Antimicrobials |
Antibiotics |
A number of novel antibiotics are in clinical trials. |
Ribaxamase |
This is a beta-lactamase that may be co-administered with systemic broad-spectrum antibiotics, with the aim of degrading the antibiotics in the gut before they can affect the gut microbiota and create a propensity to CDI. |
Immunisation |
Passive immunisation |
Co-administration of bezlotoxumab (an anti-toxin B antibody) together with conventional antibiotic therapy has been shown to reduce the rate of recurrence of CDI compared to antibiotic therapy alone22. |
Active immunisation |
Anti-toxin vaccines are now in clinical trials. However, early data suggest reduced seroconversion in older people, those most at risk of CDI. |
Microbiome manipulation |
Non-toxigenic C. difficile23
|
In a clinical trial, non-toxigenic C. difficile was administered to those with CDI, with the aim of outcompeting toxigenic C. difficile from its reservoir within the gut.
CDI recurrence rates were 30% in those receiving placebo vs 11% in those receiving non-toxigenic C. difficile.
|