Clinical trial
A Multi-center, Randomized, Active-controlled, Parallel-group, Open-label and Phase II Study to Evaluate Immunogenicity and Safety of LBVD (Fully Liquid Hexavalent Vaccine; Adsorbed Diphtheria-Tetanus-Pertussis-Hepatitis B- Inactivated Poliomyelitis (Sabin) and Haemophilus Influenzae Type b Conjugate Vaccine) Compared to Co-administration of EupentaTM Inj. and Imovax® Polio (Poliomyelitis Vaccine (Inactivated)) in Separate Injections in Healthy Infants at 6-10-14 Weeks of Age as Primary Series
NCT04073459 is registered in ClinicalTrials.gov with LG Chem as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Multi-center, Randomized, Active-controlled, Parallel-group, Open-label and Phase II Study to Evaluate Immunogenicity and Safety of LBVD (Fully Liquid Hexavalent Vaccine; Adsorbed Diphtheria-Tetanus-Pertussis-Hepatitis B- Inactivated Poliomyelitis (Sabin) and Haemophilus Influenzae Type b Conjugate Vaccine) Compared to Co-administration of EupentaTM Inj. and Imovax® Polio (Poliomyelitis Vaccine (Inactivated)) in Separate Injections in Healthy Infants at 6-10-14 Weeks of Age as Primary Series
- Lead sponsor
- LG Chem
- Phase
- Phase 2
- Overall status
- Unknown status
- Start date
- November 30, 2019
- Completion date
- August 31, 2020
- Enrollment
- 336 (estimated)
- Sites
- Not reported
Conditions
As the registry lists them; a condition with its own page is linked.
diphtheria, haemophilus influenzae type b infection, hepatitis b, pertussis, poliomyelitis, tetanus