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ph-1159

Long Acting Insulin Prior Authorization Program Summary

Policy Number: PH-1159

This program applies to Blue Partner, Commercial, GenPlus, NetResults A series, SourceRx and Health Insurance Marketplace formularies.

POLICY REVIEW CYCLE

Effective Date	Date of Origin
04-01-2024

FDA APPROVED INDICATIONS AND DOSAGE

Agent(s)	FDA Indication(s)	Notes	Ref#
Basaglar® (insulin glargine) Injection	To improve glycemic control in adults and pediatric patients with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus. Limitations of Use: Not recommended for treating diabetic ketoacidosis.		1
Lantus® (insulin glargine) Injection	To improve glycemic control in adult and pediatric patients with diabetes mellitus Limitations of Use: Not recommended for the treatment of diabetic ketoacidosis		2
Levemir® (insulin detemir) Injection	To improve glycemic control in adult and pediatric patients with diabetes mellitus. Limitations of Use: Not recommended for the treatment of diabetic ketoacidosis.		3
Rezvoglar™ (insulin glargine-aglr) Injection	To improve glycemic control in adults and pediatric patients with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus Limitation of use: Not recommended for treating diabetic ketoacidosis		9
Semglee®, Glargin-yfgn Injection	To improve glycemic control in adults and pediatric patients with type 1 diabetes mellitus and in adults with type 2 diabetes mellitus Limitation of use: Not recommended for treating diabetic ketoacidosis		4
Toujeo®, Toujeo® Max (insulin glargine) Injection	To improve glycemic control in adults and pediatric patients 6 years and older with diabetes mellitus Limitation of use: Not recommended for treating diabetic ketoacidosis		5
Tresiba®, Insulin degludec Injection	To improve glycemic control in patients 1 year of age and older with diabetes mellitus Limitation of use: Not recommended for treating diabetic ketoacidosis		6

See package insert for FDA prescribing information: https://dailymed.nlm.nih.gov/dailymed/index.cfm

CLINICAL RATIONALE

Overview

The American Diabetes Association Standards of Medical Care in Diabetes recommend the following therapy for type 1 diabetes mellitus:(7)

Most individuals with type 1 diabetes should be treated with multiple daily injections of prandial and basal insulin, or subcutaneous insulin infusion.
Most individuals with type 1 diabetes should use rapid-acting insulin analogs to reduce hypoglycemia risk.
Individuals with type 1 diabetes should receive education on how to match mealtime insulin doses to carbohydrate intake, fat and protein content, and anticipated physical activity.

For type 2 diabetes mellitus, the American Diabetes Association recommends the following:(7)

Healthy lifestyle behaviors, diabetes self-management education and support, avoidance of clinical inertia, and social determinants of health should be considered in the glucose-lowering management of type 2 diabetes. Pharmacologic therapy should be guided by person-centered treatment factors, including comorbidities and treatment goals.
In adults with type 2 diabetes and established/high risk of atherosclerotic cardiovascular disease, heart failure, and/or chronic kidney disease, the treatment regimen should include agents that reduce cardiorenal risk.
Pharmacologic approaches that provide adequate efficacy to achieve and maintain treatment goals should be considered, such as metformin or other agents, including combination therapy.
Weight management is an impactful component of glucose-lowering management in type 2 diabetes. The glucose-lowering treatment regimen should consider approaches that support weight management goals.
Metformin should be continued upon initiation of insulin therapy (unless contraindicated or not tolerated) for ongoing glycemic and metabolic benefits.
Early combination therapy can be considered in some individuals at treatment initiation to extend the time to treatment failure.
The early introduction of insulin should be considered if there is evidence of ongoing catabolism (weight loss), if symptoms of hyperglycemia are present, or when A1C levels (>10% [86 mmol/mol]) or blood glucose levels (greater than or equal to 300 mg/dL [16.7 mmol/L]) are very high.
A person-centered approach should guide the choice of pharmacologic agents. Consider the effects on cardiovascular and renal comorbidities, efficacy, hypoglycemia risk, impact on weight, cost and access, risk for side effects, and individual preferences.
Among individuals with type 2 diabetes who have established atherosclerotic cardiovascular disease or indicators of high cardiovascular risk, established kidney disease, or heart failure, a sodium–glucose cotransporter 2 inhibitor and/or glucagon-like peptide 1 receptor agonist with demonstrated cardiovascular disease benefit is recommended as part of the glucose-lowering regimen and comprehensive cardiovascular risk reduction, independent of A1C and in consideration of person-specific factors.
In adults with type 2 diabetes, a glucagon-like peptide 1 receptor agonist is preferred to insulin when possible.
If insulin is used, combination therapy with a glucagon-like peptide 1 receptor agonist is recommended for greater efficacy, durability of treatment effect, and weight and hypoglycemia benefit. Recommendation for treatment intensification for individuals not meeting treatment goals should not be delayed.
Medication regimen and medication-taking behavior should be reevaluated at regular intervals (every 3–6 months) and adjusted as needed to incorporate specific factors that impact choice of treatment.
Clinicians should be aware of the potential for overbasalization with insulin therapy. Clinical signals that may prompt evaluation of overbasalization include basal dose more than ∼0.5 units/kg/day, high bedtime–morning or postpreprandial glucose differential, hypoglycemia (aware or unaware), and high glycemic variability. Indication of overbasalization should prompt reevaluation to further individualize therapy.

The American Association of Clinical Endocrinologists and American College of Endocrinology (AACE/ACE) 2023 algorithm for type 2 diabetics (T2D) recommends the overall goal of insulin therapy is to achieve glycemic control after failure of noninsulin antihyperglycemic agents. Glycemic targets should be individualized, although an A1C of 6.5% to 7% for persons on insulin is recommended for most patients. Although A1C is a key measure, insulin titration requires use of multiple glycemic parameters including fasting blood glucose (FBG), premeal or 2-hour postprandial blood glucose, and data from continuous glucose monitoring (CGM), when available. In general, targets for fasting and premeal glucose are <110 mg/dL without hypoglycemia and can be individualized based on a person’s comorbidities and clinical status. The use of CGM is recommended for persons treated with insulin to optimize glycemic control while minimizing hypoglycemia.(8)

Given that T2D is a progressive disease, many individuals will require >1 antihyperglycemic medication to achieve their individualized A1C target over the course of the disease. Clinicians should consider multiple factors when selecting the second agent, including presence of overweight or obesity, hypoglycemia risk, access/cost, and presence of severe hyperglycemia. Patients often present with >1 of these factors, so using a patient-centered, shared decision-making approach is important. The order that medications are listed in the algorithm denotes the suggested preference hierarchy for selection. In those patients with overweight or obesity and the additional goal of weight loss, dual glucose-dependent insulinotropic polypeptide and glucagon-like peptide-1 receptor agonist (GIP/GLP-1 RA), GLP-1 RA, or sodium glucose cotransporter 2 inhibitor (SGLT2i) class are preferred options. Persons with a history of hypoglycemia, at high risk of hypoglycemia, and/or at risk for severe complications from hypoglycemia should preferentially be initiated with an agent associated with low risk for hypoglycemia, including GLP-1 RA, SGLT2i, dual GIP/GLP-1 RA, thiazolidinedione (TZD), or dipeptidyl peptidase-4 inhibitor (DPP-4i).(8)

Patients with symptomatic hyperglycemia and/or an A1C >10% suggestive of marked insulin deficiency should start basal insulin to improve glycemia as quickly as possible. Basal insulin can be initiated with or without initiation and titration of a GLP-1 RA if the patient is not already on this class of agents. Some patients with severe hyperglycemia may need simultaneous initiation of bolus insulin. Clinicians should be cognizant that combination of incretin-based therapies is not recommended (i.e., DPP-4i with GLP-1 RA or dual GIP/GLP-1 RA). Antihyperglycemic medications should be titrated to the maximally tolerated dose to achieve the individualized A1C goal, and additional antihyperglycemic agents should be considered in a timely fashion to avoid therapeutic inertia. If the A1C is >9% or >1.5% above goal, greater than 2 antihyperglycemic agents may need to be initiated at once.(8)

Basal with or without prandial insulin treatment may be needed as initial therapy if the A1C is >10% and/or glucose values are >300 mg/dL, combined with catabolic symptoms, such as weight loss. If symptomatic hyperglycemia is present, a GLP-1 RA alone is not recommended as it requires titration and may delay glucose control. The goal of initial intensive insulin therapy for symptomatic hyperglycemia is to reduce glucose levels safely and promptly. After improved glycemic control is achieved with short-term insulin therapy, especially with a new diagnosis of DM, a role for noninsulin antihyperglycemic agents could be considered. For most persons who need intensification of glycemic control and who are already undergoing 3 to 4 oral therapies, a GLP-1 RA or GIP/GLP-1 RA should be the initial choice, if not already in use. If glycemic targets are not achieved with these therapies, basal insulin should be added alone or as a basal insulin/GLP-1 RA combination injection. Stepwise addition of prandial insulin at 1 to 3 meals is recommended if additional glycemic control is required. The dose of basal insulin can be based on A1C levels at the time of initiation. For an A1C <8%, basal insulin can be started at 0.1 to 0.2 U/kg/day and for an A1C >8%, 0.2 to 0.3 U/kg/day can be considered. Analog insulins, including detemir, glargine, or degludec are preferred over human insulins such as neutral protamine Hagedorn (NPH) to reduce hypoglycemia.(8)

Safety

Basaglar, Lantus, Rezvoglar, Semglee, and Toujeo products have the following contraindications:(1,2,4,5,9)

During episodes of hypoglycemia.
Hypersensitivity to insulin glargine products or any excipients.

Levemir has the following contraindications:(3)

During episodes of hypoglycemia.
Hypersensitivity to insulin detemir products or any excipients.

Tresiba has the following contraindications:(6)

During episodes of hypoglycemia.
Hypersensitivity to insulin degludec or any excipients.

REFERENCES

Number	Reference
1	Basaglar prescribing information. Eli Lilly and Company. July 2021.
2	Lantus prescribing information. Sanofi-Aventis US, LLC. June 2023.
3	Levemir prescribing information. Novo Nordisk, Inc. December 2022.
4	Semglee prescribing information. Mylan Specialty L.P. July 2023.
5	Toujeo, Toujeo Max prescribing information. Sanofi-Aventis U.S. LLC. March 2023.
6	Tresiba prescribing information. Novo Nordisk Inc. July 2022.
7	American Diabetes Association, 9. Pharmacologic Approaches to Glycemic Treatment: Standards of Care in Diabetes—2023. Diabetes Care 1 January 2023; 46 (Supplement_1): S140–S157. https://doi.org/10.2337/dc23-S009.
8	Samson, S. L., Vellanki, P., Blonde, L., et. al. (2023). American association of clinical endocrinology consensus statement: Comprehensive type 2 diabetes management algorithm – 2023 update. Endocrine Practice: Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists, 29(5), 305–340. https://doi.org/10.1016/j.eprac.2023.02.001
9	Rezvoglar prescribing information. Sanofi-Aventis US, LLC. November 2022.

POLICY AGENT SUMMARY PRIOR AUTHORIZATION

Target Brand Agent(s)	Target Generic Agent(s)	Strength	Targeted MSC	Available MSC	Final Age Limit	Preferred Status

	insulin degludec inj ; insulin degludec soln pen-injector	100 UNIT/ML ; 200 UNIT/ML	M ; N ; O ; Y	N
Lantus ; Lantus solostar ; Rezvoglar kwikpen	insulin glargine inj ; insulin glargine soln pen-injector ; insulin glargine-aglr soln pen-injector	100 UNIT/ML ; 300 UNIT/ML	M ; N ; O ; Y	N

CLIENT SUMMARY – PRIOR AUTHORIZATION

Target Brand Agent Name(s)	Target Generic Agent Name(s)	Strength	Client Formulary
	insulin degludec inj ; insulin degludec soln pen-injector	100 UNIT/ML ; 200 UNIT/ML	Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx
Lantus ; Lantus solostar ; Rezvoglar kwikpen	insulin glargine inj ; insulin glargine soln pen-injector ; insulin glargine-aglr soln pen-injector	100 UNIT/ML ; 300 UNIT/ML	Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx

PRIOR AUTHORIZATION CLINICAL CRITERIA FOR APPROVAL

Module

Clinical Criteria for Approval

Preferred Agent(s)	Non-Preferred Target Agent(s)
Insulin glargine-yfgn Glargin-yfgn Semglee	Insulin glargine Lantus Rezvoglar
Tresiba	Insulin degludec

Non-preferred Target Agent(s) will be approved when ONE of the following is met:

The patient has an intolerance, or hypersensitivity to ALL preferred long acting insulin agents that is not expected to occur with the requested agent (medical records required) OR
The patient has an FDA labeled contraindication to ALL preferred long acting insulin agents that is not expected to occur with the requested agent (medical records required)

Length of Approval: 12 months

*Step therapy requirement may not apply if a prior health plan paid for the medication - documentation of a paid claim may be required.

This pharmacy policy is not an authorization, certification, explanation of benefits or a contract. Eligibility and benefits are determined on a case-by-case basis according to the terms of the member’s plan in effect as of the date services are rendered. All pharmacy policies are based on (i) information in FDA approved package inserts (and black box warning, alerts, or other information disseminated by the FDA as applicable); (ii) research of current medical and pharmacy literature; and/or (iii) review of common medical practices in the treatment and diagnosis of disease as of the date hereof. Physicians and other providers are solely responsible for all aspects of medical care and treatment, including the type, quality, and levels of care and treatment. The purpose of Blue Cross and Blue Shield of Alabama’s pharmacy policies are to provide a guide to coverage. Pharmacy policies are not intended to dictate to physicians how to practice medicine. Physicians should exercise their medical judgment in providing the care they feel is most appropriate for their patients. Neither this policy, nor the successful adjudication of a pharmacy claim, is guarantee of payment.