Sanofi Pasteur Presents Pediatric Data on Investigational Quadrivalent Influenza Vaccine
- Pediatric Data Supplements Prior Phase II and Phase III Studies in Adults -
May 1, 2012
SWIFTWATER, Pa., May 1, 2012 /PRNewswire/ -- Sanofi Pasteur, the vaccines division of Sanofi (EURONEXT: SAN and NYSE: SNY), announced today new Phase III data for its investigational quadrivalent influenza vaccine (QIV) in children 6 months through 8 years of age. This pediatric study evaluated the safety and immunogenicity of QIV compared to currently licensed Fluzone® (Influenza Virus Vaccine). Results of the study were presented today at the Annual Meeting of the Pediatric Academic Societies in Boston.
The data from this pediatric study of QIV support the results of prior studies in adults. The non-inferiority comparisons demonstrate that the addition of a fourth influenza strain (a second B strain) to the investigational vaccine does not adversely affect the safety and immunogenicity profiles of QIV compared to those of licensed Fluzone vaccine.
"Fluzone vaccine is the only influenza vaccine licensed and available in the U.S. for use in children as young as 6 months of age along with formulations of Fluzone vaccine available for the full spectrum of the population through the oldest adults," said David Greenberg, M.D., Senior Director, U.S. Scientific and Medical Affairs, Sanofi Pasteur. "We believe that a quadrivalent Fluzone vaccine could provide an important public health benefit for people of all ages by providing coverage against an extra B virus strain of influenza. Influenza B is responsible for a substantial burden of disease and influenza-associated complications and hospitalizations in children."
Currently, seasonal influenza vaccines contain the three influenza virus strains anticipated to circulate in a given year based on global surveillance of influenza virus activity during the prior year. The annual trivalent inactivated influenza vaccine (TIV) formulation includes two A strains and one B strain. However, for over a decade, two distinct influenza B families (lineages) have co-circulated with varying prevalence, making it difficult to predict which B-lineage strain will predominate in a given year. In fact, approximately half of the time, the B-lineage strain selected for the annual vaccine has not matched the B-lineage strain that predominately circulated in a given season. Even in years where the predominant B-lineage strain is selected for the vaccine, some influenza disease occurs from the other circulating B-lineage strain not in the vaccine. Inclusion of a strain from each of the two B lineages is a public health measure that can help reduce unnecessary cases of influenza disease that could be vaccine-preventable if the additional strain were in the vaccine.
The objectives of the study included demonstration of non-inferiority of antibody responses to each influenza strain in QIV compared with responses to each respective strain in the TIV comparators. Non-inferiority was measured in children 6 months through 8 years of age for the study population overall and separately for the youngest children 6 months through 35 months of age and older children 3 years through 8 years of age.
Additional objectives of the study were to demonstrate superiority of antibody responses to each B strain in QIV compared with antibody titers following vaccination with the TIV that did not contain the corresponding B strain. Antibody responses were assessed by both geometric mean titers (GMTs) and seroconversion rates.
Immunogenicity was assessed before and 28 days post-vaccination. Safety was assessed throughout the duration of the study.
The safety profiles of the QIV and the TIV formulations in the study did not materially differ. Across all three vaccine groups, the most frequently reported solicited injection-site reaction was pain or tenderness. Across all groups, the most frequently reported systemic reactions were irritability in the younger children and myalgia (muscle ache) and malaise (feeling unwell) in the older children. Rates of unsolicited adverse events and serious adverse events were similar among the study groups.
Important Safety Information
The most common local and systemic adverse reactions to Fluzone vaccine include soreness, pain and swelling at the vaccination site, fever, malaise and myalgia. Other adverse reactions may occur. Fluzone vaccine should not be administered to anyone with a severe allergic reaction (e.g., anaphylaxis) to any vaccine component, including egg protein or thimerosal (the multi-dose vial of Fluzone vaccine is the only presentation that contains thimerosal), or to a previous dose of any influenza vaccine.
The decision to give Fluzone vaccine should be based on the potential benefits and risks, especially if Guillain-Barre syndrome has occurred within six weeks of receipt of a prior influenza vaccine. The tip caps of the prefilled syringes may contain natural rubber latex, which may cause allergic reactions in latex sensitive individuals. Vaccination with Fluzone vaccine may not protect all individuals.
Sanofi Pasteur, the vaccines division of Sanofi, provides more than 1 billion doses of vaccine each year, making it possible to immunize more than 500 million people across the globe. A world leader in the vaccine industry, Sanofi Pasteur offers the broadest range of vaccines protecting against 20 infectious diseases. The company's heritage, to create vaccines that protect life, dates back more than a century. Sanofi Pasteur is the largest company entirely dedicated to vaccines. Every day, the company invests more than EUR 1 million in research and development. For more information, please visit: www.sanofipasteur.com or www.sanofipasteur.us.
Forward Looking Statements
SOURCE Sanofi Pasteur