S2048 Significant and Durable Microbiome Restoration in a Phase 3 Trial of Fecal Microbiota, Live-JSLM for Recurrent Clostridioides difficile Infection When Administered by Colonoscopy

Introduction: Microbiota-based products may shift the microbial composition of a recipient’s gut microbiome to suppress Clostridioides difficile outgrowth and prevent recurrent C. difficile infection (rCDI). Fecal microbiota, live-jslm (RBL) is the first FDA-approved, single-dose, microbiota-based product indicated for the prevention of rCDI in adults after standard-of-care antibiotic therapy. The safety and clinical effectiveness of RBL when administered by colonoscopy to adults with rCDI was evaluated in CDI-SCOPE (NCT05831189), a phase 3b multi-center, single-arm trial. Microbiome composition, diversity of bacterial populations, and the Microbiome Health Index for post-Antibiotic dysbiosis (MHI-A) were assessed among RBL recipients in CDI-SCOPE. Methods: These exploratory analyses included samples from 41 participants who received RBL in CDI-SCOPE. Treatment success was defined as the absence of Clostridioides difficile infection (CDI) diarrhea for 8 weeks after RBL administration. Participants were required to provide stool samples prior to bowel preparation and RBL administration by colonoscopy (baseline), at regular follow-up visits after 1, 4, and 8 weeks, after 3 and 6 months, and at the time of CDI recurrence within 8 weeks of RBL administration. Samples were extracted and sequenced using deep (>20 MM reads) shotgun methods. Class-level relative abundances and alpha diversity were evaluated, including the MHI-A—a microbiome biomarker of post-antibiotic dysbiosis and restoration. Results: Overall, 41 received RBL via colonoscopy; 39 participants completed an 8-week visit, with a treatment success rate of 95%. There were 20 participants with a full stool sample timeline (baseline, 1 week, 4 weeks, 8 weeks, 3 months, and 6 months) and 18 with a baseline sample and at least 1 post-administration sample. Compared with baseline, microbiome composition and MHI-A shifted significantly towards RBL composition among responders. Bacteroidia and Clostridia increased in abundance, whereas Gammaproteobacteria and Bacilli decreased following RBL administration via colonoscopy. MHI-A also increased from baseline to 6 months after RBL administration. Conclusion: RBL administered via colonoscopy restored microbiome composition concurrent with clinical response. These restorative changes reflect shifts from a post-antibiotic state of dysbiosis to a healthier state characterized by increased colonization resistance.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001135652.72435.3d
Citations
1
Primary Topic
Clostridium difficile and Clostridium perfringens research
Type
article
Field-Weighted Citation Impact
1.40
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article

S2048 Significant and Durable Microbiome Restoration in a Phase 3 Trial of Fecal Microbiota, Live-JSLM for Recurrent Clostridioides difficile Infection When Administered by Colonoscopy

Tonya Ward, Elizabeth M. Adamowicz, Paul Feuerstadt, Ken Blount et al.
1 citations
The American Journal of Gastroenterology
Clostridium difficile and Clostridium perfringens research
1.40
article

S2048 Significant and Durable Microbiome Restoration in a Phase 3 Trial of Fecal Microbiota, Live-JSLM for Recurrent Clostridioides difficile Infection When Administered by Colonoscopy

Tonya Ward, Elizabeth M. Adamowicz, Paul Feuerstadt, Ken Blount, Sahil Khanna, Daniel Van Handel
article en
1 citations

Abstract

Introduction: Microbiota-based products may shift the microbial composition of a recipient’s gut microbiome to suppress Clostridioides difficile outgrowth and prevent recurrent C. difficile infection (rCDI). Fecal microbiota, live-jslm (RBL) is the first FDA-approved, single-dose, microbiota-based product indicated for the prevention of rCDI in adults after standard-of-care antibiotic therapy. The safety and clinical effectiveness of RBL when administered by colonoscopy to adults with rCDI was evaluated in CDI-SCOPE (NCT05831189), a phase 3b multi-center, single-arm trial. Microbiome composition, diversity of bacterial populations, and the Microbiome Health Index for post-Antibiotic dysbiosis (MHI-A) were assessed among RBL recipients in CDI-SCOPE. Methods: These exploratory analyses included samples from 41 participants who received RBL in CDI-SCOPE. Treatment success was defined as the absence of Clostridioides difficile infection (CDI) diarrhea for 8 weeks after RBL administration. Participants were required to provide stool samples prior to bowel preparation and RBL administration by colonoscopy (baseline), at regular follow-up visits after 1, 4, and 8 weeks, after 3 and 6 months, and at the time of CDI recurrence within 8 weeks of RBL administration. Samples were extracted and sequenced using deep (>20 MM reads) shotgun methods. Class-level relative abundances and alpha diversity were evaluated, including the MHI-A—a microbiome biomarker of post-antibiotic dysbiosis and restoration. Results: Overall, 41 received RBL via colonoscopy; 39 participants completed an 8-week visit, with a treatment success rate of 95%. There were 20 participants with a full stool sample timeline (baseline, 1 week, 4 weeks, 8 weeks, 3 months, and 6 months) and 18 with a baseline sample and at least 1 post-administration sample. Compared with baseline, microbiome composition and MHI-A shifted significantly towards RBL composition among responders. Bacteroidia and Clostridia increased in abundance, whereas Gammaproteobacteria and Bacilli decreased following RBL administration via colonoscopy. MHI-A also increased from baseline to 6 months after RBL administration. Conclusion: RBL administered via colonoscopy restored microbiome composition concurrent with clinical response. These restorative changes reflect shifts from a post-antibiotic state of dysbiosis to a healthier state characterized by increased colonization resistance.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 14%
Clostridium difficile and Clostridium perfringens research
1.40
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