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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)

Collarettes are the pathognomonic sign of Demodex blepharitis. They are waxy in texture and composed of accumulated undigested material, keratinized cells, dead or living mites, eggs and egg casings of mites that form a cylindrical collar that remain at the base of the eyelash follicle. Collarettes can be readily identified at the base of the upper lash margin on downward gaze using a slitlamp. Ocular itching is the symptom most commonly associated with Demodex blepharitis, and evidence suggests that patients consider this to be one of the most bothersome symptoms associated with the disease. It is more likely to occur at night or early morning after periods of mite activity, distinguishing it from daytime, allergy-related itching. In addition to itching, other symptoms include dryness, discharge, eye redness, burning, tearing, foreign body sensation, pain, and blurred (or fluctuating) vision.(3)

The American Academy of Ophthalmology notes that a cure is usually not possible for blepharitis but many treatments or treatment combinations may be helpful including: warm compresses, eyelid cleansing, topical and/or systemic antibiotics, and topical anti-inflammatory agents. Patients with recalcitrant blepharitis have responded to therapy directed at decreasing or eradicating the Demodex mites. Oral ivermectin has been reported to be of benefit in some cases of recalcitrant Demodex blepharitis.(2) Ivermectin has long been used safely by dermatologists to treat Demodex-related skin conditions and is known to have an acaricidal effect. Ivermectin improves the signs and symptoms of Demodex blepharitis along with reducing the mite density.(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)

PREREQUISITE AGENT(S)

Xdemvy

ivermectin oral tablet

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
2. The patient has an intolerance or hypersensitivity to ONE prerequisite agent OR
3. The patient has an FDA labeled contraindication to ALL prerequisite agents

Length of Approval: 2 months

NOTE: If Quantity Limit applies, please refer to Quantity Limit Criteria.

*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:

  1. The requested quantity (dose) does NOT exceed the program quantity limit OR
  2. The requested quantity (dose) exceeds the program quantity limit AND ONE of the following:
    1. BOTH of the following:
      1. The requested agent does NOT have a maximum FDA labeled dose for the requested indication AND
      2. There is support for therapy with a higher dose for the requested indication OR
    2. The requested quantity (dose) does NOT exceed the maximum FDA labeled dose for the requested indication

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