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KD-332 Phase III study

A phase III study of KD-332 multicenter, randomized, double-blind, parallel-group, comparative study of healthy children using DTaP vaccine and live-oral Polio vaccine as comparator vaccines.

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080221042
Enrollment
315
Registered
2010-03-19
Start date
2010-03-19
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

Prophylaxis of pertussis, diphtheria, tetanus, and poliomyelitis infection.

Interventions

investigational material(s) Generic name etc : KD-332 INN of investigational material : Therapeutic category code : 631 Vaccines Dosage and Administration for Investigational material : Subcutaneous

Sponsors

The Chemo-Sero-Therapeutic Research Institute
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 3-90 months of age

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Immunogenicity Neutralizing antibody titers against type 1, type 2 and type 3 polio virus.

Outcome results

None listed

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