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FDA rejected Moderna’s mRNA flu vaccine due to flawed trial design and comparator, raising concerns over regulatory consistency and impact on innovation.
The FDA rejected Moderna’s application for its mRNA flu vaccine, citing insufficient trial design and an inadequate comparator, despite the company’s claims of meeting regulatory expectations and prior approvals in other countries.
The refusal to file, a rare move typically reserved for incomplete submissions, has raised concerns about regulatory consistency and potential political influence following Robert F. Kennedy Jr.’s appointment as HHS secretary.
Industry leaders warn the decision may deter investment in mRNA technology, slowing innovation and threatening U.S. public health preparedness, especially amid a severe flu season.
La FDA rechazó la vacuna contra la gripe por ARNm de Moderna debido a un diseño de ensayo y comparador defectuosos, lo que generó preocupaciones sobre la consistencia regulatoria y el impacto en la innovación.