Hybrid Closed Loop Pivotal Trial in Type 1 Diabetes

Type 1 Diabetes Clinical Trial

Official title:

Safety Evaluation of the Hybrid Closed Loop (HCL) System in Type 1 Diabetes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02463097
• Other study ID #: CEP 294
• Status: Completed
• Phase: N/A
• Start date: June 2015
• Est. completion date: October 2018

Study information

• Verified date: April 2019
• Source: Medtronic Diabetes
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 124
• Est. completion date: October 2018
• Est. primary completion date: March 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 14 Years to 75 Years

Eligibility

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.

Related Conditions & MeSH terms

• Diabetes Mellitus
• Diabetes Mellitus, Type 1
• Type 1 Diabetes

Intervention

Device:
• Insulin Pump
Closed Loop Algorithm

Locations

Country	Name	City	State
Israel	Institute of Endocrinology, Sheba Medical Center	Tel Aviv
United States	Atlanta Diabetes Associates	Atlanta	Georgia
United States	Barbara Davis Center for Childhood Diabetes (Adult)	Aurora	Colorado
United States	Barbara Davis Center for Childhood Diabetes (Pediatric)	Aurora	Colorado
United States	University of Virginia	Charlottesville	Virginia
United States	AMCR Institute	Escondido	California
United States	Park Nicollet Clinic-International Diabetes Center - Adult and Pediatric	Minneapolis	Minnesota
United States	Yale University School of Medicine	New Haven	Connecticut
United States	Stanford University Medical Center	Palo Alto	California
United States	Rainer Clinical Research Center	Renton	Washington

Sponsors (1)

Lead Sponsor	Collaborator
Medtronic Diabetes

Countries where clinical trial is conducted

United States,  Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in A1C	There is no statistically powered primary endpoint in this study. However, there will be a descriptive analysis of change in A1C.	Baseline and 3 months
Secondary	Number of Severe Hypoglycemia Events	There is no statistically powered secondary endpoint in this study. However, there will be a descriptive analysis of the number of Severe Hypoglycemia events.	3 months
Secondary	Number of Diabetic Ketoacidosis (DKA) Events	There is no statistically powered secondary endpoint in this study. However, there will be a descriptive analysis on number of Diabetic Ketoacidosis (DKA) Event.	3 months