Pilot and Feasibility Study of 2'-FL as a Dietary Supplement in IBD Patients Receiving Stable Maintenance Anti-TNF Therapy

Inclusion Criteria:

1. Provision of signed and dated informed consent form

2. Stated willingness to comply with all study procedures and availability for theduration of the study

3. Male or female, aged 11 - 25

4. Diagnosed with Crohns Disease or Ulcerative Colitis

5. Disease is in remission

• Adult CD (age 18-25): CDAI score < 150

• Pediatric CD (age 11-17): wPCDAI < 12.5

• Adult UC (age 18-25): Modified Mayo sub-scores: stool frequency sub-score=0,rectal bleeding sub-score=0

• Pediatric UC (age 11-17): PUCAI score < 10

6. Not receiving corticosteroids

7. Receiving a stable anti-TNF maintenance dose of adalimumab, infliximab, or thebiosimilar infliximab-dyyb for 12 weeks prior to enrollment. A stable infliximab orinfliximab-dyyb dose may range from 5 mg/kg every 8 weeks to 10 mg/kg every 4 weeks.A stable adalimumab dose may range from 20 mg every 2 weeks to 40 mg every 7 days.While therapeutic drug monitoring will not be required for inclusion, all drug andanti-drug antibody levels obtained for clinical indications within six months priorto enrollment, and from the screening visit through week 20, will be recorded.

8. If receiving mesalamine, mercaptopurine, azathioprine, or methotrexate, must be on astable dose for at least 12 weeks prior to enrollment.

9. Agreement to not make any major dietary changes throughout study duration. Thiswould include changing usual diet to a vegan diet, Specific Carbohydrate Diet (SCD),or exclusive enteral nutrition (EEN) diet.

10. We will include CD patients who have had one ileo-colic resection, as long as theresection did not include more of the colon than the cecum and ascending colon. CDpatients may be enrolled if at least six months post-surgery.

Exclusion Criteria:

1. Experienced active IBD clinical disease during the previous six months as determinedby the Principal Investigator.

2. Use of any of the following medications during the previous month: antibiotics,probiotics or prebiotics

3. Diagnosis of celiac disease, diabetes or other co-morbidity that is determined bythe PI as being exclusionary

4. Treatment with another investigational drug or other intervention within 4 weeks

5. Treatment with other biologic medication for IBD within prior 12 weeks

6. Problem with lactose breakdown

7. Currently pregnant or breast feeding

8. We will exclude CD patients with more than one IBD related surgery, or those with asub-total colectomy. We will exclude UC patients with colectomy or IBD relatedsurgery.

9. We will not allow concomitant use of anti-diarrheal medications.