<< AAPA welcomes Senate Finance Committee's vote to approve the America's Healthy Future Act | Control and coordination may aid multiple sclerosis patients perform daily activities independently >>
Read in | English | Español | Français | Deutsch | Português | Italiano | 日本語 | 한국어 | 简体中文 | 繁體中文 | Nederlands | Русский | Polski

Interim data from Sanofi Pasteur's Influenza A 2009 Monovalent Vaccine clinical trials in infants and children

Published on October 15, 2009 at 1:10 AM · No Comments

Sanofi Pasteur, the vaccines division of the sanofi-aventis Group (EURONEXT: SAN and NYSE: SNY), announced today an interim analysis of data from clinical trials of the U.S. licensed Influenza A (H1N1) 2009 Monovalent Vaccine in infants and children 6 months through 9 years of age. The data indicate the vaccine is immunogenic and that one dose may protect many children. However, the study suggests that two doses of vaccine will be required for optimal protection of children under the age of 10 years. This is consistent with the recommendations for seasonal influenza immunization in children of this age. Clinical trials are ongoing to evaluate the immunogenicity and safety in children following two doses of vaccine.

"According to the Centers for Disease Control and Prevention young children are among those of highest priority for immunization with the Influenza A (H1N1) 2009 Monovalent Vaccine, given the relatively high disease incidence and potential for transmission in this population," said Wayne Pisano, President and Chief Executive Officer of Sanofi Pasteur. "As the only company licensed in the U.S. to produce a pediatric influenza vaccine which is licensed for children as young as 6 months of age, it was the highest priority for Sanofi Pasteur to conduct clinical trials to evaluate the safety and immunogenicity of the pandemic vaccine in children to support decisions on vaccine administration."

This randomized, placebo-controlled, multicenter trial was conducted by Sanofi Pasteur to determine the immunogenicity and safety of the vaccine, given as a two-dose schedule, 21 days apart. A total of 474 children were enrolled in the trial in two age cohorts: 229 children 6 months through 35 months of age; and 245 children 3 years through 9 years of age. The trial evaluated two antigen doses: formulated as 7.5 mcg and 15 mcg hemagglutinin in each cohort (ClinicalTrials.gov registration number NCT00952419). The interim results reported today are the first data available from children under the age of 10 years. Previously, Sanofi Pasteur reported that 98 percent of adults 18 years through 64 years of age had an immune response considered protective following one 15 mcg dose of vaccine.

Comments
The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News-Medical.Net.



  Country flag

biuquote
  • Comment
  • Preview
Loading