{"id":59423,"date":"2024-05-24T04:03:29","date_gmt":"2024-05-24T02:03:29","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/celltrion-receives-european-commission-approval-of-omlyclo-ct-p39-the-first-and-only-omalizumab-biosimilar-approved-in-europe\/"},"modified":"2024-05-24T04:03:29","modified_gmt":"2024-05-24T02:03:29","slug":"celltrion-receives-european-commission-approval-of-omlyclo-ct-p39-the-first-and-only-omalizumab-biosimilar-approved-in-europe","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/celltrion-receives-european-commission-approval-of-omlyclo-ct-p39-the-first-and-only-omalizumab-biosimilar-approved-in-europe\/","title":{"rendered":"Celltrion receives European Commission approval of Omlyclo\u00ae (CT-P39), the first and only omalizumab biosimilar approved in Europe"},"content":{"rendered":"<div>\n<ul class=\"bwlistdisc\">\n<li>\nOmlyclo<sup>\u00ae<\/sup> (CT-P39), used to treat allergic asthma, chronic rhinosinusitis with nasal polyps (CRSwNP) and chronic spontaneous urticaria (CSU), becomes the first omalizumab biosimilar approved in the European Union<\/li>\n<li>\nThe European Commission (EC) decision is based on clinical evidence, including results from a Phase III clinical trial demonstrating a comparable efficacy and safety profile with the reference product Xolair<sup>\u00ae<\/sup><\/li>\n<li>\nOmlyclo<sup>\u00ae<\/sup> is the first omalizumab biosimilar in allergic diseases approved by the EC; the approval further bolsters the expansion of Celltrion\u2019s biosimilar portfolio in Europe<\/li>\n<\/ul>\n<p>INCHEON, South Korea&#8211;(BUSINESS WIRE)&#8211;Celltrion today announced that the European Commission (EC) has approved Omlyclo<sup>\u00ae<\/sup> (CT-P39), an omalizumab biosimilar referencing Xolair<sup>\u00ae<\/sup>. Omlyclo<sup>\u00ae<\/sup> is approved for the treatment of allergic asthma, chronic spontaneous urticaria (CSU), and chronic rhinosinusitis with nasal polyps (CRSwNP).<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20240521556727\/en\/2138495\/5\/Celltrion-CI.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20240521556727\/en\/2138495\/22\/Celltrion-CI.jpg\"><\/a><br \/><a href=\"https:\/\/mms.businesswire.com\/media\/20240521556727\/en\/2138495\/5\/Celltrion-CI.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20240521556727\/en\/2138495\/21\/Celltrion-CI.jpg\"><\/a><\/p>\n<p>\nThe EC approval of Omlyclo<sup>\u00ae<\/sup> follows the recommendation for marketing authorisation issued by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) in March 2024.<\/p>\n<p>\nThe decision is based on clinical evidence, including results from a global Phase III clinical trial designed to evaluate the efficacy, safety and pharmacokinetics of Omlyclo<sup>\u00ae<\/sup> compared to the reference product Xolair<sup>\u00ae<\/sup> in patients with CSU up to Week 40.<\/p>\n<p>\n\u201cFor more than two decades, omalizumab, a blockbuster monoclonal antibody anti-IgE, has revolutionised the management of chronic immune-mediated inflammatory diseases,\u201d said Professor Marcus Maurer, Professor of Dermatology and Allergy, Co-Director for the Fraunhofer Site for Immunology and Allergology of the Fraunhofer Translational Medicine and Pharmacology ITMP and Executive Director for the Institute of Allergology, Charit\u00e9 &#8211; Universit\u00e4tsmedizin Berlin, Germany. \u201cThe development of a biosimilar of omalizumab is a welcome solution to help alleviate some challenges with treatment access. The recently approved treatment Omlyclo<sup>\u00ae<\/sup> has a comparable efficacy, safety and immunogenicity profile to Xolair<sup>\u00ae<\/sup>.\u201d<\/p>\n<p>\n\u201cImmunological conditions such as asthma can have a significant impact on the day-to-day lives of patients without appropriate treatment and care. This is why we are pleased to receive the first EC approval for an omalizumab biosimilar in Europe, an important step towards improving patient access to treatment. As we continue to expand our biosimilar offerings across the globe, building on our immunology and oncology product portfolio, we look forward to making a meaningful difference for patients living with immunological conditions,\u201d said Hyoung-Ki Kim, Vice Chairman at Celltrion.<\/p>\n<p>\nOmlyclo<sup>\u00ae<\/sup> is Celltrion\u2019s sixth biosimilar, besides Remsima<sup>\u00ae<\/sup> SC, a subcutaneous formulation of infliximab, approved for use in the EU, following the approval of Remsima<sup>\u00ae <\/sup>(biosimilar infliximab), Truxima<sup>\u00ae<\/sup> (biosimilar rituximab), Herzuma<sup>\u00ae<\/sup> (biosimilar trastuzumab), Yuflyma<sup>\u00ae <\/sup>(biosimilar adalimumab), and Vegzelma<sup>\u00ae<\/sup> (biosimilar bevacizumab). Omlyclo<sup>\u00ae<\/sup> is currently under review by the U.S. Food and Drug Administration (FDA), following the submission in March 2024.<\/p>\n<p>\n<b>About OMLYCLO<sup>\u00ae<\/sup> (CT-P39, biosimilar omalizumab)<\/b><\/p>\n<p>\nOmlyclo<sup>\u00ae<\/sup> is the first European Commission (EC) approved anti-IgE antibody biosimilar referencing Xolair<b><sup>\u00ae <\/sup><\/b>(omalizumab). In the EU, Omlyclo<sup>\u00ae<\/sup> is indicated for the treatment of patients with allergic asthma, chronic spontaneous urticaria (CSU) and chronic rhinosinusitis with nasal polyps (CRSwNP).<\/p>\n<p>\n<b>About Celltrion<\/b><\/p>\n<p>\nCelltrion is a leading biopharmaceutical company based in Incheon, South Korea that specialises in researching, developing, manufacturing, marketing and sales of innovative therapeutics that improve people&#8217;s lives worldwide. The company\u2019s solutions include world-class monoclonal antibody biosimilars such as Remsima<sup>\u00ae<\/sup>, Truxima<sup>\u00ae<\/sup> and Herzuma<sup>\u00ae<\/sup>, providing broader patient access globally. Celltrion has also received U.S. FDA and EC approval for Vegzelma<sup>\u00ae<\/sup> and Yuflyma<sup>\u00ae<\/sup>, FDA approval for Zymfentra\u2122, and EC approval for Remsima<sup>\u00ae <\/sup>SC. To learn more, please visit <a target=\"_blank\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.celltrion.com%2Fen-us&amp;esheet=54013020&amp;newsitemid=20240521556727&amp;lan=en-US&amp;anchor=www.celltrion.com%2Fen-us&amp;index=1&amp;md5=9ef3d59ac459c5f7e3249fe563148d5d\" rel=\"nofollow noopener\" shape=\"rect\">www.celltrion.com\/en-us<\/a>.<\/p>\n<p>\n<b>FORWARD-LOOKING STATEMENT<\/b><\/p>\n<p>\nCertain information set forth in this press release contains statements related to our future business and financial performance and future events or developments involving Celltrion Inc. and its subsidiaries that may constitute forward-looking statements, under pertinent securities laws.<\/p>\n<p>\nThese statements may be identified by words such as \u201cprepares\u201d, \u201chopes to\u201d, \u201cupcoming\u201d, \u201dplans to\u201d, \u201caims to\u201d, \u201cto be launched\u201d, \u201cis preparing, \u201conce gained\u201d, \u201ccould\u201d, \u201cwith the aim of\u201d, \u201cmay\u201d, \u201conce identified\u201d, \u201cwill\u201d, \u201cworking towards\u201d, \u201cis due\u201d, \u201cbecome available\u201d, \u201chas potential to\u201d, the negative of these words or such other variations thereon or comparable terminology.<\/p>\n<p>\nIn addition, our representatives may make oral forward-looking statements. Such statements are based on the current expectations and certain assumptions of Celltrion Inc. and its subsidiaries&#8217; management, of which many are beyond its control.<\/p>\n<p>\nForward-looking statements are provided to allow potential investors the opportunity to understand management\u2019s beliefs and opinions in respect of the future so that they may use such beliefs and opinions as one factor in evaluating an investment. These statements are not guarantees of future performance and undue reliance should not be placed on them.<\/p>\n<p>\nSuch forward-looking statements necessarily involve known and unknown risks and uncertainties, which may cause actual performance and financial results in future periods to differ materially from any projections of future performance or result expressed or implied by such forward-looking statements.<\/p>\n<p>\nAlthough forward-looking statements contained in this presentation are based upon what management of Celltrion Inc. and its subsidiaries believes are reasonable assumptions, there can be no assurance that forward-looking statements will prove to be accurate, as actual results and future events could differ materially from those anticipated in such statements. Celltrion Inc. and its subsidiaries undertake no obligation to update forward-looking statements if circumstances or management\u2019s estimates or opinions should change except as required by applicable securities laws. The reader is cautioned not to place undue reliance on forward-looking statements.<\/p>\n<p>\n<span class=\"bwuline\"><b>Trademark<\/b><\/span><\/p>\n<p>\nXolair<sup>\u00ae<\/sup> is a registered trademark of Novartis AG.<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nHolly Barber<br \/>\n<br \/><a target=\"_blank\" href=\"&#x6d;&#x61;&#x69;&#x6c;&#116;&#111;&#58;hb&#x61;&#x72;&#x62;&#x65;&#x72;&#64;&#104;&#97;no&#x76;&#x65;&#x72;&#x63;&#x6f;&#109;&#109;&#115;&#46;c&#x6f;&#x6d;\" rel=\"nofollow noopener\" shape=\"rect\">hbarber&#64;hano&#118;&#101;&#114;&#99;&#111;&#109;&#109;&#115;&#46;&#99;&#111;&#109;<\/a><br \/>+44 (0) 7759 301620<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Omlyclo\u00ae (CT-P39), used to treat allergic asthma, chronic rhinosinusitis with nasal polyps (CRSwNP) and chronic spontaneous urticaria (CSU), becomes the first omalizumab biosimilar approved in the European Union The European Commission (EC) decision is based on clinical evidence, including results from a Phase III clinical trial demonstrating a comparable efficacy and safety profile with the &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/celltrion-receives-european-commission-approval-of-omlyclo-ct-p39-the-first-and-only-omalizumab-biosimilar-approved-in-europe\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-59423","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Celltrion receives European Commission approval of Omlyclo\u00ae (CT-P39), the first and only omalizumab biosimilar approved in Europe - Pharma Trend<\/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:\/\/pharma-trend.com\/en\/celltrion-receives-european-commission-approval-of-omlyclo-ct-p39-the-first-and-only-omalizumab-biosimilar-approved-in-europe\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Celltrion receives European Commission approval of Omlyclo\u00ae (CT-P39), the first and only omalizumab biosimilar approved in Europe - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"Omlyclo\u00ae (CT-P39), used to treat allergic asthma, chronic rhinosinusitis with nasal polyps (CRSwNP) and chronic spontaneous urticaria (CSU), becomes the first omalizumab biosimilar approved in the European Union The European Commission (EC) decision is based on clinical evidence, including results from a Phase III clinical trial demonstrating a comparable efficacy and safety profile with the ... 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