Vyepti® (Eptinezumab-Jjmr) (Intravenous) Document Number: MAYO-0527 Last Review Date: 10/01/2020 Date of Origin: 04/01/2020 Dates Reviewed: 04/2020, 10/2020
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Pharmacokinetics, Pharmacodynamics and Drug
pharmaceutics Review Pharmacokinetics, Pharmacodynamics and Drug–Drug Interactions of New Anti-Migraine Drugs—Lasmiditan, Gepants, and Calcitonin-Gene-Related Peptide (CGRP) Receptor Monoclonal Antibodies Danuta Szkutnik-Fiedler Department of Clinical Pharmacy and Biopharmacy, Pozna´nUniversity of Medical Sciences, Sw.´ Marii Magdaleny 14 St., 61-861 Pozna´n,Poland; [email protected] Received: 28 October 2020; Accepted: 30 November 2020; Published: 3 December 2020 Abstract: In the last few years, there have been significant advances in migraine management and prevention. Lasmiditan, ubrogepant, rimegepant and monoclonal antibodies (erenumab, fremanezumab, galcanezumab, and eptinezumab) are new drugs that were launched on the US pharmaceutical market; some of them also in Europe. This publication reviews the available worldwide references on the safety of these anti-migraine drugs with a focus on the possible drug–drug (DDI) or drug–food interactions. As is known, bioavailability of a drug and, hence, its pharmacological efficacy depend on its pharmacokinetics and pharmacodynamics, which may be altered by drug interactions. This paper discusses the interactions of gepants and lasmiditan with, i.a., serotonergic drugs, CYP3A4 inhibitors, and inducers or breast cancer resistant protein (BCRP) and P-glycoprotein (P-gp) inhibitors. In the case of monoclonal antibodies, the issue of pharmacodynamic interactions related to the modulation of the immune system functions was addressed. It also focuses on the effect of monoclonal antibodies on expression of class Fc gamma receptors (FcγR). Keywords: migraine; lasmiditan; gepants; monoclonal antibodies; drug–drug interactions 1. Introduction Migraine is a chronic neurological disorder characterized by a repetitive, usually unilateral, pulsating headache with attacks typically lasting from 4 to 72 h. -
Pharmacy Prior Authorization Grid ALTCS, and Pharmacy
Please Note: Refer to the other PA grids for applicable covered services that require PA. PA Grids: Medical, Behavioral Health, Pharmacy Prior Authorization Grid ALTCS, and Pharmacy. (Effective Date of Service 1/1/2021) Injectables that require Prior Authorization All chemotherapeutic drugs must be used for FDA-approved indications and/or in accordance with NCCN guidelines *Indicates prior authorization required if billed charges are greater than $400 PA Required HMO 13 HCPCS Short Description (BUCA- Code SNP) 90378 Respiratory Syncytial Virus Immune Globulin Yes C9036 Patisiran Yes C9047 Caplacizumab-yhdp Yes C9061 Teprotumumab-trbw Yes C9063 Eptinezumab-jjmr Yes C9131 Factor VIII antihemophilic factor pegylated-auci Yes C9132 Prothrombin Complex Concentrate (Human), Kcentra Yes C9133 Factor IX (Antihemophilic Factor, Recombinant), Rixibus Yes C9399 Mipomersen (Kynamro) Yes J0129 Abatacept Yes J0135 Adalimumab Yes J0178 Aflibercept Yes J0179 Brolucizumab-dbll, 1 mg Yes J0180 Agalsidase Beta Yes J0205 Alglucerase Yes J0215 Alefacept Yes J0220 Alglucosidase Alfa (Myozyme) Yes J0221 Alglucosidase Alfa (Lumizyme) Yes J0222 Patisiran, 0.1 mg Yes J0223 Givosiran 0.5 mg Yes J0256 Alpha 1-Proteinase Inhibitor Yes J0257 Alpha 1-Proteinase Inhibitor (Glassia) Yes J0275 Alprostadil Urethral Suppository Yes J0490 Belimumab Yes J0517 Benralizumab Yes J0567 Cerliponase alfa Yes J0570 Buprenorphine implant Yes J0584 Burosumab-twza 1 mg Yes J0585 Onabotulinumtoxina (Botox) Yes J0586 Abobotulinumtoxina (Dysport) Yes J0587 Rimabotulinumtoxinb (Myobloc) -
Oxford Policy Update Bulletin: April 2020
Oxford April 2020 policy update bulletin Medical & Administrative Policy Updates Take Note POLICY IMPLEMENTATION DELAYED Implementation of the changes associated with the following Clinical Policies, previously announced for an effective date on or after Apr. 1, 2020, has been delayed as noted below: Policy Title Status Effective Date Genitourinary Pathogen Nucleic Acid Detection Panel Testing New May 1, 2020 Jun. 1, 2020 Outpatient Surgical Procedures - Site of Service Revised Apr. 6, 2020 TBD Tysabri® (Natalizumab) New Apr. 1, 2020 Jul. 1, 2020 Access a policy listed below for complete details on the latest updates. A comprehensive summary of changes is provided at the bottom of every policy document for your reference. To view a detailed version of this bulletin, click here. Policy Title Status Effective Date CLINICAL POLICY Abnormal Uterine Bleeding and Uterine Fibroids Revised Jun. 1, 2020 Actemra® (Tocilizumab) Injection for Intravenous Infusion Revised May 1, 2020 Adakveo® (Crizanlizumab-Tmca) Updated Apr. 1, 2020 Adakveo® (Crizanlizumab-Tmca) Revised Jul. 1, 2020 Cell-Free Fetal DNA Testing Revised Jun. 1, 2020 Cimzia® (Certolizumab Pegol) New Jul. 1, 2020 Collagen Crosslinks and Biochemical Markers of Bone Turnover Revised May 1, 2020 Drug Coverage Criteria – New and Therapeutic Equivalent Medications Revised May 1, 2020 Drug Coverage Guidelines Revised Apr. 1, 2020 Adakveo (Crizanlizumab-Tmca) Givlaari (Givosiran) Ziextenzo (Pegfilgrastim-Bmez) Drug Coverage Guidelines Revised May 1, 2020 Adlyxin (Lixisenatide) Arnuity -
Alder Biopharmaceuticals, Inc. (Exact Name of Registrant As Specified in Its Charter)
UNITED STATES SECURITIES AND EXCHANGE COMMISSION WASHINGTON, DC 20549 FORM 10-Q ☒ QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the quarterly period ended March 31, 2019 OR ☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from to Commission File Number: 001-36431 Alder BioPharmaceuticals, Inc. (Exact name of registrant as specified in its charter) Delaware 90-0134860 (State or other jurisdiction (I.R.S. Employer of incorporation or organization) Identification No.) 11804 North Creek Parkway South Bothell, WA 98011 (Address of principal executive offices including zip code) Registrant’s telephone number, including area code: (425) 205-2900 Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐ Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐ Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. -
VYEPTI™ (EPTINEZUMAB) Policy Number: CSLA2020D0090A Effective Date: TBD
Proprietary Information of United Healthcare: The information contained in this document is proprietary and the sole property of United HealthCare Services, Inc. Unauthorized copying, use and distribution of this information are strictly prohibited. Copyright 2020 United HealthCare Services, Inc. UnitedHealthcare® Community Plan Medical Benefit Drug Policy VYEPTI™ (EPTINEZUMAB) Policy Number: CSLA2020D0090A Effective Date: TBD Table of Contents Page Commercial Policy APPLICATION ...................................................... 1 Vyepti™ (Eptinezumab) COVERAGE RATIONALE ........................................ 1 APPLICABLE CODES ............................................. 2 BACKGROUND ................................................... 43 CLINICAL EVIDENCE ............................................ 4 U.S. FOOD AND DRUG ADMINISTRATION ............ 54 CENTERS FOR MEDICARE AND MEDICAID SERVICES 54 REFERENCES ....................................................... 5 POLICY HISTORY/REVISION INFORMATION ...... 65 INSTRUCTIONS FOR USE .................................... 65 APPLICATION This Medical Benefit Drug Policy only applies to state of Louisiana. COVERAGE RATIONALE Vyepti has been added to the Review at Launch program. Please reference the Medical Benefit Drug Policy titled Review at Launch for New to Market Medications for additional details. Chronic Migraine Vyepti is proven and medically necessary for the preventive treatment of chronic migraines when all of the following criteria are met: For initial therapy, all of the -
761119Orig1s000 SUMMARY REVIEW
CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 761119Orig1s000 SUMMARY REVIEW Summary Review Summary Review Date February 21, 2020 Heather Fitter, MD From Nick Kozauer, MD Billy Dunn, MD Subject Summary Review BLA # 761119 Applicant Lundbeck Seattle BioPharmaceuticals, Inc. Date of Submission December 26, 2018 PDUFA Goal Date February 21, 2020 Proprietary Name Vyepti Established or Proper Names Eptinezumab Solution for intravenous (IV) injection (100 Dosage Form mg/mL) Applicant Proposed Prevention of migraine in adults Indication/Population 100 mg IV infusion every 3 months; 300 mg IV Applicant Proposed Dosing Regimen(s) infusion every 3 months Recommendation on Regulatory Action Approval Recommended Indication/Population Preventive treatment of migraine in adults 100 mg IV infusion every 3 months; 300 mg IV Recommended Dosing Regimen(s) infusion every 3 months 1 Reference ID: 4564908 Summary Review 1. Benefit-Risk Assessment Benefit-Risk Assessment Framework Benefit-Risk Integrated Assessment Eptinezumab is a humanized monoclonal antibody that binds to the calcitonin gene-related peptide (CGRP) ligand, and prevents CGRP binding to its receptor. The applicant provided information supporting safety and efficacy in patients with both chronic migraine (i.e., at least 15 headache days/month, with features of migraine headache on at least 8 days/month) and episodic migraine (i.e., up to 14 migraine headache days/month). There are several FDA-approved drugs for the preventive treatment of migraine. Three drugs in the anti-CGRP class were approved recently for this indication: erenumab (May 2018), fremanezumab (September 2018), and galcanezumab (September 2018). These three drugs are given by subcutaneous (SC) administration either monthly or quarterly, while eptinezumab is given intravenously (IV) quarterly. -
(CGRP) Inhibitor Criteria – Migraine and Cluster Headache Prevention Approval Date: February 24, 2021
New Hampshire Medicaid Fee-for-Service Program Calcitonin Gene-Related Peptide (CGRP) Inhibitor Criteria – Migraine and Cluster Headache Prevention Approval Date: February 24, 2021 Medications Brand Names Generic Names Dosage 70 mg/mL solution single-dose prefilled syringe or auto-injector; Aimovig® erenumab-aooe 140 mg/mL prefilled syringe and autoinjector 225 mg/1.5 mL solution single-dose prefilled syringe; Ajovy® fremanezumab-vfrm 225 mg/1.5 mL autoinjector 120 mg/mL solution single-dose prefilled syringe or prefilled pen; Emgality® galcanezumab-gnlm 100 mg/mL solution single-dose prefilled syringe Vyepti™ eptinezumab-jjmr Intravenous (IV) solution: 100 mg/mL Indication Aimovig® (erenumab-aooe): A high-affinity human immunoglobulin G2 (IgG2) monoclonal antibody that targets the calcitonin gene-related peptide (CGRP) receptor, is indicated for the preventative treatment of migraine in adults. Ajovy® (fremanezumab-vfrm): A human IgG2 monoclonal antibody that targets the CGRP receptor, is indicated for the preventative treatment of migraine in adults. Emgality® (galcanezumab-gnlm): A human immunoglobulin IgG4 monoclonal antibody that targets the CGRP ligand, is indicated for the preventative treatment of migraine and episodic cluster headaches in adults. Vyepti™ (eptinezumab-jjmr): A humanized immunoglobulin G1 (IgG1) monoclonal antibody that targets the CGRP ligand and inhibits its interaction with the receptor, is indicated for the preventative treatment of migraine in adults. Proprietary & Confidential © 2003–2021 Magellan Health, Inc. All rights reserved. Magellan Medicaid Administration, part of the Magellan Rx Management division of Magellan Health, Inc. Migraine Headache Prevention Request Criteria for Approval 1. Patient has a diagnosis of migraine with or without aura based on International Classification of Headache Disorders (ICHD-III) diagnostic criteria; AND 2. -
Monoclonal Antibodies As Neurological Therapeutics
pharmaceuticals Review Monoclonal Antibodies as Neurological Therapeutics Panagiotis Gklinos 1 , Miranta Papadopoulou 2, Vid Stanulovic 3, Dimos D. Mitsikostas 4 and Dimitrios Papadopoulos 5,6,* 1 Department of Neurology, KAT General Hospital of Attica, 14561 Athens, Greece; [email protected] 2 Center for Clinical, Experimental Surgery & Translational Research, Biomedical Research Foundation of the Academy of Athens (BRFAA), 11527 Athens, Greece; [email protected] 3 Global Pharmacovigilance, R&D Sanofi, 91385 Chilly-Mazarin, France; vid.stanulovic@sanofi.com 4 1st Neurology Department, Aeginition Hospital, National and Kapodistrian University of Athens, 11521 Athens, Greece; [email protected] 5 Laboratory of Molecular Genetics, Hellenic Pasteur Institute, 129 Vasilissis Sophias Avenue, 11521 Athens, Greece 6 Salpetriere Neuropsychiatric Clinic, 149 Papandreou Street, Metamorphosi, 14452 Athens, Greece * Correspondence: [email protected] Abstract: Over the last 30 years the role of monoclonal antibodies in therapeutics has increased enormously, revolutionizing treatment in most medical specialties, including neurology. Monoclonal antibodies are key therapeutic agents for several neurological conditions with diverse pathophysio- logical mechanisms, including multiple sclerosis, migraines and neuromuscular disease. In addition, a great number of monoclonal antibodies against several targets are being investigated for many more neurological diseases, which reflects our advances in understanding the pathogenesis of these -
Anti‐Migraine Calcitonin Gene–Related Peptide Receptor
RESEARCH ARTICLE Anti-migraine Calcitonin Gene–Related Peptide Receptor Antagonists Worsen Cerebral Ischemic Outcome in Mice † † Inge A. Mulder, MSc ,1 Mei Li, PhD,1 Tessa de Vries, MSc,2 Tao Qin,1 , Takeshi Yanagisawa, MD, PhD,1 Kazutaka Sugimoto, MD, PhD ,1 Antoon van den Bogaerdt, PhD,3 A. H. Jan Danser, MD, PhD,2 Marieke J. H. Wermer, MD, PhD,4 Arn M. J. M. van den Maagdenberg, PhD,4,5 ‡ Antoinette MaassenVanDenBrink, PhD,2 Michel D. Ferrari, MD, PhD,4 and ‡ Cenk Ayata, MD, PhD1,6 Objective: Calcitonin gene–related peptide (CGRP) pathway inhibitors are emerging treatments for migraine. CGRP- mediated vasodilation is, however, a critical rescue mechanism in ischemia. We, therefore, investigated whether gepants, small molecule CGRP receptor antagonists, worsen cerebral ischemia. Methods: Middle cerebral artery was occluded for 12 to 60 minutes in mice. We compared infarct risk and volumes, collateral flow, and neurological deficits after pretreatment with olcegepant (single or 10 daily doses of 0.1–1mg/kg) or rimegepant (single doses of 10–100mg/kg) versus vehicle. We also determined their potency on CGRP-induced relaxa- tions in mouse and human vessels, in vitro. Results: Olcegepant (1mg/kg, single dose) increased infarct risk after 12- to 20-minute occlusions mimicking transient ischemic attacks (14/19 vs 6/18 with vehicle, relative risk = 2.21, p < 0.022), and doubled infarct volumes (p < 0.001) and worsened neurological deficits (median score = 9 vs 5 with vehicle, p = 0.008) after 60-minute occlusion. Ten daily doses of 0.1 to 1mg/kg olcegepant yielded similar results. -
CDER List of Licensed Biological Products With
Center for Drug Evaluation and Research List of Licensed Biological Products with (1) Reference Product Exclusivity and (2) Biosimilarity or Interchangeability Evaluations to Date DATE OF FIRST REFERENCE PRODUCT DATE OF LICENSURE LICENSURE EXCLUSIVITY EXPIRY DATE INTERCHANGEABLE (I)/ BLA STN PRODUCT (PROPER) NAME PROPRIETARY NAME (mo/day/yr) (mo/day/yr) (mo/day/yr) BIOSIMILAR (B) WITHDRAWN 125118 abatacept Orencia 12/23/05 NA NA 103575 abciximab ReoPro 12/22/94 NA NA Yes 125274 abobotulinumtoxinA Dysport 04/29/09 125057 adalimumab Humira 12/31/02 NA NA 761071 adalimumab-adaz Hyrimoz 10/30/18 B 761058 adalimumab-adbm Cyltezo 08/25/17 B 761118 adalimumab-afzb Abrilada 11/15/19 B 761024 adalimumab-atto Amjevita 09/23/16 B 761059 adalimumab-bwwd Hadlima 07/23/19 B 125427 ado-trastuzumab emtansine Kadcyla 02/22/13 125387 aflibercept Eylea 11/18/11 103979 agalsidase beta Fabrazyme 04/24/03 NA NA 125431 albiglutide Tanzeum 04/15/14 017835 albumin chromated CR-51 serum Chromalbin 02/23/76 103293 aldesleukin Proleukin 05/05/92 NA NA 103948 alemtuzumab Campath, Lemtrada 05/07/01 NA NA 125141 alglucosidase alfa Myozyme 04/28/06 NA NA 125291 alglucosidase alfa Lumizyme 05/24/10 125559 alirocumab Praluent 07/24/15 103172 alteplase, cathflo activase Activase 11/13/87 NA NA 103950 anakinra Kineret 11/14/01 NA NA 020304 aprotinin Trasylol 12/29/93 125513 asfotase alfa Strensiq 10/23/15 101063 asparaginase Elspar 01/10/78 NA NA 125359 asparaginase erwinia chrysanthemi Erwinaze 11/18/11 761034 atezolizumab Tecentriq 05/18/16 761049 avelumab Bavencio 03/23/17 -
CGRP Inhibitors
MEDICATION POLICY: CGRP Inhibitors Generic Name: N/A Preferred: Ajovy (fremanezumab-vfrm) Therapeutic or Brand Name: Calcitonin Gene- Non-preferred: Aimovig (Erenumab-aooe), Related Peptide (CGRP) Inhibitors Emgality (galcanezumab-gnlm), Nurtec (rimegepant), Ubrelvy (ubrogepant), Vypeti Applicable Drugs (if Therapeutic Class): (eptinezumab-jjmr) AimovigTM (Erenumab-aooe), AjovyTM (fremanezumab-vfrm), Emgality™ Date of Origin: 10/2/2018 (galcanezumab-gnlm), NurtecTM (rimegepant), Date Last Reviewed / Revised: 2/11/2021 Ubrelvy TM (ubrogepant), Vypeti TM (eptinezumab-jjmr) GPI Code: 6770202010, 6770203020, 6770203530, 6740654060, 6770108000, 6770201520 PRIOR AUTHORIZATION CRITERIA (May be considered medically necessary when criteria I through V are met) I. Documented diagnosis of one of the following conditions A or B and must meet criteria listed under applicable diagnosis: A. Episodic migraine headaches (4-14 migraine days per month) or chronic migraines (15 or more headache days per month with at least 8 migraine days per month) and criteria i – IV. Is met: i. Documentation of functional impairment due to episodic or chronic migraines (eg, severe pain, missed days at school or work, impaired activities of daily living). ii. Documentation of treatment failure, intolerance, or contraindication to medications from all 3 of the following drug categories A through C for prevention of episodic or chronic migraine headaches: 1. Anticonvulsants (such as Divalproex Sodium or Topiramate) 2. Beta-blockers (such as Metoprolol or propranolol) 3. Antidepressants (such as Venlafaxine or Amitriptyline) iii. Documentation that evaluation has been performed demonstrating patient does not suffer from rebound headaches due to medication overuse (medication overuse headache, or MOH). iv. Prescription is for Ajovy OR there is a clinically significant treatment failure, intolerance or contraindication to Ajovy and the prescription is for Aimovig, Emgality, or Vyepti. -
Umpqua Health Alliance List of Medication Coverage Changes
Umpqua Health Alliance List of Medication Coverage Changes (Updated 4/1/2021) INTRODUCTION The Umpqua Health Alliance (UHA) Pharmacy and Therapeutics (P&T) Committee composed of pharmacists and physicians determine which drugs should be covered, the coverage restrictions, and the PA guidelines. The goal of the P&T Committee is to create a formulary (list of covered drugs) with medications that are safe and effective and that offer the best value. Our formulary and prior authorization guidelines are usually updated quarterly. This document contains all updates made to the UHA formulary and PA guidelines since January 1, 2020. The current versions of our formulary and PA guidelines are available on the UHA Pharmacy Services webpage: https://www.umpquahealth.com/pharmacy‐services/. LEGEND The following are restriction and coverage abbreviations found in this document: ABBREVIATIONS DEFINITION EXPLANATION PA Prior Authorization Required Prior authorization (e.g. prior approval) is required before filling a prescription for this drug. Without prior authorization, we may not cover this drug. The provider must submit a request for prior authorization with the appropriate documentation (including recent chart notes) before the drug is covered. A specific PA guideline policy number beginning with “RX” may be referenced in the “Description” column. Visit the UHA Pharmacy Services webpage for our PA guidelines: https://www.umpquahealth.com/pharmacy‐services/. ST Step Therapy Restriction We require trial and failure of one or more lower‐cost or preferred drug(s) (“Step 1 drug”) before using the more expensive or non‐preferred drug (“Step 2 drug”). If it is medically necessary for a member to use a Step 2 drug first, the prescriber will need to submit a request for prior authorization.