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The Safety and Immunogenicity of DTP/Hepatitis B 10ug Hib Vaccine (Bio Farma)

Primary Purpose

Healthy

Status
Completed
Phase
Phase 1
Locations
Indonesia
Study Type
Interventional
Intervention
DPT/HepatitisB/Hib vaccine
Sponsored by
PT Bio Farma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Healthy focused on measuring DTB/HB/Hib vaccine, Infants, Phase I

Eligibility Criteria

6 Weeks - 11 Weeks (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Infant 6-11 week of age
  • Infant born after 37-42 week of pregnancy
  • Infant weighting more than 2.5 kg at birth
  • Father, mother or legally acceptable representative properly informed about the study and having signed the informed consent form
  • Parents commit themselves to comply with the indication of the investigator and with the schedule of the trial

Exclusion Criteria:

  • Child concomitantly enroll or schedule to be enroll in another trial
  • Evolving moderate or severe illness, especially infectious diseases or fever (axillary temperature >=37.5 Celsius on Day 0)
  • Known history of allergy to any component of the vaccine component (e.g.formaldehyde)
  • History of uncontrolled coagulopathy or blood disorder contraindicating intramuscular injection
  • Known history of congenital or acquired immunodeficiency (including HIV infection)
  • Child who has received in the previous 4 weeks a treatment likely to alter the immune response (intravenous immunoglobulin, blood derived product or long term corticotherapy (>2 minggu)
  • Other vaccination within the 7 days prior to inclusion 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 objective
  • Infant with a known history of diphteria, tetanus, pertussis, Hib, Hepatitis B infection

Sites / Locations

  • Hasan Sadikin Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

DTP/HepatitisB/Hib vaccine

Arm Description

Purified diphteria toxoid Purified tetanus toxoid Inactivated Bordetella pertussis HbsAg PRP-TT Aluminum phosphate Natrium Chloride Thimerosal

Outcomes

Primary Outcome Measures

Incidence rate of adverse event of DTP/Hepatitis B/Hib vaccine (Bio Farma)
Local and systemic reactions

Secondary Outcome Measures

Incidence rate of adverse event of DTP/Hepatitis B/Hib vaccine (Bio Farma)
Local and systemic reaction
To asses the immunogenicity
Percentage of infants with increasing antibody

Full Information

First Posted
October 30, 2013
Last Updated
November 5, 2013
Sponsor
PT Bio Farma
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1. Study Identification

Unique Protocol Identification Number
NCT01977196
Brief Title
The Safety and Immunogenicity of DTP/Hepatitis B 10ug Hib Vaccine (Bio Farma)
Official Title
Phase 1 of DTP/Hepatitis B 10ug Hib Vaccine
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this study was to know the safety of DTP/Hepatitis B and Hib/PRP-T vaccine and immediate reactions within the first 30 minutes after injection.
Detailed Description
This trial was an open-label study, no randomization, and no placebo or control group. Total 30 healthy infants (age 6-11 weeks) followed this trial. The safety was assessed within 24 hours, 48 hours, 72 hours, and 28 days after injection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy
Keywords
DTB/HB/Hib vaccine, Infants, Phase I

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
DTP/HepatitisB/Hib vaccine
Arm Type
Experimental
Arm Description
Purified diphteria toxoid Purified tetanus toxoid Inactivated Bordetella pertussis HbsAg PRP-TT Aluminum phosphate Natrium Chloride Thimerosal
Intervention Type
Biological
Intervention Name(s)
DPT/HepatitisB/Hib vaccine
Other Intervention Name(s)
Pentavalent
Intervention Description
DPT/HepatitisB/Hib vaccine (Bio Farma)
Primary Outcome Measure Information:
Title
Incidence rate of adverse event of DTP/Hepatitis B/Hib vaccine (Bio Farma)
Description
Local and systemic reactions
Time Frame
30 minutes
Secondary Outcome Measure Information:
Title
Incidence rate of adverse event of DTP/Hepatitis B/Hib vaccine (Bio Farma)
Description
Local and systemic reaction
Time Frame
28 hours, 48 hours, 72 hours, 28 days
Title
To asses the immunogenicity
Description
Percentage of infants with increasing antibody
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Weeks
Maximum Age & Unit of Time
11 Weeks
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Infant 6-11 week of age Infant born after 37-42 week of pregnancy Infant weighting more than 2.5 kg at birth Father, mother or legally acceptable representative properly informed about the study and having signed the informed consent form Parents commit themselves to comply with the indication of the investigator and with the schedule of the trial Exclusion Criteria: Child concomitantly enroll or schedule to be enroll in another trial Evolving moderate or severe illness, especially infectious diseases or fever (axillary temperature >=37.5 Celsius on Day 0) Known history of allergy to any component of the vaccine component (e.g.formaldehyde) History of uncontrolled coagulopathy or blood disorder contraindicating intramuscular injection Known history of congenital or acquired immunodeficiency (including HIV infection) Child who has received in the previous 4 weeks a treatment likely to alter the immune response (intravenous immunoglobulin, blood derived product or long term corticotherapy (>2 minggu) Other vaccination within the 7 days prior to inclusion 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 objective Infant with a known history of diphteria, tetanus, pertussis, Hib, Hepatitis B infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kusnandi Rusmil, PhD
Organizational Affiliation
Faculty of Medicine UNPAD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hasan Sadikin Hospital
City
Bandung
State/Province
West Java
ZIP/Postal Code
40161
Country
Indonesia

12. IPD Sharing Statement

Learn more about this trial

The Safety and Immunogenicity of DTP/Hepatitis B 10ug Hib Vaccine (Bio Farma)

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