Gan & Lee Insulin Glargine Target Type (2) Evaluating Research

Inclusion Criteria

• Male or nonpregnant, nonlactating female subjects between the ages of 18 and 75 years, inclusive.
• Ability to provide written, personally signed, and dated informed consent to participate in the study, in accordance with the ICH GCP Guideline E6 and all applicable regulations, before initiating any study related procedures.
• Ability to understand and fully comply with all study procedures and restrictions.
• Subjects with a confirmed diagnosis of type 2 diabetes mellitus who meet one of the following:
• If insulin-naïve, subjects should have been on at least 2 approved OAMs for at least 12 weeks before screening, and the clinician has decided to add insulin therapy.
• If already being treated with a basal and/or bolus insulin, subjects should have been treated with insulin for at least 6 months in addition to at least 1 approved OAM, and must not have changed the type or brand of insulin within 6 months prior to screening.
• HbA1c values as follows:
• If insulin-naïve, HbA1c ≤ 11.0%.
• If previously on a basal insulin regimen, HbA1c ≥ 7.0% and ≤ 11.0%.
• Body mass index (BMI) ≤ 45 kg/m2.
• Adherence to a prudent diet and exercise regimen recommended by the medical provider, and willingness to maintain these consistently for the duration of the study.
• Concomitant medications are allowed, provided that no significant dosing changes are anticipated during the study (see the exclusion criteria below for specific prohibited concomitant medications); for concomitant thyroid medications, subjects must have been on a stable dosage for 90 days before screening.

Exclusion Criteria

• Participation in another clinical study or use of any study drug within 30 days before screening.
• Previous use of a biosimilar insulin, either basal or bolus.
• Diabetic ketoacidosis within a year before screening.
• Brittle type 2 diabetes mellitus within the year before screening (e.g., multiple hospitalizations related to diabetes mellitus and/or severe hypoglycemia for which the subject required 3rd party assistance).
• Any severe, delayed sequela of diabetes mellitus, e.g., worsening end-stage renal disease, advanced coronary artery disease, or myocardial infarction within the year before screening, or autonomic peristaltic problems, e.g., gastroparesis.
• Anticipated change in insulin used during the study (change in dosage is allowed, but change in type or brand of insulin will result in the subject being withdrawn from the study).
• Inadequately controlled thyroid disease, defined as a TSH or free T4 value > the upper limit of normal.
• BMI > 45 kg/m2.
• Any clinically significant (in the opinion of the Investigator) hematology or chemistry test results at screening, including any liver function test > 3x the upper limit of normal (subjects with elevated bilirubin due to Gilbert syndrome are eligible to participate).
• Documented history of anti-insulin antibodies.
• Treatment with glucocorticosteroids, immunosuppressants, or cytostatic agents within 60 days before screening (newly-prescribed or high-dose corticosteroids are prohibited; chronically administered oral, inhaled, topical, or intra-articular corticosteroids at a stable dosage are allowed if no increase in dose is anticipated during the study; See Appendix 3 [Section 17.3] for a list of allowed and prohibited concomitant medications).
• Current use of medication intended to cause weight loss or weight gain.
• Alcohol or substance use disorder within the 2 years before screening.
• Any previous or anticipated treatment with interferons.
• Any history of malignant disease within 5 years before screening, except for adequately treated basal cell carcinoma.
• Severe concomitant physical or psychiatric diseases or conditions.
• A history of a positive test result for HIV, hepatitis B, or hepatitis C; any subject who has a positive test result during the study may continue at the discretion of the Investigator.
• Any histor