Effect of Duodenal Mucosal Resurfacing (DMR) Using the Revita System in the Treatment of Type 2 Diabetes (T2D)

Not Applicable

Completed

• Conditions: Diabetes Mellitus, Type 2; Noninsulin-Dependent Diabetes Mellitus
• Interventions: Procedure: Sham Procedure; Procedure: DMR Procedure

• Registration Number: NCT02879383
• Lead Sponsor: Fractyl Health Inc.

Brief Summary

The purpose of this study is to demonstrate the efficacy and safety of the Fractyl duodenal mucosal resurfacing (DMR) Procedure using the Revita System compared to a sham procedure for the treatment of uncontrolled type 2 diabetes.

Subjects randomized to the DMR procedure are followed per protocol for 48 Weeks. The Sham treatment arm will cross over to receive the DMR treatment at 24 weeks with background medications held constant from 24-48 weeks of follow up.

Detailed Description

The study is a multi-center, randomized, prospective, double-blinded (subject and endocrinologist) trial of type 2 diabetes patients sub-optimally controlled on 1 or more oral anti-diabetic medications comparing the Fractyl DMR procedure to sham procedure. Randomization will be 1:1 DMR treatment to sham. All subjects will participate in a 4 week oral anti-diabetic medication run-in period before the index procedure to confirm lack of blood glucose control in conjunction with medication compliance and nutritional counseling. The Sham treatment arm will cross-over to receive the DMR treatment at 24 weeks with background medications held constant 24weeks of follow up after the cross-over DMR procedure. The DMR treatment arm will be managed according to current diabetes standard of care.

Subjects randomized to the DMR procedure are followed per protocol for 48 Weeks. The Sham treatment arm will cross over to receive the DMR treatment at 24 weeks with background medications held constant from 24-48 weeks of follow up.

Study Timeline

• Study First Submitted: 2016-08-04
• Study First Submitted QC: 2016-08-22
• Study First Posted: 2016-08-25
• Study Start: 2017-03-01
• Primary Completion: 2019-12-20
• Study Completion: 2019-12-20
• Results First Submitted: 2021-02-12
• Results First Submitted QC: 2021-04-30
• Results First Posted: 2021-05-25
• Status Verified: 2024-02
• Last Update Submitted: 2024-02-12
• Last Update Posted: 2024-02-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 109

Inclusion Criteria

1. 28-75 years of age
2. Diagnosed with Type 2 Diabetes and evidence of preserved insulin secretion. Fasting insulin > 7 μU/ mL.
3. Glycated Hemoglobin (HbA1c) of 7.5 - 10.0% (59-86 mmol/mol)
4. Body Mass Index (BMI) ≥ 24 and ≤ 40 kg/m2
5. Currently taking one or more oral glucose lowering medications of which one must be Metformin, with no changes in dose or medication in the previous 12 Weeks prior to study entry
6. Able to comply with study requirements and understand and sign the informed consent

Exclusion Criteria

1. Diagnosed with Type 1 Diabetes or with a history of ketoacidosis
2. Current use of Insulin
3. Current use of Glucagon-like peptide-1 (GLP-1) analogues
4. Hypoglycemia unawareness or a history of severe hypoglycemia (more than 1 severe hypoglycemic event, as defined by need for third-party-assistance, in the last year)
5. Known autoimmune disease, as evidenced by a positive Anti- Glutamic Acid Decarboxylase (GAD) test, including Celiac disease, or pre-existing symptoms of systemic lupus erythematosus, scleroderma or other autoimmune connective tissue disorder
6. Active H. pylori infection (Participants with active H. pylori may continue with the screening process if they are treated via medication and re-testing verifies the condition has resolved.)
7. Previous GI surgery that could affect the ability to treat the duodenum such as subjects who have had a Bilroth 2, Roux-en-Y gastric bypass, or other similar procedures or conditions
8. History of chronic or acute pancreatitis
9. Known active hepatitis or active liver disease
10. Symptomatic gallstones or kidney stones, acute cholecystitis or history of duodenal inflammatory diseases including Crohn's Disease and Celiac Disease
11. History of coagulopathy, upper gastro-intestinal bleeding conditions such as ulcers, gastric varices, strictures, congenital or acquired intestinal telangiectasia
12. Use of anticoagulation therapy (such as warfarin) which cannot be discontinued for 7 days before and 14 days after the procedure
13. Use of P2Y12 inhibitors (clopidogrel, pasugrel, ticagrelor) which cannot be discontinued for 14 days before and 14 days after the procedure. Use of aspirin is allowed.
14. Unable to discontinue NSAIDs (non-steroidal anti-inflammatory drugs) during treatment through 4 weeks post procedure phase
15. Taking corticosteroids or drugs known to affect GI motility (e.g. Metoclopramide)
16. Receiving weight loss medications such as Meridia, Xenical, or over the counter weight loss medications
17. Persistent Anemia, defined as Hgb<10 g/dl
18. Estimated Glomerular Filtration Rate (eGFR) or Modified of Diet in Renal Diseae (MDRD) <30 ml/min/1.73m^2
19. Active systemic infection
20. Active malignancy within the last 5 years
21. Not potential candidates for surgery or general anesthesia
22. Active illicit substance abuse or alcoholism
23. Participating in another ongoing clinical trial of an investigational drug or device
24. Any other mental or physical condition which, in the opinion of the Investigator, makes the subject a poor candidate for clinical trial participation

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Sham Procedure	Sham Procedure	Subjects are unblinded at 24 Weeks. Sham subjects to cross over to receive DMR treatment at 24 Weeks and followed up for additional 24 weeks.
DMR Procedure	DMR Procedure	Subjects randomized to the DMR procedure are unblinded at 24 weeks and followed for an additional 24 weeks.

Primary Outcome Measures

Name	Time	Method
Change From Baseline at 12 Weeks in MR-PDFF, DMR vs Sham	Baseline and 12 Weeks post-procedure	The absolute change from baseline at 12 weeks in MR-PDFF in patients with baseline MR-PDFF \> 5% , DMR vs Sham
Change From Baseline at 24 Weeks in Hemoglobin A1c (HbA1c), DMR vs Sham.	Baseline and 24 Weeks post-procedure	The primary efficacy endpoint is the change from baseline at 24 weeks in HbA1c, DMR vs Sham

Trial Locations

Locations (11)

University College London Hospitals; 🇬🇧 London, United Kingdom

Policlinico Gemelli (Sacro Cuore); 🇮🇹 Rome, Lazio, Italy

Hopital Erasme; 🇧🇪 Brussels, Belgium

King's College, Denmark Hill; 🇬🇧 London, United Kingdom

ABC Hospital; 🇧🇷 São Paulo, Brazil

Humanitas Research Hospital & Humanitas University Via Manzoni 56, Rozzano; 🇮🇹 Milano, Italy

Glasgow Royal Infirmary; 🇬🇧 Glasgow, United Kingdom

Hospital das Clinicas da Faculdade de medicina da Universidade de São Paulo; 🇧🇷 Sao Paulo, Brazil

UZ Leuven; 🇧🇪 Leuven, Belgium

Queens Medical Centre campus, Nottingham University Hospitals NHS Trust, Derby Road; 🇬🇧 Nottingham, United Kingdom

Amsterdam University Medical Center; 🇳🇱 Amsterdam, Netherlands