{"id":29501,"date":"2024-09-10T17:49:20","date_gmt":"2024-09-10T12:19:20","guid":{"rendered":"https:\/\/www.delveinsight.com\/blog\/?p=29501"},"modified":"2024-09-10T17:49:21","modified_gmt":"2024-09-10T12:19:21","slug":"pharma-news-for-biogen-travere-gsk","status":"publish","type":"post","link":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk","title":{"rendered":"Biogen&#8217;s SPINRAZA Phase II\/III Trial Results; Travere\u2019s FILSPARI FDA Approval; GSK&#8217;s NUCALA Succeeds in COPD Trial; Summit&#8217;s NSCLC Win Over KEYTRUDA Raises Caution; FDA Lifts Hold on RZ358 for Congenital Hyperinsulinism"},"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-6a0fee96681e7\" 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-6a0fee96681e7\"  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-biogen-travere-gsk\/#Biogens_Higher_SPINRAZA_Dose_Shows_Improved_Efficacy_in_Phase_IIIII_Trial\" >Biogen&#8217;s Higher SPINRAZA Dose Shows Improved Efficacy in Phase II\/III Trial<\/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-biogen-travere-gsk\/#Travere_Secures_FDA_Approval_for_FILSPARI_in_IgAN_After_FSGS_Setback\" >Travere Secures FDA Approval for FILSPARI in IgAN After FSGS Setback<\/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-biogen-travere-gsk\/#GSKs_NUCALA_Achieves_Success_in_COPD_Phase_III_Trial\" >GSK&#8217;s NUCALA Achieves Success in COPD Phase III Trial<\/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-biogen-travere-gsk\/#Summits_NSCLC_Success_Against_KEYTRUDA_Draws_Caution_Over_China-Only_Data\" >Summit&#8217;s NSCLC Success Against KEYTRUDA Draws Caution Over China-Only Data<\/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-biogen-travere-gsk\/#FDA_Lifts_Partial_Hold_on_RZ358_for_Congenital_Hyperinsulinism_US_Phase_III_Study_to_Continue\" >FDA Lifts Partial Hold on RZ358 for Congenital Hyperinsulinism, U.S. Phase III Study to Continue<\/a><\/li><\/ul><\/nav><\/div>\n\n<h2 class=\"wp-block-heading\" id=\"h-biogen-s-higher-spinraza-dose-shows-improved-efficacy-in-phase-ii-iii-trial\"><span class=\"ez-toc-section\" id=\"Biogens_Higher_SPINRAZA_Dose_Shows_Improved_Efficacy_in_Phase_IIIII_Trial\"><\/span>Biogen&#8217;s Higher SPINRAZA Dose Shows Improved Efficacy in Phase II\/III Trial<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>A trial studying a higher dose of Biogen\u2019s <a href=\"https:\/\/www.delveinsight.com\/report-store\/spinal-muscular-atrophy-market-insights-epidemiology-and-market-forecast\">spinal muscular atrophy<\/a> drug SPINRAZA (nusinersen) has met the primary endpoint in a cohort of infants with SMA. The Phase II\/III DEVOTE study, which included 145 patients across various ages and SMA types, revealed that infants receiving the elevated dose exhibited a significant improvement in motor function compared to a prespecified, untreated control group from the ENDEAR study. The investigational regimen involved a faster loading phase with two 50 mg doses given 14 days apart, followed by a higher maintenance dose of 28 mg every four months, compared to the standard 12 mg dose regimen.<\/p>\n\n\n\n<p>In the study, patients receiving the higher dose showed an adjusted average difference of 26.19 in CHOP-INTEND scores\u2014a measure of motor function in infants with neuromuscular disorders\u2014compared to the sham group. Secondary outcomes also indicated a positive trend for the higher dose, with favorable results on key biomarker and efficacy measures. The higher dose regimen was generally well tolerated, with fewer serious adverse events (60%) compared to the 12 mg group (72%).<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>Stephanie Fradette, head of Biogen&#8217;s neuromuscular development unit, commented, \u201cWhile there has been remarkable progress in the treatment of SMA, there remains significant unmet need. Building on the well-characterized profile of SPINRAZA established over the past 10 years, we continue to explore the potential for maximizing efficacy outcomes while maintaining our commitment to safety.\u201d Biogen now plans to seek regulatory approval for this higher dose regimen. SPINRAZA, which generated $1.74 billion in sales for Biogen in 2023, is expected to see a decline in revenue, projected to reach $1.13 billion by 2030, due to shipment timing issues, increased competition, and pricing pressures outside the U.S.<\/em><\/p>\n<\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-travere-secures-fda-approval-for-filspari-in-igan-after-fsgs-setback\"><span class=\"ez-toc-section\" id=\"Travere_Secures_FDA_Approval_for_FILSPARI_in_IgAN_After_FSGS_Setback\"><\/span>Travere Secures FDA Approval for FILSPARI in IgAN After FSGS Setback<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The FDA has granted full approval to Travere Therapeutics\u2019 FILSPARI (sparsentan) for the treatment of primary <a href=\"https:\/\/www.delveinsight.com\/report-store\/iga-nephropathy-igan-market\">IgA nephropathy (IgAN)<\/a>, upgrading its previous accelerated approval status. This decision broadens the drug&#8217;s use by eliminating the prior requirement of a urine protein-to-creatinine ratio (UPCR) above 1.5g\/g, making it available to a wider range of patients at risk of disease progression.<\/p>\n\n\n\n<p>The full approval comes with a boxed warning for potential hepatotoxicity and birth defects, leading to FILSPARI being distributed under a Risk Evaluation and Mitigation Strategies (REMS) program. The FDA requires kidney function monitoring before initiating treatment, with monthly tests during the first year and quarterly checks thereafter.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>Stephanie Fradette, head of the neuromuscular development unit at Biogen, stated, \u201cWhile there has been remarkable progress in the treatment of SMA, there remains significant unmet need. Building on the well-characterized profile of SPINRAZA established over the past 10 years, we continue to explore the potential for maximizing efficacy outcomes while maintaining our commitment to safety.\u201d In related news, Travere had previously sought approval for sparsentan for focal segmental glomerulosclerosis (FSGS) but faced additional data requests, leading the company to streamline its operations and focus on FILSPARI\u2019s IgAN launch. Meanwhile, FILSPARI will compete with <\/em><a href=\"https:\/\/www.delveinsight.com\/blog\/crovalimab-for-pnh-treatment\"><em>Novartis\u2019s FABHALTA<\/em><\/a><em> (iptacopan), atrasentan, and zigakibart, with recent advancements in these therapies adding to the dynamic treatment landscape for IgAN.<\/em><\/p>\n<\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-gsk-s-nucala-achieves-success-in-copd-phase-iii-trial\"><span class=\"ez-toc-section\" id=\"GSKs_NUCALA_Achieves_Success_in_COPD_Phase_III_Trial\"><\/span>GSK&#8217;s NUCALA Achieves Success in COPD Phase III Trial<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>GSK\u2019s asthma medication NUCALA (mepolizumab) has achieved its primary endpoint in a Phase III trial for <a href=\"https:\/\/www.delveinsight.com\/report-store\/chronic-obstructive-pulmonary-disease-copd-market\">chronic obstructive pulmonary disease (COPD)<\/a>. The MATINEE study demonstrated that adding NUCALA to inhaled maintenance therapy significantly reduced the annualized rate of moderate or severe COPD exacerbations compared to a placebo. While GSK has not released detailed data, they reported a &#8220;statistically significant and clinically meaningful reduction&#8221; in exacerbations over up to two years, with preliminary safety results aligning with NUCALA\u2019s established profile.<\/p>\n\n\n\n<p>The late-stage trial, involving 806 patients aged 40 and older, was conducted globally across the Americas, Europe, and Asia. NUCALA was administered as a subcutaneous injection every four weeks in addition to standard therapy. GSK plans to submit regulatory filings for NUCALA\u2019s COPD indication in the EU and Canada by 2025, although a specific timeline was not confirmed.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>GSK spokesperson said, \u201cWe are pleased with the results of the MATINEE study and are committed to advancing NUCALA as a treatment option for COPD. Our next steps include further data analysis to fully understand the benefits and safety of NUCALA in this new indication.\u201d NUCALA, which generated \u00a31.6 billion ($2.1 billion) in revenue in 2023, is forecasted to peak at $2.35 billion in sales by 2026. Meanwhile, Sanofi\u2019s DUPIXENT (dupilumab) recently became the first targeted therapy approved for adults with uncontrolled COPD, underscoring the growing competition in this therapeutic area.<\/em><\/p>\n<\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-summit-s-nsclc-success-against-keytruda-draws-caution-over-china-only-data\"><span class=\"ez-toc-section\" id=\"Summits_NSCLC_Success_Against_KEYTRUDA_Draws_Caution_Over_China-Only_Data\"><\/span>Summit&#8217;s NSCLC Success Against KEYTRUDA Draws Caution Over China-Only Data<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Summit Therapeutics has unveiled promising data from its Phase III HARMONi-2 trial, indicating that its investigational bispecific antibody, ivonescimab, significantly outperforms Merck\u2019s KEYTRUDA (pembrolizumab) in treating advanced <a href=\"https:\/\/www.delveinsight.com\/report-store\/non-small-cell-lung-cancer-nsclc-market\">non-small cell lung cancer (NSCLC)<\/a>. Ivonescimab showed a 49% reduction in the risk of disease progression or death compared to KEYTRUDA, with a median progression-free survival (PFS) of 11.14 months versus 5.82 months for KEYTRUDA. The results, presented at the International Association for the Study of Lung Cancer\u2019s 2024 World Conference on Lung Cancer, are statistically significant with a p-value of less than 0.0001.<\/p>\n\n\n\n<p><em>Despite these impressive results, analysts urge caution. BMO Capital Markets\u2019 Evan Seigerman emphasized that while ivonescimab shows strong performance, it is &#8220;not yet the KEYTRUDA slayer.&#8221; He pointed out that the trial was conducted exclusively in China, which may limit the generalizability of the findings to other populations. Additionally, Summit has yet to release overall survival (OS) data, which is crucial for treatment decisions.<\/em><\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>Summit CEO Maky Zanganeh expressed optimism, stating, \u201cHARMONi-2 clearly demonstrates that ivonescimab has the potential to be the next generation in PD-1 directed immunotherapy.\u201d Zanganeh also highlighted the potential for ivonescimab to extend beyond lung cancer to other tumors. Summit plans to advance ivonescimab into the multi-regional HARMONi-7 study, set to begin in early 2025, with the goal of securing broader regulatory approval. However, analysts like Truist Securities\u2019 Srikripa Devarakonda caution that the current regional focus of the study may impact U.S. approval timelines, given the need for additional global data.<\/em><\/p>\n<\/blockquote>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-fda-lifts-partial-hold-on-rz358-for-congenital-hyperinsulinism-u-s-phase-iii-study-to-continue\"><span class=\"ez-toc-section\" id=\"FDA_Lifts_Partial_Hold_on_RZ358_for_Congenital_Hyperinsulinism_US_Phase_III_Study_to_Continue\"><\/span>FDA Lifts Partial Hold on RZ358 for Congenital Hyperinsulinism, U.S. Phase III Study to Continue<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>Rezolute, Inc. announced a significant regulatory milestone: the FDA has lifted the partial clinical holds on RZ358 (ersodetug), a novel therapy for treating <a href=\"https:\/\/www.delveinsight.com\/report-store\/hypoglycemia-market\">hypoglycemia<\/a> associated with congenital hyperinsulinism (HI). This decision clears the way for Rezolute to move forward with the U.S. component of the global Phase III sunRIZE study, which is a multi-center, double-blind, randomized, placebo-controlled trial assessing the safety and efficacy of ersodetug.<\/p>\n\n\n\n<p>With the partial holds removed, Rezolute will begin preparations to enroll U.S. participants in early 2025, aiming to include them in the ongoing sunRIZE study. The company expects to announce topline results from the study in the latter half of 2025. The FDA\u2019s decision also allows the inclusion of participants as young as three months old and confirms that the liver toxicity observed in preclinical studies with Sprague Dawley rats is considered strain-specific and not applicable to humans.<\/p>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><em>Rezolute CEO and Founder Nevan Charles Elam expressed enthusiasm about the development, stating, \u201cWe are delighted that the FDA has completely removed the partial clinical holds and are allowing us to proceed in the U.S. at all doses and in participants as young as three months of age. The FDA\u2019s conclusion that the liver toxicity observed in rats is likely strain-specific is particularly encouraging.\u201d Elam also highlighted the recent FDA clearance for a separate Phase III study in tumor-associated HI, positioning Rezolute to advance ersodetug in two significant Phase III programs both in the U.S. and globally.<\/em><\/p>\n<\/blockquote>\n","protected":false},"excerpt":{"rendered":"<p>Biogen&#8217;s Higher SPINRAZA Dose Shows Improved Efficacy in Phase II\/III Trial A trial studying a higher dose of Biogen\u2019s spinal muscular atrophy drug SPINRAZA (nusinersen) has met the primary endpoint in a cohort of infants with SMA. The Phase II\/III DEVOTE study, which included 145 patients across various ages and SMA types, revealed that infants [&hellip;]<\/p>\n","protected":false},"author":20,"featured_media":29502,"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":[719,718,204,704,17539,18841,349,420,639,5789,2031],"industry":[17225],"therapeutic_areas":[17240,17245,17228],"class_list":["post-29501","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-notizia","tag-chronic-obstructive-pulmonary-disease","tag-copd","tag-delveinsight","tag-fda","tag-hypoglycemia","tag-iga-nephropathy","tag-latest-pharma-news","tag-news","tag-pharma-news","tag-recent-pharma-news","tag-spinal-muscular-atrophy","industry-pharmaceutical","therapeutic_areas-endocrinology-and-metabolic-disorders","therapeutic_areas-neurology","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 | Biogen, Travere, GSK<\/title>\n<meta name=\"description\" content=\"Biogen\u2019s SPINRAZA, Travere\u2019s FILSPARI\u2019s FDA Approval, GSK\u2019s NUCALA, Summit\u2019s NSCLC victory, FDA\u2019s hold on Rezolute\u2019s RZ358\" \/>\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-biogen-travere-gsk\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Pharma News | Biogen, Travere, GSK\" \/>\n<meta property=\"og:description\" content=\"Biogen\u2019s SPINRAZA, Travere\u2019s FILSPARI\u2019s FDA Approval, GSK\u2019s NUCALA, Summit\u2019s NSCLC victory, FDA\u2019s hold on Rezolute\u2019s RZ358\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk\" \/>\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=\"2024-09-10T12:19:20+00:00\" \/>\n<meta property=\"article:modified_time\" content=\"2024-09-10T12:19:21+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/09\/10174849\/Pharma-news-for-biogen-travere-GSK.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=\"Jatin Vimal\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:creator\" content=\"@DelveInsight\" \/>\n<meta name=\"twitter:site\" content=\"@DelveInsight\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Jatin Vimal\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"4 minutes\" \/>\n<!-- \/ Yoast SEO Premium plugin. -->","yoast_head_json":{"title":"Pharma News | Biogen, Travere, GSK","description":"Biogen\u2019s SPINRAZA, Travere\u2019s FILSPARI\u2019s FDA Approval, GSK\u2019s NUCALA, Summit\u2019s NSCLC victory, FDA\u2019s hold on Rezolute\u2019s RZ358","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk","og_locale":"en_US","og_type":"article","og_title":"Pharma News | Biogen, Travere, GSK","og_description":"Biogen\u2019s SPINRAZA, Travere\u2019s FILSPARI\u2019s FDA Approval, GSK\u2019s NUCALA, Summit\u2019s NSCLC victory, FDA\u2019s hold on Rezolute\u2019s RZ358","og_url":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk","og_site_name":"DelveInsight Business Research","article_publisher":"https:\/\/www.facebook.com\/DelveInsight-1423323754607782\/","article_published_time":"2024-09-10T12:19:20+00:00","article_modified_time":"2024-09-10T12:19:21+00:00","og_image":[{"width":772,"height":482,"url":"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/09\/10174849\/Pharma-news-for-biogen-travere-GSK.png","type":"image\/png"}],"author":"Jatin Vimal","twitter_card":"summary_large_image","twitter_creator":"@DelveInsight","twitter_site":"@DelveInsight","twitter_misc":{"Written by":"Jatin Vimal","Est. reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk","url":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk","name":"Pharma News | Biogen, Travere, GSK","isPartOf":{"@id":"https:\/\/www.delveinsight.com\/blog\/#website"},"primaryImageOfPage":{"@id":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk#primaryimage"},"image":{"@id":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk#primaryimage"},"thumbnailUrl":"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/09\/10174849\/Pharma-news-for-biogen-travere-GSK.png","datePublished":"2024-09-10T12:19:20+00:00","dateModified":"2024-09-10T12:19:21+00:00","author":{"@id":"https:\/\/www.delveinsight.com\/blog\/#\/schema\/person\/c846f0323e948c55336d657b654f3158"},"description":"Biogen\u2019s SPINRAZA, Travere\u2019s FILSPARI\u2019s FDA Approval, GSK\u2019s NUCALA, Summit\u2019s NSCLC victory, FDA\u2019s hold on Rezolute\u2019s RZ358","inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk"]}]},{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.delveinsight.com\/blog\/pharma-news-for-biogen-travere-gsk#primaryimage","url":"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/09\/10174849\/Pharma-news-for-biogen-travere-GSK.png","contentUrl":"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/09\/10174849\/Pharma-news-for-biogen-travere-GSK.png","width":772,"height":482,"caption":"Pharma-news-for-biogen-travere-GSK"},{"@type":"WebSite","@id":"https:\/\/www.delveinsight.com\/blog\/#website","url":"https:\/\/www.delveinsight.com\/blog\/","name":"DelveInsight Business Research","description":"Blog","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/www.delveinsight.com\/blog\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Person","@id":"https:\/\/www.delveinsight.com\/blog\/#\/schema\/person\/c846f0323e948c55336d657b654f3158","name":"Jatin Vimal","image":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/www.delveinsight.com\/blog\/#\/schema\/person\/image\/","url":"https:\/\/secure.gravatar.com\/avatar\/10dcf4b5071c366691525fa20af33b87e8a3897e6d0acc1a2b09a7b99b8d8ae1?s=96&d=mm&r=g","contentUrl":"https:\/\/secure.gravatar.com\/avatar\/10dcf4b5071c366691525fa20af33b87e8a3897e6d0acc1a2b09a7b99b8d8ae1?s=96&d=mm&r=g","caption":"Jatin Vimal"},"sameAs":["https:\/\/www.delveinsight.com"]}]}},"author_meta":{"display_name":"Jatin Vimal","author_link":"https:\/\/www.delveinsight.com\/blog\/author\/jatin"},"featured_img":"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2024\/09\/10174849\/Pharma-news-for-biogen-travere-GSK-300x187.png","coauthors":[],"tax_additional":{"categories":{"linked":["<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">Notizia - Recent Pharma, Healthcare and Biotech Happenings<\/a>"],"unlinked":["<span class=\"advgb-post-tax-term\">Notizia - Recent Pharma, Healthcare and Biotech Happenings<\/span>"]},"tags":{"linked":["<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">Chronic Obstructive Pulmonary Disease<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">COPD<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">DelveInsight<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">FDA<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">Hypoglycemia<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">IgA Nephropathy<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">Latest pharma news<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">news<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">pharma news<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">recent pharma news<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">spinal muscular atrophy<\/a>"],"unlinked":["<span class=\"advgb-post-tax-term\">Chronic Obstructive Pulmonary Disease<\/span>","<span class=\"advgb-post-tax-term\">COPD<\/span>","<span class=\"advgb-post-tax-term\">DelveInsight<\/span>","<span class=\"advgb-post-tax-term\">FDA<\/span>","<span class=\"advgb-post-tax-term\">Hypoglycemia<\/span>","<span class=\"advgb-post-tax-term\">IgA Nephropathy<\/span>","<span class=\"advgb-post-tax-term\">Latest pharma news<\/span>","<span class=\"advgb-post-tax-term\">news<\/span>","<span class=\"advgb-post-tax-term\">pharma news<\/span>","<span class=\"advgb-post-tax-term\">recent pharma news<\/span>","<span class=\"advgb-post-tax-term\">spinal muscular atrophy<\/span>"]}},"comment_count":"0","relative_dates":{"created":"Posted 2 years ago","modified":"Updated 2 years ago"},"absolute_dates":{"created":"Posted on Sep 10, 2024","modified":"Updated on Sep 10, 2024"},"absolute_dates_time":{"created":"Posted on Sep 10, 2024 5:49 pm","modified":"Updated on Sep 10, 2024 5:49 pm"},"featured_img_caption":"Pharma-news-for-biogen-travere-GSK\n","series_order":"","_links":{"self":[{"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/posts\/29501","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/users\/20"}],"replies":[{"embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/comments?post=29501"}],"version-history":[{"count":1,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/posts\/29501\/revisions"}],"predecessor-version":[{"id":29503,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/posts\/29501\/revisions\/29503"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/media\/29502"}],"wp:attachment":[{"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/media?parent=29501"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/categories?post=29501"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/tags?post=29501"},{"taxonomy":"industry","embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/industry?post=29501"},{"taxonomy":"therapeutic_areas","embeddable":true,"href":"https:\/\/www.delveinsight.com\/blog\/wp-json\/wp\/v2\/therapeutic_areas?post=29501"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}