Awiqli (insulin icodec-abae)
Indications for Prior Authorization
Awiqli (insulin icodec-abae)
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For diagnosis of Type 2 diabetes mellitus
Indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
Criteria
Awiqli
Prior Authorization (Initial Authorization)
Length of Approval: 12 Month(s)
- Diagnosis of Type 2 Diabetes Mellitus AND
- Patient is 18 years of age or older AND
- Inadequate glycemic control on non-insulin antidiabetic therapy (i.e., HbA1c greater than or equal to 7%) AND
- One of the following:
- Trial and inadequate response (minimum 90-day supply) or contraindication to one of the following basal insulin:
- Lantus (insulin glargine)
- Toujeo (insulin glargine)
- Basaglar Kwikpen (insulin glargine)
- Rezvoglar Kwikpen (insulin glargine)
- Tresiba (insulin degludec)
- Patient has a barrier that prevents safe self-administration of daily insulin (e.g., non-adherence to daily basal insulin, visual impairment, need for caregiver assistance, physical or cognitive limitations, etc)
- Patient or caregiver has been counseled on all of the following:
- Once weekly administration
- Risk, recognition, and management of hypoglycemia
- Not to be used in combination with any other basal insulin
Awiqli
Prior Authorization (Reauthorization)
Length of Approval: 12 Month(s)
- Patient demonstrates positive clinical response to therapy (e.g., decrease in HbA1c from baseline)
P & T Revisions
2026-07-14, 2026-07-14
References
- Awiqli Prescribing Information. Novo Nordisk Inc. Plainsboro, NJ. March 2026.
Revision History
- 2026-07-14: New Program for Awiqli
- 2026-07-14: New Program for Awiqli
HEALTHY LIVING