Clinical trials
Follow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
fecal microbiota spores, live-brpk (marketed as Vowst, formerly known as SER-109) is an orally administered live biotherapeutic product consisting of a purified consortium of bacterial spores (primarily Firmicutes) derived from healthy human donor fecal matter. It is developed by Seres Therapeutics and Nestlé Health Science (which acquired full global rights to the product in 2024). Vowst is FDA-approved for the prevention of recurrence of Clostridioides difficile infection (CDI) in adults following antibacterial treatment for recurrent CDI. The therapeutic works by restoring the gut microbiome, thereby increasing colonization resistance against C. difficile.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on fecal microbiota spores, live-brpk.