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A Phase II/III Study to Evaluate the Immunogenicity, Safety and Lot-to-lot Consistency of LBVD, a Fully Liquid Hexavalent Diphtheria-tetanus-whole Cell Pertussis-hepatitis B-poliovirus-Haemophilus Influenzae Type b Conjugate (DTwP-HepB-IPV-Hib) Vaccine, in Healthy Infants as Primary Series

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NCT06947499 · readout ≤ 103 d

Sponsored by LG Chem (industry) · 051910.KS — their whole pipeline →.

Phase
Phase 2/3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Prevention
Enrollment
1,186estimated
Sites
1
Country
Philippines

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-05-30actualWhen the study began enrolling
Primary completionNov 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionApr 2027estimatedThe whole study's end, after follow-up
First posted2025-04-27actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-07-03actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Diphtheria
  • Tetanus
  • Pertussis
  • Hepatitis B
  • Poliomyelitis
  • Haemophilus Influenzae Type b

Interventions

  • Biological: LBVD
  • Biological: Pentavalent vaccine and Inactivated Polio vaccine

Primary outcomes

what the primary-completion date above is the date OF
Seroprotection/seroconversion rate
measured 4 weeks after a three-dose primary series
Geometric mean concentration (GMC) for pertussis
measured 4 weeks after a three-dose primary series

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