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Seres pioneered the first-ever FDA-approved oral live biotherapeutic (VOWST™, formerly SER-109) for recurrent C. difficile infection. Their pipeline includes programs in preclinical through Phase 3 development targeting gastrointestinal, inflammatory, metabolic, and immuno-oncology indications, with SER-109 demonstrating positive Phase 3 results and receiving approval; SER-262 and SER-287 are in early to mid-clinical stages, while SER-401 is preclinical[2].
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