A Research Study to See How Well Weekly Insulin Icodec Maintains Blood Sugar Levels Compared to Daily Basal Insulins in Adults With Type 2 Diabetes

What this study is about

This study compares insulin icodec, taken once a week, with other basal insulins, taken once a day, in people with type 2 diabetes.The purpose of this study is to see how well the approved injectable weekly insulin icodec maintains blood sugar levels when compared to approved and available daily injectable basal insulins in people with type 2 diabetes. The participants will either be prescribed weekly insulin icodec or a daily basal insulin (insulin glargine, insulin detemir or insulin degludec) based on current standards for the treatment of type 2 diabetes. The study will last for about 13 months.

Who can join (things the study team will check)

✅ You may be able to join if…

• Diagnosed with T2D greater than or equal to (≥) 180 days prior to the day of screening.
• Treatment with any of the following non-insulin glucose-lowering medication(s) or combination regimen(s) at the time of screening: Metformin, Sulfonylureas, Meglitinides (glinides), dipeptidyl peptidase-4 (DPP-4) inhibitors, sodium-glucose cotransporter-2 (SGLT2) inhibitors, Thiazolidinediones, Alpha-glucosidase inhibitors, Oral combination products (for the allowed individual oral antidiabetic drugs), Oral or injectable glucagon-like peptide-1 (GLP-1) receptor agonists and Injectable dual glucose-dependent insulinotropic polypeptides (GIP) and GLP-1 receptor agonist.
• Need of intensification with basal insulin, as indicated at the discretion of the investigator.
• Recorded HbA1c value ≥7% within the last 90 days prior to randomization.

🚫 You may not be able to join if…

• Known or suspected hypersensitivity to study intervention(s) or related products.
• Previous participation in this study. Participation is defined as signed informed consent.
• Female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using adequate contraceptive method.
• Participation (i.e., received any study intervention) in any interventional clinical study within 90 days before screening.
• Any disorder which in the investigator's opinion might jeopardize participant's safety.

Where this trial is running

• Centricity Research Calgary Endocrinology, Calgary, Alberta, Canada
• Alta Clinical Research at Hermitage Medicentre, Edmonton, Alberta, Canada
• Fraser Clinical Trials Inc., New Westminster, British Columbia, Canada
• Winnipeg Clinic, Winnipeg, Manitoba, Canada
• G.A. Research Associates Ltd., Moncton, New Brunswick, Canada
• Centricity Research Brampton Endocrinology, Brampton, Ontario, Canada
• Centricity Clinical Research Burlington, Burlington, Ontario, Canada
• Centricity Research Vaughn Endocrinology, Concord, Ontario, Canada
• Medical Trust Clinics, Inc., Courtice, Ontario, Canada
• Centricity Research Etobicoke Endocrinology, Etobicoke, Ontario, Canada
• Janik Research, Greater Sudbury, Ontario, Canada
• Premier Clinical Trial Research Network (PCTRN), Hamilton, Ontario, Canada

+ 63 more sites.

Who to contact

Novo Nordisk · (+1) 866-867-7178 · clinicaltrials@novonordisk.com

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT07112339.