drugset / Trial / NCT04263597

Oral Supplementation of 2'-Fucosyllactose in Allogeneic Bone Marrow Transplant Recipients

NCT04263597 ↗

Phase 1/2 Completed 70 enrolled Children's Hospital Medical Center, Cincinnati
Non-randomizedParallel-groupOpen-labelPrevention

Summary

High dose chemotherapy and radiation used as preparative regimens in patients undergoing an allogeneic hematopoietic stem cell transplant (HSCT) disrupts intestinal homeostasis by damaging the intestinal epithelium and altering the intestinal microbiome. The investigators hypothesize that 2'-fucosyllactose (2FL) supplementation will be safe and tolerable and result in an increase in the relative abundance of intestinal Bifidobacteria. The investigators also hypothesize that 2FL supplementation will lead to reduction of Firmicutes and/or Proteobacteria, and improved intestinal homeostasis at day+30 as measured by lower pro-inflammatory cytokines, reduced levels of T-cell activation, lower markers of intestinal injury (fecal human DNA and plasma reg-3-alpha), increased fecal butyrate levels and ultimately lower incidence of acute GVHD and BSI at day+100. Phase II: The investigators hypothesize that 2FL supplementation will be safe and tolerable and result in an increase in the relative abundance of fecal short chain fatty acids such as butyrate, acetate and propionate at day+7 compared to baseline values.

Timeline

Start
2020-08-26
Primary completion
2025-05-23
Completion
2025-05-23

Drugs

EvaluationDrugModalityDoseRoute
Subject 2'-Fucosyllactose Other / unclassified 2.5 g Oral
Subject 2'-Fucosyllactose Other / unclassified 5 g Oral
Subject 2'-Fucosyllactose Other / unclassified 10 g Oral