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Comparison of Immunogenicity and Safety of DTP-HB-Hib Using New Hepatitis B Bulk (Bio Farma) With Pentabio® Vaccine Primed With Recombinant Hepatitis B at Birth Dose Using New Hepatitis B Bulk (Bio Farma), in Indonesian Infants

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05482282
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:43.584576+00:00
Published At
2025-06-05T00:00:00+00:00
Record Updated At
2025-06-05
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Diphtheria Vaccine Adverse Reaction", "Tetanus Vaccine Adverse Reaction", "Pertussis Vaccine Adverse Reaction", "Haemophilus Influenzae Type B Vaccine Adverse Reaction", "Hepatitis B Vaccine Adverse Reaction"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-06-05"
protocolSection.identificationModule.nctId
"NCT05482282"
protocolSection.identificationModule.officialTitle
"Comparison of Immunogenicity and Safety of DTP-HB-Hib Using New Hepatitis B Bulk (Bio Farma) With Pentabio\u00ae Vaccine Primed With Recombinant Hepatitis B at Birth Dose Using New Hepatitis B Bulk (Bio Farma), in Indonesian Infants"
protocolSection.statusModule.overallStatus
"WITHDRAWN"
protocolSection.designModule.phases
["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Diphtheria Vaccine Adverse Reaction (protocolSection.conditionsModule.conditions)
  • Tetanus Vaccine Adverse Reaction (protocolSection.conditionsModule.conditions)
  • Pertussis Vaccine Adverse Reaction (protocolSection.conditionsModule.conditions)
  • Haemophilus Influenzae Type B Vaccine Adverse Reaction (protocolSection.conditionsModule.conditions)
  • Hepatitis B Vaccine Adverse Reaction (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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