Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adults and Pediatrics Utilizing Lyumjev®
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|ClinicalTrials.gov Identifier: NCT05325294|
Recruitment Status : Recruiting
First Posted : April 13, 2022
Last Update Posted : April 24, 2023
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|Condition or disease||Intervention/treatment||Phase|
|Type 1 Diabetes||Device: MiniMed 780G System||Not Applicable|
This study is a multi-center, single arm study in insulin-requiring adult and pediatric subjects with type 1 diabetes on the MiniMed™ 780G system using Lyumjev® insulin lispro-aabc and Medtronic Extended infusion set and reservoir. The run-in period and study period will be approximately 120 days long.
A total of up to 250 subjects with insulin-requiring type 1 diabetes age 7-80 will be enrolled at up to 25 investigational centers across the United States in order to have at least 200 subjects enter the study period. Up to 125 subjects will be enrolled in the pediatric age group (7-17 years of age) and up to 125 in the adult age group (18 years or older).
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||250 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Evaluation of the Advanced Hybrid Closed Loop (AHCL) System in Type 1 Adult and Pediatric Subjects Utilizing Lyumjev® Insulin Lispro-aabc|
|Actual Study Start Date :||May 5, 2022|
|Estimated Primary Completion Date :||December 1, 2023|
|Estimated Study Completion Date :||December 1, 2023|
Experimental: MiniMed 780G System Utilizing Insulin Lyumjev®
Subjects with insulin-requiring type 1 diabetes age 7-80 using the MiniMed 780G system with Insulin Lyumjev® for a period of three months.
Device: MiniMed 780G System
MiniMed™ 780G Insulin Pump, Guardian™ 4 Glucose Sensor, and Guardian 4 Transmitter; used with Insulin Lyumjev® insulin lispro-aabc
- Primary Safety Endpoint for Age 18-80 - Change in HbA1c [ Time Frame: 3 months ]Age 18-80: The overall mean change in HbA1c from baseline to end of 3-month study period. Non-inferiority test.
- Primary Safety Endpoint for Age 7-17 - Change in HbA1c [ Time Frame: 3 months ]Age 7-17: The overall mean change in HbA1c from baseline to end of 3-month study period. Non-inferiority test.
- Primary Effectiveness Endpoint for Age 18-80 - Percent of Time in Range (TIR 70-180 mg/dL) [ Time Frame: 3 months ]Age 18-80: The mean % of time in range (TIR 70-180 mg/dL). Non-inferiority test.
- Primary Effectiveness Endpoint for Age 7-17 - Percent of Time in Range (TIR 70-180 mg/dL) [ Time Frame: 3 months ]Age 7-17 : The mean % of time in range (TIR 70-180 mg/dL). Non-inferiority test.
- Secondary Effectiveness Endpoint 1 for Age 18-80 - Percent of Time in Hypoglycemia (< 54 mg/dL) [ Time Frame: 3 months ]Age 18-80: The mean % of time in hypoglycemia (< 54 mg/dL). Non-inferiority test.
- Secondary Effectiveness Endpoint 1 for Age 7-17 - Percent of Time in Hypoglycemia (< 54 mg/dL) [ Time Frame: 3 months ]Age 7-17: The mean % of time in hypoglycemia (< 54 mg/dL). Non-inferiority test.
- Secondary Effectiveness Endpoint 2 for Age 18-80 - Percent of Time in Range (TIR 70-180 mg/dL) [ Time Frame: 3 months ]Age 18-80: The mean % of time in range (TIR 70-180 mg/dL). Superiority test.
- Secondary Effectiveness Endpoint 2 for Age 7-17 - Percent of Time in Range (TIR 70-180 mg/dL) [ Time Frame: 3 months ]Age 7-17: The mean % of time in range (TIR 70-180 mg/dL). Superiority test.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
|Ages Eligible for Study:||7 Years to 80 Years (Child, Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Age 7-80 years at time of screening.
Has a clinical diagnosis of type 1 diabetes:
- 14-80 years of age: 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.
- 7-13 years of age: A clinical diagnosis of type 1 diabetes for 1 year or more as determined via medical record or source documentation by an individual qualified to make a medical diagnosis.
- Does not require a legally authorized representative to consent on their behalf due to mental or intellectual disability.
- Subject or parent/caregiver is literate and able to read the language offered in the pump or pump materials.
- Subject and/or legally authorized representative is willing to provide informed consent for participation.
- Is willing to perform fingerstick blood glucose measurements as needed.
- Is willing to wear the system continuously throughout the study.
- Must have a minimum daily insulin requirement (Total Daily Dose) of greater than or equal to 8 units and a maximum total daily dose of 250 units or less.
Has a Glycosylated hemoglobin (HbA1c) less than 10% (as processed by Central Lab) at time of screening visit.
Note: All HbA1c blood specimens will be sent to and tested by a National Glycohemoglobin Standardization Program (NGSP) certified Central Laboratory. HbA1c testing must follow NGSP standards.
- Has thyroid-stimulating hormone (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.
- Uses pump therapy for greater than 6 months (with or without CGM experience) prior to screening
- Is willing to upload data from the study pump, must have Internet access, and a computer system, or compatible smartphone that meets the requirements for uploading the study pump.
Is willing to take one of the following insulins and can financially support the use of insulin preparations as required during the run-in period:
- Humalog (insulin lispro injection)
- NovoLog (insulin aspart injection)
- Admelog(insulin lispro injection)
- Is willing to take Lyumjev insulin during the study period (supplied via Sponsor).
- Has hypersensitivity to insulin lispro or one of the excipients in Lyumjev®
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)
- Has been hospitalized or has visited the ER in the 6 months prior to screening resulting in a primary diagnosis of uncontrolled diabetes.
- Has had DKA in the last 6 months prior to screening visit.
- Will not tolerate tape adhesive in the area of sensor placement as assessed by a qualified individual.
- Has any unresolved adverse skin condition in the area of sensor placement (e.g., psoriasis, dermatitis herpetiformis, rash, Staphylococcus infection).
- Is female of child-bearing potential and result of pregnancy test is positive at screening.
- Is sexually active female of child-bearing potential and is not using a form of contraception deemed reliable by the investigator.
- Is female and plans to become pregnant during the course of the study
- Is being treated for hyperthyroidism at time of screening.
- Has diagnosis of adrenal insufficiency.
- Has taken any oral, injectable, or intravenous (IV) glucocorticoids within 8 weeks from time of screening visit, or plans to take any oral, injectable, or IV glucocorticoid during the course of the study.
- Is using hydroxyurea at time of screening or plans to use it during the study.
- Is 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.
- Is currently abusing illicit drugs.
- Is currently abusing marijuana.
- Is currently abusing prescription drugs.
- Is currently abusing alcohol.
- Using pramlintide (Symlin), DPP-4 inhibitor, liraglutide (Victoza or other GLP-1 agonists), metformin, canagliflozin (Invokana or other SGLT2 inhibitors) at time of screening.
- 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.
- Has elective surgery planned that requires general anesthesia during the course of the study.
- Has sickle cell disease, hemoglobinopathy; or has received red blood cell transfusion or erythropoietin within 3 months prior to time of screening.
- Plans to receive red blood cell transfusion or erythropoietin over the course of study participation.
- Is diagnosed with current eating disorder such as anorexia or bulimia.
- Has been diagnosed with chronic kidney disease that results in chronic anemia.
- Has a hematocrit that is below the normal reference range of lab used.
- Is on dialysis.
- Has serum creatinine of >2 mg/dL.
- Has celiac disease that is not adequately treated as determined by the investigator.
- 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, or ventricular rhythm disturbances.
Has had history of cardiovascular event 1 year or more from the time of screening without
- a normal EKG and stress test within 6 months prior to screening or during screening or
- clearance from a qualified physician prior to receiving the study devices if there is an abnormal EKG or stress test.
Has 3 or more cardiovascular risk factors listed below without a normal EKG within 6 months prior to screening or during screening or clearance from a qualified physician if there is an abnormal EKG:
- 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
- Is a member of the research staff involved with the study.
- Has used a MiniMed 780G pump prior to screening
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05325294
|Contact: Thomas Troub||818 576 firstname.lastname@example.org|
|Contact: Shannon Bondy||818 576 email@example.com|
|Responsible Party:||Medtronic Diabetes|
|Other Study ID Numbers:||
|First Posted:||April 13, 2022 Key Record Dates|
|Last Update Posted:||April 24, 2023|
|Last Verified:||January 2023|
|Studies a U.S. FDA-regulated Drug Product:||No|
|Studies a U.S. FDA-regulated Device Product:||Yes|
|Device Product Not Approved or Cleared by U.S. FDA:||Yes|
Diabetes Mellitus, Type 1
Glucose Metabolism Disorders
Endocrine System Diseases
Immune System Diseases