Study Testing Prebiotic Supplementation for Inflammatory Bowel Disease Moves to Pediatric Phase
Researchers are one step closer to developing personalized microbial therapeutic interventions for inflammatory bowel disease (IBD) thanks to a novel study co-sponsored by Cincinnati Children’s and two other pediatric institutions.
The study is exploring the potential benefits of the prebiotic 2'-fucosyllactose (2’FL) in restoring a healthy microbiome in children and young adults with IBD. It is the first National Institutes of Health-sponsored, randomized controlled trial to study 2’FL.
Phase one concluded in 2022. Study participants were young adults 18-25 with Crohn’s disease or ulcerative colitis who were doing well on Remicade (infliximab) or Humira (adalimumab). Two of the three doses tested met the required endpoints for safety, tolerability and effectiveness. In 2023, researchers at Cincinnati Children’s, Nationwide Children’s and Connecticut Children’s launched the study’s next phase, which is testing the two doses in children ages 11-17.
2’FL is an oligosaccharide that is present in breast milk. Synthetic 2’FL is available in powdered form and can be mixed into a beverage. Patients assigned to one of the 2’FL groups continue to follow their established treatment plan and take the supplement for one month (others take a placebo). Three months after their last dose, they return to the clinic for testing to see if their biome shows beneficial changes.



