| Eligibility |
Inclusion Criteria:
- Diagnosed (clinically) with type 1 diabetes (T1D) for at least 1 year or type 2
diabetes (T2D) for at least 6 months.
- Using insulin injection regimen of basal/bolus or basal only for 3 months prior to
screening, which includes:
- for bolus insulin (U-100) - a rapid-acting insulin analog (glulisine, lispro, or
aspart).
- for basal insulin - degludec (U-100 or U-200), detemir (U-100), or glargine (U-
100 or U-300).
- Participants with T2D may be on = 3 anti-hyperglycemic medications in addition to
insulin, including alpha-glucosidase inhibitors, dipeptidyl peptidase 4 (DPP-4)
inhibitors, glucagon-like peptide 1 receptor agonist (GLP-1 RA; oral or injectable),
meglitinides, metformin, sodium-glucose cotransporter-2 inhibitors (SGLTi-2),
sulfonylureas, or thiazolidinediones consistent with product labeling.
- Participants with T1D must be on insulin only.
- Have point-of-care hemoglobin A1c (HbA1c) value of =11% at screening.
- Must be able to self-inject insulin dose (basal or basal/bolus) without assistance.
- If using Continuous Glucose Monitoring or Flash Glucose Monitoring device, must agree
to stop use throughout duration of trial.
- Must be able to read and speak English.
- Able and willing to use only study-provided insulin Basaglar and/or Humalog for
duration of trial.
- Able and willing to follow insulin regimen specified by investigator throughout
duration of trial, insulin dose may be titrated at investigator's discretion.
- Have no physical or cognitive disabilities that would, in the opinion of the
investigator, preclude participant from using sponsor-provided iOS device for study
activities and comply with study requirements.
- Agree not to post any personal medical data, pictures of the IIM system or information
related to the study on any website or social media site (for example, Facebook,
Twitter, LinkedIn, etc.).
- Have refrigeration in home for storage of insulin.
- Women of childbearing potential participating:
- Cannot be pregnant or intend to become pregnant during the trial period
- Cannot be breastfeeding (including the use of a breast pump)
- Must remain abstinent or
- Must use 1 highly effective method (less than 1% failure rate) of contraception
or a combination of 2 effective methods of contraception for the entirety of the
study and
- Test negative for pregnancy based on a urine pregnancy test at the time of
screening. Additional local urine pregnancy tests may be conducted for duration
of trial at discretion of investigator.
Exclusion Criteria:
- If not able to take the basal insulin dose in 1 injection per day.
- Have experienced an episode of severe hypoglycemia (defined as requiring assistance
due to neurologically disabling hypoglycemia) within 3 months prior to screening.
- Have hypoglycemia unawareness as judged by the investigator.
- Have had 1 or more emergency room visits or hospitalization due to poor glucose
control (hyperglycemia or diabetic ketoacidosis [DKA]) within 3 months prior to
screening.
- History of renal transplantation, receiving renal dialysis, or diagnosed with stage IV
chronic kidney disease.
- Any of the following cardiovascular conditions within 6 months prior to screening: i.
acute myocardial infarction (MI) ii. cerebrovascular accident (stroke) iii. unstable
angina, or iv. hospitalization due to congestive heart failure (CHF)
- Presence or history of severe congestive heart failure (New York Heart Association
Class IV [CCNYHA 1994]).
- Have history of or clinical signs of liver disease (for example, acute or chronic
hepatitis, or cirrhosis).
- Have active or untreated malignancy except basal cell or squamous cell skin cancer.
- Have any hypersensitivity or allergy to any of the insulins or excipients used in this
trial.
- Have vision loss or vision impairment that does not allow recognition of MMA screen
features.
- Have impaired dexterity which limits ability to use injection device or mobile MMA.
- Are currently enrolled in any other clinical study involving an investigational
product or any other type of medical research judged not to be scientifically or
medically compatible with this study.
- Have participated, within the last 30 days, in a clinical study involving an
investigational product. If the previous investigational product has a long halflife,
5 half-lives or 30 days (whichever is longer) should have passed.
- Have previously completed or withdrawn from this study.
- Have previously used or are currently using an approved or investigational connected
pen system.
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