Immunogenicity and tolerability of a bivalent virus-like particle norovirus vaccine candidate in children from 6 months up to 4 years of age: A phase 2 randomized, double-blind trial
We conducted a dose-finding phase 2 study of the HilleVax bivalent virus-like particle (VLP) vaccine candidate (HIL-214) in two cohorts of children, 6-≤12 months and 1-≤4 years of age (N = 120 per cohort), in Panama and Colombia (ClinicalTrials.gov, identifier NCT02153112). On Day 1, children random...
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Taylor & Francis Group,
2023-01-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_8bdc7287d8f147359bc3a2bc68a345d5 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Pio López |e author |
700 | 1 | 0 | |a Eduardo López-Medina |e author |
700 | 1 | 0 | |a Xavier Sáez-Llorens |e author |
700 | 1 | 0 | |a Rodrigo deAntonio |e author |
700 | 1 | 0 | |a Taisei Masuda |e author |
700 | 1 | 0 | |a Paul M. Mendelman |e author |
700 | 1 | 0 | |a James Sherwood |e author |
700 | 1 | 0 | |a Frank Baehner |e author |
700 | 1 | 0 | |a Astrid Borkowski |e author |
245 | 0 | 0 | |a Immunogenicity and tolerability of a bivalent virus-like particle norovirus vaccine candidate in children from 6 months up to 4 years of age: A phase 2 randomized, double-blind trial |
260 | |b Taylor & Francis Group, |c 2023-01-01T00:00:00Z. | ||
500 | |a 2164-5515 | ||
500 | |a 2164-554X | ||
500 | |a 10.1080/21645515.2023.2204787 | ||
520 | |a We conducted a dose-finding phase 2 study of the HilleVax bivalent virus-like particle (VLP) vaccine candidate (HIL-214) in two cohorts of children, 6-≤12 months and 1-≤4 years of age (N = 120 per cohort), in Panama and Colombia (ClinicalTrials.gov, identifier NCT02153112). On Day 1, children randomized to one of the four equal groups received intramuscular injections of four different HIL-214 formulations containing 15/15, 15/50, 50/50, or 50/150 μg of GI.1/GII.4c genotype VLPs and 0.5 mg Al(OH)3. On Day 29, half the children in each group received a second vaccination (N = 60), while the other half received saline placebo injections to maintain the blind. VLP-specific ELISA Pan-Ig and histo-blood group binding antigen-blocking antibodies (HBGA) were measured on Days 1, 29, 57 and 210. On Day 29, after one dose, there were large Pan-Ig and HBGA responses in both age cohorts with some indication of dose-dependence, and higher geometric mean titers (GMT) in the older children. A further increase in titers was observed 28 days after a second dose in the 6-≤12-month-old groups, but less so in the 1-≤4-year-old groups; GMTs at Day 57 were broadly similar across doses and in both age groups. GMTs of Pan-Ig and HBGA persisted above baseline up to Day 210. All formulations were well tolerated with mostly mild-to-moderate transient solicited adverse events reported by parents/guardians, and no vaccine-related serious adverse events occurred. Further development of HIL-214 is warranted to protect the most susceptible young children against norovirus. | ||
546 | |a EN | ||
690 | |a norovirus | ||
690 | |a vaccine | ||
690 | |a children | ||
690 | |a immunogenicity | ||
690 | |a reactogenicity | ||
690 | |a virus-like particles | ||
690 | |a Immunologic diseases. Allergy | ||
690 | |a RC581-607 | ||
690 | |a Therapeutics. Pharmacology | ||
690 | |a RM1-950 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Human Vaccines & Immunotherapeutics, Vol 19, Iss 1 (2023) | |
787 | 0 | |n http://dx.doi.org/10.1080/21645515.2023.2204787 | |
787 | 0 | |n https://doaj.org/toc/2164-5515 | |
787 | 0 | |n https://doaj.org/toc/2164-554X | |
856 | 4 | 1 | |u https://doaj.org/article/8bdc7287d8f147359bc3a2bc68a345d5 |z Connect to this object online. |