Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Introduction to Biosimilars A Clinician’s Perspective Steven Lucio, PharmD, BCPS December 9, 2015 1 ©2014 Novation Confidential. Question #1: Why Do We Need Biosimilars? 2 ©2014 Novation Confidential. Medication Costs in the US Continue to Increase! SURPRISE!?!?!!? • Spending on pharmaceuticals reached $374 billion, an increase of 13.1% • Largest increase since 2001 • Price increases for “protected” brands increased spending $26.3 billion • Compared to $11.9 billion lower spending due to loss of patent exclusivity Report available at: www.imshealth.com/portal/site/imshealth/menuitem.762a961826aad98f53c7 53c71ad8c22a/?vgnextoid=3f140a4331e8c410VgnVCM1000000e2e2ca2R CRD&vgnextchannel=736de5fda6370410VgnVCM10000076192ca2RCRD& vgnextfmt=default, accessed, October 31, 2015. 3 ©2014 Novation Confidential. • New medicines for hepatitis C, multiple sclerosis, cancer, and diabetes drove over $21 billion in increased spending How Much Have Drug Prices Increased? (Oncology Example) • Letter from 118 physicians of the Mayo Clinic, calling for lower prices of oncology drugs • In the US, the average price of new cancer drugs increased 5- to 10- fold over 15 years, to more than $100,000 per year in 2012. • The cost of drugs for each additional year lived (after adjusting for inflation) has increased from $54,000 in 1995 to $207,000 in 2013. • In 2014, all new FDA approved cancers drugs were priced above $120,000 per year of use. 4 ©2014 Novation Confidential. Mayo Clin Proc. 2015;90:996-1000. The Value of Generic Drugs • From 2004 to 2013, generic drugs have saved the U.S. health system approximately $1.5 trillion • $239 billion saved in 2013 alone • $140 billion saved in 2013 due to new generic introductions • 86% of prescriptions dispensed in the US are filled with generic drugs Report available at www.gphaonline.org/media/cms/GPhA_ Savings_Report.9.10.14_FINAL.pdf, accessed October 31, 2015 5 ©2014 Novation Confidential. Top Pharmaceutical Sales (2010) When Small Molecule Drugs Dominated Drug Spend Drug US Sales (millions) 1 SM Clopidogrel (Plavix®) $6,154 2 SM Atorvastatin (Lipitor®) $5,329 3 SM Fluticasone/ salmeterol inhaler (Advair®) $4,026 4 SM Aripiprazole (Abilify®) $3,606 5 SM Pioglitazone (Actos®) $3,582 6 B Etanercept (Enbrel®) $3,304 7 SM Montelukast (Singulair®) $3,219 8 SM Quetiapine (Seroquel®) $3,107 9 B Infliximab (Remicade®) $3,099 10 B Bevacizumab (Avastin®) $3,068 SM = small molecule drug, B = biologic drug EvaluatePharma. Available at info.evaluategroup.com/rs/evaluatepharmaltd/images/SV2014.pdf. Accessed July 2015. Top Pharmaceutical Sales (2014) Biologics Now Represent More Top Spend Pharmaceuticals Drug US Sales (millions) 1 SM Sofosbuvir (Sovaldi®) $10,098 2 B Adalimumab (Humira®) $6,078 3 SM Glargine insulin (Lantus®) $5,759 4 B Etanercept (Enbrel®) $4,311 5 B Infliximab (Remicade®) $4,154 6 SM Aripiprazole (Abilify®) $3,886 7 B Rituximab (Rituxan®) $3,707 8 B Pegfilgrastim (Neulasta®) $3,523 9 SM Fluticasone/ salmeterol (Advair®) $3,325 10 B Bevacizumab (Avastin®) $2,928 SM = small molecule drug, B = biologic drug EvaluatePharma. Available at info.evaluategroup.com/rs/evaluatepharmaltd/images/SV2014.pdf. Accessed July 2015. Question #2: When can we Expect the First Generic Biologic Drug? Answer: It’s complicated! 8 ©2014 Novation Confidential. While Many Biologic Drugs Are Nearing The End of Their Exclusivities Global Sales 2013, US$ Billion 9.1 Adalimumab (Humira) Etanercept (Enbrel) Infliximab (Remicade) Insulin Glargine (Lantus) Rituximab (Mabthera) Bevacizumab (Avastin) Interferon Beta-1A (Avonex,… Trastuzumab (Herceptin) Glatiramer Acetate (Copaxone) Ranibizumab (Lucentis) Pegfilgrastim (Neulasta) 7.7 7.5 7.1 6.2 5.6 5.4 5.1 4.7 4.2 4.2 EU Expiry Date US Expiry Date 2018 2016 2015 2028 2015 2018 Expired Expired Expired 2016 2019 2017 Expired Expired Expired 2019 2015 Expired 2016 2016 2015 Expired 0 1 2 3 4 5 6 7 8 9 10 Adapted from IMS Health. http://www.imshealth.com/deployedfiles/imshealth/Global/Content/Healthcare/ Life%20Sciences%20Solutions/Generics/IMSH_Biosimilars_WP.pdf. Accessed June 2015. 9 ©2014 Novation Confidential. Biologic Drugs are Much More Complex Molecules Aspirin N Engl J Med 2011;365:385-388. 10 ©2014 Novation Confidential. Monoclonal antibody biologic Biologics Are More Difficult to Manufacture (and Subject to Variability) Small molecule drugs Biologic medications • Well understood organic medicinal chemistry reactions • Very complex manufacturing steps that require various stages of purification, production, and validation • Since the product is less complicated, easier to ensure structure is not altered due to manufacturing changes • Given simplicity of the molecules, it is possible to create a “generic” or bioequivalent version. • Rely on living organisms • Any modification can alter the final structure and function of the protein • Due to the size, complexity, and inherent variability of biologics, can only create “highly similar” or “biosimilar” version of originator molecule. NCCN biosimilars white paper, J Natl Compr Canc Netw. 2011;9(suppl 4):S1-S22. 11 ©2014 Novation Confidential. Due to Differences in Small Molecules and Biologics, Different Legislation Was Needed Hatch-Waxman, 1984 Biosimilars Act, 2010 http://www.gpo.gov/fdsys/pkg/STATUTE-98/pdf/STATUTE-98-Pg1585.pdf; http://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/UCM216146.pdf 12 ©2014 Novation Confidential. Question #3: How easy will it be to adopt and use biosimilars? Answer: That’s a great question! 13 ©2014 Novation Confidential. Differentiating Generics and Biosimilars Key Attributes Generics Biosimilars Approval No clinical trials required Must conduct at least one trial Indications (Uses) Same as originator May not include all indications Same generic name Yes Probably not Interchangeable Yes, upon approval Possible, but not granted immediately Cost to develop $1 to $4 million $100 to $250 million Price discounts 50% to 90% 15% to 30% Formulary Review Required No Yes Role of the Branded Company Limited or non-existent Prominent Lucio SD, Stevenson JG, Hoffman JM. Biosimilars: implications for health-system pharmacists. Am J Health Syst Pharm. 2013;70(22):2004-2017. 14 ©2014 Novation Confidential. The Mystery of Interchangeability Biosimilar Interchangeability (per FDA) Means • The interchangeable biosimilar can be expected to produce the same clinical result in any given patient, • Can be substituted without the intervention of the health care provider (states may have different ideas) • For a biological administered more than once to a patient, the is no greater risk of switching or alternating between products (biosimilar and originator), than using the originator without switching http://www.fda.gov/Drugs/DevelopmentApprovalProcess/HowDrugsareDevelopedandApproved/ApprovalApplications/Thera peuticBiologicApplications/Biosimilars/ucm241719.htm The Mystery of Interchangeability What Do We Mean By Generic Interchangeability • Generic drug – A drug that is identical – or bioequivalent – to a brand name drug in dosage form, safety, strength, route of administration, quality, performance characteristics and intended use. • “Therapeutic equivalence” code (ie. “A” rating) • Metformin, simvastatin, linezolid, vancomycin Understanding Generic Drugs, www.fda.gov The Mystery of Interchangeability Can all Generic Drugs be Substituted? • Critical dose drugs – Drugs in which comparatively small differences in dose or concentration may lead to serious therapeutic failures and/or serious drug reactions • Examples • Coumadin vs. warfarin • Prograf vs. tacrolimus • Anti-seizure medications ACCF/AHA 2011 Health Policy Statement on Therapeutic Interchange and Substitution, available at: http://circ.ahajournals.org/content/124/11/1290.extract Examples of Therapeutic Interchange Of Distinct Molecules Non-acute setting Acute care/Hospital setting • Diabetes • Topic agents to prevent of slow bleeding (i.e. thrombins) • Insulins • Inhalers • Asthma • COPD • Cholesterol • Statins • PCSK9 inhibitors? • Human growth hormone • Intravenous immune globulins • Injectable and oral anticoagulants • Antifungals • Echinocandins • Lipid amphotericin B • Injectable antibiotics Where do biosimilars fit on the continuum of interchangeability and substitution? 18 ©2014 Novation Confidential. How Much Progress Have We Made in the Last Five Years? • One official biosimilar approved • Filgrastim-sndz (Zarxio; Sandoz), competing version of branded product Neupogen (filgrastim; Amgen) • Six other biosimilar applications pending before the Food and Drug Administration; one application received complete response letter • Many unknowns remain • When will additional biosimilars be approved? • Will more complex biosimilars be approved for all of the uses of the branded biologic? • What will biosimilars be called? (naming) • What information is required to deem a biosimilar interchangeable? • How will FDA’s decision align with actions of state legislatures? • How will biosimilars be labeled? Novartis (press release), September 3, 2015; The Pink Sheet, Pending Biosimilar FDA Performance Tracker, accessed December 1, 2015.; http://www.fiercebiotech.com/story/novartis-comes-enbrel-latest-biosimilar-shot-amgen/2015-10-02 19 ©2014 Novation Confidential. Challenges for Physicians and Others • Lack of familiarity with the biosimilar paradigm and the processes for biologic manufacturing and approval • Differences between small molecule drugs and biologics • Inherent variability of all biologics (branded and biosimilar) • Understanding of the biosimilar approval pathway • Appropriate extrapolation of indications • Absence of final definition for critical biosimilar attributes • In the absence of definition, many organizations attempting to define the narrative of biosimilars • Acceptance of the biosimilar paradigm includes a willingness to trust more in analytical evaluation rather than relying solely on clinical studies • Many aspects of the financial attributes of biosimilars (costs and reimbursements) remain to be defined 20 ©2014 Novation Confidential. Challenge (Sorting Through the Messages) • Branded Companies • Genentech • Hospira • AbbVie • Teva • Janssen Biotech • Sandoz • Pfizer • Apotex • Amgen 21 • Generic Companies ©2014 Novation Confidential. Biosimilar Companies? • Teva • Sandoz • Amgen • Pfizer • Baxalta • Celltion The “Biosimilar” Pyramid Clinical Animal Studies Clinical Immunogenicity …the less you should have to do here. Clinical Knowledge (e.g., Post-Market Experience) The more work you do here… Human Pharmacokinetics and Pharmacodynamics Structural and Functional Characterization Adapted from FDA Webinar: Biosimilar Biological Products 22 ©2014 Novation Confidential. Biosimilars Balancing Act How do clinicians become comfortable relying on analytical data to greater extent? Clinical Analytical Summary • The biosimilar pathway continues to progress, even though at a less than desirable pace. • The increasing costs of pharmaceuticals necessitate that a concerted and continued effort be made to support biosimilar introduction and use in order to create competition and lower comparative expense for similar biologic drugs. • Health care organizations and providers will have to invest greater resources to biosimilar evaluation prior to use than what currently occurs with generic drugs. • Regulatory, legal, financial, and clinical practice factors will all influence the extent to which biosimilars are truly viable in the US. 24 ©2014 Novation Confidential.