Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
IMM-529 is an oral polyclonal antibody therapy developed to target and neutralize the main virulence factors of *Clostridioides difficile* (C. difficile), specifically for the prevention and treatment of recurrent C. difficile infection (CDI). The drug contains bovine colostrum-derived antibodies generated by immunizing dairy cows, resulting in hyperimmune bovine colostrum that targets three essential components of C. difficile pathogenesis: Toxin B, spores, and surface layer proteins of vegetative cells[1][3][5][6]. This triple-target approach aims to neutralize Toxin B locally in the gut while binding spores and vegetative cells to prevent colonization and recurrence without disrupting the normal gut microbiome[5][6]. Preclinical studies have shown efficacy in preventing primary disease, protecting against recurrence, and treating active infection[3][7]. IMM-529 is being developed as an adjunctive therapy alongside standard-of-care antibiotics for CDI[3]. The developer is Immuron, an Australian biopharmaceutical company; manufacturing has involved CSIRO Agriculture and Food as well as collaboration with Monash University for vaccine manufacture support[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 IMM-529.