Diabetic GLP-1's
Indications for Prior Authorization
Bydureon BCise
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Adjunctive therapy to diet and exercise to improve glycemic control in adults and pediatric patients aged 10 years and older with type 2 diabetes mellitus
Byetta, Rybelsus, Mounjaro
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Adjunctive therapy to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus
Ozempic, Trulicity
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Adjunctive therapy to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus
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To reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke) in adults with type 2 diabetes mellitus and established cardiovascular disease
Victoza
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Adjunctive therapy to diet and exercise to improve glycemic control in adults and pediatric patients 10 years of age and older with type 2 diabetes mellitus
-
To reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke) in adults with type 2 diabetes mellitus and established cardiovascular disease
Criteria
Bydureon BCise, Byetta, Ozempic, Rybelsus, Trulicity, Generic/Brand liraglutide, Mounjaro
Prior Authorization (Initial Authorization)
Length of Approval: 1 Year(s)
For diagnosis of Diagnosis of type 2 diabetes mellitus (DM2)
- Patient has a documented diagnosis of type 2 diabetes mellitus as evidenced by medical records documenting one of the following:
- A1C ≥ 6.5%
- Fasting plasma glucose (FPG) ≥ 126 mg/dL
- 2-hour plasma glucose ≥ 200 mg/dL during OGTT
- Random plasma glucose ≥ 200 mg/dL
- Minimum duration of a 30-day trial and failure, contraindication, or intolerance to metformin or another diabetic product (e.g. SGLT-2 Inhibitors, DPP4 Inhibitors, Glinides, Sulfonylureas, Alpha Glucosidase Inhibitors)
Bydureon BCise, Byetta, Ozempic, Rybelsus, Trulicity, Generic/Brand liraglutide, Mounjaro
Prior Authorization (Reauthorization)
Length of Approval: 1 Year(s)
For diagnosis of Diagnosis of type 2 diabetes mellitus (DM2)
- Documentation of a positive clinical response to therapy (e.g., reduction in HbA1c from baseline)
Brand Victoza
Non Formulary (Initial Authorization)
Length of Approval: 1 Year(s)
For diagnosis of Diagnosis of type 2 diabetes mellitus (DM2)
- Patient has a documented diagnosis of type 2 diabetes mellitus as evidenced by medical records documenting one of the following:
- A1C ≥ 6.5%
- Fasting plasma glucose (FPG) ≥ 126 mg/dL
- 2-hour plasma glucose ≥ 200 mg/dL during OGTT
- Random plasma glucose ≥ 200 mg/dL
- Minimum duration of a 30-day trial and failure, contraindication, or intolerance to metformin or another diabetic product (e.g., SGLT-2 Inhibitors, DPP4 Inhibitors, Glinides, Sulfonylureas, Alpha Glucosidase Inhibitors) AND
- Trial and intolerance to generic liraglutide AND
- Trial and failure, contraindication, or intolerance to two of the following:
- Mounjaro
- Ozempic or Rybelsus
- Trulicity
- Byetta or Bydureon BCise
Brand Victoza
Non Formulary (Reauthorization)
Length of Approval: 1 Year(s)
For diagnosis of Diagnosis of type 2 diabetes mellitus (DM2)
- Documentation of a positive clinical response to therapy (e.g., reduction in HbA1c from baseline)
P & T Revisions
2025-03-17, 2025-03-04, 2024-11-05
References
- Byetta Prescribing Information. AstraZeneca Pharmaceuticals LP. Wilmington, DE. December 2022.
- Victoza Prescribing Information. Novo Nordisk Inc. Plainsboro, NJ. July 2023
- Trulicity Prescribing Information. Eli Lily and Company. Indianapolis, IN. April 2023
- Bydureon BCise Prescribing Information. AstraZeneca Pharmaceuticals LP. Wilmington, DE. May 2023
- Ozempic Prescribing Information. Novo Nordisk Inc. Plainsboro, NJ. September 2023.
- Mounjaro Prescribing Information. Eli Lily and Company. Indianapolis, IN. September 2023.
- Rybelsus Prescribing Information. Novo Nordisk Inc. Plainsboro, NJ. January 2024.
- 8. American Diabetes Association (ADA) 2023 Standards of Care in Diabetes to Guide Prevention, Diagnosis, and Treatment for People Living with Diabetes. Accessed May 18, 2023.
Revision History
- 2025-03-17: Update Program
- 2025-03-04: Updated criteria
- 2024-11-05: New Program