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    CHICAGO — In a Healio video exclusive, Ken Blount, PhD, discusses successful restoration of gut microbiota and clonal engraftment as soon as 1 week after treatment with Rebyota in those with recurrent Clostridioides difficile infection. Blount and colleagues sought to quantify and define clonal engraftment and durable microbiome compositional changes with FDA-approved Rebyota (fecal

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    • #ICYMI with @KenBlountPhD at #DDW23: ‘Distinctive shift’ in #gutmicrobiota after #Rebyota ( @FerringMBiome) treatment for #Cdifficile @DDWMeeting https://t.co/5OfW7hBH0A

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    The FDA has approved Vowst, the first orally administered fecal microbiota product indicated for the prevention of recurrent Clostridioides difficile infection in adults following antibacterial treatment. With this approval, Vowst ( SER-109, Seres Therapeutics) becomes the second microbiota-based live biotherapeutic approved for recurrent C. difficile infection following the

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    • #ICYMI: @US_FDA approves Vowst (@SeresTX) as first oral microbiota biotherapeutic for recurrent #Cdifficile #GITwitter #MedTwitter https://t.co/1WvG0plks2

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    The FDA has approved Rebyota, a microbiota-based live biotherapeutic indicated for the prevention of recurrent Clostridioides difficile infection in adults after antibiotic treatment, Ferring Pharmaceuticals announced in a press release. The approval comes after an FDA panel voted in favor of Rebyota (fecal microbiota, live-jslm; Ferring Pharmaceuticals) in September 2022, with the Vaccines and

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    • #ICYMI: @US_FDA approves fecal microbiota biotherapeutic for recurrent #Cdifficile infection @ferring #GITwitter #Medtwitter https://t.co/XimIH2blxH