Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
EBS-C12 is a small molecule organoselenium compound developed by EBS Pharma as a non-antibiotic treatment for *Clostridioides difficile* infection (CDI). Unlike standard-of-care antibiotics that target the bacteria and disrupt the gut microbiome, EBS-C12 functions as a toxin-neutralizing agent. It specifically inhibits the cysteine protease domain (CPD) of *C. difficile* toxin B (TcdB), which is essential for the toxin's autoprocessing and the subsequent release of its cytotoxic glucosyltransferase domain into the host cell. By blocking this activation step, EBS-C12 prevents the cellular damage and inflammation that drive CDI symptoms and recurrence, while sparing the beneficial gut microbiota. The drug has received Fast Track designation from the U.S. FDA.
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 EBS-C12.