search
Back to results

Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) With Pentabio® Vaccine Primed With Recombinant Hepatitis B

Primary Purpose

Immunogenicity, Safety

Status
Completed
Phase
Phase 3
Locations
Indonesia
Study Type
Interventional
Intervention
Recombinant Hepatitis B + DTP-HB-Hib
Hep B + Pentabio (registered)
Sponsored by
PT Bio Farma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Immunogenicity

Eligibility Criteria

0 Days - 3 Days (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy, full term, newborns infants.
  • Infant born after 37-42 weeks of pregnancy.
  • Infant weighing 2500 gram or more at birth.
  • Father, mother or legally acceptable representative properly informed about the study and having signed the informed consent form.
  • Parents will commit themselves to comply with the indications of the investigator and with the schedule of the trial.

Exclusion Criteria:

  • Child concomitantly enrolled or scheduled to be enrolled in another trial.
  • Mother with HBsAg positive.
  • Evolving mild, moderate or severe illness, especially infectious diseases or fever (axillary temperature >37.5C on Day 0).
  • Suspected of allergy to any component of the vaccines (e.g. formaldehyde).
  • Suspected of uncontrolled coagulopathy or blood disorders contraindicating intramuscular injection.
  • Newborn suspected of congenital or acquired immunodeficiency (including HIV infection).
  • Received or plans to receive any treatment likely to alter the immune response (intravenous immunoglobulins, blood-derived products or long term corticotherapy (> 2 weeks)).
  • Received other vaccination with the exception of BCG and poliomyelitis.
  • Any abnormality or chronic disease which according to the investigator might interfere with the assessment of the trial objectives.

Sites / Locations

  • Garuda Primary Health Centre
  • Ibrahim Adjie Primary Health Centre
  • Puter Primary Health Care

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

HepB + Penta batch 1

Hep B + Pentabio (registered)

Arm Description

Recombinant Hepatitis B + DTP-HB-Hib batch 1

Recombinant Hepatitis B + Pentabio (registered)

Outcomes

Primary Outcome Measures

To evaluate protectivity of DTP-HB-Hib Vaccine (Bio Farma) with new Hepatitis B bulk
Percentage of infants with anti-diphtheria titer and anti-tetanus titer > 0.01 IU/ml, anti HbsAg titer > 10 mIU/ml, and anti PRP-T titer > 0.15 ug/ml 28 days after the last injection of DTP/HB/Hib with different source of Hepatitis B bulk vaccine group.

Secondary Outcome Measures

Describes antibody response to diphtheria toxoid, tetanus toxoid in both group with the evaluation criteria
Serological response to diphtheria toxoid, tetanus toxoid: GMT, percentage of infants with titer > 0.01 IU/ml, > 0.1 IU/ml percentage of infants with increasing antibody titer > 4 times and/or percentage of infants with transition of seronegative to seropositive
Serological response to the pertussis component (agglutinins)
Serological response to the pertussis component (agglutinins): GMT, percentage of infants with titer > 40, > 80, > 160 and > 320 (1/dil.), percentage of infants with increasing antibody titer > 4 times
Geometric mean of anti-HbsAg
Geometric mean of anti-HbsAg, percentage of infants with titer > 10mIU/ml, percentage of infants with increasing antibody titer > 4 times and/ or percentage of infants with transition of seronegative to seropositive
Serological response to Hib/PRP
Serological response to Hib/PRP: GMT, percentage of infants with titer >1 ug /ml ; > 0.15 ug /ml percentage of infants with increasing antibody titer > 4 times and/or percentage of infants with transition of seronegative to seropositive
Seroconversion
Comparison of GMT, seroprotection, percentage of subjects with increasing antibody titer > 4 times and/ or percentage of subjects with transition of seronegative to seropositive following primary series of investigational product compare to control.

Full Information

First Posted
August 26, 2019
Last Updated
January 13, 2022
Sponsor
PT Bio Farma
search

1. Study Identification

Unique Protocol Identification Number
NCT04071379
Brief Title
Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) With Pentabio® Vaccine Primed With Recombinant Hepatitis B
Official Title
Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) With Pentabio® Vaccine Primed With Recombinant Hepatitis B at Birth Dose (Using Different Source of Hepatitis B), in Indonesian Infants
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
October 13, 2020 (Actual)
Primary Completion Date
April 6, 2021 (Actual)
Study Completion Date
December 16, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
PT Bio Farma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) with Pentabio® vaccine Primed with Recombinant Hepatitis B
Detailed Description
Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) with Pentabio® vaccine Primed with Recombinant Hepatitis B at Birth dose (using different source of Hepatitis B), in Indonesian Infants

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Immunogenicity, Safety

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Subjects neonates: Randomized, double blind, 2 arms parallel groups, prospective intervention Study
Masking
ParticipantInvestigator
Masking Description
Randomized, double blind, 2 arms parallel group, prospective intervention study This study will do the lot to lot consistency and will be compared to registered product
Allocation
Randomized
Enrollment
220 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HepB + Penta batch 1
Arm Type
Experimental
Arm Description
Recombinant Hepatitis B + DTP-HB-Hib batch 1
Arm Title
Hep B + Pentabio (registered)
Arm Type
Active Comparator
Arm Description
Recombinant Hepatitis B + Pentabio (registered)
Intervention Type
Biological
Intervention Name(s)
Recombinant Hepatitis B + DTP-HB-Hib
Other Intervention Name(s)
Hep B + DTP-HB-Hib
Intervention Description
1 dose of 0.5 ml Recombinant Hepatitis B + 3 dose of 0.5 ml of DTP-HB-Hib
Intervention Type
Biological
Intervention Name(s)
Hep B + Pentabio (registered)
Other Intervention Name(s)
Recombinant Hepatitis B (Bio Farma) + Pentabio (Bio Farma)
Intervention Description
1 dose of 0.5 ml Recombinant Hepatitis B (registered) + 3 dose of 0.5 ml of Pentabio (registered)
Primary Outcome Measure Information:
Title
To evaluate protectivity of DTP-HB-Hib Vaccine (Bio Farma) with new Hepatitis B bulk
Description
Percentage of infants with anti-diphtheria titer and anti-tetanus titer > 0.01 IU/ml, anti HbsAg titer > 10 mIU/ml, and anti PRP-T titer > 0.15 ug/ml 28 days after the last injection of DTP/HB/Hib with different source of Hepatitis B bulk vaccine group.
Time Frame
28 days after immunization
Secondary Outcome Measure Information:
Title
Describes antibody response to diphtheria toxoid, tetanus toxoid in both group with the evaluation criteria
Description
Serological response to diphtheria toxoid, tetanus toxoid: GMT, percentage of infants with titer > 0.01 IU/ml, > 0.1 IU/ml percentage of infants with increasing antibody titer > 4 times and/or percentage of infants with transition of seronegative to seropositive
Time Frame
28 days after immunization
Title
Serological response to the pertussis component (agglutinins)
Description
Serological response to the pertussis component (agglutinins): GMT, percentage of infants with titer > 40, > 80, > 160 and > 320 (1/dil.), percentage of infants with increasing antibody titer > 4 times
Time Frame
28 days after immunization
Title
Geometric mean of anti-HbsAg
Description
Geometric mean of anti-HbsAg, percentage of infants with titer > 10mIU/ml, percentage of infants with increasing antibody titer > 4 times and/ or percentage of infants with transition of seronegative to seropositive
Time Frame
28 days after immunization
Title
Serological response to Hib/PRP
Description
Serological response to Hib/PRP: GMT, percentage of infants with titer >1 ug /ml ; > 0.15 ug /ml percentage of infants with increasing antibody titer > 4 times and/or percentage of infants with transition of seronegative to seropositive
Time Frame
28 days after immunization
Title
Seroconversion
Description
Comparison of GMT, seroprotection, percentage of subjects with increasing antibody titer > 4 times and/ or percentage of subjects with transition of seronegative to seropositive following primary series of investigational product compare to control.
Time Frame
28 days after immunization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Days
Maximum Age & Unit of Time
3 Days
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy, full term, newborns infants. Infant born after 37-42 weeks of pregnancy. Infant weighing 2500 gram or more at birth. Father, mother or legally acceptable representative properly informed about the study and having signed the informed consent form. Parents will commit themselves to comply with the indications of the investigator and with the schedule of the trial. Exclusion Criteria: Child concomitantly enrolled or scheduled to be enrolled in another trial. Mother with HBsAg positive. Evolving mild, moderate or severe illness, especially infectious diseases or fever (axillary temperature >37.5C on Day 0). Suspected of allergy to any component of the vaccines (e.g. formaldehyde). Suspected of uncontrolled coagulopathy or blood disorders contraindicating intramuscular injection. Newborn suspected of congenital or acquired immunodeficiency (including HIV infection). Received or plans to receive any treatment likely to alter the immune response (intravenous immunoglobulins, blood-derived products or long term corticotherapy (> 2 weeks)). Received other vaccination with the exception of BCG and poliomyelitis. Any abnormality or chronic disease which according to the investigator might interfere with the assessment of the trial objectives.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eddy Fadliyana
Organizational Affiliation
Hasan Sadikin General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Garuda Primary Health Centre
City
Bandung
State/Province
West Java
Country
Indonesia
Facility Name
Ibrahim Adjie Primary Health Centre
City
Bandung
State/Province
West Java
Country
Indonesia
Facility Name
Puter Primary Health Care
City
Bandung
State/Province
West Java
Country
Indonesia

12. IPD Sharing Statement

Learn more about this trial

Comparison of Immunogenicity and Safety of DTP-HB-Hib (Bio Farma) With Pentabio® Vaccine Primed With Recombinant Hepatitis B

We'll reach out to this number within 24 hrs