This is really quite bad. The FDA’s Prasad succeeded in creating enough regulatory roadblocks such that Pfizer gave up on its #covid #covid19 vaccine trial for healthy adults.

https://www.reuters.com/business/healthcare-pharmaceuticals/pfizer-biontech-halt-us-covid-vaccine-study-after-recruitment-struggles-2026-04-01/

@cremevax lots if people aged 50-64 have chronic illnesses. By demanding enrolment of 25,000 50-64yo's without chronic illnesses, Trump's FDA killed Pfizer's COVID vaccine.

@DavidPenington I wouldn’t say that the Pfizer covid vax has been killed — not yet, anyway.

But by imposing new, large trial requirements for an annual strain revision for a given population subset, the FDA is doing its best to make up-to-date Covid vaccines uneconomical to produce. If they are successful, then that impacts vaccine access for everyone.

But! FDA decisions are not set in stone. See for example the pending Moderna mRNA flu application, about which they originally said they wouldn’t even look at the application, promptly ate shit on, and then decided to review after all. Trump is only getting weaker, and therefore is more susceptible to pushback — before the midterms at least.

https://www.cidrap.umn.edu/influenza-vaccines/double-reverse-fda-now-says-it-will-review-moderna-s-mrna-flu-vaccine

Double-reverse: FDA now says it will review Moderna’s mRNA flu vaccine

CIDRAP