Approval of a drug under this criteria document does not ensure full coverage of the drug.

Similar documents
BIOLOGIC MEDICATIONS IN THE TREATMENT OF IBD. crohnsandcolitis.ca

Treatment: Nutrition and Medication

REFERENCE CODE GDHC218CFR PUBLICAT ION DATE FEBRUARY 2014 ULCERATIVE COLITIS - US DRUG FORECAST AND MARKET ANALYSIS TO 2022

NEUTRALIZING ANTIBODY TESTS FOR INTERFERON

REFERENCE CODE GDHC1180DFR PUBLICATION DATE M AY 2013

REFERENCE CODE GDHC1106CFR PUBLICATION DATE M AY 2013

Emerging Medical Therapies in Inflammatory Bowel Disease

A Physician s consideration towards Biosimilars. João Eurico Fonseca

HIGHLIGHTS OF PRESCRIBING INFORMATION REMICADE

Drug Development in Inflammatory Bowel Disease: The FDA Perspective

National MS Society Information Sourcebook

Clinical Policy: Octreotide Acetate (Sandostatin Injection, Sandostatin LAR Depot) Reference Number: CP.PHAR.40

Medical Policy An independent licensee of the Blue Cross Blue Shield Association

There are currently 4 US Food and Drug

Quantification of Neutralizing Antibodies to Biopharmaceuticals using a Novel Cell- Bassed Assay Platform Technology

Pipeline Drug Evidence Review: Ocrevus (ocrelizumab) vs. Tysabri, Lemtrada, Rebif and Tecfidera June 8, 2016

8/14/2017 FOLLOW-ON BIOLOGICS: HOW BIOSIMILAR ARE THEY? STEPHANIE A. KLEPSER, PHARM.D. OPTIMED SPECIALTY PHARMACY OBJECTIVES OBJECTIVES

Office for Human Subject Protection. University of Rochester

NRCS Standards and Criteria for Dead Animal Composting

Sovaldi Pegasys Ribavirin

A GUIDE TO THIS REFLECTIONS B RESEARCH STUDY IF YOU RE FIGHTING BREAST CANCER, YOU RE NOT ALONE

ACG Public Forum. Join ACG, the FDA, and EMA for a discussion on biosimilars and IBD. Monday, 12:45 pm 2:15 pm

Regulatory Pathways for Rare Diseases

Naming, tracing, switching and other safety issues after 10 years learning

The Future of the U.S. Biosimilars Market: Development, Education, and Utilization. October 18, 2016

WORKFORCE CONNECTIONS, INC. GRIEVANCE PROCEDURES

Baek, Kyung-min. Recombinant Protein Products Division. Ministry of Food and Drug Safety

Learn more about why severe RSV disease APPROVED USE

BUDGET BASICS TRAINING TOPIC: DIRECT AND INDIRECT COSTS. Child and Adult Care Food Program (CACFP)

Professor Kimme Hyrich, MD, PhD, FRCPC, UK

Texas Vendor Drug Program Fee-For-Service Medicaid Synagis Authorization Request

The rheumatoid arthritis drug development model: a case study in Bayesian clinical trial simulation

PHYSICIAN OFFICE BILLING INFORMATION SHEET FOR IMLYGIC (talimogene laherparepvec)

FDA Update on Compounding

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE ) ) ) ) ) ) ) ) ) ) ) ) COMPLAINT INTRODUCTION

Tysedmus, a Registry of Multiple Sclerosis patients exposed to Natalizumab

Biogen Idec Synergy Creation in the move to the Big League. Activities, Assets and Sales Figures

BL-7040: Oligonucleotide for Inflammatory Bowel Disease

Package leaflet: Information for the user. Remicade 100 mg powder for concentrate for solution for infusion Infliximab

Professor Ahmed H Al-jedai, PharmD, MBA, BCPS, FCCP, FAST, Saudi Arabia

MEDICATION GUIDE RIBAVIRIN TABLETS Rx Only Read this Medication Guide carefully before you start taking ribavirin tablets and read the Medication

Clinical Policy: Humate-P (Antihemophiliac Factor/von Willebrand Factor Complex Human) Reference Number: CP.MP.404

STATEMENT SANDRA KWEDER, M.D DEPUTY DIRECTOR, OFFICE OF NEW DRUGS CENTER FOR DRUG EVALUATION AND RESEARCH U.S. FOOD AND DRUG ADMINISTRATION BEFORE THE

Water Talk Series

Announcement of Class and Component Prices United States Department of Agriculture

[Year] Delegating and Empowering. National Food. Ins. The National Food Service Management Institute. The University of Mississippi

Ideally located at the heart of Europe Liège

Is FMT A Drug? Lance Shea, M.S., J.D. Washington Square, Suite Connecticut Ave., NW Washington, DC, D

WIOA PROGRAM GRIEVANCE PROCEDURES

TRACKING EXPENSES. All Programs/SPSP

Case 2:17-cv JCJ Document 1 Filed 09/20/17 Page 1 of 51 UNITED STATES DISTRICT COURT EASTERN DISTRICT OF PENNSYLVANIA. Case No.

Doctor of Pharmacy Course Descriptions

Original Article. Abstract. 1. Introduction

Ambrogio Orlando. L esperienza clinica con il biosimilare in Italia. IBD Unit U.O. Medicina Interna 2a A.O. Osp.Riuniti Villa Sofia-Cervello Palermo

Copyright. Jeremiah J. Kelly (2015). All rights reserved. Further dissemination without express written consent strictly prohibited.

MRC Technology. A Life Science Specialist Technology Transfer Company. Skaggs School of Pharmacy and Pharmaceutical Sciences, December 2011

Mithra manages today multiple synergistic innovation streams for R&D, manufacturing or commercial partnering

Antibody Decisions and the Written Description Requirement. Workgroup

Update from the Center for Biologics Evaluation and Research (CBER): Advancing the Development of Complex Biologic Products

San Francisco Health Service System

Safety Data Sheet European Format

Regulatory Updates for Biopharmaceutical Products:FDA Perspective

Drug Development: Why Does it Cost so Much? Lewis J. Smith, MD Professor of Medicine Director, Center for Clinical Research Associate VP for Research

SYNAGIS (palivizumab) injection, for intramuscular use Initial U.S. Approval: 1998

Calendar Year 2018 Medicare Hospital Outpatient Prospective Payment System Proposed Rule

1 st Quarter 2007 Earnings. April 19, 2007

Overview of Biologics Testing and Evaluation: Regulatory Requirements and Expectations. Audrey Chang, PhD, Senior Director Development Services

TOP PAPERS FROM 2016: IBD & BIOSIMILARS CYNTHIA SEOW MBBS(HONS), MSC, FRACP UNIVERSITY OF CALGARY CDDW, BANFF, AB MARCH 5, 2017

Guideline on the clinical investigation of human normal immunoglobulin for subcutaneous and/or intramuscular administration (SCIg/IMIg)

Investigator-Initiated INDs

Phase 1 SMA Type 2 Trial Initiation and Study Design. December 2017

The Science of Monoclonal Antibody Therapy: Introducing Canine Atopic Dermatitis Immunotherapeutic*

Together, all nine participants have reduced infusions of factor IX concentrates by 99 percent over cumulative 1,650 days

Cellular Tumor Antigen P53 (Tumor Suppressor P53 or Antigen NY-CO-13) - Pipeline Review, H1 2016

Locally Led Conservation & The Local Work Group. Mark Habiger NRCS

Quo vadis Pharma industry. Vladimír Král, 2015

uniqure Announces First Clinical Data From Second Dose Cohort of AMT-060 in Ongoing Phase I/II trial in Patients with Severe Hemophilia B

Update on New MS Therapeutics

Specialty Drug Spending

Guideline on similar biological medicinal products containing interferon beta

Decision Notice and Finding of No Significant Impact

Center for Drug Evaluation and Research. CDER Small Business and Industry Assistance. (CDER SBIA) and New Drug Review.

Credit Suisse 7 th Annual European Large Cap Pharmaceutical Conference. November 6, 2007

Filed on behalf of: Boehringer Ingelheim International GmbH and Boehringer Ingelheim Pharmaceuticals, Inc.

TNFα-Blocker-Monitoring (drug-level e.g. Remicade) ELISA Kit

Participant Copy. No. Participation is voluntary. Your decision will not affect your health care at Mayo Clinic in any way.

Developing innovative new medicines for acute and chronic neurological and psychiatric conditions Larry Glass, CEO

Understanding Biosimilars and Projecting the Cost Savings to Employers Update

Reward Your Health. Live well. Get rewarded.

* * * Calculation of the Indirect Cost PE RVUs Expected Specialty for Low-Volume Services

Seasonal High Tunnels. Conservation Benefits Interim Practice Standard Financial Assistance Guidance

ANTIBODY IMMUNOGENICITY

Biosimilars: An Update on Clinical Trials (Review of Published and Ongoing Studies)

Transcription:

Criteria Document: Reference #: PC/B006 Page 1 of 5 and Therapeutics Quality PRODUCT APPLICATION: PreferredOne Administrative Services, Inc. (PAS) ERISA PreferredOne Administrative Services, Inc. (PAS) Non-ERISA PreferredOne Community Health Plan (PCHP) PreferredOne Insurance Company (PIC) Individual PreferredOne Insurance Company (PIC) Large Group PreferredOne Insurance Company (PIC) Small Group Coverage is subject to the terms of a member s benefit plan. To the extent there is any inconsistency between this criteria document or policy and the terms of a member s benefit plan, the member s benefit plan govern. Approval of a drug under this criteria document does not ensure full coverage of the drug. PURPOSE: The intent of the Biologics for Crohn s Disease criteria document is to: Ensure the intended use is medically necessary; and Require a failed trial of oral/self-administered drug(s) before a provider administered drug; and Consider overall cost effectiveness where appropriate. GUIDELINES: Medical Necessity Criteria Must satisfy any of the following: I-III Table 1: First-Line Provider Administered Biologics Biologics Entyvio Inflectra Remicade Renflexis Stelara Route of Administration Recommended Age Generic Name(s) FYI ONLY Biosimilar(s) adult vedolizumab N Drug Class integrin receptor antagonist not age specific infliximab-dyyb Y TNFα blocker not age specific infliximab Y TNFα blocker not age specific infliximab-abda Y TNFα blocker adult ustekinumab N I. Initial request for Entyvio, infliximab, or Stelara - must meet: A and one of B-D A. Ordered (or followed) by a gastroenterologist; and B. The request is for infliximab and the member has had an ileocolonic resection; or IL-12 and IL-23 antagonist C. If the member is 18 years of age or older, the member has not responded to, is intolerant to, responds to but cannot taper off without recurrent symptoms, or is a poor candidate for one self-administered biologic (see Table 3); or D. The request is for infliximab and the member is 17 years of age or younger, either of the following: 1 or 2 1. Ordered (or followed) by a pediatric gastroenterologist; or

Criteria Document: Reference #: PC/B006 Page 2 of 5 and Therapeutics Quality 2. There must be documentation of both of the following: a and b a. Symptomatic disease - such as, but not limited to, fever, abdominal distention, pain, diarrhea, bleeding, weight loss, intestinal fistula, intestinal obstruction; and b. The member has not responded to, is intolerant to, responds to but cannot taper off without recurrent symptoms, or is a poor candidate for both of the following: i and ii i. One corticosteroid; and ii. One of the following: a) e) a) Aminosalicylates; or b) Azathioprine (Imuran); or c) Cyclosporine (Sandimmune); or d) Methotrexate (Trexall, Rheumatrex); or e) 6-mercaptopurine (6MP). Table 2: Second-Line Provider Administered Biologic Biologic Tysabri Route of Administration Recommended Age II. Initial request for Tysabri - must meet: A and B A. Ordered (or followed) by a gastroenterologist; and Generics Available FYI ONLY Generic Name Biosimilar Drug Class adult N natalizumab N α4-integrin blocker B. The member has not responded to, is intolerant to, or responds to but cannot taper off without recurrent symptoms, or is a poor candidate for one first-line provider administered biologic: Entyvio, infliximab or Stelara (see Table 1). III. Continuation request Allow an additional 24 months Table 3: Self-Administered Biologics* Biologics Cimzia Humira Route of Administration subcutaneous injection subcutaneous injection Recommended Age Generics available FYI ONLY Generic Name Biosimilar Drug Class adult N certolizumab N TNFα blocker adult or child 6 years of age or older N adalimumab N TNFα blocker subcutaneous Stelara adult N ustekinumab N injection * Listing of drugs in table above does not ensure coverage. Please check member s prescription benefit. IL-12 and IL-23 antagonist

Criteria Document: Reference #: PC/B006 Page 3 of 5 and Therapeutics Quality DEFINITIONS: Biologic/biological: Biological products include a wide range of products such as vaccines, blood and blood components, allergenics, somatic cells, gene therapy, tissues, and recombinant therapeutic proteins. Infliximab: Reference product or biosimilar BACKGROUND: This criteria document is based on U.S. Food and Drug Administration (FDA) approved indications and dosing, expert consensus opinion and/or available reliable evidence.

Criteria Document: Reference #: PC/B006 Page 4 of 5 and Therapeutics Quality FOR INTERNAL USE ONLY COVERAGE: Prior Authorization: Yes Entyvio or infliximab - initial, authorize for 12 months; continued use, authorize for 24 months Stelara - initial, authorize one dose, only - not FDA approved for continued administration Tysabri initial, approve for 3 months; continued use, authorize for 3 months if patient receiving corticosteroids or 6 months if not receiving corticosteroids Coverage is subject to the member s contract benefits. CODING: HCPCS - 2017 J1745 Injection, infliximab, excludes biosimilar, 10mg NDC Remicade J2323 Injection, natalizumab, 1 mg (Tysabri) J3357 Injection, ustekinumab, 1mg (Stelara) J3380 Injection, vedolizumab, 1mg (Entyvio) Q5102 Injection, infliximab, biosimilar, 10mg (Inflectra, Renflexis) RELATED CRITERIA/POLICIES: Integrated Healthcare Services Process Manual: UR015 Use of Medical Policy and Criteria REFERENCES: 1. Yoshida EM. The Crohn s Disease Activity Index, its derivatives and the Inflammatory Bowel Disease Questionnaire: a review of instruments to assess Crohn s disease. 2. Entyvio [package insert]. Deerfield, IL:Takeda Pharmaceuticals America, Inc.; 2014 3. Cheifetz, AS. Management of active Crohn disease. JAMA. 2013;309(20). 4. Remicade [package insert]. Horsham, PA: Janssen Biotech Inc. 2015. 5. Tysabri [package insert]. Cambridge, MA. Biogen Idec Inc. 2017. 6. ClearScript. Prior Authorization. Infliximab (Remicade). Revision Date 8/31/2016. 7. ClearScript. Prior Authorization. Tysabri (natalizumab). 09/15/2016. 8. American Gastroenterological Association (AGA). American Gastroenterological Association Institute Technical Review on the Use of Thiopurines, Methotrexate, and Anti-TNF-α Biologic Drugs for the Induction and Maintenance of Remission of Inflammatory Crohn s Disease. Gastroenterology 2013;145:1464-1478. Retrieved from http://www.gastrojournal.org/article/s0016-5085(13)01520-5/pdf 9. Singh S, Garg SK, Pardi DS, et al. Comparative efficacy of biologic therapy in biologic-naïve patients with Crohn disease: a systematic review and network meta-analysis. Mayo Clin Proc. 2014 Dec;89(12):1621-35. doi: 10.1016/j.mayocp.2014.08.019. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/25441399 10. Stelara [package insert]. Horsham, PA: Janssen Biotech Inc. 2016. 11. Inflectra (infliximab-dyyb) [package insert]. Lake Forest, IL. CELLTRION, Inc. 2016. 12. Renflexis (infliximab-abda) [package insert]. 2017. Kenilworth, NJ. Merck & Co., Inc. 2017. DOCUMENT HISTORY: Created Date: 05/17/06 Reviewed Date: 12/27/12, 12/27/13, 12/22/14, 12/22/15, 09/23/16, 09/19/17 Revised Date: 04/18/07, 04/23/08, 3/26/09, 06/02/09, 03/25/10, 01/13/11, 06/08/11, 09/07/11, 01/02/12, 08/01/12, 12/27/12, 05/02/13, 07/01/13, 12/22/14, 03/21/16, 04/11/16, 09/23/16, 04/14/17, 07/10/17, 10/25/17

Attachment A Tumor Necrosis Factor (TNF) Blockers FDA Contraindications and Warnings Drug FDA Contraindications FDA Warnings Cimzia None Serious active infection and/or invasive fungal infections Central Nervous System demyelinating disease (exacerbation or onset) Formation of autoantibodies (Lupus-like syndrome) Live or live-attenuated vaccines Enbrel Sepsis Serious active infection and/or invasive fungal infections Known hypersensitivity to Enbrel components Wegener's Granulomatosis Moderate to severe alcoholism Humira None Serious active infection and/or invasive fungal infections Formation of autoantibodies (Lupus-like syndrome) Live vaccines Remicade > 5mg/kg doses in moderate to severe heart failure Known hypersensitivity to Remicade components Serious active infection and/or invasive fungal infections Formation of autoantibodies (lupus-like syndrome) Hepatoxicity Live vaccines Simponi None Serious active infection and/or invasive fungal infections Live vaccines For more details, check each drug's FDA-approved label on the FDA's website: http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=search.search_drug_name

PreferredOne Community Health Plan Nondiscrimination Notice PreferredOne Community Health Plan ( PCHP ) complies with applicable Federal civil rights laws and does not discriminate on the basis of race, color, national origin, age, disability, or sex. PCHP does not exclude people or treat them differently because of race, color, national origin, age, disability, or sex. PCHP: Provides free aids and services to people with disabilities to communicate effectively with us, such as: Qualified sign language interpreters Written information in other formats (large print, audio, accessible electronic formats, other formats) Provides free language services to people whose primary language is not English, such as: Qualified interpreters Information written in other languages If you need these services, contact a Grievance Specialist. If you believe that PCHP has failed to provide these services or discriminated in another way on the basis of race, color, national origin, age, disability, or sex, you can file a grievance with: Grievance Specialist PreferredOne Community Health Plan PO Box 59052 Minneapolis, MN 55459-0052 Phone: 1.800.940.5049 (TTY: 763.847.4013) Fax: 763.847.4010 customerservice@preferredone.com You can file a grievance in person or by mail, fax, or email. If you need help filing a grievance, a Grievance Specialist is available to help you. You can also file a civil rights complaint with the U.S. Department of Health and Human Services, Office for Civil Rights, electronically through the Office for Civil Rights Complaint Portal, available at https://ocrportal.hhs.gov/ocr/portal/lobby.jsf, or by mail or phone at: U.S. Department of Health and Human Services 200 Independence Avenue, SW Room 509F, HHH Building Washington, D.C. 20201 1-800-368-1019, 800-537-7697 (TDD) Complaint forms are available at http://www.hhs.gov/ocr/office/file/index.html. Language Assistance Services NDR PCHP LV (10/16)

PreferredOne Insurance Company Nondiscrimination Notice PreferredOne Insurance Company ( PIC ) complies with applicable Federal civil rights laws and does not discriminate on the basis of race, color, national origin, age, disability, or sex. PIC does not exclude people or treat them differently because of race, color, national origin, age, disability, or sex. PIC: Provides free aids and services to people with disabilities to communicate effectively with us, such as: Qualified sign language interpreters Written information in other formats (large print, audio, accessible electronic formats, other formats) Provides free language services to people whose primary language is not English, such as: Qualified interpreters Information written in other languages If you need these services, contact a Grievance Specialist. If you believe that PIC has failed to provide these services or discriminated in another way on the basis of race, color, national origin, age, disability, or sex, you can file a grievance with: Grievance Specialist PreferredOne Insurance Company PO Box 59212 Minneapolis, MN 55459-0212 Phone: 1.800.940.5049 (TTY: 763.847.4013) Fax: 763.847.4010 customerservice@preferredone.com You can file a grievance in person or by mail, fax, or email. If you need help filing a grievance, a Grievance Specialist is available to help you. You can also file a civil rights complaint with the U.S. Department of Health and Human Services, Office for Civil Rights, electronically through the Office for Civil Rights Complaint Portal, available at https://ocrportal.hhs.gov/ocr/portal/lobby.jsf, or by mail or phone at: U.S. Department of Health and Human Services 200 Independence Avenue, SW Room 509F, HHH Building Washington, D.C. 20201 1-800-368-1019, 800-537-7697 (TDD) Complaint forms are available at http://www.hhs.gov/ocr/office/file/index.html. Language Assistance Services NDR PIC LV (10/16)