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Related: Editorials & Other Articles, Issue Forums, Alliance Forums, Region ForumsFDA refuses to review Moderna's application for mRNA flu vaccine, company says
Reposted by We Left With All Of My Popehats
https://bsky.app/profile/kenwhite.bsky.social
@hammbear2024.bsky.social
This isnt a setback. This is deliberately thwarting the research and development of safe and effective medicine.
CNN
@cnn.com
· 5h
The FDA has refused to accept an application from Moderna to review its first mRNA seasonal flu vaccine, the company said, in another setback for the technology thats been a target of some Trump administration health officials.
https://www.cnn.com/2026/02/10/health/fda-moderna-mrna-flu-vaccine
6:46 PM · Feb 10, 2026
This isnât a setback. This is deliberately thwarting the research and development of safe and effective medicine.
— Clean Observer (@hammbear2024.bsky.social) 2026-02-10T23:46:58.337Z
@cnn.com
The FDA has refused to accept an application from Moderna to review its first mRNA seasonal flu vaccine, the company said, in another setback for the technology thats been a target of some Trump administration health officials.
https://www.cnn.com/2026/02/10/health/fda-moderna-mrna-flu-vaccine
6:19 PM · Feb 10, 2026
The FDA has refused to accept an application from Moderna to review its first mRNA seasonal flu vaccine, the company said, in another setback for the technology thatâs been a target of some Trump administration health officials. https://cnn.it/4kt8iyn
— CNN (@cnn.com) 2026-02-10T23:19:23.9388563Z
FDA refuses to review Modernas application for mRNA flu vaccine, company says
By Meg Tirrell
Updated 2 hr ago
Updated Feb 10, 2026, 9:24 PM ET
PUBLISHED Feb 10, 2026, 6:06 PM ET
The US Food and Drug Administration has refused to accept an application from Moderna to review its first mRNA seasonal flu vaccine, the company said Tuesday, in another setback for the technology thats been a target of some Trump administration health officials.
The agency told Moderna that its application didnt contain an adequate and well-controlled trial because the control arm didnt reflect the best-available standard of care in the United States at the time of the study, according to a letter dated February 3 that Moderna posted online. It didnt identify any safety or efficacy concerns, the company said.
Moderna said that the refusal was inconsistent with previous feedback from the agency and that it had requested a meeting with FDA officials to understand how to proceed. ... The complete stunner here is at no point in any of this did anybody say that it was not adequate to run its clinical trial the way it had discussed with the agency, Modernas president, Dr. Stephen Hoge, told CNN on Tuesday. ... The US Department of Health and Human Services said the FDA generally does not comment on regulatory communications to individual sponsors. Its rare for the FDA to issue a refuse-to-file letter; a 2021 study of almost 2,500 applications submitted to the agency found that only 4% received such letters.
Moderna used a standard-dose seasonal flu vaccine called Fluarix as a comparator in a 40,700-person clinical trial to demonstrate the experimental mRNA vaccines safety and efficacy. The company said the FDA had agreed with that plan in April 2024 but suggested it also include data comparing its vaccine with an approved high-dose flu vaccine for people over 65, which the company said it did.
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AZJonnie
(3,277 posts)durablend
(9,045 posts)LudwigPastorius
(14,396 posts)...and Trump put him in power to do it because, like a true Nazi, he views them as "unnütze Esser".
BlueWaveNeverEnd
(13,492 posts)LetMyPeopleVote
(177,018 posts)While the Trump administration focuses on a deworming medication as a possible cancer cure, its taking a different approach to a potential flu vaccine.
FDAâs refusal to review Moderna flu vaccine generates immediate political backlash While the Trump administration focuses on a deworming medication as a possible cancer cure, itâs taking a diff...
— Cancer-Vaccine (@cancer-vaccine.activitypub.awakari.com.ap.brid.gy) 2026-02-11T14:55:00.000Z
#Maddowblog #Politics
Origin | Interest | Match
https://www.ms.now/rachel-maddow-show/maddowblog/fdas-refusal-to-review-moderna-flu-vaccine-generates-immediate-political-backlash
Ordinarily, the FDA wouldnt have to remind people that theyre not livestock, but it became necessary for an unfortunate reason: An alarming number of people were trying to treat Covid-19 by voluntarily taking a medicine known as ivermectin, which is generally a deworming medication intended for horses and cows.....
Making matters spectacularly worse, while the Trump administration takes seriously the idea that a livestock deworming medication might cure cancer, the same administration is taking a very different approach to a potential vaccine for influenza. The New York Times reported:
The vaccine maker Moderna said on Tuesday that the Food and Drug Administration had notified the company that the agency would not review its mRNA flu vaccine, the latest sign of federal health policy that has become hostile to vaccine development.
Dr. Vinay Prasad, the agencys top vaccine regulator, rejected the companys application for approval over a concern that Modernas clinical trial had compared its experimental vaccine against a product the agency did not consider the best on the market. People in the comparison group received Fluarix Quadrivalent, a flu vaccine sold by GSK.
The Times report added that Moderna had spent years and hundreds of millions of dollars testing its flu vaccine. Evidently, the Trump administration doesnt care.....
Democratic Sen. Patty Murray of Washington wrote online on Tuesday night that Health and Human Services Secretary Robert F. Kennedy Jr. is now blocking an updated flu vaccine for no reason grounded in science. American vaccine policy has been hijacked by a conspiracy theorist yet most Republicans are happy to just sit on their hands. They are allowing FDA policy to be dictated by DELUSION.
Murray, in a message directed at Republican Sen. Bill Cassidy of Louisiana, who chairs the Senates Health, Education, Labor and Pensions Committee, added, If I were the Chair of the Senate HELP Committee, I would have moved to subpoena RFK Jr. a LONG time ago, but the next best time is NOW. [Cassidy], what happened to those quarterly oversight hearings? You and I both know its well past time for Congress to step in.
Cassidy has not yet responded. Watch this space
