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Explore some of our expert contributions, media coverage, and related content that showcased our commitment to helping our biopharma partners accelerate product success. 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In 2020, Xcenda evaluated the formulary exclusion lists of the 3 PBMs and found that the their standard formularies excluded almost 850 unique prescription drugs that year. Since then, the pace of formulary exclusions has continued at an astonishing rate. Download the white paper below to learn about the proliferation of PBM exclusions and their implications for patient access.","img":{"alt":"AB abstract","src":"-/media/assets/xcenda/english/images/01-home-page-new-images/gettyimages-1139001612_rgb_large_jpg-(2).jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/skyrocketing-growth-pbm-formulary-exclusions-concerns-patient-access","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Skyrocketing growth in PBM formulary exclusions continues to raise concerns about patient access"},"categories":["affordability","commercialization","legislation","managed care","policy","product access","regulatory"],"segments":[],"timestamp":637889934700000000,"title":"skyrocketing growth in pbm formulary exclusions continues to raise concerns about patient access"},{"card":{"key":"44d1bac7-b3d6-46c9-a148-ddc54d81b7eb","authorName":"Tasmina Hydery","authorCompany":"","date":"June 2022","description":"Download the webinar slides from the Xcenda and FormularyDecisions discussion: “Navigating Reimbursement and Access Challenges for Novel Cell and Gene Therapies.” ","img":{"alt":"abstract lines ","src":"-/media/assets/xcenda/english/images/insights/ab-colors-abstract-lines.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/webinar-slides-navigating-reimbursement-and-access-challenges-for-novel-cell-and-gene-therapies","linkText":"Download slides","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Webinar slides: Navigating Reimbursement and Access Challenges for Novel Cell and Gene Therapies"},"categories":["cell and gene therapy","commercialization","market access"],"segments":[],"timestamp":637914326220000000,"title":"webinar slides: navigating reimbursement and access challenges for novel cell and gene therapies"},{"card":{"key":"1eb52eae-fe07-4653-a1d0-769a54a4d8ab","authorName":"Xcenda","authorCompany":null,"date":"June 2021","description":"In January 2021, Xcenda developed a model to estimate the number of fewer hospitalizations, intensive-care unit admissions, and deaths if the prevalence of obesity were reduced at the start of the pandemic. We refreshed the model to include adverse outcomes due to COVID-19 as of April 2021. The results are sobering: if the prevalence of obesity were reduced by 25% at the start of the pandemic, the US would have had 119,000 fewer hospitalizations, almost 45,000 ICU admissions, and 65,000 fewer deaths.

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","img":{"alt":"image of a patient with alopecia areata","src":"-/media/assets/xcenda/english/images/insights/aa_image.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/alopecia-areata-a-global-perspective-of-a-disease-that-extends-beyond-hair-loss","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Alopecia areata: A global perspective of a disease that extends beyond hair loss"},"categories":["advocacy","commercialization","managed care","policy","market access"],"segments":[],"timestamp":637927514400000000,"title":"alopecia areata: a global perspective of a disease that extends beyond hair loss"},{"card":{"key":"ad91ba77-cb69-43e1-b194-501789a50fe5","authorName":"Xcenda","authorCompany":null,"date":"May 2022","description":"The National Institute for Health and Care Excellence (NICE) recently published two new health technology assessment (HTA) manuals detailing updates and changes in the way it carries out the evaluation of health technologies. 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New NICE HTA manuals"},"categories":[],"segments":[],"timestamp":637883064600000000,"title":"the answer to the ultimate question of life, the universe, and everything? new nice hta manuals"},{"card":{"key":"8f237cd6-59f8-4fdf-be7e-c6355eab8bbe","authorName":"Amanda OHora","authorCompany":"","date":"July 2022","description":"Cell and gene-based therapies (CGTs) have captured our imagination for their potential to cure disease after a single course of therapy but have also raised eyebrows for their astronomical price tags.","img":{"alt":"Business meeting","src":"-/media/assets/gnp/images/01-home-page-new-images/home-page-service-images/business-meeting.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/navigating-reimbursement-and-access-challenges-for-novel-cell-and-gene-therapies","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Navigating reimbursement and access challenges for novel cell and gene therapies"},"categories":["cell and gene therapy","reimbursement"],"segments":[],"timestamp":637934028190000000,"title":"navigating reimbursement and access challenges for novel cell and gene therapies"},{"card":{"key":"0aae6981-27d4-4879-af4f-7be8cac19595","authorName":"Xcenda","authorCompany":null,"date":"August 2020","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-fall-2020-hta-policy-market-access-south-korea","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Feature Article: 20 Years After the National Health Insurance Act, HTA Policy Changes Reshape Market Access in South Korea"},"categories":["market access","policy"],"segments":[],"timestamp":637334556000000000,"title":"feature article: 20 years after the national health insurance act, hta policy changes reshape market access in south korea"},{"card":{"key":"a71c88b0-4a81-4d7e-9e42-05a0882b1c0f","authorName":"Xcenda","authorCompany":null,"date":"May 2023","description":"Is artificial intelligence (AI) set to take over the world? In this article, we reflect on an interview we conducted with one of the current AI tools, in which we explored its “knowledge” of and potential role in health technology assessment (HTA).","img":{"alt":"HTAQ AI File 1","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-ai-file-1.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2023-ai-and-hta","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Reflections on an interview with a ghost "},"categories":[],"segments":[],"timestamp":638185384200000000,"title":"reflections on an interview with a ghost "},{"card":{"key":"bd49b044-70ca-4a60-8bfe-8b6133cb39a7","authorName":"Xcenda","authorCompany":null,"date":"February 2021","description":"Real-world evidence (RWE) has garnered increased attention in recent years to advance drug development. The framework for the Food and Drug Administration’s (FDA’s) RWE Program, published in 2018, serves as a roadmap for the inclusion of real-world data (RWD) and RWE in regulatory decisions, including standards on how RWD are defined, collected, and analyzed. This article reviews the use of RWE in United States (US) regulatory decisions after the publication of the FDA’s RWE framework and describes how manufacturers can leverage RWE to optimize their product launch. ","img":{"alt":"Man with digital corporate symbols ","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-spring-2021/shutterstock_1048013563.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-spring-2021-rwe-us-regulatory-decisions","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Real-world evidence in United States regulatory decisions "},"categories":[],"segments":[],"timestamp":637498656600000000,"title":"real-world evidence in united states regulatory decisions "},{"card":{"key":"b5ba0654-ba59-4cbc-856a-b07cc7d54ad9","authorName":"AmerisourceBergen","authorCompany":null,"date":"November 2022","description":"The right global market access partner will move beyond talk and into action. 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This article discusses ICER’s approach to the UPI assessment, considerations for manufacturers, and reactions from stakeholders.","img":{"alt":"Abstract figure pushing pill up with US dollar sign","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-fall-2021/htaq_fall_2021-_valq_icer_article_image.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-fall-2021-valq-icer","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Elucidating ICER’s methodologies for Unsupported Price Increase assessments "},"categories":["commercialization","analytics","market access","managed care","policy","product access","regulatory"],"segments":[],"timestamp":637656778200000000,"title":"elucidating icer’s methodologies for unsupported price increase assessments "},{"card":{"key":"657999c2-1f5b-4744-b757-93902b8bfcd7","authorName":"Tasmina Hydery; Sara Linnerooth","authorCompany":"","date":"March 2022","description":"Discussing the transition of going from platform users to employees of FormularyDecisions with the power to affect change.","img":{"alt":"Coworkers at meeting","src":"-/media/assets/xcenda/english/images/insights/gettyimages-1179568324_srgb_jpg-(1).jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/6-insights-driving-formularydecisions-evolution","linkText":"Read more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Six insights driving the evolution of FormularyDecisions®"},"categories":["market access","product access","technology"],"segments":[],"timestamp":637843252400000000,"title":"six insights driving the evolution of formularydecisions®"},{"card":{"key":"bd9d6eba-3ac7-40a3-88ad-a6bca8e1c68d","authorName":"Xcenda","authorCompany":null,"date":"May 2022","description":"The Institute for Clinical and Economic Review (ICER) explores the “Grand Bargain” in a recently published assessment of fair access criteria among select US health plans. As predicted, plans may fall short in offering fair cost-sharing to patients. However, biopharma companies can encourage fair access by communicating a comprehensive product value proposition.","img":{"alt":"White tablet pc and access security concept on media screen","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/shutterstock_568790215.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2022-supporting-access-with-a-comprehensive-value-proposition","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Do fair prices lead to fair access? Supporting access with a comprehensive value proposition to bridge the gap"},"categories":[],"segments":[],"timestamp":637883182800000000,"title":"do fair prices lead to fair access? supporting access with a comprehensive value proposition to bridge the gap"},{"card":{"key":"1faea7bd-1efb-44a5-a365-cefe0c073144","authorName":"Xcenda","authorCompany":null,"date":"August 2021","description":"Increasingly the US healthcare system is acknowledging that there is an need to consider and address health disparities and healthcare inequality. A logical place to start is with payers and the tools they are using to make coverage decisions. Xcenda reviewed reports from several value assessment frameworks to determine if they considered health disparities in their framework. 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How can manufacturers avoid common pitfalls on the journey toward product success? Strategic Partnerships for Unlocking Product Potential explores how manufacturers can benefit from integrated commercialization solutions. 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To evaluate the impact of government-mandated price reductions on coverage and patient affordability and access, Xcenda surveyed advisors from health plans, integrated delivery networks (IDNs), and pharmacy benefit managers (PBMs) and asked questions about the impact of government price regulation on access, including cost-sharing and benefit design. 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Manufacturers offering copay assistance for medical benefit products will need to stay aware of these trends and closely monitor the impact these policies may have on their brand and the programs that serve their patients. Xcenda recently conducted research to find out how copay accumulator programs are currently being applied and possible trends in the future. 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","img":{"alt":"Globe with communication lines from UK","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-winter-2021/htaqwinter2021_nice_image.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-winter-2021-nice-becoming-nicer","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Is NICE becoming nicer?"},"categories":["market access","product access","regulatory","commercialization","data"],"segments":[],"timestamp":637732956000000000,"title":"is nice becoming nicer?"},{"card":{"key":"52dea110-5672-4507-96c2-14025ee5eb9c","authorName":"Xcenda","authorCompany":null,"date":"October 2022","description":"In this issue our editors provide insights on the new European Union Health Technology Assessment regulation, the United Kingdom's Innovative Licensing and Access Pathway, and the drug reimbursement environment in Canada.","img":{"alt":"HTA Quarterly Logo","src":"-/media/assets/xcenda/german/images/home---about-us/xcenda_2_3_card-02.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-winter-2022-summary-page","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"HTA Quarterly | Winter 2022"},"categories":["market access","regulatory","reimbursement","commercialization"],"segments":[],"timestamp":638023899600000000,"title":"hta quarterly | winter 2022"},{"card":{"key":"29a49b49-9419-48e2-900e-2005e8f004b5","authorName":"Xcenda","authorCompany":null,"date":"October 2019","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-fall-2019-summary-page","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"HTA Quarterly | Fall 2019"},"categories":["market access","commercialization"],"segments":[],"timestamp":637079292000000000,"title":"hta quarterly | fall 2019"},{"card":{"key":"56c2cb96-9028-4cd9-814a-052efc15a1ca","authorName":"Xcenda","authorCompany":null,"date":"May 2020","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2020-emerging-gene-therapies-hemophilia-us-value-drivers","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Emerging Gene Therapies for Hemophilia in the United States—Value Drivers in a Crystal Ball"},"categories":["analytics","cell and gene therapy","commercialization","market access"],"segments":[],"timestamp":637254684000000000,"title":"emerging gene therapies for hemophilia in the united states—value drivers in a crystal ball"},{"card":{"key":"cafc4054-288a-4708-bacd-0de63710aac0","authorName":"Xcenda","authorCompany":null,"date":"May 2021","description":"","img":{"alt":"vaccines on top of US dollars","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-summer-2021/htaq_vaccines.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2021-value-vaccines-hta-perspective","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Assessing the value of vaccines: Considerations from the HTA perspective"},"categories":[],"segments":[],"timestamp":637564608000000000,"title":"assessing the value of vaccines: considerations from the hta perspective"},{"card":{"key":"3ec87561-84d9-4b67-a716-224c1b15988d","authorName":"Xcenda","authorCompany":null,"date":"January 2017","description":"It is not uncommon for a single health technology to have clinical benefit in multiple indications or patient populations. The magnitude of clinical benefit and value of a technology may vary substantially across indications, which can complicate pricing strategies. Indication-specific pricing (ISP) of health technologies, however, may better align reimbursement with value. In this article, we describe models in which ISP may be implemented, and the pricing policies and use of ISP in France, Germany, Italy, Spain, the United Kingdom (UK) (EU-5), and the United States (US).","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-winter-2017-indication-specific-pricing","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Indication-specific Pricing: What should manufacturers expect in key markets"},"categories":["commercialization","market access"],"segments":[],"timestamp":636204327000000000,"title":"indication-specific pricing: what should manufacturers expect in key markets"},{"card":{"key":"af4a2c8e-a375-45fa-beef-011503680515","authorName":"Xcenda","authorCompany":null,"date":"May 2020","description":"Technology has the potential to make healthcare delivery more effective, efficient, and patient-centric through improved access to an abundance of data. As digital health technology (DHT) innovations become increasing inseparable from healthcare, a paradigm shift is imminent. This article examines the opportunities and challenges for mobile health (mHealth).","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2020-era-mhealth-global-perspective","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"The Era of mHealth: A Global Perspective"},"categories":["analytics","commercialization","market access"],"segments":[],"timestamp":637254576000000000,"title":"the era of mhealth: a global perspective"},{"card":{"key":"284f258a-8d03-452c-a5c6-2379e7763921","authorName":"Xcenda","authorCompany":null,"date":"August 2017","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2017-colombia-a-unique-universal-healthcare-model-in-latin-america","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Understanding the Columbian Health Care Market"},"categories":["commercialization","market access"],"segments":[],"timestamp":636379271400000000,"title":"understanding the columbian health care market"},{"card":{"key":"5cb36cf6-d7ad-44bc-84fe-10726c259dd5","authorName":"Xcenda","authorCompany":null,"date":"August 2017","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2017-duchenne-muscular-dystrophy-new-and-revitalized-drugs-bring-hope-to-patients","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"HTAQ Summer 2017 Duchenne Muscular Dystrophy New and Revitalized Drugs Bring Hope to Patients"},"categories":["commercialization","market access","orphan drugs"],"segments":[],"timestamp":636379200000000000,"title":"htaq summer 2017 duchenne muscular dystrophy new and revitalized drugs bring hope to patients"},{"card":{"key":"51d7dff3-9f5b-446f-977d-012dafb896d8","authorName":"Xcenda","authorCompany":null,"date":"October 2016","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-fall-2016-rapid-access-in-the-us-uk-france","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Rapid Access in the US, UK, and France"},"categories":["commercialization","market access"],"segments":[],"timestamp":636119697600000000,"title":"rapid access in the us, uk, and france"},{"card":{"key":"7264d941-4a16-4a9f-a0b5-e9b4c3a14128","authorName":"Xcenda","authorCompany":null,"date":"February 2023","description":"For many rural populations, cancer mortality is not decreasing; it is steady and, in some cases, rising. This issue brief seeks to compare the rates of diagnosed cancers in metropolitan vs non-metropolitan areas to help quantify the disparity in cancer burden for patients living in non-metro areas.","img":{"alt":"Rural landscape","src":"-/media/assets/xcenda/english/images/insights/rural-landscape.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/cancer-disproportionately-impacts-adults-living-in-rural-areas","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Cancer disproportionately impacts adults living in rural areas"},"categories":[],"segments":[],"timestamp":638108814710000000,"title":"cancer disproportionately impacts adults living in rural areas"},{"card":{"key":"f28a3625-ea3c-4996-8ebc-162012db6b63","authorName":"Xcenda","authorCompany":null,"date":"September 2018","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2018-japan-novel-cost-effectiveness-submission-requirement","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Japan’s Ongoing Shift From a Traditional Reimbursement Assessment to a Novel Cost-Effectiveness Submission Requirement"},"categories":[],"segments":[],"timestamp":636723739800000000,"title":"japan’s ongoing shift from a traditional reimbursement assessment to a novel cost-effectiveness submission requirement"},{"card":{"key":"bde5d60b-07bb-4bb8-a7c0-1ce350441281","authorName":"Xcenda","authorCompany":null,"date":"November 2021","description":"Atherosclerotic cardiovascular disease (ASCVD) is insidiously common—it is the leading cause of death in the US and the underlying cause in about 50% of all deaths in Western societies. It is known more commonly by its myriad and negative outcomes, including myocardial infarction (MI), angina, stroke/transient ischemic attack, peripheral artery disease, heart failure, and atrial fibrillation, than by the collective term ASCVD. Unfortunately, there is no magic bullet to improve outcomes. Many of the first-line prescription drugs to lower risk factors for ASCVD are low-cost generics and thus have broad coverage among payers. Despite the easy access to high-value drugs, there are persistent gaps in adherence. Other patients with adverse outcomes simply do not respond—or respond well—to the available therapies, despite fully complying with their physicians’ instruction. This biologic basis for a less-than-average response shows the need and opportunity for continued innovation to develop treatments for the spectrum of people with ASCVD. Read Xcenda’s white paper for our analysis about the need for continued innovation to treat ASCVD.","img":{"alt":"abstract waves","src":"-/media/assets/xcenda/english/images/01-home-page-new-images/gettyimages-1153883015_rgb_large_jpg.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/ascvd-needs-innovation","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"ASCVD needs innovation"},"categories":["innovation","managed care","medication adherence","patient care","product access","commercialization","advocacy"],"segments":[],"timestamp":637715364000000000,"title":"ascvd needs innovation"},{"card":{"key":"a709d216-db35-4ec0-8327-b4021a56ae3a","authorName":"Lung-I Cheng","authorCompany":"Biopharma Services","date":"April 2023","description":"","img":{"alt":"insights","src":"-/media/assets/amerisourcebergen/insights/gettyimages-1158524088-rt-rgb_jpg.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/three-opportunities-and-three-challenges-in-the-cell-and-gene-therapy-market","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Three opportunities and three challenges in the cell and gene therapy market"},"categories":["cell and gene therapy"],"segments":[],"timestamp":638180419180000000,"title":"three opportunities and three challenges in the cell and gene therapy market"},{"card":{"key":"40045d25-a192-4ee5-9a83-89bbf86d8b3d","authorName":"Xcenda","authorCompany":null,"date":"August 2020","description":"By the numbers: Field reimbursement and access support for pharmaceutical products in the new normal of COVID-19.","img":{"alt":"Male doctor speaking to patient on a tablet","src":"-/media/assets/xcenda/english/images/insights/telehealth.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/solving-access-reimbursement-and-pap-awareness-problems","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Solving access, reimbursement, and PAP awareness problems"},"categories":["reimbursement","patient support services","covid-19","product access","market access"],"segments":[],"timestamp":637338783070000000,"title":"solving access, reimbursement, and pap awareness problems"},{"card":{"key":"2ab34e20-124f-43f7-af7a-855de9350f16","authorName":"Xcenda","authorCompany":null,"date":"September 2017","description":"Medical nutritional therapy (MNT) is intended to meet specific nutritional requirements of a disease or condition that cannot be met by normal foods alone and should be used only under medical supervision. MNT can serve as the sole source of nourishment for prolonged periods, with balanced nutritional composition of macro- and micro-nutrients that reflect dietary recommendations. We examine the reimbursement landscape for this non-drug therapy option.","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-late-summer-2017-medical-nutritional-therapy","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Medical Nutritional Therapy: Achieving Reimbursement Across the Globe for Unique Non-drug Therapy Options"},"categories":["market access"],"segments":[],"timestamp":636416297400000000,"title":"medical nutritional therapy: achieving reimbursement across the globe for unique non-drug therapy options"},{"card":{"key":"64d2a14e-fb7e-437b-830d-c749a92d8a4d","authorName":"Xcenda","authorCompany":null,"date":"March 2023","description":"President Joe Biden signed the Inflation Reduction Act (IRA) into law in August 2022. Since then, many in biopharma have been assessing how the law might affect drug pricing and drug spending. Even though several components of the IRA's drug pricing measure go into effect in 2023, several outstanding questions for biopharma still remain. Join AmerisourceBergen's Jennifer Snow, Vice President of Market Economics, and Corey Ford, Vice President of Reimbursement and Policy Insights, as they discuss what's next for IRA.
","img":{"alt":"An abstract image with colorful waves","src":"-/media/assets/amerisourcebergen/dei/dei-health-equity-carousel-full-image-abstract-4.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/webinar-ira-update-key-considerations-for-2023","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Webinar: IRA Update: Key considerations for 2023"},"categories":["policy"],"segments":[],"timestamp":638143281140000000,"title":"webinar: ira update: key considerations for 2023"},{"card":{"key":"50f0991e-4480-47a3-879e-1ebc32f39681","authorName":"Xcenda","authorCompany":null,"date":"June 2023","description":"The Part B Home Infusion Therapy benefit addresses some gaps but has provider qualifications and excludes drug and pump coverage. For a comprehensive understanding of access options, download this white paper for valuable insights.","img":{"alt":"Abstract","src":"-/media/assets/amerisourcebergen/about-us/abstract.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/reimbursement-considerations-for-home-infusions","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Reimbursement considerations for home infusions"},"categories":["commercialization","consulting","managed care","reimbursement"],"segments":[],"timestamp":638213086680000000,"title":"reimbursement considerations for home infusions"},{"card":{"key":"e99c7d52-9d41-47f5-9bab-0e024056eb50","authorName":"Xcenda","authorCompany":null,"date":"October 2016","description":"","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-fall-2016-singapore-worlds-most-efficient-healthcare-systems","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Singapore: Key Insights Into One of the World’s Most Efficient Healthcare Systems"},"categories":[],"segments":[],"timestamp":636119836200000000,"title":"singapore: key insights into one of the world’s most efficient healthcare systems"},{"card":{"key":"a3b05bd0-7e91-45ed-883a-4f430f9fe832","authorName":"Xcenda","authorCompany":null,"date":"November 2022","description":"Establishment of the Danish Medicines Council (DMC) in 2017 was intended to ensure transparent assessment of hospital medicines and rapid, consistent access to effective medicines across Denmark, while balancing healthcare costs against demand. Five years later, we consider what impact the DMC has had on market access and implications for drug developers.","img":{"alt":"Danish Pig","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-winter-2022/danish-pig.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-winter-2022-hta-market-access-denmark","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Has mandatory HTA improved access to new medicine in Denmark? Learnings from the first 5 years with the Danish Medicines Council"},"categories":[],"segments":[],"timestamp":638034689400000000,"title":"has mandatory hta improved access to new medicine in denmark? learnings from the first 5 years with the danish medicines council"},{"card":{"key":"2d77a076-cba3-44f3-8d07-c835119377c9","authorName":"Xcenda","authorCompany":null,"date":"February 2021","description":"In this issue, our editors examine how real-world evidence impacts regulatory decisions in the United States, the current state of reimbursement for Advanced Therapy Medicinal Products (ATMPs) in Germany, and a look at two value assessment frameworks, Innovation and Value Initiative (IVI) and the Institute for Clinical and Economic Review (ICER).","img":{"alt":"Xcenda_2_3_Card-02","src":"-/media/assets/xcenda/english/images/xcenda_2_3_card-02.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-spring-2021-summary-page","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"HTA Quarterly | Spring 2021"},"categories":[],"segments":[],"timestamp":637498640400000000,"title":"hta quarterly | spring 2021"},{"card":{"key":"a665311e-1dcf-4c54-ac80-d9ad937f1e49","authorName":"Xcenda","authorCompany":null,"date":"September 2022","description":"","img":{"alt":"Patient support services","src":"-/media/assets/amerisourcebergen/insights/images-for-insights/gettyimages-1055509742_srgb_jpg.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/youve-created-a-good-patient-support-program-now-make-it-great","linkText":"Watch on demand","hasImage":true,"isImageMode":true,"label":"Insight","headline":"On-demand webinar: You’ve created a good patient support program, now make it great"},"categories":["commercialization","marketing","patient support services"],"segments":[],"timestamp":638001437840000000,"title":"on-demand webinar: you’ve created a good patient support program, now make it great"},{"card":{"key":"5a62053c-5706-4191-9d96-455f73f3d580","authorName":"Xcenda","authorCompany":null,"date":"May 2023","description":"Project Orbis was launched by the FDA Oncology Center of Excellence to facilitate faster patient access to innovative cancer therapies in multiple countries. Leveraging a consortium of participating countries, Project Orbis aims for concurrent submission, review, and regulatory action for high-impact clinically significant marketing applications among participating countries. ","img":{"alt":"htaq project orbis","src":"-/media/assets/xcenda/english/images/hta-quarterly-images/htaq-project-orbis.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2023-project-orbis","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Project Orbis: A three-year review"},"categories":[],"segments":[],"timestamp":638185383600000000,"title":"project orbis: a three-year review"},{"card":{"key":"401301ec-d01e-4d7b-8407-fd80b5a02008","authorName":"AmerisourceBergen","authorCompany":null,"date":"May 2023","description":"","img":{"alt":"Amerisourcebergen representatives at Asembia","src":"-/media/assets/amerisourcebergen/manufacturer/asembia-hero.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/recap-asembia-2023","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Recap Asembia 2023: Our impactful contributions to the premier specialty pharmacy conference"},"categories":["commercialization","commercial supply chain","cell and gene therapy","biosimilars","consulting","distribution","specialty pharmacy"],"segments":[],"timestamp":638188891230000000,"title":"recap asembia 2023: our impactful contributions to the premier specialty pharmacy conference"},{"card":{"key":"5307c4e7-ce63-4f92-b79c-6f871d9b6cb4","authorName":"Xcenda","authorCompany":null,"date":"January 2022","description":"Xcenda and FormularyDecisions joined AMCP for a live webinar on January 19, 2022 titled, “Bridging the HCEI Divide – Insights on an Effective Healthcare Economic Information (HCEI) Exchange.”","img":{"alt":"AB-Business-Meeting-2_RGB_card","src":"-/media/assets/sustainability/images/ab-business-meeting-2_rgb_card.png?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/bridging-the-hcei-divide-webinar","linkText":"Download slides","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Webinar: Bridging the HCEI Divide – Insights on an Effective Healthcare Economic Information (HCEI) Exchange"},"categories":[],"segments":[],"timestamp":637781981400000000,"title":"webinar: bridging the hcei divide – insights on an effective healthcare economic information (hcei) exchange"},{"card":{"key":"6856ad6e-4642-4985-b779-70c9f3131c1e","authorName":"Xcenda","authorCompany":null,"date":"June 2020","description":"FormularyDecisions is a secure, online platform facilitating the bi-directional exchange of information between life sciences companies and over 2,100 qualified, active healthcare decision-makers. From pre-approval to post-launch, get unrivaled insight into what payers think of your product and those of your competitors, and gain feedback to better inform your market access strategies. ","img":{"alt":"CircularModule_TYPage_Refresh","src":"-/media/assets/xcenda/english/images/paid-media/circularmodule_typage_refresh.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/formularydecisions-amcp-pie-webinar-june-3-2020","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Now Available: Out in Front Effective Pre-approval Communication with Payers Webinar Slides"},"categories":[],"segments":[],"timestamp":637269601800000000,"title":"now available: out in front effective pre-approval communication with payers webinar slides"},{"card":{"key":"658a40d3-28a5-4334-bfb1-6618b3c3c761","authorName":"Tommy Bramley, PhD; Corey Ford, MHA","authorCompany":"Lash Group","date":"August 2020","description":"The COVID-19 pandemic continues to leave its mark on American life. As the larger healthcare system looks for ways to alleviate challenges brought on by the coronavirus, patient support providers are shifting how they work with manufacturers to increase impact and provide ongoing support for patients.","img":{"alt":"GettyImages-1136331627","src":"-/media/assets/lashgroup/images/about/gettyimages-1136331627.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/webinar-navigating-covid-19-simplifying-the-path-to-better-patient-outcomes","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Webinar | Navigating COVID-19: Simplifying the Path to Better Patient Outcomes"},"categories":["market access","patient care","patient support services","medication adherence","covid-19"],"segments":[],"timestamp":637333955400000000,"title":"webinar | navigating covid-19: simplifying the path to better patient outcomes"},{"card":{"key":"79cbf232-6764-4964-a398-6f18fbda74c3","authorName":"Xcenda","authorCompany":null,"date":"August 2019","description":"Precision medicine has rapidly evolved in the field of oncology, with therapeutic interventions being specifically selected to target molecular features associated with malignancy. Although cancer genome sequencing is a relatively new endeavor, it already has great potential to impact the clinical care of patients with cancer from diagnosis through treatment. For this reason, it is important to understand the current reimbursement climate for genetic testing within oncology—in particular, next-generation sequencing (NGS).","img":{"alt":"","src":""},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/htaq-summer-2019-hta-decision-for-next-generation-sequencing","linkText":"Learn more","hasImage":false,"isImageMode":true,"label":"Insight","headline":"Review of HTA Frameworks and Decisions for Next-Generation Sequencing in Precision Oncology"},"categories":["oncology","commercialization","market access"],"segments":[],"timestamp":637024860000000000,"title":"review of hta frameworks and decisions for next-generation sequencing in precision oncology"},{"card":{"key":"b2ed2e7e-a344-40ed-b85e-c49e1416ed3c","authorName":"Xcenda","authorCompany":null,"date":"September 2020","description":"","img":{"alt":"Physician's hand with healthcare blocks","src":"-/media/assets/xcenda/english/images/insights/pbm_exclusion_whitepaper_cover.jpg?h=320&w=540"},"link":"https://xcenda-prod-cd.cmsmartech.com/insights/skyrocketing-growth-in-pbm-formulary-exclusions-raises-concerns-about-patient-access","linkText":"Learn more","hasImage":true,"isImageMode":true,"label":"Insight","headline":"Skyrocketing Growth in PBM Formulary Exclusions Raises Concerns About Patient Access"},"categories":["affordability","managed care","product access"],"segments":[],"timestamp":637358148000000000,"title":"skyrocketing growth in pbm formulary exclusions raises concerns about patient access"},{"card":{"key":"9b3d9df5-01d5-49d1-9c07-a62370cfe7e5","authorName":"Corey Ford, MHA","authorCompany":"","date":"June 2021","description":"In recent years, commercial health plans and their pharmacy benefit managers (PBMs) have launched copay accumulator adjustment programs (AAPs), insurance designs that exclude the value of manufacturer-sponsored copay assistance from a patient’s accrual of out-of-pocket (OOP) expenses toward OOP limits throughout a plan benefit year. The restriction on copay assistance may have an adverse impact on patients’ adherence to prescribed therapy regimens and therefore may affect patient health and overall healthcare costs. While large, self-funded, employer-sponsored plans have led the charge in saturating the commercial market with these designs, recent federal regulation has given way to even more plans adopting AAPs and threatened the beneficial impact of copay assistance to patients on a long-term basis. 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