Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes

• ClinicalTrials.gov Identifier: NCT02463097
• Recruitment Status: Completed
• First Posted: June 4, 2015
• Results First Posted: April 18, 2017
• Last Update Posted: April 15, 2019
• Sponsor: Medtronic Diabetes
• Information provided by (Responsible Party): Medtronic Diabetes

Tracking Information

• First Submitted Date: May 28, 2015
• First Posted Date: June 4, 2015
• Results First Submitted Date: March 7, 2017
• Results First Posted Date: April 18, 2017
• Last Update Posted Date: April 15, 2019
• Study Start Date: June 2015
• Actual Primary Completion Date: March 2016 (Final data collection date for primary outcome measure)

Current Primary Outcome Measures (submitted: May 12, 2017)

Change in A1C [ Time Frame: Baseline and 3 months ]

There is no statistically powered primary endpoint in this study. However, there will be a descriptive analysis of change in A1C.

Original Primary Outcome Measures (submitted: June 2, 2015)

Reduction in A1C [ Time Frame: 1 year ]

There is no statistically powered primary endpoint in this study. However, there will be a descriptive analysis of reduction in A1C.

• Change History: Complete list of historical versions of study NCT02463097 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures (submitted: May 12, 2017)

• Number of Severe Hypoglycemia Events [ Time Frame: 3 months ]
  There is no statistically powered secondary endpoint in this study. However, there will be a descriptive analysis of the number of Severe Hypoglycemia events.
• Number of Diabetic Ketoacidosis (DKA) Events [ Time Frame: 3 months ]
  There is no statistically powered secondary endpoint in this study. However, there will be a descriptive analysis on number of Diabetic Ketoacidosis (DKA) Event.

Original Secondary Outcome Measures (submitted: June 2, 2015)

• Event Rate of Severe Hypoglycemia [ Time Frame: 1 year ]
  There is no statistically powered secondary endpoint in this study. However, there will be a descriptive analysis of the event rate of Severe Hypoglycemia.
• Event Rate of Diabetic Ketoacidosis (DKA) [ Time Frame: 1 year ]
  There is no statistically powered secondary endpoint in this study. However, there will be a descriptive analysis of the event rate of DKA.

• Current Other Pre-specified Outcome Measures: Not Provided
• Original Other Pre-specified Outcome Measures: Not Provided

Descriptive Information

• Brief Title: Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes
• Official Title: Safety Evaluation of the Hybrid Closed Loop (HCL) System in Type 1 Diabetes
• Brief Summary: This study is a single-arm, multi-center, Home and Hotel Clinical Investigation in subjects with type 1 diabetes on insulin pump therapy. The purpose of this study is to demonstrate that the closed loop algorithm that is built into the 670G insulin pump is safe as part of the overall system.

Detailed Description

The study will proceed as follows:

Run-in Period:

A total of up to 150 subjects (age 14 - 75) will be enrolled at up to 10 investigational centers (9 in the US, 1 in the Europe, Middle East and Africa (EMEA) region) in order to reach 100 subjects who will complete the HCL study. The 2-week run-in period will be used to allow subjects to become familiar with new study devices. During the two week run-in period subjects will be using the Study Pump (670G) with the Sensor Augmented Pump function only activated (i.e. SmartGuard OFF and HCL OFF).

Study Period - At Home:

Following the two week run-in period using the Study Pump (670G), all subjects will participate in a 3-month study period.

Subjects will be required to have a companion with them during the night for the duration of the study period. Companions will need to be under the same roof, but not necessarily in the same bedroom. During the Hotel stay where subjects are monitored closely, the presence of a companion is not necessary.

Study Period - Hotel Study Subjects will participate in a Hotel study (6 days, 5 nights), with the remainder of the study period to be spent at home.

All subjects will undergo daytime and nighttime Frequent Sample Testing (FST) for approximately 24 hours during the Hotel study with YSI or i-STAT® used as a reference value.

With respect to meals, subjects will be allowed to eat as they normally do.

Continued Access Program Subjects will be given the opportunity to extend use of their study devices for a period of 3 years. If subjects choose to participate in the continuation period, they will retain the study devices at the end of study period visit or receive them back in the event they have been returned to study staff already. During the continuation period, subjects will come in for office visits every 3 months. At each of the quarterly visits, subjects will be asked about the occurrence of adverse events and device complaints.

• Study Type: Interventional
• Study Phase: Not Applicable
• Study Design: Intervention Model: Single Group Assignment; Masking: None (Open Label); Primary Purpose: Treatment
• Condition: Type 1 Diabetes

Intervention

Device: Insulin Pump

Closed Loop Algorithm

Other Name: MMT-670G

Study Arms

Experimental: Study Arm

All subjects wearing the MMT-670G insulin pump, using it with the closed loop algorithm

Intervention: Device: Insulin Pump

Publications *

• Cordero TL, Garg SK, Brazg R, Bailey TS, Shin J, Lee SW, Kaufman FR. The Effect of Prior Continuous Glucose Monitoring Use on Glycemic Outcomes in the Pivotal Trial of the MiniMed(™) 670G Hybrid Closed-Loop System. Diabetes Technol Ther. 2017 Dec;19(12):749-752. doi: 10.1089/dia.2017.0208. Epub 2017 Nov 17.
• Garg SK, Weinzimer SA, Tamborlane WV, Buckingham BA, Bode BW, Bailey TS, Brazg RL, Ilany J, Slover RH, Anderson SM, Bergenstal RM, Grosman B, Roy A, Cordero TL, Shin J, Lee SW, Kaufman FR. Glucose Outcomes with the In-Home Use of a Hybrid Closed-Loop Insulin Delivery System in Adolescents and Adults with Type 1 Diabetes. Diabetes Technol Ther. 2017 Mar;19(3):155-163. doi: 10.1089/dia.2016.0421. Epub 2017 Jan 30.

Recruitment Information

• Recruitment Status: Completed
• Actual Enrollment (submitted: March 7, 2017): 124
• Original Estimated Enrollment (submitted: June 2, 2015): 150
• Actual Study Completion Date: October 2018
• Actual Primary Completion Date: March 2016 (Final data collection date for primary outcome measure)

Eligibility Criteria

Inclusion Criteria:

1. Is age 14 - 75 years at time of screening
2. Has a clinical diagnosis of type 1 diabetes for 2 years or more as determined via medical record or source documentation by an individual qualified to make a medical diagnosis
3. Is willing to participate in a hotel study for the specified duration of hotel stay.
4. Must have companion who will sleep in the same dwelling place every night during the study period and should also be able to call the subject daily in the event the subject is traveling.
5. Is willing to perform ≥ 4 finger stick blood glucose measurements daily
6. Is willing to perform required sensor calibrations
7. Is willing to wear the system continuously throughout the study
8. Has a Glycosylated hemoglobin (A1C) value less than 10.0% (as processed by Central Lab) at time of screening visit
9. Has TSH in the normal range OR if the TSH is out of normal reference range the Free T3 is below or within the lab's reference range and Free T4 is within the normal reference range.
10. Pump therapy for greater than 6 months prior to screening (with or without CGM experience)
11. Is willing to upload data from the study pump, must have Internet access and a computer system that meets the requirements for uploading the study pump
12. If subject has celiac disease, it has been adequately treated as determined by the investigator

13. Is willing to take one of the following insulins and can financially support the use of either of the 2 insulin preparations throughout the course of the study (i.e. co-payments for insulin with insurance or able to pay full amount)

    • Humalog® (insulin lispro injection)
    • NovoLog® (insulin aspart)
14. With history of cardiovascular event 1 year or more from the time of screening must have an EKG within 6 months prior to screening or during screening. If subject has an abnormal EKG, participation is allowed if there is clearance from a cardiologist

15. With 3 or more cardiovascular risk factors listed below must have an EKG within 6 months prior to screening or during screening. If subject has an abnormal EKG, participation is allowed if there is clearance from a cardiologist

    Cardiovascular risk factors include:

    • Age >35 years
    • Type 1 diabetes of >15 years' duration
    • Presence of any additional risk factor for coronary artery disease
    • Presence of microvascular disease (proliferative retinopathy or nephropathy, including microalbuminuria)
    • Presence of peripheral vascular disease
    • Presence of autonomic neuropathy
16. With history of cardiovascular event 1 year or more from the time of screening must have a stress test within 6 months prior to screening or during run in period. If subject fails stress test, participation is allowed if there is clearance from a cardiologist
17. Must be able to speak and be literate in English

Exclusion Criteria:

1. Has a history of 2 or more episodes of severe hypoglycemia, which resulted in any the following during the 6 months prior to screening:

   • Medical assistance (i.e. Paramedics, Emergency Room ( ER) or Hospitalization)
   • Coma
   • Seizures
2. Is unable to tolerate tape adhesive in the area of sensor placement
3. Has any unresolved adverse skin condition in the area of sensor placement (e.g., psoriasis, dermatitis herpetiformis, rash, Staphylococcus infection)
4. Females who are sexually active and able to conceive will be excluded if they are not using an effective method of contraception and do not agree to continue using an effective method of contraception for the duration of the study as determined by investigator.
5. Has had any of the following cardiovascular events within 1 year of screening: myocardial infarction, unstable angina, coronary artery bypass surgery, coronary artery stenting, transient ischemic attack, cerebrovascular accident, angina, congestive heart failure, ventricular rhythm disturbances or thromboembolic disease
6. Is being treated for hyperthyroidism at time of screening
7. Has diagnosis of adrenal insufficiency
8. Has had DKA in the 6 months prior to screening visit.
9. Has taken any oral, injectable, or intravenous (IV) steroids within 8 weeks from time of screening visit, or plans to take any oral, injectable, or IV steroids during the course of the study
10. Actively participating in an investigational study (drug or device) wherein he/she has received treatment from an investigational study drug or investigational study device in the last 2 weeks
11. Has been hospitalized or has visited the ER in the 6 months prior to screening resulting in a primary diagnosis of uncontrolled diabetes
12. Currently abusing illicit drugs
13. Currently abusing marijuana.
14. Currently abusing prescription drugs
15. Currently abusing alcohol
16. Using pramlintide (Symlin), DPP-4 inhibitor, liraglutide (Victoza or other GLP-1 agonists), metformin, canagliflozin (Invokana or other SGLT2 inhibitors) at time of screening
17. Has a history of visual impairment which would not allow subject to participate in the study and perform all study procedures safely, as determined by the investigator
18. Has elective surgery planned that requires general anesthesia during the course of the study
19. Has a sickle cell disease, hemoglobinopathy; or has received red blood cell transfusion or erythropoietin within 3 months prior to time of screening
20. Plans to receive red blood cell transfusion or erythropoietin over the course of study participation
21. Diagnosed with current eating disorder such as anorexia or bulimia
22. Diagnosed with chronic kidney disease that results in chronic anemia
23. Hematocrit that is below the normal reference range of lab used.
24. On dialysis
25. Serum creatinine of >2 mg/dL.

Sex/Gender

• Sexes Eligible for Study: All

• Ages: 14 Years to 75 Years (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Contacts: Contact information is only displayed when the study is recruiting subjects
• Listed Location Countries: Israel, United States

Administrative Information

• NCT Number: NCT02463097
• Other Study ID Numbers: CEP 294
• Has Data Monitoring Committee: Yes
• U.S. FDA-regulated Product: Not Provided
• IPD Sharing Statement: Not Provided
• Responsible Party: Medtronic Diabetes
• Study Sponsor: Medtronic Diabetes
• Collaborators: Not Provided
• Investigators: Not Provided
• PRS Account: Medtronic Diabetes
• Verification Date: April 2019