Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MBX-SD-201 is an investigational whole microbiome therapeutic developed by MyBiotics for the treatment of *Clostridium difficile* infection (CDI). It is designed as an oral, feces-free alternative to traditional fecal microbiota transplantation (FMT), utilizing a proprietary technology that enables the industrial-scale production of a powder closely resembling a selected human microbiome sample. This approach aims to restore and maintain healthy gut flora, providing long-term recovery and potentially replacing FMT in clinical practice. The product leverages MyBiotics' MyCrobe technology, which enhances bacterial colonization and survival in the human body. As of early 2021, MBX-SD-201 was in preclinical development for CDI[1][2][3][4][5].
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 MBX-SD-201.