Study to Evaluate the Immunogenicity and Safety of LBVD(Hexavalent Vaccine), Given to Healthy Infants at Primary Series
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Phase
Phase 2/3
Status
Unknown status
Study type
Interventional
Design
Randomized · None · Prevention
Enrollment
1,438estimated
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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2023-04-01 | estimated | When the study began enrolling |
| Primary completion | 2025-09-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-09-30 | estimated | The whole study's end, after follow-up |
| First posted | 2022-07-14 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2023-03-10 | actual | The 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 Infection
Interventions
- Biological: LBVD (Hexavalent vaccine)
- Biological: Pentavalent vaccine and Inactivated Polio vaccine (Sabin strains)
Primary outcome
what the primary-completion date above is the date OFSeroprotection/seroconservison/ vaccine-response rate
measured 4 weeks after three-dose primary series
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