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Research Study to Look at Fast-acting Insulin Aspart With the Insulin Pump System 'iLet™' in Adults With Type 1 Diabetes

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ClinicalTrials.gov Identifier: NCT03816761
Recruitment Status : Completed
First Posted : January 25, 2019
Last Update Posted : June 20, 2019
Sponsor:
Information provided by (Responsible Party):
Novo Nordisk A/S

Brief Summary:
The iLet™ is a new insulin pump that is programmed to work with a Continuous Glucose Monitoring (CGM) device. This is to give participants insulin automatically. The CGM device is already available for sale. The iLet™ is not yet approved for use. Fast-acting insulin aspart is a type of insulin that doctors can already prescribe for use with insulin pens, but not for use in an insulin pump. This study is to test how safe fast acting insulin aspart is when used with different insulin delivery settings in the iLet™ in people with type 1 diabetes. Participants will get fast-acting insulin aspart as participants' insulin and use the iLet™ as participants' insulin pump with a CGM device. Participants' iLet™ will be set to 2 different insulin delivery settings for 7 days on each setting. The setting participants get first is decided by chance. The study will last for about 5 to 9 weeks. Participants will have 4 visits and 1 phone contact with the study or staff.

Condition or disease Intervention/treatment Phase
Diabetes Mellitus, Type 1 Drug: Fast-acting insulin aspart Device: iLet™ Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 24 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double (Participant, Outcomes Assessor)
Masking Description: Sponsor staff involved in the clinical trial is masked according to company standard procedures.
Primary Purpose: Treatment
Official Title: An Exploratory Trial Investigating the Safety and Efficacy of Fast-acting Insulin Aspart in a Closed-loop Insulin Delivery System (Bionic Pancreas) in Adults With Type 1 Diabetes
Actual Study Start Date : February 25, 2019
Actual Primary Completion Date : May 31, 2019
Actual Study Completion Date : June 10, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Diabetes Type 1

Arm Intervention/treatment
Experimental: Fast-acting insulin aspart, default tmax setting
Participants will receive fast-acting insulin aspart using the iLet™ with default tmax setting (t65 = 65 minutes) in two different treatment periods in a cross-over manner. There will be 3 different cohorts with 2 treatment periods in each cohort.
Drug: Fast-acting insulin aspart
In each cohort, participants will receive fast-acting insulin aspart using the iLet™ in a cross-over manner for 14 days (7days per period). Dose modification will be handled autonomously by the iLet™ based on the CGM sensor readings and the user interaction with the iLet™ e.g. meal announcements.

Device: iLet™
The bionic pancreas including pigtail adapters, used in insulin-only configuration

Experimental: Fast-acting insulin aspart, non-default tmax setting
Participants will receive fast-acting insulin aspart using the iLet™ with non-default tmax setting (t50 = 50 minutes, t40 = 40 minutes or t30 = 30 minutes) in two different treatment periods in a cross-over manner. There will be 3 different cohorts with 2 treatment periods in each cohort.
Drug: Fast-acting insulin aspart
In each cohort, participants will receive fast-acting insulin aspart using the iLet™ in a cross-over manner for 14 days (7days per period). Dose modification will be handled autonomously by the iLet™ based on the CGM sensor readings and the user interaction with the iLet™ e.g. meal announcements.

Device: iLet™
The bionic pancreas including pigtail adapters, used in insulin-only configuration




Primary Outcome Measures :
  1. Time in low interstitial glucose (defined as <54 mg/dL; 3 mmol/L) [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Measured as percentage of time.


Secondary Outcome Measures :
  1. Number of treatment emergent severe hypoglycaemic episodes [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  2. Number of self-manageable (able to self-treat) treatment emergent hypoglycaemic episodes that require oral carbohydrate intervention per day [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  3. Number of treatment emergent overall hypoglycaemic episodes classified according to the American Diabetes Association (ADA) definition [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  4. Number of treatment emergent overall hypoglycaemic episodes classified according to the Novo Nordisk classification [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  5. Number of treatment emergent daytime hypoglycaemic episodes classified according to the ADA definition [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  6. Number of treatment emergent daytime hypoglycaemic episodes classified according to the Novo Nordisk classification [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  7. Number of treatment emergent nocturnal hypoglycaemic episodes (00:01-05:59 both inclusive) classified according to the ADA definition [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  8. Number of treatment emergent nocturnal hypoglycaemic episodes (00:01-05:59 both inclusive) classified according to the Novo Nordisk classification [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of episodes.

  9. Time in interstitial glucose range defined as 70-180 mg/dL (3.9-10 mmol/L) [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Measured as percentage of time.

  10. Mean interstitial-glucose level [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Measured in mg/dL.

  11. Number of treatment emergent adverse events [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of events.

  12. Number of treatment emergent infusion site reactions [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Count of reactions.

  13. Total insulin dose per day [ Time Frame: Day 1 to day 7 (in both the treatment periods) ]
    Measured in U/Kg/day.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Informed consent obtained before any trial-related activities. Trial-related activities are any procedures that are carried out as part of the trial, including activities to determine suitability for the trial
  • Male or female, age more than or equal to 18 years and less than or equal to 75 years at the time of signing informed consent
  • Diagnosed with type 1 diabetes mellitus more than or equal to 1 year prior to the day of screening
  • Treated with continuous subcutaneous insulin infusion more than or equal to 1 year prior to the day of screening
  • Have a mean total daily dose of insulin more than or equal to 20 units
  • Familiar with continuous glucose monitoring as judged by the investigator
  • Has someone over 18 years of age who (i) lives with them, (ii) has access to where they sleep, (iii) is willing to be in the house when the subject is sleeping, and (iv) is willing to receive calls from the study staff and check the welfare of the study subject
  • Body mass index (BMI) less than or equal to 35.0 kg/m^2 at screening
  • Glycated haemoglobin (HbA1c) more than or equal to 6.5% (47 mmol/mol) and less than or equal to 9% (75 mmol/mol) at screening
  • Able and willing to remain in a designated place for the specified duration of the 'in-patient' periods
  • Lives within a 120-minute drive away from the central monitoring location (site)

Exclusion Criteria:

  • Known or suspected hypersensitivity to trial product(s) or related products
  • Previous participation in this trial. Participation is defined as signed informed consent
  • Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using an adequate contraceptive method (adequate contraceptive measures as required by local regulation or practice)
  • Participation in any clinical trial of an approved or non-approved investigational medicinal product within 30 days before screening
  • Any disorder, except for conditions associated with diabetes mellitus, which in the investigator's opinion might jeopardise subject's safety or compliance with the protocol
  • Anticipated initiation or change in concomitant medications known to affect weight or glucose metabolism during the trial
  • Impaired liver function, defined as Alanine Aminotransferase (ALT) more than or equal to 2.5 times or Bilirubin more than 1.5 times upper normal limit at screening
  • Renal impairment measured as estimated Glomerular Filtration Rate (eGFR) value of eGFR less than 60 ml/min/1.73 m^2
  • Any episodes of diabetic ketoacidosis within the past 90 days prior to the day of screening
  • Known hypoglycaemic unawareness as indicated by the Investigator according to Clarke's questionnaire question 8
  • Recurrent severe hypoglycaemic episodes within the last year as judged by the Investigator
  • Any of the following: myocardial infarction, stroke, hospitalization for unstable angina pectoris or transient ischaemic attack within the past 180 days prior to the day of screening
  • Subjects presently classified as being in New York Heart Association (NYHA) Class IV
  • Planned coronary, carotid or peripheral artery revascularisation known on the day of screening
  • Inadequately treated blood pressure defined as Grade 3 hypertension or higher (systolic more than or equal to 180 mmHg or diastolic more than or equal to 110 mmHg) at screening
  • Unwilling or unable to avoid acetaminophen throughout the trial

Information from the National Library of Medicine

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): NCT03816761


Locations
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United States, Massachusetts
Novo Nordisk Investigational Site
Boston, Massachusetts, United States, 02114
Sponsors and Collaborators
Novo Nordisk A/S
Investigators
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Study Director: Clinical Reporting Anchor and Disclosure (1452) Novo Nordisk A/S

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Responsible Party: Novo Nordisk A/S
ClinicalTrials.gov Identifier: NCT03816761     History of Changes
Other Study ID Numbers: NN1218-4360
U1111-1205-1788 ( Other Identifier: World Health Organization (WHO) )
First Posted: January 25, 2019    Key Record Dates
Last Update Posted: June 20, 2019
Last Verified: June 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: According to the Novo Nordisk disclosure commitment on novonordisk-trials.com
URL: http://novonordisk-trials.com/sharing-results

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: Yes
Device Product Not Approved or Cleared by U.S. FDA: Yes
Additional relevant MeSH terms:
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Insulin
Insulin, Globin Zinc
Insulin Aspart
Insulin, Long-Acting
Insulin degludec, insulin aspart drug combination
Diabetes Mellitus
Diabetes Mellitus, Type 1
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Autoimmune Diseases
Immune System Diseases
Hypoglycemic Agents
Physiological Effects of Drugs