3 Key Takeaways
- The primary goal of the phase 3 trial of VE303 is to prevent the recurrence of CDI, building on promising phase 2 trial results.
- The phase 2 trial demonstrated that a high dose of VE303 prevented recurrent CDI among adults, showed a significant reduction in CDI recurrence rates compared to placebo. These findings are crucial as they support the rationale for the larger-scale phase 3 trial.
- Success in this trial could transform the management of CDI, offering a new avenue for patients struggling with this condition.
Findings in the phase 2 trial from 2023 indicate that a high dose of VE303 is effective in preventing recurrent CDI in adults with laboratory-confirmed CDI, including those with one or more prior CDI episodes in the last 6 months, as well as those with primary CDI who are at high risk for recurrence, when compared to a placebo.
Based on a previous report by Contagion, in the phase 2 trial CDI recurrence was reported among 13.8% of participants in the high-dose group, 37% in the low-dose group, and 45.5% in the placebo group. In the high-dose group, all recurrences occurred by Day 11. Most participants experienced sustained cures through Week 24, with only 2 CDI recurrences reported. The investigators also analyzed the fecal microbiota of participants. Those in the high-dose group had a significantly increased detection of VE303 strains, and early colonization was associated with greater treatment efficacy. Microbial diversity recovered most notably in the high-dose group. The adjusted absolute risk reduction was 30.5% in the high-dose group, compared with other treatment options, including fecal microbial transplant (28%), bezlotoxumab (10%), and RBX2660 (12.3%). The treatment was well-tolerated, with no serious treatment-emergent adverse events or deaths reported. 3
“The notorious difficulty of preventing recurrent CDI creates a large population of patients struggling with the condition, with few therapeutic options. VE303 provides an approach that is designed to address the underlying biology in a novel way,” said Darrell Pardi, MD, chair of the division of gastroenterology and hepatology at the Mayo Clinic. “The clinical data to date have been extremely promising, and we are eager to see future updates on this program as it progresses through the clinic.” 3
Overall, in the phase 2 trial in patients at high risk of recurrent CDI, VE303 met its primary efficacy endpoint of preventing CDI recurrence at 8 weeks. The phase 3 trial, expected to be completed in October 2027, aims to confirm these results in a larger population. This trial is important for understanding VE303’s safety and efficacy. Results from this trial could provide a new option for CDI management.
References
- Vedanta Biosciences. VE303 for Prevention of Recurrent Clostridioides Difficile Infection (RESTORATiVE303). Clincaltrials.gov. Published February 2, 2024. Accessed March 12, 2024. https://classic.clinicaltrials.gov/ct2/show/NCT03788434
- CDC. C diff (Clostridiodes difficile). Published December 7, 2023. Accessed March 12, 2024. https://www.cdc.gov/cdiff/what-is.html
- Lorenz J. Oral Bacterial Therapy for Recurrent CDI Shows Promise in Phase 2 Trial. Contagion. Published May 3, 2024. Accessed March 12, 2024. https://www.contagionlive.com/view/oral-bacterial-therapy-for-recurrent-cdi-shows-promise-in-phase-2-trial