Lead Sponsor

ProgenaBiome

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

•1. Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study
•2. Male or female patients age 12 and older. (interest is given to children 12 and older to compare with mothers).
•3. Diagnosis of Non-Fistulating Crohn's disease confirmed by at least one of the following
•1. Colonoscopy
•2. Capsule Endoscopy
•3. Computerized Tomography (CT) Scan
•4. Magnetic Resonance Imaging (MRI)
•5. Balloon-assisted enteroscopy

•1. Refusal to sign informed consent form
•2. Presence of Fistulating Crohn's disease
•3. Treatment with antibiotics within 2 weeks prior to screening
•4. Treatment with probiotics within 6 weeks prior to screening.
•5. History of bariatric surgery, total colectomy with ileorectal anastomosis or proctocolectomy.
•6. Postoperative stoma, ostomy, or ileoanal pouch
•7. Participation in any experimental drug protocol within the past 12 weeks
•8. Treatment with total parenteral nutrition
•9. Any clinically significant evidence of disease that could interfere with the subject's ability to enter the trial
•10. Inability to adequately communicate with the investigator or their respective designee and/or comply with the requirements of the entire study