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Xdemvy Step Therapy with Quantity Limit Program Summary
Policy Number: PH-91217
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 |
01-01-2025 |
04-01-2024 |
FDA LABELED INDICATIONS AND DOSAGE
Agent(s) |
FDA Indication(s) |
Notes |
Ref# |
Xdemvy® (lotilaner) Ophthalmic solution |
An ectoparasiticide (anti-parasitic) indicated for the treatment of Demodex blepharitis. |
|
1 |
See package insert for FDA prescribing information: https://dailymed.nlm.nih.gov/dailymed/index.cfm
CLINICAL RATIONALE
Demodex blepharitis |
Demodex blepharitis is a common disease of the eyelid, affecting approximately 25 million Americans.(3) Blepharitis is a chronic inflammation of the eyelid margin and a common cause of chronic ocular inflammation.(2) It is characterized by erythema, ocular irritation and discomfort, discharge and debris on the eyelids and lashes and eyelash anomalies. In more advanced stages, there may be corneal involvement. Although blepharitis can have various etiologies, including allergic, staphylococcal and seborrheic, one of the most common is Demodex mite infestation and accounts for more than 60% of those with blepharitis. It has long been accepted that the prevalence of Demodex increase with age, affecting more than 80% of those older than 60 years and 100% of those older than 70 years. Demodex prevalence is lower among younger university-based populations and reported between 2% and 27%. Demodex blepharitis is equally present in both sexes and infestation was similar regardless of ethnicity.(3) |
Efficacy |
The safety and efficacy of Xdemvy for the treatment of Demodex blepharitis was evaluated in a total of 833 patients (415 of which received Xdemvy) in two 6-week, randomized, multicenter, double-masked, vehicle-controlled studies (Saturn-1 and Saturn-2). Patients with Demodex blepharitis were randomized to either Xdemvy or Vehicle at a 1:1 ratio dosed twice daily in each eye. Efficacy was demonstrated by improvement in lids (reduction of collarettes to no more than 2 collarettes per upper lid) in each study (Saturn-1 and Saturn-2) by Day 43. The endpoints of mite eradication (mite density of 0 mites/lash) and erythema cure (Grade 0) of Xdemvy vs. Vehicle demonstrated statistically significant improvement at Day 43 across both Saturn-1 (Table 1) and Saturn-2 (Table 2) studies.(1) |
Safety |
Xdemvy has no FDA labeled contraindications for use. |
REFERENCES
Number |
Reference |
1 |
Xdemvy prescribing information. Tarsus Pharmaceuticals, Inc. July 2023. |
2 |
Amescua G, Akpek EK, Farid M, et al. Blepharitis Preferred Practice Pattern®. Ophthalmology. 2019;126(1):P56-P93. doi:10.1016/j.ophtha.2018.10.019 |
3 |
Rhee MK, Yeu E, Barnett M, et al. Demodex Blepharitis: A Comprehensive review of the disease, current management, and emerging therapies. Eye & Contact Lens. 2023;49(8):311-318. doi:10.1097/icl.0000000000001003 |
POLICY AGENT SUMMARY STEP THERAPY
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
Targeted MSC |
Available MSC |
Final Age Limit |
Preferred Status |
|
||||||
Xdemvy |
lotilaner ophth soln |
0.25 % |
M ; N ; O ; Y |
N |
|
|
POLICY AGENT SUMMARY QUANTITY LIMIT
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
QL Amount |
Dose Form |
Day Supply |
Duration |
Addtl QL Info |
Allowed Exceptions |
Targeted NDCs When Exclusions Exist |
|
|||||||||
Xdemvy |
lotilaner ophth soln |
0.25 % |
1 |
Bottle |
50 |
DAYS |
|
|
|
CLIENT SUMMARY – STEP THERAPY
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
Client Formulary |
Xdemvy |
lotilaner ophth soln |
0.25 % |
Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx |
CLIENT SUMMARY – QUANTITY LIMITS
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
Client Formulary |
Xdemvy |
lotilaner ophth soln |
0.25 % |
Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx |
STEP THERAPY CLINICAL CRITERIA FOR APPROVAL
Module |
Clinical Criteria for Approval |
||||
Step Therapy |
Target Agent(s) will be approved when ONE of the following is met: 1. The patient has a medication history of use in the past 90 days with ONE prerequisite agent OR Length of Approval: 2 months *Step therapy requirement may not apply if a prior health plan paid for the medication - documentation of a paid claim may be required. |
QUANTITY LIMIT CLINICAL CRITERIA FOR APPROVAL
Module |
Clinical Criteria for Approval |
QL |
Quantity limit for the Target Agent(s) will be approved when ONE of the following is met:
Length of Approval: up to 12 months |
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.
Commercial _ CSReg _ Xdemvy__STQL _ProgSum_ 01-01-2025