{"id":970480,"date":"2026-06-04T07:04:31","date_gmt":"2026-06-04T11:04:31","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\/"},"modified":"2026-06-04T07:04:31","modified_gmt":"2026-06-04T11:04:31","slug":"regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\/","title":{"rendered":"Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO"},"content":{"rendered":"<h2>\nLatest clinical data and research illustrate Regeneron\u2019s advancement of innovative science for diverse and serious diseases with significant unmet needs<br \/>\n<\/h2>\n<div class=\"mw_release\">\n<p>TARRYTOWN, N.Y., June  04, 2026  (GLOBE NEWSWIRE) &#8212; Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that new clinical data and research from its metabolic disease, ophthalmology and rare disease pipelines will be presented at two major medical meetings in June 2026. These include the American Diabetes Association (ADA) 86th Scientific Sessions, June 5-8 in New Orleans, and the Endocrine Society Annual Meeting (ENDO 2026), June 13-16 in Chicago.<\/p>\n<p>\u201cOur presentations at ADA and ENDO reflect the rapid progress of our diverse pipeline across diseases where we see both significant unmet need and a real opportunity to make a meaningful impact on patients&#8217; lives,\u201d said Boaz Hirshberg, M.D., Senior Vice President, Clinical Development, Internal Medicine, Regeneron. \u201cAt ADA, we\u2019re advancing the healthcare community\u2019s understanding of how muscle and metabolic health intersect \u2014 an area where Regeneron is uniquely positioned to advance research using innovative approaches. And at ENDO, we\u2019re sharing early insights from a novel program in Graves&#8217; and thyroid eye disease, as well as pivotal Phase 3 results for garetosmab in fibrodysplasia ossificans progressiva, or FOP \u2013 a devastating ultra-rare genetic disorder in which muscles, tendons and ligaments are progressively replaced by bone.<\/p>\n<p>\n        <strong>New Research on Muscle Biology and Body Composition in Metabolic Disease\u00a0at ADA<\/strong><br \/>\n        <br \/>Four abstracts at ADA reflect Regeneron&#8217;s investment in understanding and addressing muscle loss across metabolic disease. Three abstracts from the Phase 2 COURAGE trial examine the effects of\u00a0trevogrumab\u00a0(anti-GDF8) on lean mass in people with obesity treated with semaglutide, and an additional abstract will provide early preclinical research on muscle biology.<\/p>\n<p>\n        <strong>Novel Ophthalmology Program and Phase 3 FOP Data at ENDO<\/strong><br \/>\n        <br \/>Regeneron will also present 5 abstracts at ENDO, focused on its expanding ophthalmology pipeline and pivotal Phase 3 clinical data for garetosmab as a treatment for FOP. Specifically, two presentations feature early preclinical data from Regeneron&#8217;s investigational antibody program targeting Graves&#8217; disease and thyroid eye disease \u2013 two conditions driven by the same underlying biology that can cause hyperthyroidism and painful eye protrusion. In addition, three presentations from the garetosmab program in FOP will be featured in:<\/p>\n<ul type=\"disc\">\n<li>An oral presentation of the Week 56 efficacy and safety primary analysis data from the OPTIMA trial<\/li>\n<li>A rapid-fire oral presentation of preclinical data showing that blocking activin A prevents heterotopic bone from regrowing after surgical removal in a mouse model<\/li>\n<li>A poster presentation of qualitative interviews from OPTIMA trial participants on their experience during the Phase 3 trial\n<\/li>\n<\/ul>\n<p>\n        <strong>Regeneron Presentations:<\/strong>\n      <\/p>\n<table style=\"border-collapse: collapse;width:100%;border-collapse:collapse\">\n<tr>\n<td style=\"max-width:46%;width:46.0248%;min-width:46%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">\n            <strong>Abstract Title<\/strong>\u00a0<\/td>\n<td style=\"max-width:18%;width:18.0097%;min-width:18%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">\n            <strong>Presenter<\/strong>\u00a0<\/td>\n<td style=\"max-width:18%;width:18.0097%;min-width:18%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">\n            <strong>Session Type<\/strong>\u00a0<\/td>\n<td style=\"max-width:18%;width:18.0097%;min-width:18%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">\n            <strong>Date \/ Time (CT)<\/strong>\u00a0<\/td>\n<\/tr>\n<tr>\n<td colspan=\"4\" style=\"width:100.054%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">\n            <strong><br \/>\n              <em>ADA 2026 Scientific\u00a0Sessions <\/em><br \/>\n            <\/strong>\n          <\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Lean Mass Effects of Anti-GDF8 (Trevogrumab) \u00b1 Anti-activin A (Garetosmab) in People Living with Obesity Treated with Semaglutide\u00a0with\u00a0or without Low Lean Mass at Baseline<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Jesse Chao, PharmD., MBA<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Oral Presentation<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Sunday, June 7, <br \/>9:00 &#8211; 9:15 am<\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Double Knockout of INHBC and INHBE Protect Against Diet-Induced Obesity and<br \/>Insulin Resistance in Mice<\/p>\n<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Diana Li, PhD<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Poster\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Monday, June 8, 12:30 &#8211; 1:30 pm<\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Optimizing\u00a0DXA Imaging in Obese Populations: Lessons from the COURAGE Study\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Andrea Vavere, PhD\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Poster\u00a0\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Monday, June 8, 12:30 &#8211; 1:30 pm<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Population-normed Z-scores for Body Composition Enhance Sensitivity and Effect Size: Analysis of a Phase 2 RCT Testing Anti-GDF8 and Anti-activin A on Top of Semaglutide (COURAGE)\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Jos\u00e9 G. Raya, PhD\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Poster\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Monday, June 8, 12:30 -1:30 pm<\/td>\n<\/tr>\n<tr>\n<td colspan=\"4\" style=\"width:100.054%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">\n            <strong><br \/>\n              <em>ENDO\u00a02026<\/em><br \/>\n            <\/strong>\n          <\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-right: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Inhibition of Activin A Stops the Regrowth of Surgically Resected Heterotopic Bone in a Mouse Model of Fibrodysplasia Ossificans Progressiva<strong><em><br \/><\/em><\/strong><\/td>\n<td style=\"width:18.0097%;border-right: solid black 1pt;vertical-align: top\">Aris N. Economides, PhD\u00a0<strong><em><br \/><\/em><\/strong><\/td>\n<td style=\"width:18.0097%;border-right: solid black 1pt;vertical-align: top\">Rapid-Fire Oral\u00a0Presentation<strong><em><br \/><\/em><\/strong><\/td>\n<td style=\"width:18.0097%;border-right: solid black 1pt;vertical-align: top\">Saturday, June 13 9:50 &#8211; 9:55 am<strong><em><br \/><\/em><\/strong><\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Safety and Efficacy of\u00a0Garetosmab\u00a0in Adults with Fibrodysplasia Ossificans Progressiva: Week 56 Results from the Phase 3 OPTIMA Study\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Richard Keen, MD\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Oral Presentation\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Saturday, June 13 10:00 &#8211; 10:15 am \u00a0<\/p>\n<\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Assessing the Participant Experience with Fibrodysplasia Ossificans Progressiva: Qualitative Interviews from the OPTIMA Trial\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Jing Gu, PhD\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Poster<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Monday, June 15 9:00 am \u2013 2:00 pm<\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">A Novel TSHR Blocking Antibody Effectively Reduces Hyperthyroidism and Proptosis in a Mouse Model of Graves\u2019 and Thyroid Eye Disease\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Mutayyaba Adnan, MPH<\/p>\n<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Oral Presentation\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Sunday, June 14<br \/>3:30 &#8211; 4:15 pm<\/td>\n<\/tr>\n<tr>\n<td style=\"width:46.0248%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">In-Vitro Properties of REGN24493, a Novel TSHR Blocking\u00a0mAb\u00a0for the Treatment of Graves\u2019 Disease and Thyroid Eye Disease\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Bristol Denlinger, PhD\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Poster\u00a0<\/td>\n<td style=\"width:18.0097%;border-top: solid black 1pt;border-right: solid black 1pt;border-bottom: solid black 1pt;border-left: solid black 1pt;vertical-align: top\">Sunday, June 14<br \/>9:00 am \u2013 4:00 pm<\/td>\n<\/tr>\n<\/table>\n<p>\n        <strong><br \/>\n          <br \/>About Regeneron<\/strong><br \/>\n        <br \/>Regeneron (NASDAQ: REGN) is a leading biotechnology company that invents, develops and commercializes life-transforming medicines for people with serious diseases. Founded and led by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to numerous approved treatments and\u202fproduct candidates in development, most of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurological diseases, hematologic conditions, infectious diseases, and rare diseases.<\/p>\n<p>Regeneron\u202fpushes the boundaries of scientific discovery and\u202faccelerates drug development\u202fusing\u202four proprietary technologies, such as\u202f<em>VelociSuite<\/em><sup>\u00ae<\/sup>, which produces optimized fully human antibodies and new classes of bispecific antibodies.\u202fWe are shaping the next frontier of medicine with data-powered insights from the\u202fRegeneron Genetics Center<sup>\u00ae<\/sup>\u202fand pioneering genetic medicine platforms, enabling us to identify innovative targets and complementary approaches to potentially treat or cure diseases.<\/p>\n<p>For more information, please visit <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=kGRrXlgGjDmAfSPGrHavSlMv404dyxxnEhNW4ZyRHiRm-4OKr-uB_mvT6MpLc44u2i7KhIa6_DNAwfZaD5XCUcwCDTBpfmDNE65lhJ5d6EomERzGs3T1ZmRlVnoPId3zeFgxotsWBaZkCNeJGalKktc-tBcIXEzOPwEoaf3xKlefaKSIx0UHnB5lp7rAF1GnzmDOubEvZ_ADNtQwDf6hhyEsvxWYBtgUx6a8FD67yhs-5TzKCoLvXrDAkTUwEMR57rL-e4pHOlcHHb3DwyKH5w==\" rel=\"nofollow\" target=\"_blank\">www.Regeneron.com<\/a> or follow Regeneron on <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=4AW_HO8Pn4P4WJazaReX6mdgxSK0HjZZLXVfKkSw-DOi27iSTXhiIM7ipFWnYrl28DXJP5BS_t22PgW5vaxeWBhNOmLzUx0TUqW74DWNq25RW4RypDQ5jJHG6rsuUYmnKxv2QrQu_3ytRG52w3Sk_yMTYS6JwfXfS470o1r_6WMprwRZjFo5I94-Xpwmqu0YcJSi_CwqHHxv16ycMlwuVsjn4dDctNmpJR4XvpELjWreK1-nu5SRvbZzwlzXyJpCTn1HknMtUSeAaYycWWl-YA==\" rel=\"nofollow\" target=\"_blank\">LinkedIn<\/a>, <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=wr-nzsqPsnoS67XwOucyvZ-hyyfhor8IWMREMlH5NgP49ZzYTKhOmfdGrj1CeRAToiNf-AQCo1OVC98B9HlbaL_VC3b5hRaypWLszptPMXD6ILd2NykLoEmbVs2WcdH3xx675vCJIchH6jIJnc28IjYNmvz6b0TfKfxrUpt2TMGuJOMsKXkLZzXs_bxs3vuJ2bI18drf_4j3LUljJTJm3xmziZyNkuuJGP7aVcHQmf7wCPnLZOCCXcb2lrM70OBU\" rel=\"nofollow\" target=\"_blank\">Instagram<\/a>, <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=L68PAev5VWNJMgNrseBTT_JJdRO6pi5apkcROCMtZD5oKEdV6l3NkhucIQmO9a04LlzDYsEvSJHcvY2Qu97OYaNQ4H7VTcA1S4qAtNxxbNOrn_jwNi3OilXN8pX65ClbeTvzaOO3yFNM_oOwW_w3Pj76G6ylgBiWwKJJ1wPJNkIr2kMy7UapR_7cjTSiV-fZJnyeA8SQNMVyKk96rwUFqh5MAE6jPZ_E-nrcq7W4L0VhDFGSRIYfS_twKkM7KNBE\" rel=\"nofollow\" target=\"_blank\">Facebook<\/a> or <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=ak9FZq0mv6rxhRuv-UZFs-TioX8bKF72iU2j5iTyyKezl5S2JE9oDeI221AcOGxSdJfLgeWffXn0nVjJ1uOTlaNKPTnVCn21QU-lFwUlyEJkq1wDcm_CGyQmMyGYJ8gkbMH29M7n6jL1xMM7JcXZDRwkKhWyr1j8SxvWrJKkbG3X6uoUuoreQleylp__aRoDmX5hsjHyjinGbc17VQe3jg==\" rel=\"nofollow\" target=\"_blank\">X<\/a>.<\/p>\n<p>\n        <strong>Forward-Looking Statements and Use of Digital Media<\/strong><br \/>\n        <br \/>\n        <em>This press release includes forward-looking statements that involve risks and uncertainties relating to future events and the future performance of Regeneron Pharmaceuticals, Inc. (\u201cRegeneron\u201d or the \u201cCompany\u201d), and actual events or results may differ materially from these forward-looking statements. Words such as \u201canticipate,\u201d \u201cexpect,\u201d \u201cintend,\u201d \u201cplan,\u201d \u201cbelieve,\u201d \u201cseek,\u201d \u201cestimate,\u201d variations of such words, and similar expressions are intended to identify such forward-looking statements, although not all forward-looking statements contain these identifying words. These statements concern, and these risks and uncertainties include, among others, the nature, timing, and possible success and therapeutic applications of products marketed or otherwise commercialized by Regeneron and\/or its collaborators or licensees (collectively, \u201cRegeneron\u2019s Products\u201d) and product candidates being developed by Regeneron and\/or its collaborators or licensees (collectively, \u201cRegeneron\u2019s Product Candidates\u201d) and research and clinical programs now underway or planned, including without limitation garetosmab, trevogrumab, and the other clinical programs discussed or referenced in this press release;<\/em><br \/>\n        <em>uncertainty of the utilization, market acceptance, and\/or commercial success of Regeneron\u2019s Products and Regeneron\u2019s Product Candidates and the impact of studies (whether conducted by Regeneron or others and whether mandated or voluntary), including the studies discussed or referenced in this press release, on any of the foregoing or any potential regulatory approval of Regeneron\u2019s Products and Regeneron\u2019s Product Candidates (such as those referenced above); the likelihood, timing, and scope of possible regulatory approval and commercial launch of Regeneron\u2019s Product Candidates and new indications for Regeneron\u2019s Products, such as garetosmab for the treatment of fibrodysplasia ossificans progressiva; the ability of Regeneron\u2019s collaborators, licensees, suppliers, or other third parties (as applicable) to perform manufacturing, filling, finishing, packaging, labeling, distribution, and other steps related to Regeneron\u2019s Products and Regeneron\u2019s Product Candidates; the ability of Regeneron to manage supply chains for multiple products and product candidates and risks associated with tariffs and other trade restrictions; safety issues resulting from the administration of Regeneron\u2019s Products and Regeneron\u2019s Product Candidates (such as those referenced above) in patients, including serious complications or side effects in connection with the use of Regeneron\u2019s Products and Regeneron\u2019s Product Candidates in clinical trials; determinations by regulatory and administrative governmental authorities which may delay or restrict Regeneron\u2019s ability to continue to develop or commercialize Regeneron\u2019s Products and Regeneron\u2019s Product Candidates; ongoing regulatory obligations and oversight impacting Regeneron\u2019s Products, research and clinical programs, and business, including those relating to patient privacy; the availability and extent of reimbursement or copay assistance for Regeneron\u2019s Products from third-party payors and other third parties, including private payor healthcare and insurance programs, health maintenance organizations, pharmacy benefit management companies, and government programs such as Medicare and Medicaid; coverage and reimbursement determinations by such payors and other third parties and new policies and procedures adopted by such payors and other third parties; changes to drug pricing regulations and requirements and Regeneron\u2019s pricing strategy, including in connection with Regeneron\u2019s April 2026 agreements with the U.S. government; other changes in laws, regulations, and policies affecting the healthcare industry; competing products and product candidates (including biosimilar products) that may be superior to, or more cost effective than, Regeneron\u2019s Products and Regeneron\u2019s Product Candidates; the extent to which the results from the research and development programs conducted by Regeneron and\/or its collaborators or licensees may be replicated in other studies and\/or lead to advancement of product candidates to clinical trials, therapeutic applications, or regulatory approval; unanticipated expenses; the costs of developing, producing, and selling products; the ability of Regeneron to meet any of its financial projections or guidance and changes to the assumptions underlying those projections or guidance; the potential for any license, collaboration, or supply agreement, including Regeneron\u2019s agreements with Sanofi and Bayer (or their respective affiliated companies, as applicable), to be cancelled or terminated; the impact of public health outbreaks, epidemics, or pandemics on Regeneron&#8217;s business; and risks associated with litigation and other proceedings and government investigations relating to the Company and\/or its operations (including the pending civil proceedings initiated or joined by the U.S. Department of Justice and the U.S. Attorney&#8217;s Office for the District of Massachusetts), risks associated with intellectual property of other parties and pending or future litigation relating thereto (including without limitation the patent litigation and other related proceedings relating to EYLEA<\/em><br \/>\n        <sup><br \/>\n          <em>\u00ae<\/em><br \/>\n        <\/sup><br \/>\n        <em> (aflibercept) Injection), the ultimate outcome of any such proceedings and investigations, and the impact any of the foregoing may have on Regeneron\u2019s business, prospects, operating results, and financial condition. A more complete description of these and other material risks can be found in Regeneron\u2019s filings with the U.S. Securities and Exchange Commission, including its Form 10-K for the year ended December 31, 2025 and its Form 10-Q for the quarterly period ended March 31, 2026. Any forward-looking statements are made based on management\u2019s current beliefs and judgment, and the reader is cautioned not to rely on any forward-looking statements made by Regeneron. Regeneron does not undertake any obligation to update (publicly or otherwise) any forward-looking statement, including without limitation any financial projection or guidance, whether as a result of new information, future events, or otherwise.<\/em>\n      <\/p>\n<p>\n        <em>Regeneron uses its media and investor relations website and social media outlets to publish important information about the Company, including information that may be deemed material to investors. Financial and other information about Regeneron is routinely posted and is accessible on Regeneron&#8217;s media and investor relations website (<\/em><br \/>\n        <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=OERkmaB4CbMTuC4VtKLVMKbxh5KNSckGOhksnlIvoPvtyCjmYU_CGSbh1Y4OsKDF8uRa0ezRnRL59ppEaBajKyZlWllg8i9CmdoCH-UpW7dxUwiZHni9b-OPZw-ZxbY1\" rel=\"nofollow\" target=\"_blank\"><br \/>\n          <em>https:\/\/investor.regeneron.com<\/em><br \/>\n        <\/a><br \/>\n        <em>) and its LinkedIn page (<\/em><br \/>\n        <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=OERkmaB4CbMTuC4VtKLVMF7xIh_Hxi4aZ8jKkOCFH0OO9VyshXIgpSjcMES6MaxDwkZ1BK_ASOGp6eI1AhMr2jXROq8MTUO6VuPQ_2Bt2pd9YHxluYzeK8abHLxslpT0mAtprWmb2UbMxrcVU62qNWKrtSMh-gpdapJfY0oVOOccH_a_giRkBQZR9rSgsjW9\" rel=\"nofollow\" target=\"_blank\"><br \/>\n          <em>https:\/\/www.linkedin.com\/company\/regeneron-pharmaceuticals<\/em><br \/>\n        <\/a><br \/>\n        <em>)<\/em>\n      <\/p>\n<table style=\"border-collapse: collapse;width:100%;border-collapse:collapse\">\n<tr>\n<td style=\"vertical-align: top\">\n            <strong>Contacts:<br \/><\/strong><br \/>\n            <br \/>\n            <strong>Media Relations<\/strong><br \/>\n            <br \/>Mary Heather<br \/>Tel: +1 914-847-8650<br \/><a href=\"mailto:mary.heather@regeneron.com\" rel=\"nofollow\" target=\"_blank\">mary.heather@regeneron.com<\/a><\/td>\n<td style=\"vertical-align: top\">\n            <strong><\/p>\n<p>Investor Relations<\/strong><br \/>\n            <br \/>Matthew Feeney <br \/>Tel: + 1 914-847-1004<br \/><a href=\"mailto:matthew.feeney@regeneron.com\" rel=\"nofollow\" target=\"_blank\">matthew.feeney@regeneron.com<\/a><\/td>\n<\/tr>\n<\/table>\n<p>\n        \n      <\/p>\n<p>      <img decoding=\"async\" alt=\"\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTczMTc4NiM3NjM2Mjc4IzIwMDYyNTA=\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" alt=\"\" src=\"https:\/\/ml.globenewswire.com\/media\/NzNhNDY0NzctNjYxYS00NWQ0LWEzMmMtMDdlZDE3YTI3ZGVkLTEwMTc4MjMtMjAyNi0wNi0wNC1lbg==\/tiny\/Regeneron-Pharmaceuticals-Inc-.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Latest clinical data and research illustrate Regeneron\u2019s advancement of innovative science for diverse and serious diseases with significant unmet needs TARRYTOWN, N.Y., June 04, 2026 (GLOBE NEWSWIRE) &#8212; Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that new clinical data and research from its metabolic disease, ophthalmology and rare disease pipelines will be presented at two major medical meetings in June 2026. These include the American Diabetes Association (ADA) 86th Scientific Sessions, June 5-8 in New Orleans, and the Endocrine Society Annual Meeting (ENDO 2026), June 13-16 in Chicago. \u201cOur presentations at ADA and ENDO reflect the rapid progress of our diverse pipeline across diseases where we see both significant unmet need and a real opportunity to make a meaningful impact &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO&#8221;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[],"tags":[],"class_list":["post-970480","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO - Market Newsdesk<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.marketnewsdesk.com\/index.php\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Latest clinical data and research illustrate Regeneron\u2019s advancement of innovative science for diverse and serious diseases with significant unmet needs TARRYTOWN, N.Y., June 04, 2026 (GLOBE NEWSWIRE) &#8212; Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that new clinical data and research from its metabolic disease, ophthalmology and rare disease pipelines will be presented at two major medical meetings in June 2026. These include the American Diabetes Association (ADA) 86th Scientific Sessions, June 5-8 in New Orleans, and the Endocrine Society Annual Meeting (ENDO 2026), June 13-16 in Chicago. \u201cOur presentations at ADA and ENDO reflect the rapid progress of our diverse pipeline across diseases where we see both significant unmet need and a real opportunity to make a meaningful impact &hellip; Continue reading &quot;Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2026-06-04T11:04:31+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=OTczMTc4NiM3NjM2Mjc4IzIwMDYyNTA=\" \/>\n<meta name=\"author\" content=\"Newsdesk\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Newsdesk\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"9 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO\",\"datePublished\":\"2026-06-04T11:04:31+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\\\/\"},\"wordCount\":1816,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=OTczMTc4NiM3NjM2Mjc4IzIwMDYyNTA=\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/regeneron-to-highlight-progress-across-its-metabolic-disease-ophthalmology-and-rare-disease-pipelines-at-ada-and-endo\\\/\",\"name\":\"Regeneron to Highlight Progress Across Its Metabolic Disease, Ophthalmology and Rare Disease Pipelines at ADA and ENDO - 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