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The US Food and Drug Administration (FDA) has approved a drug made from human poop to treat a critical type of diarrheal infection. The new drug, Rebyota, is produced from a blend of human poop donated by screened donors, saline, and laxative solution; and is manufactured by Switzerland-based Ferring Pharmaceuticals. Rebyota is administered as an enema –
Ferring's novel first-in-class REBYOTA is indicated for the prevention of recurrence of Clostridioides difficile infection (CDI) in individuals 18 years of age and older, following antibiotic treatment
Ferring to share insights and expertise across a range of timely and critical topics at the Women’s Health Innovation Summit in Boston As the headline sponsor, Ferring will have a significant presence with executives providing the keynote address, participating on several panels and hosting an Innovation Council.