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OpenTrials
Completed

NCT Number: NCT02095314

Antibody Persistence, Immune Response and Safety After Doses of Pentabio Vaccine

Measure antibody persistence prior to booster administration of Pentabio vaccine.

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Key information

Conditions

Age range

18 month–24 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Jatinegara Primary Health Center, Jakarta, Jakarta Special Capital Region, Indonesia

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About this study

Number and percentage of children with anti diphtheria, titer and anti tetanus titer >= 0.01 IU/ml, anti HBs >=10mIU/ml, anti Hib >=0.15ug/ml prior to booster administration.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children, 18-24 months of age
  • Subjects who had completed the primary series of Pentabio vaccine in the previous trial
  • Father, mother, or legally acceptable representative have been informed properly regarding the study and signed the informed consent form
  • Subject's parents commit to comply with the instruction

Exclusion criteria

  • Subjects concomitantly enrolled or scheduled to be enrolled in another trial
  • Evolving mild, moderate or severe illness, especially infectious diseases or fever (axillary temperature >=37.5oC on Day 0)
  • Known history of uncontrolled coagulopathy or blood disorders contraindicating intramuscular injection
  • Known history of allergy to any component of the vaccines (e.f. formaldehyde)
  • Known history of acquired immunodeficiency (including HIV infection)
  • Subject who has received a treatment likely to alter immune response in the previous 4 weeks (e.g intravenous immunoglobulin, blood-derived products or long term corticotherapy (>2 weeks)
  • Subject receives other vaccination within 1 month prior to inclusion
  • Any abnormality or chronic disease justified by investigator that might interfere assessment of the trial objectives
  • Infant with a known history of diphtheria, tetanus, pertussis, Hepatitis B and Hib infection

Treatment and study plan

Pentavalen

Biological

Batch 5010613

Other names: Pentabio vaccine, DPT-HB-Hib

Primary outcomes

  1. Geomoteric mean titer prior to booster administration of Pentabio vaccine

    Time frame: visit 1

    The number and percentage of children with anti diphtheria titer and anti tetanus titer >=0.01 IU/ml anti HBs >=10 mIU/ml, anti Hib >=0.15 ug/ml prior to booster administration.

Secondary outcomes

  1. Protectivity of Pentabio vaccine 1 month after the booster dose

    Time frame: 1 month

    Serological response to diphtheria, tetanus, pertussis and Hib (Geometric Mean Titer)

  2. Serological response to diphtheria, tetanus, pertussis, hepatitis B and PRP-T before and 1 month after the booster dose

    Time frame: 1 month

    Geometric mean titer to diphtheria, tetanus, pertussis, Hepatitis B and Hib before immunization and 1 month after immunization

  3. Seroconversion and seroprotection before and 1 month after the booster dose

    Time frame: 1 month

    The changes of serological response before and after booster dose

  4. Number of participants with adverse events

    Time frame: 1 month

    Local and systemic reaction within 28 days after immunization.

Sponsors and collaborators

Lead sponsor

PT Bio Farma

Industry

Registry information

Official study title

Antibody Persistence After Primary Doses, Immune Response and Safety After Doses of Pentabio Vaccine in Indonesian Children at 18-24 Months of Age

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Mar 24, 2014
Registry last updated
Dec 18, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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