HLA Demographics Study in Adults With Type 1 Diabetes

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• Participant is an employee of, or an immediate family member of an employee, of the Sponsor, study site, or of a contractor/vendor who is involved in direct study conduct for this protocol.
• Participant is unwilling or unable to comply with the study visit assessments.

• Male and female participants aged ≥ 18 to ≤ 55 years, with type 1 DM meeting American Diabetes Association criteria at diagnosis:
  • Fasting glucose ≥ 126 mg/dL (7.0 mmol/L), or
  • 2-hour oral glucose tolerance test plasma glucose ≥ 200 mg/dL (11.0 mmol/L), or
  • Hemoglobin A1c ≥ 6.5%, or
  • Random plasma glucose ≥ 200 mg/dL (11.1 mmol/L) (with documented classic hyperglycemia symptoms or hyperglycemic crisis).
• Date of T1D diagnosis within 6 months of the study visit.
• Able and willing to provide written, informed consent as approved by the institutional review board (IRB). Participants must be able to consent directly; no other person or guardian may consent for them in this study.