RESET System Pivotal Trial (Rev F)

Not Applicable

Recruiting

• Conditions: Diabetes type2; Obesity

• Registration Number: NCT04101669
• Lead Sponsor: Morphic Medical Inc.

Brief Summary

A Randomized, Multi-Center, Pivotal Efficacy and Safety Study Evaluating the RESET System for Glycemic Improvement in Patients with Inadequately Controlled Type 2 Diabetes and Obesity, the STEP-1 Study.

A multi-center, double-blinded, randomized, sham-controlled trial to evaluate the safety and effectiveness of the RESET System plus moderate intensity lifestyle and dietary counseling compliant with 2024 ADA Standard of Care as compared to a sham control receiving moderate intensity lifestyle and dietary counseling. Both the treatment and sham group will practice medical management compliant with STEP-1 Study Guidelines. Patients will be randomized 3 (RESET):1 (Sham).

Detailed Description

The objective of this study is to evaluate the safety and effectiveness of the RESET System when used with moderate intensity lifestyle and dietary counseling and medical management, in patients with baseline HbA1c ≥ 7.5% and ≤10%, and BMI ≥ 30 kg/m2 and ≤ 50kg/m2, whose diabetes medications consist of at least dual therapy for 3 months, yet have not achieved adequate HbA1c control (\<7%).

Specific objectives of this study are:

1. To determine if the RESET System significantly improves glycemic control

2. To determine that the RESET System can be safely used to improve glycemic control

Study Timeline

• Study Start: 2019-09-09
• Study First Submitted: 2019-09-20
• Study First Submitted QC: 2019-09-23
• Study First Posted: 2019-09-24
• Status Verified: 2024-07
• Last Update Submitted: 2024-07-16
• Last Update Posted: 2024-07-18
• Primary Completion: 2025-12-01
• Study Completion: 2026-12-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 264

Inclusion Criteria

1. Age ≥22 years and ≤ 65 years
2. Have understood and signed the approved informed consent form
3. Diagnosis of type 2 diabetes
4. HbA1c ≥ 7.5% and ≤10%
5. BMI ≥30kg/m2 and ≤ 50kg/m2
6. Willing and able to comply with study requirements
7. Documented negative pregnancy test in women of childbearing potential
8. Women of childbearing potential not intending to become pregnant (continue to be on an approved form of birth control) for the duration of their trial participation, including post explant period. Women of child-bearing age without known sterilization will be placed on 1 form of birth-control to prevent unwanted pregnancies
9. At least one year of medical records available, including detailed medical therapy and dosing information
10. Failed to achieve adequate HbA1c reduction (<7.5%) after dual therapy for at least 3-month stable dosage of diabetes medication(s), including insulin, metformin, SGLT-2 inhibitor, GLP-1 RA, Dual GLP-1/GIPR agonist or, other medications including meglitinides, sulfonylureas, thiazolidinediones, or DPP-4s.

Exclusion Criteria

1. Previous treatment with the RESET System

2. Previous GI surgery that could preclude the ability to place the RESET Liner or affect the function of the RESET Liner, or abnormal GI anatomical finding that could preclude the ability to place the RESET Liner or affect the function of the RESET Liner

3. Hypoglycemia and/or DKA/HHNK in the last 6 months requiring 3rd party assistance

4. Known history of liver disease (e.g., viral or autoimmune etiology, METAVIR grade 2 or higher fibrosis/cirrhosis from a biopsy within the past 6 months, but not including incidental fatty liver)

5. eGFR of less than 45 ml/min/1.73 m2

6. Prior history of an abscess requiring hospitalization, intravenous antibiotics or drainage

7. Previous treatment for severe liver disease and/or biliary tract disease, including but not limited to, surgery, bile duct dilatation, and stent placement

8. Diagnosis of type 1 diabetes mellitus or having any history of ketoacidosis

9. Fasting C-peptide < 1.0 ng/mL

10. Triglyceride level > 600 mg/dL

11. Vitamin D deficiency (<20ng/ml)

12. Uncorrectable bleeding diathesis, platelet dysfunction, thrombocytopenia with platelet count less than 100,000/microliter, or known coagulopathy

13. Height < 5 feet (152.4 cm)

14. Current alcohol addiction, current drug addiction or usage, of drugs such as, narcotics, opiates, or benzodiazepines and other addictive tranquilizers

15. History of pancreatitis, including gallstone related pancreatitis (subsequent to which patient has cholecystectomy)

16. Diagnosis of osteopenia or osteoporosis or currently taking denosumab, romosozumab-aqqg, bisphosphonates or teriparatide

17. Diagnosis of autoimmune connective tissue disorder (e.g. lupus erythematosus, scleroderma)

18. Active or recent (less than 12 months) gastroesophageal reflux disease (GERD) unless treated with H2RAs not PPI.

19. Uncontrolled thyroid disease, including a history of thyroid cancer, hyperthyroidism, or taking thyroid hormone for any reason other than primary hypothyroidism (TSH level must be between 0.4-4)

20. Currently taking prescription antithrombotic therapy (e.g. anticoagulant or antiplatelet agent) within 10 days prior to randomization and/or there is a need or expected need to use during the trial 9 months post implant procedure

21. Currently taking the following medications (within 30 days prior to randomization) and/or there is a need or expected need to use these medications during the trial 12 months post index procedure:

    Restricted Medications/Supplements Systemic corticosteroids Proton Pump Inhibitor (PPI) Drugs known to affect GI motility (e.g.metoclopramide) Prescription or over-the-counter weight loss medication(s) Non-Steroidal Anti-Inflammatory Drugs (NSAIDs), aspirin, ibuprofen, and other anti-inflammatory medication for study duration Medications known to cause significant weight gain or weight loss (e.g. chemotherapeutics)

    Supplements that are known or suspected to increase bleeding risk including but not limited to:

    Gingko biloba Ginseng Vitamins C & E Turmeric St. John's wort Evening primrose oil Feverfew Green Tea Extract

22. Active H. pylori

23. History of Crohn's disease, atresias or untreated stenoses

24. Abnormal pathologies or conditions of the gastrointestinal tract, including ulcers or upper gastrointestinal bleeding conditions within 3 months of randomization

25. Patients may be disqualified for study inclusion for any condition determined by the PI that places the patient at undue risk

26. Poor dentition not allowing complete chewing of food

27. Enrolled in another investigational study within 3 months of screening for this study (enrollment in observational studies is permitted)

28. Residing in a location without ready access to study site medical resources

29. Documented weight loss of 5% total body weight (TBW) anytime during the 3 months preceding randomization

30. Positive Fecal Immunochemical Test (FIT) at time of screening

31. History or observation of psychological disorder or behavior which could preclude compliance to the treatment and follow up plan

32. No access to an active telephone and internet service for provision of Follow Up Schedule calls and electronic diary

33. Having donated blood or received a blood transfusion in the 90 days prior to baseline labs. Patients should agree not to donate blood during the study

34. Any condition that increases red cell turnover, such as thalassemia

35. Existence of (>5 cm string test) Pseudomonas aeruginosa, Stenotrophomonas maltophilia and/or Klebsiella pneumoniae serotype K1 and K2

36. A known sensitivity to nickel or titanium

37. Do not meet the screening criteria for MRI (i.e., MRI unsafe, or MRI conditional but not appropriate for the region of interest)

38. Patients with history or suspicion of coronary artery disease

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change in HbA1c	9 Months	Change in HbA1c value from baseline to 9 months.

Secondary Outcome Measures

Name	Time	Method
HbA1c value	9 and 21 months	Proportion of patients who achieve an HbA1c value of \< 7 %
Weight Loss	9 and 21 months	Proportion of patients who achieve percent total body weight loss ≥ 5% from baseline
Change in Nonalcoholic Steatohepatitis (NASH)	9 and 21 months	NASH- liver fibrosis % compared to baseline using using MRE measured in kPa
Triglycerides	9 and 21 months	Change in triglycerides
Insulin use	9 and 21 months	Proportion of patients reducing insulin dosage
LDL cholesterol	9 and 21 months	Chnage in LDL cholesterol
Blood pressure	9 and 21 months	Change in systolic blood pressure values
Vitamin D	9 and 21 months	Change in vitamin D levels
Refractory to Vitamin D Supplementation	9 and 21 months	Proportion of patients refractory to vitamin D supplementation
Serum Creatinine	9 and 21 months	Change in serum creatinine levels
Fasting blood glucose level	9 and 21 months	Change in fasting blood glucose values
Vitamin D Supplementation	9 and 21 months	Average vitamin D levels required to maintain normal vitamin D levels
eGFR	9 and 21 months	Change in eGFR levels
Change in Nonalcoholic Fatty Liver Disease (NAFLD)	9 and 21 months	Change in NAFLD, change in % liver fat using MRI (proton density fat fraction)
DTSQ Questionnaire	9 and 21 months	Change from baseline in treatment satisfaction using Diabetes Treatment Satisfaction Questionnaire (DTSQ)
IWQOL Questionnaire	9 and 21 months	Impact of weight on quality of life (IWQOL)

Trial Locations

Locations (7)

MedStar Health Research Institute; 🇺🇸 Washington, District of Columbia, United States

University of Miami Hospital; 🇺🇸 Miami, Florida, United States

Brigham and Women's Hospital; 🇺🇸 Boston, Massachusetts, United States

Michigan Medicine, Division of Gastroenterology and Hepatology; 🇺🇸 Ann Arbor, Michigan, United States

Weill Cornell Medicine; 🇺🇸 New York, New York, United States

Cleveland Clinic; 🇺🇸 Cleveland, Ohio, United States

Baylor College of Medicine; 🇺🇸 Houston, Texas, United States