Gan & Lee Insulin Glargine Target Type (1) Evaluating Research

Exclusion Criteria

• •1. Participation in another clinical study or use of any study drug within 30 days before screening.
• •2. Previous use of a biosimilar insulin, either basal or bolus.
• •3. Diabetic ketoacidosis within a year before screening.
• •4. Brittle type 1 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).
• •5. 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.
• •6. 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during the study (change in dosage is allowed, but change in type or brand of insulin will result in the subject being withdrawn from the study).
• •7. Inadequately controlled thyroid disease, defined as a TSH or free T4 value \> the upper limit of normal.
• •8. BMI \< 19 kg/m2 or \> 35 kg/m2.
• •9. 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).
• •10. Documented history of anti-insulin antibodies.
• •11. 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 medications).
• •12. Current use of medication intended to cause weight loss or weight gain.
• •13. Alcohol or substance use disorder within the 2 years before screening.
• •14. Any previous or anticipated treatment with interferons.
• •15. Any history of malignant disease within 5 years before screening, except for adequately treated basal cell carcinoma.
• •16. Severe concomitant physical or psychiatric diseases or conditions
• •17. 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.
• •18. Any history of pancreatitis or pancreatectomy.
• •19. Any diagnosis or condition that requires the subject to undergo procedures that could decrease antibodies in plasma or that would require treatment with immunosuppressant agents.
• •20. Any condition e.g., splenectomy, autoimmune disease, or rheumatologic disease, that could affect immunologic responses, could indicate an altered immune system, or could require treatment with a prohibited medication.
• •21. Any unresolved infection or a history of active infection within 30 days before screening other than mild or viral illness (as judged by the Investigator).
• •22. Any other disease or condition that in the opinion of the Investigator could confound the study results or limit the subject's ability to participate in the study or comply with follow-up procedures; or any other factor that would indicate a significant risk of loss to follow up.
• •23. Intolerance or history of hypersensitivity to insulin glargine or any excipient of IP.
• •24. Inability or unwillingness to wear the CGM sensor as required for the study, or to comply with the concomitant medication requirements in the FreeStyle Libre Pro Indications and Important Safety Information, during the CGM periods.