{"id":76809,"date":"2026-06-03T09:51:11","date_gmt":"2026-06-03T09:51:11","guid":{"rendered":"https:\/\/www.europesays.com\/ch\/76809\/"},"modified":"2026-06-03T09:51:11","modified_gmt":"2026-06-03T09:51:11","slug":"novartis-data-at-eular-2026-demonstrates-momentum-for-broad-immunology-portfolio-for-complex-high-unmet-need-diseases-2","status":"publish","type":"post","link":"https:\/\/www.europesays.com\/ch\/76809\/","title":{"rendered":"Novartis data at EULAR 2026 demonstrates momentum for broad immunology portfolio for complex, high unmet need diseases"},"content":{"rendered":"<p>New Cosentyx\u00ae (secukinumab) data from REPLENISH, largest ever global Phase III trial in polymyalgia rheumatica, to be highlighted in oral sessionNew ianalumab interim results from Sj\u00f6gren\u2019s Phase III extension study up to week 108 and Phase II data in systemic lupus erythematosus will be presented    <\/p>\n<p>Basel, June 1, 2026 \u2013 Novartis will present new data from 31 abstracts across its industry-leading immunology portfolio at the European Alliance of Associations for Rheumatology (EULAR) Congress on June 3-6 in London, advancing scientific insight into high-burden autoimmune diseases.<\/p>\n<p>\u201cNovartis is committed to shaping the future of immunology. From small molecules to biologics and CAR-T cell therapy, our pioneering science is focused on where we can have the greatest impact on patient outcomes,\u201d said Angelika Jahreis, Global Head, Immunology Development, Novartis. \u201cAt EULAR, we will share compelling new data for Cosentyx, ianalumab and our CAR-T therapy rap-cel across diseases where there is high unmet need. These data demonstrate how Novartis innovation can have meaningful impact for people living with autoimmune diseases like polymyalgia rheumatica, Sjogren\u2019s disease, systemic lupus erythematosus and systemic sclerosis.\u201d<\/p>\n<p>Key abstracts accepted by EULAR include:<\/p>\n<p>                Molecule\/Disease                        Abstract Title                        Number\/Presentation Details                        Cosentyx\u00ae (secukinumab)                        Polymyalgia Rheumatica<\/p>\n<p>\u00a0            <\/p>\n<p>            Secukinumab in polymyalgia rheumatica: Results of the phase 3 REPLENISH trial                        OP0116<br \/>Oral Presentation<br \/>June 3, 4:30pm-4:40pm BST                        Secukinumab in patients with polymyalgia rheumatica: Subgroup analyses of Week 52 results of a Phase 3, multicentre, randomised, double-blind, placebo-controlled trial (REPLENISH)                        POS0019<br \/>Poster Tour Presentation<br \/>June 3, 3:30pm-4:30pm BST                        Psoriatic Arthritis                        Impact of Early Biologic Use With Secukinumab on Radiographic Progression in Psoriatic Arthritis: A Pooled Analysis of the FUTURE 1 and FUTURE 5 Trials                        POS0474<br \/>Poster Tour Presentation<br \/>June 3, 3:30pm-4:50pm BST\u00a0                        Rap-cel (rapcabtagene autoleucel, YTB323)                        Systemic Sclerosis and Severe Refractory Idiopathic Inflammatory Myopathies                        Safety and Early Efficacy of Rapcabtagene Autoleucel, an Autologous CD19 Directed Chimeric Antigen Receptor T-Cell Therapy, in Severe Refractory Idiopathic Inflammatory Myopathies and Diffuse Cutaneous Systemic Sclerosis: Preliminary Analysis of the Open-Label AUTOGRAPH-IIM and \u2013SSC studies                        OP077<br \/>Oral Abstract Presentation<br \/>June 3, 4:40pm-4:50pm BST                        Systemic Lupus Erythematosus                        Clinical, Cellular Kinetics, Pharmacodynamics and Biomarker Data Up to 24 Months After Rapcabtagene Autoleucel (YTB323), a Rapidly Manufactured CD19 CAR-T Therapy, From an Open-Label, Phase 1\/2 Study in Severe Refractory SLE                        POS0303<br \/>Poster Tour Presentation<br \/>June 5, 4:00pm-5:00pm BST                        Ianalumab                         <br \/>\u00a0                        <br \/>\u00a0                        Sj\u00f6gren&#8217;s Disease                        Efficacy and Safety of the Ianalumab Global Phase 3 Studies (NEPTUNUS-1 and NEPTUNUS-2) and Their Extension Study in Patients With Sj\u00f6gren&#8217;s Disease                        OP0126<br \/>Oral Presentation<br \/>June 3, 4:50pm-5:00pm BST                        Systemic Lupus Erythematosus                        Safety and Efficacy of Subcutaneous Ianalumab (VAY736) Post-B Cell Recovery in Patients with Systemic Lupus Erythematosus: End of Study Results from a Phase 2 Study                        OP0335<br \/>Oral Presentation<br \/>June 5, 8:15am-8:25am BST              <\/p>\n<p>About Novartis Immunology\u00a0<br \/>At Novartis, we\u2019re advancing bold science with the goal of bringing relief and a renewed sense of hope to people living with autoimmune diseases. Building on our legacy of first-in-class innovation across rheumatology, dermatology and allergy, and a diverse industry-leading pipeline, we\u2019re committed to shaping what\u2019s next in Immunology.<\/p>\n<p>Product Information<br \/>For full prescribing information, including approved indications and important safety information about marketed products, please visit <a href=\"https:\/\/www.novartis.com\/about\/products\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">https:\/\/www.novartis.com\/about\/products<\/a>.<\/p>\n<p>Disclaimer<br \/>This press release contains forward-looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements can generally be identified by words such as \u201cpotential,\u201d \u201ccan,\u201d \u201cwill,\u201d \u201cplan,\u201d \u201cmay,\u201d \u201ccould,\u201d \u201cwould,\u201d \u201cexpect,\u201d \u201canticipate,\u201d \u201clook forward,\u201d \u201cbelieve,\u201d \u201ccommitted,\u201d \u201cinvestigational,\u201d \u201cpipeline,\u201d \u201claunch,\u201d or similar terms, or by express or implied discussions regarding potential marketing approvals, new indications or labeling for the investigational or approved products described in this press release, or regarding potential future revenues from such products. You should not place undue reliance on these statements. Such forward-looking statements are based on our current beliefs and expectations regarding future events, and are subject to significant known and unknown risks and uncertainties. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those set forth in the forward-looking statements. There can be no guarantee that the investigational or approved products described in this press release will be submitted or approved for sale or for any additional indications or labeling in any market, or at any particular time. Nor can there be any guarantee that such products will be commercially successful in the future. In particular, our expectations regarding such products could be affected by, among other things, the uncertainties inherent in research and development, including clinical trial results and additional analysis of existing clinical data; regulatory actions or delays or government regulation generally; global trends toward health care cost containment, including government, payor and general public pricing and reimbursement pressures and requirements for increased pricing transparency; our ability to obtain or maintain proprietary intellectual property protection; the particular prescribing preferences of physicians and patients; general political, economic and business conditions, including the effects of and efforts to mitigate pandemic diseases; safety, quality, data integrity or manufacturing issues; potential or actual data security and data privacy breaches, or disruptions of our information technology systems, and other risks and factors referred to in Novartis AG\u2019s current Form 20-F on file with the US Securities and Exchange Commission. Novartis is providing the information in this press release as of this date and does not undertake any obligation to update any forward-looking statements contained in this press release as a result of new information, future events or otherwise.<\/p>\n<p>About Novartis <br \/>Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people\u2019s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 300 million people worldwide.<\/p>\n<p>Reimagine medicine with us: Visit us at <a href=\"https:\/\/www.novartis.com\/\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">https:\/\/www.novartis.com<\/a> and connect with us on <a href=\"https:\/\/www.linkedin.com\/company\/novartis\/\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">LinkedIn<\/a>, <a href=\"https:\/\/www.facebook.com\/novartis\/\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">Facebook<\/a>, <a href=\"https:\/\/twitter.com\/Novartis\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">X\/Twitter<\/a> and <a href=\"https:\/\/instagram.com\/novartis?igshid=MzRlODBiNWFlZA==__;!!N3hqHg43uw!pjp8z253J5NjaOYrW65UbAAlHeHRdQ-w0m4ezZxEQEl0ptafXN2M99VRIk39pf49PAc8NbK93Pxp3uaSBQkAf8oEnzWXG8Sk$\" rel=\"nofollow noopener\" target=\"_blank\" title=\"\">Instagram<\/a>.<\/p>\n<p># # #<\/p>\n<p><img decoding=\"async\" alt=\"\" src=\"https:\/\/www.europesays.com\/ch\/wp-content\/uploads\/2026\/06\/1780480271_904_Novartis-Pharma-AG.png\"\/><script async src=\"https:\/\/platform.twitter.com\/widgets.js\" charset=\"utf-8\"><\/script><script async src=\"\/\/www.instagram.com\/embed.js\"><\/script><\/p>\n","protected":false},"excerpt":{"rendered":"New Cosentyx\u00ae (secukinumab) data from REPLENISH, largest ever global Phase III trial in polymyalgia rheumatica, to be highlighted&hellip;\n","protected":false},"author":2,"featured_media":76810,"comment_status":"","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":"","_share_on_mastodon":"0"},"categories":[127],"tags":[1792,1288,1101,206,1100],"class_list":["post-76809","post","type-post","status-publish","format-standard","has-post-thumbnail","category-novartis","tag-chronic-illness","tag-clinical-trials","tag-innovation","tag-novartis","tag-reimagine-medicine"],"share_on_mastodon":{"url":"https:\/\/pubeurope.com\/@ch\/116685562690181986","error":""},"_links":{"self":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts\/76809","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/comments?post=76809"}],"version-history":[{"count":0,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/posts\/76809\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/media\/76810"}],"wp:attachment":[{"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/media?parent=76809"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/categories?post=76809"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.europesays.com\/ch\/wp-json\/wp\/v2\/tags?post=76809"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}