For all requests for Multiple Sclerosis Medications all of the following criteria must be met:

Similar documents
Calcitonin Gene Related Peptide Receptor Inhibitors Prior Authorization Criteria:

Prior Authorization. Drug Name (select from list of drugs shown) Gilenya (fingolomid) Quantity Frequency Strength. Physician Name:

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

2. Has this plan authorized this medication in the past for this member (i.e., previous authorization is on file under this plan)?

Galafold (migalastat) or Fabrazyme (agalsidase beta) Prior Authorization Criteria:

Pharmacy Prior Authorization

Gilenya. Gilenya (fingolimod) Description

GILENYA (fingolimod) oral capsule

Gilenya. Gilenya (fingolimod) Description

Gilenya. Gilenya (fingolimod) Description

GILENYA (fingolimod) oral capsule

Circle Yes or No Y N. [If no, then no further questions.]

APPENDIX D SASKATCHEWAN MS DRUGS PROGRAM

Circle Yes or No Y N. [If no, skip to question 8.] 2. Has the patient been compliant with therapy as verified by the prescriber?

Request for Prior Authorization for PCSK9 inhibitor therapy Website Form Submit request via: Fax

REQUESTED DRUG INFORMATION

MEDICAL ASSISTANCE HANDBOOK PRIOR AUTHORIZATION OF PHARMACEUTICAL SERVICES. I. Requirements for Prior Authorization of Multiple Sclerosis Agents

MULTIPLE SCLEROSIS - REVIEW AND UPDATE

* Note: please reference the Highmark Health Options Gender Transition Services (MP- 033-MD-DE) policy for all gender dysphoria requests.

Section I. Short-acting opioid Prior Authorization Criteria

PATIENT INFORMATION: Patient Surname First Name Middle Initial Sex Date of Birth Alberta Personal Health Number M / F Year Month Day

Deaths Patients with events (%) 0 vs. 0 n.r.

Prior Authorization Conditions for Approval of Enbrel (etanercept) Website Form Submit request via: Fax

Biologics and Beyond: Treatment of Multiple Sclerosis. Rita Jebrin, PharmD, BCPS

Clinical Policy: Natalizumab (Tysabri) Reference Number: ERX.SPA.162 Effective Date:

Regulatory Status FDA-approved indication: Tysabri is an integrin receptor antagonist indicated for treatment of (1):

Regulatory Status FDA-approved indication: Tysabri is an integrin receptor antagonist indicated for treatment of:

Medication Policy Manual. Topic: Aubagio, teriflunomide Date of Origin: November 9, 2012

Updated: 08/2017 DMMA Approved: 11/2017

Prior Authorization Conditions for Approval of Humira (adalimumab) Website Form Submit request via: Fax

Hot Topics Multiple Sclerosis. Natalie Parks, MD, FRCPC Assistant Professor, Dalhousie University June 27, 2018

FINGOLIMOD (GILENYA) CLINICIAN INFORMATION

Clinical Policy: Natalizumab (Tysabri) Reference Number: ERX.SPA.162 Effective Date:

Clinical Policy: Mitoxantrone (Novantrone) Reference Number: CP.PHAR.258 Effective Date: Last Review Date: Line of Business: Medicaid

2. Does the patient have a diagnosis of Crohn s disease? Y N

Updates to the Alberta Human Services Drug Benefit Supplement

Clinical Policy: Mitoxantrone (Novantrone) Reference Number: CP.CPA.334 Effective Date: Last Review Date: Line of Business: Commercial

Current Enrolling Clinical Trials

CLINICAL MEDICAL POLICY

Medical Policy An Independent Licensee of the Blue Cross and Blue Shield Association

TYSABRI (natalizumab) BENEFIT INVESTIGATION WORKSHEET GUIDE

PRODUCT MONOGRAPH GILENYA. Fingolimod (as fingolimod hydrochloride) Oral capsules, 0.5 mg fingolimod (as fingolimod hydrochloride)

Pediatric MS treatments: What do you start with, when do you switch?

See Important Reminder at the end of this policy for important regulatory and legal information.

TECFIDERA (dimethyl fumarate) oral capsule

Address: City: State: ZIP code: Inferferon Product Requested (Include Strength):

Medication Policy Manual. Topic: Tecfidera, dimethyl fumarate Date of Origin: May 16, 2013

Objectives. There Aren t Enough Hours in the Day

AMPYRA (dalfampridine) extended release oral tablet Dalfampridine ER oral tablet

PRODUCT MONOGRAPH. Pr GILENYA. Fingolimod capsules mg and 0.5 mg fingolimod (as fingolimod hydrochloride)

NBPDP FORMULARY UPDATE

Molina Healthcare of Texas

Hepatitis C Medications Hawaii PRIOR AUTHORIZATION REQUEST FORM

Neurological Assessment for Multiple Sclerosis and Extended Disability Scale Score

Pharmacy Prior Authorization

Clinical Policy: Natalizumab (Tysabri) Reference Number: ERX.SPA.162 Effective Date:

Committee Approval Date: December 12, 2014 Next Review Date: December 2015

See Important Reminder at the end of this policy for important regulatory and legal information.

AUBAGIO (teriflunomide) oral tablet

3. Does the member continue to receive nutritional or psychological counseling?

CORLANOR (ivabradine) oral tablet

Clinical Policy: Natalizumab (Tysabri) Reference Number: CP.PHAR.259 Effective Date: Last Review Date: Line of Business: Medicaid

Priority Health Medicare prior authorization form Fax completed form to: toll free, or

Per Soelberg Sørensen

2. Did the member receive this medication during a recent hospitalization? Y N

2. Did the patient receive this medication during a recent hospitalization? Y N

Regulatory Status FDA-approved indication: Tecfidera is indicated for the treatment of patients with relapsing forms of multiple sclerosis (1).

2. Is the patient responding to medication? Y N

Progress in MS: Current and Emerging Therapies. Presented by: Dr. Kathryn Giles, MD MSc FRCPC Cambridge, Ontario, Canada

Multiple Sclerosis Update

Demyelinating Diseases: Multiple Sclerosis January 10, 2018 Dr. Ostrow

3. Has the patient had a sustained improvement in Pain or Function (e.g. PEG scale with a 30 percent response from baseline)?

See Important Reminder at the end of this policy for important regulatory and legal information.

Updates to the Alberta Drug Benefit List. Effective August 1, 2018

Ocrevus. (ocrelizumab) New Product Slideshow

3. Does the patient continue to receive nutritional or psychological counseling? Y N

Ocrevus (ocrelizumab)

Le Hua, MD. Disclosures Teaching and Speaking: Teva Neurosciences, Genzyme, Novartis Advisory Board: Genzyme, EMD Serono

2. Does the patient have chronic urticaria? Y N

Pharmacy Prior Authorization

Pharmacy Management Drug Policy

Pharmacy Prior Authorization

HIGHLIGHTS OF PRESCRIBING INFORMATION

2. Is this request for a preferred medication? Y N

SAVAYSA (edoxaban tosylate) oral tablet

3. Has the patient shown improvement in signs and symptoms of the disease? Y N

Multiple Sclerosis , The Patient Education Institute, Inc. nr Last reviewed: 04/17/2017 1

3. Has the patient shown improvement in signs and symptoms of the disease? Y N

TREATING MULTIPLE SCLEROSIS The Current Disease Modifying Therapies Beverly Gilder, M.D. Blue Sky Neurology MS Center

NDMP Multiple Sclerosis Treatment Protocol. Alemtuzumab THERAPY

Pharmacy Prior Authorization

2. Does the patient have a diagnosis of ulcerative colitis or Crohn s? Y N

1. Has this plan authorized this medication in the past for this patient (i.e., previous authorization is on file under this plan)?

2. Does the patient have a diagnosis of chronic idiopathic thrombocytopenic purpura (ITP)?

Acthar Gel. H. P. Acthar Gel (corticotropin; ACTH) Description

HIGHLIGHTS OF PRESCRIBING INFORMATION WARNINGS AND PRECAUTIONS

Immune Modulating Drugs Prior Authorization Request Form

Subject: Natalizumab (Tysabri ) IV

Transcription:

Request for Prior Authorization for Multiple Sclerosis Medications Website Form www.highmarkhealthoptions.com Submit request via: Fax - 1-855-476-4158 All requests for Multiple Sclerosis Medications require a prior authorization and will be screened for medical necessity and appropriateness using the criteria listed below. Multiple Sclerosis Medications Prior Authorization Criteria: Multiple Sclerosis Medications addressed in this policy include: Avonex (interferon beta-1a), Copaxone (glatiramer acetate), Gilenya (fingolimod), Tecfidera (dimethyl fumarate), and Ocrevus (Ocrelizumab) Disclaimer: All requests for Multiple Sclerosis Medications require a prior authorization and will be screened for medical necessity and appropriateness using the criteria listed below. For all requests for Multiple Sclerosis Medications all of the following criteria must be met: One of the following: o Member is 18 years of age or older o Request is for Gilenya and member is 10 years of age or older Must be prescribed by, or in consultation with, a neurologist or a physician that specializes in the treatment of MS The drug will not be given in combination with other disease modifying therapies approved for the treatment of MS o Gilenya and Tecfidera must not be given in combination with any antineoplastic, non-corticosteroid immunosuppressive or immune-modulating therapies used for the treatment of MS The requested dose and frequency is in accordance with FDA-approved labeling, nationally recognized compendia, and/or evidence-based practice guidelines If the request is for a non-preferred medication, must provide documentation showing one of the following: o The member has tried and failed (which will be verified via pharmacy claims if available) or had an intolerance to a preferred agent o All of the preferred agents would be contraindicated. If member is new to the plan and requests a continuation of therapy, must provide chart documentation indicating member is currently on requested therapy Coverage may be provided with a diagnosis of relapsing forms of multiple sclerosis (e.g. relapsing-remitting, secondary-progressive, or progressive-relapsing multiple sclerosis) and the following criteria is met:

For members initiating therapy for the first time, must provide documentation of one of the following: o One clinical relapse (e.g. functional disability, hospitalization, acute steroid therapy, etc.) during the prior year o Two relapses within the prior two years o A single clinical demyelinating event and 2 or more brain lesions characteristic of MS Coverage provided for situations in which there is functional status that can be preserved o Member must still either be able to walk at least a few steps OR alternatively must have some functional arm/hand use consistent with performing activities of daily living Requests for Ocrevus must also meet the following criteria: o Must provide documentation of Hepatitis B Virus (HBV) screening confirming negative HBsAg and anti-hb. Requests for Gilenya must also meet the following criteria: o Member must have documentation of positive antibodies for varicella zoster virus (VZV) if there is no documentation of a healthcare professional confirmed history of chickenpox or documentation of a full course of vaccination against VZV o Member must have a recent ECG (within 6 months) with no evidence of heart block or bradycardia and has had an ophthalmologic exam of the macula prior to treatment initiation o Member does not have any contraindications to Gilenya including: Recent myocardial infarction, unstable angina, stroke, transient ischemic attack, decompensated heart failure with hospitalization, or Class III/IV heart failure History of Mobitz Type II 2nd degree or 3rd degree AV block or sick sinus syndrome, unless patient has a pacemaker Baseline QTc interval 500 msec Treatment with Class Ia or Class III anti-arrhythmic drugs Initial Duration of Approval: 12 months Reauthorization criteria o Documentation of clinical response defined as: Member continues to receive benefit from treatment by having the ability to walk at least a few steps or alternatively have some functional arm/hand use consistent with performing activities of daily living. Member did not experience 1 or more relapses Member does not have 2 or more unequivocally new MRI-detected lesions Reauthorization Duration of Approval: 12 months Coverage may be provided with a diagnosis of primary progressive multiple sclerosis (MS) and the following criteria is met: Request must be for Ocrevus

Must provide documentation of Hepatitis B Virus (HBV) screening confirming negative HBsAg and anti-hb. Must have one year of disease progression (retrospectively or prospectively determined), independent of clinical relapse, plus two of the following: o One or more hyperintense T2 lesions characteristics of MS in one or more of the periventricular, cortical, juxtacortical, or infratentorial areas o Two or more hyperintense T2 lesions in the spinal cord o Presence of cerebrospinal fluid-specific oligoclonal bands Coverage provided for situations in which there is functional status that can be preserved o Member must still either be able to walk at least a few steps OR alternatively must have some functional arm/hand use consistent with performing activities of daily living Initial Duration of Approval: 12 months Reauthorization criteria o Documentation of clinical response defined as: Member continues to receive benefit from treatment by having the ability to walk at least a few steps or alternatively have some functional arm/hand use consistent with performing activities of daily living. Reauthorization Duration of Approval: 12 months Coverage may be provided for any non-fda labeled indication if it is determined that the use is a medically accepted indication supported by nationally recognized pharmacy compendia or peer-reviewed medical literature for treatment of the diagnosis(es) for which it is prescribed. These requests will be reviewed on a case by case basis to determine medical necessity.

MULTIPLE SCLEROSIS MEDICATIONS PRIOR AUTHORIZATION FORM Please complete and fax all requested information below including any progress notes, laboratory test results, or chart documentation as applicable to Highmark Health Options Pharmacy Services. FAX: (855) 476-4158 If needed, you may call to speak to a Pharmacy Services Representative. PHONE: (844) 325-6253 Monday through Friday 8:30am to 5:00pm PROVIDER INFORMATION Requesting Provider: NPI: Provider Specialty: Office Address: Office Contact: Office Phone: Office Fax: MEMBER INFORMATION Member Name: DOB: Health Options ID: Member weight: pounds or kg REQUESTED DRUG INFORMATION Medication: Strength: Frequency: Duration: Is the member currently receiving requested medication? Yes No Date Medication Initiated: Is this medication being used for a chronic or long-term condition for which the medication may be necessary for the life of the patient? Yes No Billing Information This medication will be billed: at a pharmacy OR medically (if medically please provide a JCODE: Place of Service: Hospital Provider s office Member s home Other Place of Service Information Name: NPI: Address: Phone: MEDICAL HISTORY (Complete for ALL requests) Diagnosis: Relapsing Multiple Sclerosis Primary-Progressive Multiple Sclerosis Other: ICD-10 Code: Is there functional status that can be preserved? Yes No Member is able to walk at least a few steps Member has functional use of arm/hand consistent with performing activities of daily living Will the medication be administered by a health care provider? Yes No Please provide a medication list of any concurrent medications that the member will be taking. For Relapsing Multiple Sclerosis: Check any of the applicable statements: Member had at least one clinical relapse (e.g. functional disability, hospitalization, acute steroid therapy, etc.) during the prior year Member had two relapses within the prior two years Member had a single clinical demyelinating event and 2 or more brain lesions characteristic of MS

MULTIPLE SCLEROSIS MEDICATIONS PRIOR AUTHORIZATION FORM (CONTINUED) PAGE 2 OF 2 Please complete and fax all requested information below including any progress notes, laboratory test results, or chart documentation as applicable to Highmark Health Options Pharmacy Services. FAX: (855) 476-4158 If needed, you may call to speak to a Pharmacy Services Representative. PHONE: (844) 325-6253 Monday through Friday 8:30am to 5:00pm MEMBER INFORMATION Member Name: Health Options ID: DOB: Member weight: pounds or kg MEDICAL HISTORY (Complete for ALL requests) For Primary Progressive Multiple Sclerosis: Check any of the applicable statements: Member has one year of disease progression (retrospectively or prospectively determined) independent of clinical relapse Member has one or more hyperintense T2 lesions characteristics of MS in one or more of the periventricular, cortical, juxtacortical, or infratentorial areas Member has two or more hyperintense T2 lesions in the spinal cord Cerebrospinal fluid-specific oligoclonal bands are present Requests for Ocrevus: Has the member been screened for Hepatitis B Virus (HBV)? Yes No Date of screening: Does the patient have active HBV? Yes No Requests for Gilenya: Does the member have documentation of receiving a full course of vaccination against varicella zoster virus? Yes No If not, please provide documentation of positive antibodies for varicella zoster virus Has the member had an ophthalmologic exam of the macula? Yes No Has the member had a ECG within the last 6 months? Yes No Please check any of the applicable statements: ECG has evidence of heart block or bradycardia Member has baseline QTc interval 500 msec Member has a history of Mobitz Type II 2nd degree or 3rd degree AV block or sick sinus syndrome without a pacemaker Member had a recent myocardial infarction, unstable angina, stroke, transient ischemic attack, decompensated heart failure with hospitalization, or Class III/IV heart failure CURRENT or PREVIOUS THERAPY Medication Name Strength/ Frequency Dates of Therapy Status (Discontinued & Why/Current) REAUTHORIZATION Has the member experienced a significant improvement with treatment? Yes No Please describe: For Relapsing Multiple Sclerosis: How many relapses has the member had in the last year? How many unequivocally new MRI-detected lesions has the member had in the last year? Prescribing Provider Signature Date