A Research Study to See How Insulin Icodec Helps People With Type 1 Diabetes Control Their Blood Sugar

Prior treatment

• Previous participation in this study. Participation is defined as having given informed consent in this study.
• Treatment with any investigational drug within 30 days prior to enrolment into the study.

Other

• Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation.

• Signed consent obtained before any study-related activities (study-related activities are any procedures related to recording of data according to the protocol).
• The decision to initiate treatment with commercially available insulin icodec has been made by the participant/legally acceptable representative (LAR) and the treating physician before and independently from the decision to include the participant in this study.
• Male or female, age greater than or equal to (≥) 18 years at the time of signing informed consent.
• Diagnosed with T1D ≥ 1 year before signing informed consent.
• Treated with multiple daily insulin injections (daily basal insulin analogue and bolus insulin analogue regimen) ≥ 6 months before signing informed consent.
• Available HbA1c value less than or equal to (≤) 90 days prior to the 'Initiation visit' (V1) or HbA1c measurement taken in relation with the 'Initiation visit' (V1) if in line with local clinical practice.
• Treatment naïve to once-weekly insulin prior to the 'Initiation Visit' (V1).