{"id":27413,"date":"2024-03-26T15:08:05","date_gmt":"2024-03-26T09:38:05","guid":{"rendered":"https:\/\/www.delveinsight.com\/blog\/?p=27413"},"modified":"2024-03-26T15:08:07","modified_gmt":"2024-03-26T09:38:07","slug":"pharma-news-for-regeneron-novartis-novo-nordisk-abbvie","status":"publish","type":"post","link":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie","title":{"rendered":"Regeneron\u2019s Odronextamab BLA; Novo Nordisk\u2019s Cardior Pharmaceuticals Acquisition; Novartis\u2019 Fabhalta CHMP Approval; Idorsia\u2019s TRYVIO FDA Approval; AbbVie\u2019s Landos Biopharma Acquisition"},"content":{"rendered":"<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_76 counter-hierarchy ez-toc-counter ez-toc-white ez-toc-container-direction\">\n<p class=\"ez-toc-title\" style=\"cursor:inherit\">Table of Contents<\/p>\n<label for=\"ez-toc-cssicon-toggle-item-6a2c44c960e46\" class=\"ez-toc-cssicon-toggle-label\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/label><input type=\"checkbox\"  id=\"ez-toc-cssicon-toggle-item-6a2c44c960e46\"  aria-label=\"Toggle\" \/><nav><ul class='ez-toc-list ez-toc-list-level-1 ' ><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\/#Regeneron_Updates_Progress_on_Biologics_License_Application_for_Odronextamab\" >Regeneron Updates Progress on Biologics License Application for Odronextamab<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\/#Novo_Nordisk_Bolsters_Cardiovascular_Disease_Portfolio_with_Cardior_Pharmaceuticals_Acquisition\" >Novo Nordisk Bolsters Cardiovascular Disease Portfolio with Cardior Pharmaceuticals Acquisition<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\/#CHMP_Greenlights_Novartis_Fabhalta_%E2%80%93_First-Ever_Oral_Monotherapy_for_Adult_PNH_Patients\" >CHMP Greenlights Novartis Fabhalta &#8211; First-Ever Oral Monotherapy for Adult PNH Patients<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\/#Idorsias_TRYVIO_Gets_FDA_Nod_First-of-Its-Kind_Endothelin_Receptor_Antagonist_for_High_Blood_Pressure_When_Other_Antihypertensives_Fall_Short\" >Idorsia\u2019s TRYVIO Gets FDA Nod, First-of-Its-Kind Endothelin Receptor Antagonist for High Blood Pressure When Other Antihypertensives Fall Short<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\/#AbbVie_Grows_Its_Presence_in_Inflammatory_and_Autoimmune_Diseases_with_Landos_Biopharma_Acquisition\" >AbbVie Grows Its Presence in Inflammatory and Autoimmune Diseases with Landos Biopharma Acquisition<\/a><\/li><\/ul><\/nav><\/div>\n\n<h2 class=\"wp-block-heading\" id=\"h-regeneron-updates-progress-on-biologics-license-application-for-odronextamab\"><span class=\"ez-toc-section\" id=\"Regeneron_Updates_Progress_on_Biologics_License_Application_for_Odronextamab\"><\/span><strong>Regeneron Updates Progress on Biologics License Application for Odronextamab<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>Regeneron Pharmaceuticals, Inc.<\/strong> has announced that the FDA has issued Complete Response Letters (CRLs) regarding the Biologics License Application (BLA) for <strong>odronextamab <\/strong>in cases of relapsed\/refractory (R\/R) follicular lymphoma (FL) and relapsed\/refractory (R\/R) diffuse large B-cell lymphoma (DLBCL), each occurring after two or more lines of systemic therapy. The sole concern for approval is associated with the status of enrollment in the confirmatory trials. The CRLs, one for R\/R FL and one for R\/R DLBCL did not highlight any concerns regarding the clinical effectiveness or safety of odronextamab, trial structure, labeling, or manufacturing.<\/p>\n\n\n\n<p>Regeneron has actively been enrolling patients in multiple Phase III trials for odronextamab within the OLYMPIA program, one of the largest clinical initiatives in lymphoma treatment. The OLYMPIA program aims to revolutionize the treatment approach for various <a href=\"https:\/\/www.delveinsight.com\/report-store\/b-cell-non-hodgkin-lymphoma-market\">B-cell non-Hodgkin lymphoma subtypes<\/a>, including those in earlier stages of therapy. To participate in this program, the FDA mandated that these trials include both sections for determining the appropriate dosage and for confirming efficacy. While enrollment for the dosage determination stage has commenced, the Complete Response Letters (CRLs) suggest that the confirmatory phases of these trials should be in progress, with agreed-upon timelines for completion before resubmission. Regeneron is dedicated to closely collaborating with the FDA and researchers to expedite the availability of odronextamab for <a href=\"https:\/\/www.delveinsight.com\/report-store\/follicular-lymphoma-market-insights\">patients with R\/R FL<\/a> and R\/R DLBCL. Updates on enrollment progress and regulatory timelines will be shared by Regeneron later this year.<\/p>\n\n\n\n<p>The European Medicines Agency (EMA) is still in the process of reviewing odronextamab for its effectiveness in treating Relapsed or Refractory Diffuse Large B-cell lymphoma (R\/R DLBCL) and Relapsed or Refractory Follicular Lymphoma (R\/R FL). Within the European Union, odronextamab has received special status as an Orphan Drug for DLBCL and FL. However, its potential use for R\/R DLBCL and R\/R FL is presently being studied in clinical trials and has not yet been approved by any regulatory body.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-novo-nordisk-bolsters-cardiovascular-disease-portfolio-with-cardior-pharmaceuticals-acquisition\"><span class=\"ez-toc-section\" id=\"Novo_Nordisk_Bolsters_Cardiovascular_Disease_Portfolio_with_Cardior_Pharmaceuticals_Acquisition\"><\/span><strong>Novo Nordisk Bolsters Cardiovascular Disease Portfolio with Cardior Pharmaceuticals Acquisition<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>Novo Nordisk and Cardior Pharmaceuticals<\/strong> have revealed that Novo Nordisk will be acquiring Cardior for a sum of up to <strong>1.025 billion Euros<\/strong>. This includes an initial payment as well as potential additional payments contingent upon the accomplishment of specific milestones in development and commercialization. Cardior stands at the forefront of pioneering treatments that focus on RNA to prevent, repair, and reverse heart diseases. Through targeting unique non-coding RNAs, the company aims to tackle the fundamental reasons behind cardiac dysfunctions, with the ultimate goal of creating enduring benefits for patients.<\/p>\n\n\n\n<p>The deal encompasses Cardior&#8217;s primary drug candidate <strong>CDR132L<\/strong>, presently undergoing phase II clinical trials for heart failure treatment. This acquisition marks a significant advancement in Novo Nordisk&#8217;s plan to enter the <a href=\"https:\/\/www.delveinsight.com\/blog\/cardiovascular-diseases\">cardiovascular disease sector<\/a>. Novo Nordisk is dedicated to creating a purposeful and influential collection of treatments, utilizing both internal research and external collaborations, to tackle the substantial gaps that remain in addressing cardiovascular disease, the leading cause of mortality worldwide.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><strong><em>Martin Holst Lange, Novo Nordisk&#8217;s executive vice president for Development<\/em><\/strong><em>, stated that by incorporating Cardior into Novo Nordisk, they aim to fortify their lineup of projects in cardiovascular disease. Novo Nordisk already has ongoing programs in all stages of clinical development in this area. Lange emphasized their admiration for Cardior&#8217;s scientific endeavors, particularly highlighting CDR132L. This treatment boasts a unique mechanism of action and the potential to be a pioneering therapy intended to slow down or partially reverse the progression of heart failure in individuals.<\/em><\/p>\n<\/blockquote>\n\n\n\n<p>Novo Nordisk intends to start another phase II study focusing on CDR132L in <a href=\"https:\/\/www.delveinsight.com\/report-store\/chronic-heart-failure-market\">individuals with chronic heart failure<\/a> and cardiac hypertrophy, a condition leading to thickened and rigid heart muscle walls, which hampers the heart&#8217;s pumping function. This move will not influence Novo Nordisk&#8217;s earlier projected operating profit for 2024 or its current share buy-back program. The funding for this acquisition by Novo Nordisk will come from its existing financial reserves.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-chmp-greenlights-novartis-fabhalta-first-ever-oral-monotherapy-for-adult-pnh-patients\"><span class=\"ez-toc-section\" id=\"CHMP_Greenlights_Novartis_Fabhalta_%E2%80%93_First-Ever_Oral_Monotherapy_for_Adult_PNH_Patients\"><\/span><strong>CHMP Greenlights Novartis Fabhalta &#8211; First-Ever Oral Monotherapy for Adult PNH Patients<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>Novartis <\/strong>has reported that the European Medicines Agency&#8217;s Committee for Medicinal Products for Human Use (CHMP) has issued a favorable recommendation for the approval of <strong>Fabhalta (iptacopan)<\/strong>. This recommendation is for its use in treating hemolytic anemia in <a href=\"https:\/\/www.delveinsight.com\/report-store\/paroxysmal-nocturnal-hemoglobinuria-market\">adults with paroxysmal nocturnal hemoglobinuria (PNH)<\/a>.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>According to <\/em><strong><em>Antonio Risitano, M.D., Ph.D., President of the International PNH Interest Group and Head of the Hematology and Hematopoietic Transplant Unit at the AORN San Giuseppe Moscati in Avellino, Italy<\/em><\/strong><em>, Fabhalta has the potential to significantly impact patient care by alleviating the challenges faced by individuals with PNH. Backed by substantial evidence and a proven track record of safety, Fabhalta may revolutionize treatment approaches. Clinical trials have shown that oral iptacopan offers superior improvement in hemoglobin levels without necessitating red blood cell transfusions, surpassing the performance of anti-C5 therapies. This could lead to the normalization of hemoglobin levels for most patients, marking a potentially groundbreaking advancement for those managing this persistent blood disorder.<\/em><\/p>\n<\/blockquote>\n\n\n\n<p>The CHMP&#8217;s positive decision was influenced by strong data from two Phase III trials: APPLY-PNH, which involved patients with persistent anemia despite prior anti-C5 therapy, comparing those who switched to Fabhalta with those who continued anti-C5 treatment; and APPOINT-PNH, which focused on patients new to complement inhibitors. In APPLY-PNH, after 24 weeks, 82.3% of Fabhalta patients previously on anti-C5 treatment achieved a sustained increase in Hb levels of \u22652 g\/dL without needing transfusions, compared to only 2.0% of those on anti-C5 (a significant difference of 80.2%, P&lt;0.0001). In APPOINT-PNH, 92.2% of patients new to complement inhibitors, and using Fabhalta achieved this same outcome. APPLY-PNH also revealed a notable transfusion avoidance rate of 94.8% for Fabhalta patients previously on anti-C5, compared to 25.9% for those continuing anti-C5 treatment (a significant difference of 68.9%, P&lt;0.0001). Both studies demonstrated Fabhalta&#8217;s effectiveness in controlling intravascular hemolysis (IVH), indicated by maintaining mean lactate dehydrogenase (LDH) levels below 1.5 times the upper limit of normal. APPLY-PNH patients also reported feeling less fatigued, as shown by improvements in Functional Assessment of Chronic Illness Therapy \u2013 Fatigue (FACIT-F) scores. Across both APPLY-PNH and APPOINT-PNH, the safety profile of iptacopan remained consistent.<\/p>\n\n\n\n<p>After the CHMP suggests approving Fabhalta for <a href=\"https:\/\/www.delveinsight.com\/report-store\/paroxysmal-nocturnal-hemoglobinuria-market\">adult PNH patients<\/a> with hemolytic anemia, the European Commission (EC) will make a conclusive judgment in around two months.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-idorsia-s-tryvio-gets-fda-nod-first-of-its-kind-endothelin-receptor-antagonist-for-high-blood-pressure-when-other-antihypertensives-fall-short\"><span class=\"ez-toc-section\" id=\"Idorsias_TRYVIO_Gets_FDA_Nod_First-of-Its-Kind_Endothelin_Receptor_Antagonist_for_High_Blood_Pressure_When_Other_Antihypertensives_Fall_Short\"><\/span><strong>Idorsia\u2019s TRYVIO Gets FDA Nod, First-of-Its-Kind Endothelin Receptor Antagonist for High Blood Pressure When Other Antihypertensives Fall Short<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>Idorsia Ltd<\/strong> has revealed that the FDA granted approval for <strong>TRYVIO (aprocitentan)<\/strong> to address hypertension in conjunction with additional antihypertensive medications, aimed at decreasing blood pressure in adult patients whose current drug regimens are not effectively managing their condition. Lowering blood pressure diminishes the likelihood of fatal and non-fatal cardiovascular incidents, notably strokes and heart attacks. The suggested dose for TRYVIO is 12.5 mg taken orally once per day, with or without food.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>&#8220;Presently, there exist millions of Americans whose blood pressure remains inadequately managed despite available treatments. This poses a significant public health concern, contributing to a heightened occurrence of cardiovascular and cerebrovascular incidents. To combat this challenge, Idorsia has developed aprocitentan, an endothelin receptor antagonist designed for these particular patients. Idorsia undertook an extensive clinical initiative involving patients who continued to experience <\/em><a href=\"https:\/\/www.delveinsight.com\/report-store\/hypertension-market\"><em>hypertension<\/em><\/a><em> despite being on at least three medications at their optimal doses, and at times even four, five, or six antihypertensives. I am immensely proud of the Idorsia team and delighted that physicians will soon have a fresh therapeutic avenue for patients grappling with uncontrolled blood pressure.&#8221;<\/em><\/p>\n<cite><strong><em>Jean-Paul Clozel, MD and Chief Executive Officer of Idorsia<\/em><\/strong><\/cite><\/blockquote>\n\n\n\n<p>TRYVIO (aprocitentan) is a type of endothelin receptor antagonist that works by blocking the interaction between endothelin (ET)-1 and the ETA and ETB receptors. The actions of ET-1 closely resemble the mechanisms behind hypertension, and ET-1 plays a significant role in stimulating the production of aldosterone. Before the approval of TRYVIO, no systemic medications for lowering blood pressure specifically targeted the ET pathway. Instead, approved antihypertensive treatments focused on methods such as controlling salt and water balance (diuretics), countering the renin-angiotensin-aldosterone system (RAAS), reducing the entry of extracellular calcium into cells (calcium channel blockers), decreasing sympathetic activity (beta blockers, central alpha-agonist agents), or inducing non-selective vasodilation.<\/p>\n\n\n\n<p>TRYVIO underwent assessment as a standalone treatment in a Phase II investigation involving individuals with hypertension. Additionally, it was examined as an additional therapy in a Phase III trial named PRECISION among patients with confirmed resistant hypertension. During PRECISION, aprocitentan was not only well received but also demonstrated superiority over a placebo in reducing blood pressure by week 4, maintaining this effect through week 40.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-abbvie-grows-its-presence-in-inflammatory-and-autoimmune-diseases-with-landos-biopharma-acquisition\"><span class=\"ez-toc-section\" id=\"AbbVie_Grows_Its_Presence_in_Inflammatory_and_Autoimmune_Diseases_with_Landos_Biopharma_Acquisition\"><\/span><strong>AbbVie Grows Its Presence in Inflammatory and Autoimmune Diseases with Landos Biopharma Acquisition<\/strong><span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>AbbVie Inc. and Landos Biopharma, Inc.<\/strong> have revealed a firm arrangement in which AbbVie is set to purchase Landos, a clinical-stage biopharmaceutical enterprise concentrating on pioneering oral treatments for individuals with autoimmune illnesses. At the forefront of Landos&#8217; portfolio is NX-13, a groundbreaking oral NLRX1 agonist (a part of the NOD-like receptor family) with a dual-action mechanism that is both anti-inflammatory and aids in the restoration of epithelial tissue.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>&#8220;We are acquiring Landos with the goal of advancing the clinical development of NX-13, an innovative, first-of-its-kind oral medication that holds promise for improving the lives of individuals with ulcerative colitis and Crohn&#8217;s disease,&#8221; stated <\/em><strong><em>Dr. Roopal Thakkar, Senior Vice President and Chief Medical Officer of Global Therapeutics at AbbVie<\/em><\/strong><em>.<\/em><\/p>\n<\/blockquote>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>&#8220;This announcement underscores the exceptional capabilities of Landos&#8217; skilled team and their dedication to our shared mission of developing oral therapies to address unmet medical needs,&#8221; remarked <\/em><strong><em>Gregory Oakes, President and CEO of Landos<\/em><\/strong><em>. &#8220;NX-13, with its unique bimodal mechanism of action, could offer a fresh approach to treating ulcerative colitis and Crohn&#8217;s disease. With AbbVie&#8217;s expertise in therapeutic areas and global development, we believe they are well-positioned to propel NX-13 forward.&#8221;<\/em><\/p>\n<\/blockquote>\n\n\n\n<p>NLRX1 plays a role in controlling the balance between immune function and metabolism, as well as in regulating inflammation. Its activation affects various aspects of how <a href=\"https:\/\/www.delveinsight.com\/report-store\/inflammatory-bowel-disease-market\">inflammatory bowel disease (IBD)<\/a> develops. The NEXUS clinical trial, a randomized Phase II study of NX-13 for ulcerative colitis (UC), is presently accepting participants in the United States and Europe (NCT05785715). AbbVie has agreed to acquire Landos for <strong>$20.42 per share<\/strong> in cash upon completion, totaling approximately <strong>$137.5 million<\/strong>, along with an additional non-tradable contingent value right per share worth up to <strong>$11.14<\/strong>, around<strong> $75 million<\/strong> in total. This contingent value right is based on achieving a clinical development milestone. The transaction is anticipated to be finalized in the second quarter of 2024, pending customary closing requirements and approval from Landos&#8217; shareholders.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Regeneron Updates Progress on Biologics License Application for Odronextamab Regeneron Pharmaceuticals, Inc. has announced that the FDA has issued Complete Response Letters (CRLs) regarding the Biologics License Application (BLA) for odronextamab in cases of relapsed\/refractory (R\/R) follicular lymphoma (FL) and relapsed\/refractory (R\/R) diffuse large B-cell lymphoma (DLBCL), each occurring after two or more lines of [&hellip;]<\/p>\n","protected":false},"author":14,"featured_media":27415,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_editorskit_title_hidden":false,"_editorskit_reading_time":0,"_editorskit_is_block_options_detached":false,"_editorskit_block_options_position":"{}","advgb_blocks_editor_width":"","advgb_blocks_columns_visual_guide":"","footnotes":""},"categories":[32],"tags":[56,21920,21921,704,21922,2595,349,420,21919,2699,639,5789,21923],"industry":[17225],"therapeutic_areas":[17242,17233,17228],"class_list":["post-27413","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-notizia","tag-abbvie","tag-b-cell-non-hodgkin-lymphoma","tag-chronic-heart-failure","tag-fda","tag-idorsia","tag-inflammatory-bowel-disease","tag-latest-pharma-news","tag-news","tag-odronextamab","tag-paroxysmal-nocturnal-hemoglobinuria","tag-pharma-news","tag-recent-pharma-news","tag-tryvio","industry-pharmaceutical","therapeutic_areas-cardiovascular-diseases","therapeutic_areas-hematological-disorders","therapeutic_areas-oncology"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v25.8 (Yoast SEO v25.8) - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Pharma News | Regeneron, Novartis, Novo Nordisk, AbbVie<\/title>\n<meta name=\"description\" content=\"Regeneron\u2019s Odronextamab; Novo Nordisk\u2019s Acquisition; Novartis\u2019 Fabhalta; Idorsia\u2019s TRYVIO; AbbVie\u2019s Acquisition\" \/>\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.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pharma News | Regeneron, Novartis, Novo Nordisk, AbbVie\" \/>\n<meta property=\"og:description\" content=\"Regeneron\u2019s Odronextamab; Novo Nordisk\u2019s Acquisition; Novartis\u2019 Fabhalta; Idorsia\u2019s TRYVIO; AbbVie\u2019s Acquisition\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie\" \/>\n<meta property=\"og:site_name\" content=\"DelveInsight Business Research\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/DelveInsight-1423323754607782\/\" \/>\n<meta property=\"article:published_time\" content=\"2024-03-26T09:38:05+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-03-26T09:38:07+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/03\/26150750\/pharma-news-for-regeneron-novartis-novo-nordisk-abbvie.png\" \/>\n\t<meta property=\"og:image:width\" content=\"772\" \/>\n\t<meta property=\"og:image:height\" content=\"482\" \/>\n\t<meta property=\"og:image:type\" content=\"image\/png\" \/>\n<meta name=\"author\" content=\"Sandeep Joshi\" \/>\n<meta name=\"twitter:card\" 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