MedPath

Vaccine Updates: FDA Approves Self-Administered FluMist, Updated Novavax COVID-19 Vaccine

• The FDA has approved FluMist, a nasal spray flu vaccine, for self- or caregiver-administration, making it the first flu vaccine with this capability, indicated for individuals aged 2 to 49 years. • Novavax's updated COVID-19 vaccine has received FDA emergency use authorization for individuals aged 12 years and older, set to be available in pharmacies and grocers across the United States. • GSK reported positive topline data from a phase 3 study for co-administration of its RSV vaccine (Arexvy) with its shingles vaccine (Shingrix) in adults 50 years and older. • The WHO has added the MVA-BN (Imvanex) vaccine to its prequalification list, marking the first mpox vaccine to receive this designation, indicated for adults and potentially for off-label use in younger populations.

The FDA has approved several key vaccine updates, including a first-of-its-kind self-administered flu vaccine and an updated COVID-19 vaccine, alongside positive data for RSV and shingles co-administration and a WHO prequalification for an mpox vaccine.

Self-Administered FluMist Approved

The FDA has approved FluMist, a nasal spray influenza vaccine, for self- or caregiver-administration. This marks the first time a flu vaccine has been approved for administration outside of a healthcare setting. FluMist is indicated for individuals aged 2 to 49 years for the prevention of influenza virus subtypes A and B. The vaccine contains weakened, live strains of the influenza virus. It was initially approved in 2003 for those aged 5-49, with the approval expanded in 2007 to include children aged 2-5.

Updated Novavax COVID-19 Vaccine Authorized

Novavax announced that the FDA has granted emergency use authorization (EUA) to its updated COVID-19 vaccine for individuals aged 12 years and older. The updated vaccine will be available at pharmacies and grocery stores throughout the United States, pending release by the Center for Biologics Evaluation and Research.

GSK Reports Positive Co-Administration Data for RSV and Shingles Vaccines

GSK has announced positive topline data from a phase 3 study evaluating the immunogenicity, reactogenicity, and safety of its respiratory syncytial virus (RSV) vaccine (Arexvy) when co-administered with its recombinant zoster vaccine for shingles (Shingrix) in adults aged 50 years and older. The results will be submitted for publication in a peer-reviewed journal and will support regulatory submissions to the FDA, European Medicines Agency, and other regulatory bodies.

WHO Adds First Mpox Vaccine to Prequalification List

The MVA-BN (Imvanex) vaccine has been added to the WHO’s prequalification list. Manufactured by Bavarian Nordic, the vaccine is a two-dose injection given four weeks apart and is intended for adults. It is the first mpox vaccine to be added to the list and is indicated for active immunization against smallpox, mpox, and related orthopoxvirus infections and disease in adults. The WHO also noted that the vaccine can be used off-label in individuals under 18 years of age and in pregnant and immunocompromised individuals, particularly in outbreak settings where the benefits outweigh the potential risks.
Subscribe Icon

Stay Updated with Our Daily Newsletter

Get the latest pharmaceutical insights, research highlights, and industry updates delivered to your inbox every day.

Related Topics

Reference News

[1]
Immunization Roundup: FDA Approves FluMist, Updated Novavax COVID-19 Vaccine
drugtopics.com · Sep 25, 2024

FDA approves FluMist for self- or caregiver-administration, Novavax updates COVID-19 vaccine, GSK reports positive data ...

© Copyright 2025. All Rights Reserved by MedPath