Seqirus today announced that the U.S. Food and Drug Administration (FDA) has approved FLUCELVAX® QUADRIVALENT
- Approval aligns with universal age recommendation for all eligible people six months and older to receive annual influenza vaccination[1]
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[15-October-2021] |
SUMMIT, N.J., Oct. 15, 2021 /PRNewswire/ -- Seqirus, a global leader in influenza prevention, and a business of CSL Limited (ASX: CSL), today announced that the U.S. Food and Drug Administration (FDA) has approved FLUCELVAX® QUADRIVALENT (Influenza Vaccine), the company’s cell-based quadrivalent influenza vaccine, for an expanded age indication for children as young as six months old.4 With this approval, FLUCELVAX QUADRIVALENT, the first and only cell-based influenza vaccine in the U.S., is now indicated for everyone eligible to receive an influenza vaccine in the U.S.4 Experience the interactive Multichannel News Release here: The expanded age indication is supported by a Phase 3 clinical study demonstrating that FLUCELVAX QUADRIVALENT was as safe and immunogenic as a standard quadrivalent seasonal influenza vaccine (QIV) in children six months to <four years of age during the U.S. 2019/20 influenza season.5 These data, presented at the Pediatric Academic Society (PAS) virtual Annual Meeting on May 1, 2021, represent the first U.S. Phase 3 study of a cell-based influenza vaccine in this population. “As one of the world’s largest influenza vaccine manufacturers, we continually seek to apply new technologies and evolve our vaccine portfolio to help address challenges associated with seasonal influenza vaccine effectiveness,” said Dave Ross, Vice President, North America Commercial Operations at Seqirus. “The FLUCELVAX QUADRIVALENT expanded age indication for children as young as six months of age now allows all eligible people to receive a differentiated influenza vaccine option.” FLUCELVAX QUADRIVALENT utilizes a cell-based influenza vaccine manufacturing process, an alternative to traditional egg-based manufacturing.2 Traditional egg-based vaccine production can cause the strain to mutate at several steps throughout the manufacturing process, which may lead to an antigenic mismatch between the circulating strains and the inactivated influenza strains contained within the seasonal influenza vaccine.2 Cell-based influenza vaccines are designed to produce an exact match to WHO-selected influenza virus strains by avoiding egg-adapted changes, and therefore may have the potential for greater vaccine effectiveness.2,3 Cell-based influenza vaccine technology may offer additional advantages over the standard influenza manufacturing process, including increased scalability and production speed in the event of an influenza pandemic.2 “Throughout our company’s long history as a leader in influenza prevention, we have remained committed to delivering safe and effective vaccines to as many eligible people as possible,” said Gregg Sylvester, MD, Chief Medical Officer at Seqirus. “And while we can never predict how each influenza season will unfold, we could possibly be faced with unique challenges and increased cases this upcoming season as COVID-19 mitigation tactics relax. Therefore, it is critical that all eligible people receive their annual flu vaccine.” Children younger than five years old, particularly those younger than two, are at increased risk of developing serious influenza-related complications, including pneumonia, brain dysfunction and in rare cases, even death.6 Children six months to five years of age who are otherwise healthy are at a high risk of influenza-related complications simply due to their lack of prior immunity.7 According to the U.S. Centers for Disease Control and Prevention (CDC), it is estimated that nearly 50,000 hospitalizations occurred in children younger than 18 years of age during the 2019/20 U.S. influenza season, and there were approximately over 486 influenza-related deaths in this age group.8 The CDC recommends everyone six months of age and older without contraindications receive an influenza vaccine annually as the best way to prevent influenza.1 In the U.S., Seqirus operates a state-of-the-art cell-based manufacturing facility in Holly Springs, North Carolina, purpose-built in partnership with the Biomedical Advanced Research and Development Authority (BARDA), a component of the Office of the Assistant Secretary for Preparedness and Response within the U.S. Department of Health and Human Services, to increase cell-based vaccine manufacturing capacity and combat pandemic influenza threats.9 Last year, Seqirus announced plans to build a new, world-class cell-based manufacturing facility in Australia, which will be the only cell-based influenza vaccine manufacturing facility in the Southern Hemisphere.10 About Seasonal Influenza About Seqirus About CSL For more information visit www.seqirus.com and www.csl.com. Intended Audience Forward-Looking Statements FLUCELVAX® QUADRIVALENT (Influenza What is FLUCELVAX® QUADRIVALENT (Influenza Vaccine)? Who should not get FLUCELVAX QUADRIVALENT? Before receiving FLUCELVAX QUADRIVALENT, tell your healthcare provider about all medical conditions, including if you:
What are the most common side effects of FLUCELVAX QUADRIVALENT?
Additional side effects seen in children include:
These are not all of the possible side effects of FLUCELVAX QUADRIVALENT. You can ask your healthcare provider for more information and for advice about any side effects that concern you. To report SUSPECTED ADVERSE REACTIONS, contact Seqirus at 1–855–358-8966 or VAERS at 1–800–822–7967 or www.vaers.hhs.gov. You are also encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1–800–FDA–1088. Before receiving this vaccine, please see the full US Prescribing Information for FLUCELVAX QUADRIVALENT. The information provided here does not include all that is known about FLUCELVAX QUADRIVALENT. To learn more, talk with your healthcare provider or pharmacist. FLUCELVAX® QUADRIVALENT is a trademark of Seqirus UK Limited or its affiliates. USA-QIVc-21-0096 MEDIA CONTACT 1 Centers for Disease Control and Prevention (CDC). (2021). Who Needs a Flu Vaccine and When. Retrieved from: https://www.cdc.gov/flu/prevent/vaccinations.htm. Accessed September 2021. 2 CDC. (2021). Cell-Based Flu Vaccines. Retrieved from: https://www.cdc.gov/flu/prevent/cell-based.htm. Accessed September 2021. 3 Rajaram, S., Boikos, C., Gelone, et al. (2020). Influenza Vaccines: The Potential Benefits of Cell-Culture Isolation and Manufacturing. 4 FLUCELVAX® QUADRIVALENT (Influenza Vaccine) [package insert]. Holly Springs, NC: Seqirus Inc; 2021. 5 Essink, B., Herringa, M., Jeanfreau, R., et al. (2021). Immunogenicity and Safety of Cell-derived Quadrivalent Influenza Vaccine in Children 6 through 47 Months of Age: A Randomized Controlled Non-Inferiority Trial. Presented at Pediatric Academic Societies 2021. 6 CDC. (2021). Protect Against Flu: Caregivers of Infants and Young Children. Retrieved from: https://www.cdc.gov/flu/highrisk/infantcare.htm. Accessed September 2021. 7 Munoz, F. (2002). The impact of influenza in children. Seminars in Pediatric Infectious Diseases. 8 CDC. (2021). Estimated Influenza Illnesses, Medical visits, Hospitalizations, and Deaths in the United States — 2019–2020 Influenza Season. Retrieved from: https://www.cdc.gov/flu/about/burden/2019-2020.html. Accessed September 2021. 9 This project has been funded in whole or in part with Federal funds from the Office of the Assistant Secretary for Preparedness and Response, Biomedical Advanced Research and Development Authority, under contract numbers HHSO10020060001F2C, HHSO100200700030C, HHSO100200900101C and HHSO100201200003I. 10 Data on file. (2020). Seqirus USA Inc. 11 CDC. (2021). Key Facts about Influenza (Flu). Retrieved from: https://www.cdc.gov/flu/about/keyfacts.htm Accessed September 2021.
SOURCE Seqirus | ||
Company Codes: Australia:CSL, OTC-PINK:CSLLY |