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Randomized Double-Blind Phase III Pivotal Field Trial of the Comparative Immunogenicity Safety and Tolerability of Two Yellow Fever 17D Vaccines (ARILVAX(Trademark) and YF-VAX(Trademark)) in Healthy Infants and Children in Peru. Preview this item
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Randomized Double-Blind Phase III Pivotal Field Trial of the Comparative Immunogenicity Safety and Tolerability of Two Yellow Fever 17D Vaccines (ARILVAX(Trademark) and YF-VAX(Trademark)) in Healthy Infants and Children in Peru.

Author: Vivian E Belmusto-WornJoel L SanchezKaren McCarthyRichard NicholsChristian T BaustistaAll authors
Publisher: Ft. Belvoir Defense Technical Information Center 17 AUG 2004.
Edition/Format:   eBook : English
Database:WorldCat
Summary:
We conducted a randomized, double-blind, phase III yellow fever (YF) vaccine trial among 1,107 healthy children in Sullana in northern Peru. The safety and efficacy (by measurement of geometric mean neutralizing antibody titer responses) were determined for two YF vaccines, ARILVAX (exp Trademark)" (n 738) and YF-VAX (n 369). Seroconversion rates were higher (94.9%) in ARILVAX(EXP TRADEMARK)" than in YF-VAX (90.6%)  Read more...
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Material Type: Internet resource
Document Type: Internet Resource
All Authors / Contributors: Vivian E Belmusto-Worn; Joel L Sanchez; Karen McCarthy; Richard Nichols; Christian T Baustista; Alan J Magill; Giovanna Pastor-Cauna; Carlos Echevarria; Victor A Laguna-Torres; Billey K Samame; SUTTER INST FOR MEDICAL RESEARCH SACRAMENTO CA.
OCLC Number: 227937417
Notes: Pub. in American Journal Tropical Medicine Hygiene, v72 n2, p.189-197, 2005.
Description: 10 pages

Abstract:

We conducted a randomized, double-blind, phase III yellow fever (YF) vaccine trial among 1,107 healthy children in Sullana in northern Peru. The safety and efficacy (by measurement of geometric mean neutralizing antibody titer responses) were determined for two YF vaccines, ARILVAX (exp Trademark)" (n 738) and YF-VAX (n 369). Seroconversion rates were higher (94.9%) in ARILVAX(EXP TRADEMARK)" than in YF-VAX (90.6%) recipients. The two-sided 95% confidence interval (YF-VAX ARILVAX(EXP TRADEMARK)") was (12.8% to 2.5%), indicating that the higher seroconversion rate for Arilvax" was significant. Post-vaccination (30-day) mean log10 neutralization indices were found to be similar for both products: 1.32 for ARILVAX(EXP TRADEMARK)" and 1.26 for YF-VAX (P 0.1404, by analysis of variance). A similar number of subjects in each group reported at least one adverse event (AE); 441 (59.8%) for ARILVAX(EXP TRADEMARK)" versus 211 (59.9%) for YF-VAX . Most (591; 96.7%) of these were of a mild nature and resolved without treatment. There were no treatment-related serious AEs. This is the first randomized, double-blind comparison of two YF vaccines in a pediatric population; both vaccines were shown to be highly immunogenic and well-tolerated.

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<http://www.worldcat.org/oclc/227937417> # Randomized Double-Blind Phase III Pivotal Field Trial of the Comparative Immunogenicity Safety and Tolerability of Two Yellow Fever 17D Vaccines (ARILVAX(Trademark) and YF-VAX(Trademark)) in Healthy Infants and Children in Peru.
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