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Phase 2 study of BK1901 as a Booster in Japanese children

Phase 2 study of BK1901 as a Booster in Japanese children

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2031200412
Enrollment
200
Registered
2021-03-11
Start date
2021-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prevention of pertussis, diphtheria, tetanus, and acute poliomyelitis

Interventions

Subcutaneous injection of DPT-IPV(0.5 mL) , DPT(0.5 mL) and IPV(0.5mL).

Sponsors

Fuji Hideyuki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese healthy children aged 5 to less than 7 years old on the day of injection. 2. Subjects who has written informed consent from legal guardian and has obtained an assent from subject. 3. Subjects are able to comply with the study procedures. 4. Subjects who had been vaccinated 3 or 4 times DPT-IPV with the same products at <30 months old and have not been vaccinated DPT-IPV since then.

Exclusion criteria

Exclusion criteria: 1. Subjects who had history of diphtheria, pertussis, tetanus or acute poliomyelitis. 2. Subjects who had history of diphteria, pertussis, tetanus or polio vaccination except DPT-IPV. 3. Subjects who had history of COVID-19. 4. Subjects who had history of anaphylaxis to the components of the study drug. 5. Subjects who had histories of cardiovascular disease, blood system, liver, kidney, digestive system, metabolism, neuropsychiatric disease. 6. Subjects who have a current history of apparent immunologic disorder and/or under immunosuppressive therapy. 7. Subjects who received blood transfusion and/or gamma globulin preparation from Day-90 or less, and/or received high-dose therapy (200mg/kg or more) of gamma globulin preparation from Day-180 or less prior to study administration. 8. Subjects who have received other investigational products from Day-120 or less prior to study administration. 9. Subjects who have been considered to be not eligible by the principal investigators (sub-investigators) for the enrollment.

Design outcomes

Primary

MeasureTime frame
1. Booster response rates against diphtheria toxin,tetanus toxin, pertussis(PT,FHA), and polio virus(types 1, 2 or 3) . 2. Adverse events and adverse reactions.

Secondary

MeasureTime frame
1. Antibody prevalence rate, geometric mean titer (GMT) and GMT increase against diphtheria toxin, tetanus toxin and pertussis(PT,FHA). 2. Antibody prevalence rate, geometric mean titer (GMT) and GMT increase against polio virus(types 1, 2 or 3).

Contacts

Public ContactHideyuki Fuji

The Research Foundation for Microbial Diseases of Osaka University

clinicaldevelopment@mail.biken.or.jp+81-6-6877-4812

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026