preceding the first trial vaccination. Planned participation in another clinical trial during the present trial period. Personal or immediate family history of congenital or acquired immunodeficiency, immunosuppressive therapy such as long-term systemic corticosteroids therapy. Known or suspected systemic hypersensitivity to any of the vaccine components or history of a life-threatening reaction to a vaccine containing the same substances as the trial vaccine(s). Chronic illness that could interfere with trial conduct or completion. Received blood or blood-derived products since birth. Any vaccination preceding the first trial vaccination or planned in the 4 weeks after any trial vaccination (flu vaccine may be given a minimum of 4 weeks prior to the first study vaccination). Previous vaccination with any acellular pertussis- (DTaP) or whole cell pertussis- (DTwP) based combination vaccines, Haemophilus influenzae type b (Hib)-conjugate, poliovirus, hepatitis B, or pneumococcal conjugate vaccines. Coagulation disorder contraindicating IM vaccination. Clinically significant findings on review of systems (determined by investigator or sub-investigator to be sufficient for exclusion). Developmental delay or neurological disorder. Any condition which, in the opinion of the investigator, would interfere with the evaluation of the vaccine or pose a health risk to the subject. Documented Hepatitis B surface Antigen (HBsAg) seropositivity in the child or his/her mother. History of Hib, hepatitis B, diphtheria, tetanus, pertussis or poliovirus disease.
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
Coquitlam
State/Province
British Columbia
ZIP/Postal Code
V3C 4J2
Country
Canada
City
Surrey
State/Province
British Columbia
ZIP/Postal Code
V3R 8P8
Country
Canada
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3E 3P4
Country
Canada
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3K 6R8
Country
Canada
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1S 0G8
Country
Canada
City
Beauport
State/Province
Quebec
ZIP/Postal Code
G1E 7G9
Country
Canada
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3H 1P3
Country
Canada
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3T 1C5
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
24346596
Citation
Halperin SA, Tapiero B, Dionne M, Meekison W, Diaz-Mitoma F, Zickler P, Rubin E, Embree J, Bhuyan P, Lee A, Li M, Tomovici A. Safety and immunogenicity of a toddler dose following an infant series of a hexavalent diphtheria, tetanus, acellular pertussis, inactivated poliovirus, Haemophilus influenzae type b, hepatitis B vaccine administered concurrently or at separate visits with a heptavalent pneumococcal conjugate vaccine. Pediatr Infect Dis J. 2014 Jan;33(1):73-80. doi: 10.1097/01.inf.0000437806.76221.20.
Results Reference
derived
PubMed Identifier
23241989
Citation
Tapiero B, Halperin SA, Dionne M, Meekison W, Diaz-Mitoma F, Zickler P, Rubin E, Embree J, Bhuyan P, Lee AW, Li M, Tomovici A. Safety and immunogenicity of a hexavalent vaccine administered at 2, 4 and 6 months of age with or without a heptavalent pneumococcal conjugate vaccine: a randomized, open-label study. Pediatr Infect Dis J. 2013 Jan;32(1):54-61. doi: 10.1097/INF.0b013e3182717edf.
Results Reference
derived
Links:
URL
http://www.sanofipasteur.com
Description
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Study of PR5I, a Pediatric Combination Vaccine With Enhanced Hepatitis B Component Given Concomitantly With Prevnar®

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