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Dr. Jeff Barke – Reasons to be Concerned about the New RSV Vaccine Approved by FDA on June 9, 2025
On June 9, 2025, the FDA approved a New RSV Monclonal Treatment for Neonates and Infants called Enflonsia.
ENFLONSIA is a respiratory syncytial virus (RSV) F protein-directed fusion inhibitor indicated for the prevention of RSV lower respiratory tract disease in neonates and infants who are born during or entering their first RSV season.
ENFLONSIA – Clesrovimab-cfor is a respiratory syncytial virus F protein-directed fusion inhibitor. Clesrovimab-cfor is a fully human immunoglobulin G1 kappa (IgG1κ) monoclonal antibody produced in recombinant Chinese hamster ovary (CHO) cells. The molecular weight is approximately 149 kDa.
Technically, ENFLONSIA is not a Vaccine, as it doesn’t stimulate the immune system, but is monoclonal antibody to “prevent” RSV.
It’s crazy they would approve this without any long-term studies considering some shady history with RSV Vaccines in the past.
Dr. Jeffrey Barke goes over 10 Reasons why this could be another disaster approved by the incompetent FDA.
Source:
1. Jeffrey Barke -- https://www.facebook.com/watch/?v=3935721996680551
2. Jeffrey Barke Substack – 10 Reasons to be Deeply Concerned about ENFLONSIA -- https://substack.com/home/post/p-166174541
3. U.S Food and Drug Administration. “Package Insert – ENFLONSIA.” FDA.Gov, https://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761432s000lbl.pdf. Accessed 7 Jul. 2025. *FDA Enflonsia Package Insert for RSV – Monoclonal Antibody. Approved on June 9, 2025.
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