Nirsevimab, a monoclonal antibody used to protect infants from respiratory syncytial virus (RSV), is in limited supply, according to a CDC announcement.
The CDC announced on Monday, October 23, 2023, that there is a limited supply of nirsevimab, a monoclonal antibody that is recommended for use in infants to prevent lower respiratory tract disease associated with respiratory syncytial virus (RSV).
RSV is the most common cause of respiratory infection in the United States, primarily in infants within the first year of their life. The FDA approved nirsevimab, also known as Beyfortus, in July 2023 to give infants passive immunization against lower respiratory tract infections brought on by RSV. The CDC Advisory Committee on Immunization Practices (ACIP) recommended the antibody for infants younger than 8 months during or entering their first season of RSV, as well as infants aged 8 to 19 months who were at risk for severe RSV. RSV transmission is expected to increase nationwide within the next 1 to 2 months.
Doctor Examining Toddler Listening To Lungs With Stethoscope In Clinic | Image credit: Prostock-studio - stock.adobe.com
According to the CDC’s announcement, there is a limited supply of nirsevimab from the manufacturer for the 2023-2024 RSV season, with prefilled syringes of 100-mg doses in especially short supply. Although the shortage of of 50-mg dose prefilled syringes is not as severe, supply will likely be limited during the RSV season. The CDC is working with the manufacturer on strategies to boost the supply of nirsevimab, but in the meantime issued several suggestions for both health care providers and the public on how to adapt to the shortage.
The CDC is currently recommending that the ACIP recommendations remain unchanged for infants who weigh less than 5 kg. Infants born before October 2023 should receive a 50-mg dose now and infants born in October and later this RSV season should receive a 50-mg dose within their first week of life. For infants who weigh 5 kg or more, health care providers should prioritize giving the 100-mg dose to those at highest risk of severe disease. This includes all infants younger than 6 months, American Indian and Alaska Native infants younger than 8 months, and infants aged 6 to 8 months who have conditions that give them a higher overall risk of severe RSV.
Doctors should use palivizumab instead of nirsevimab in eligible children aged 8 to 19 months, the CDC noted, but nirsevimab should be offered to American Indian and Alaska Native infants aged 8 to 19 months who are not eligible for palivizumab. Recommendations from the American Academy of Pediatrics should be followed when offering palivizumab to infants younger than 8 months. Doctors should also avoid using two 50-mg doses for any infants who weigh 5 kg or more in order to preserve the supply as much as possible. Pregnant women should also be encouraged to receive Pfizer’s RSVpreF vaccine (Abrysvo) to protect their child from RSV once born. Administration of both the preventive vaccine in pregnant women and nirsevimab in the infant is not needed; a single dose of 1 vaccine is sufficient.
The CDC also recommends that the public take precautions to limit the spread of RSV. During pregnancy, patients should ask their health care provider about receiving an RSV vaccine to protect their child from the virus. Parents should also ask about the availability of nirsevimab for their child.
Reference
Limited availability of nirsevimab in the United States—interim CDC recommendations to protect infants from respiratory syncytial virus (RSV) during the 2023-2024 respiratory virus season. News release. CDC. October 23, 2023. Accessed October 24, 2023. https://emergency.cdc.gov/han/2023/han00499.asp
Conflicts of Interest in Federal Vaccine Advisory Committees at Historic Lows Despite RFK Jr Claims
August 19th 2025Research reveals a significant decline in reported conflicts of interest among the CDC's and FDA's vaccine advisory committees, challenging Robert F. Kennedy Jr's claims.
Read More
Prenatal PFAS Exposure Alters Infant Vaccine-Related Immune Cells
August 1st 2025Prenatal exposure to per- and polyfluoroalkyl substances (PFAS), a class of persistent environmental pollutants, was linked to significant shifts in infant T helper cell development, raising concerns about long-term effects on vaccine response, immune regulation, and disease susceptibility.
Read More
Updated mRNA Vaccines Against JN.1 Show Strong Safety Signal in Real-World Data
July 31st 2025A nationwide Danish cohort study demonstrated no increased risk of serious adverse events following vaccination with JN.1-updated mRNA COVID-19 vaccines, reinforcing their safety profile and supporting continued use in high-risk populations amid ongoing viral evolution.
Read More