{"id":730000,"date":"2023-02-09T02:33:10","date_gmt":"2023-02-09T07:33:10","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\/"},"modified":"2023-02-09T02:33:10","modified_gmt":"2023-02-09T07:33:10","slug":"ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\/","title":{"rendered":"EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab)"},"content":{"rendered":"<div class=\"mw_release\">\n<ul>\n<li>Partners Alvotech and STADA have marketing authorization application (MAA) for ustekinumab accepted for filing by the European Medicines Agency (EMA)<\/li>\n<\/ul>\n<ul>\n<li style=\"margin-bottom:12pt\">EMA opinion on AVT04 could come as soon as the second half of 2023<\/li>\n<li>Reference product Stelara<sup>\u00ae<\/sup>\u00a0(ustekinumab) is prescribed to treat a variety of inflammatory conditions<\/li>\n<\/ul>\n<p>REYKJAVIK, Iceland and BAD VILBEL, Germany, Feb.  09, 2023  (GLOBE NEWSWIRE) &#8212; Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, and global pharmaceutical company STADA Arzneimittel (STADA) today announced that the European Medicines Agency (EMA) has accepted a Marketing Authorization Application for AVT04, Alvotech\u2019s proposed biosimilar to Stelara<sup>\u00ae<\/sup> (ustekinumab). The companies anticipate that the EMA could recommend approving a marketing authorization for AVT04 as soon as in the second half of 2023.<\/p>\n<p>\u201cWe are pleased to be able to move closer to making AVT04 available to patients in Europe,&#8221; said Joseph McClellan, Chief Scientific Officer of Alvotech. &#8220;Our goal is to meet an increasing need for broader access to affordable biologic medicines and Alvotech\u2019s end-to-end biosimilars platform is designed to support the development and manufacture of multiple products simultaneously.\u201d<\/p>\n<p>\u201cThe EMA\u2019s acceptance for filing marks a key milestone in making an additional treatment option for inflammatory conditions available to patients and physicians in Europe,\u201d commented STADA\u2019s Head of Specialty, Bryan Kim. \u201cAuthorization for ustekinumab would add to STADA\u2019s extensive range of six approved biosimilars in Europe, a portfolio that includes a high-concentration, citrate-free of adalimumab brought to market through our strategic partnership with Alvotech.\u201d<\/p>\n<p>In <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=lRibjcYKb6-7L848jTC66SDkaEv6_Raea4--3VuqdETKOsaWjVETLBzep6wkYGLpqENpR51vJO6wdxOEXKScF8A1_j7Z99IUtNKuxkoV04tlonBwK9bj6-ciVkbrVWbuTgQI79zd8-yZHCO1wrcdsmjvIt_qXDiYOdA3h7uYeZSw3eoOUy6_-AkkiuH5ofT6\" rel=\"nofollow noopener\" target=\"_blank\">November 2019<\/a>, Alvotech and STADA announced a strategic partnership to commercialize eight biosimilar candidates developed by Alvotech in Europe. As of December 2022, the companies had launched marketing and sales of the first biosimilar in the partnership, high-concentration adalimumab, in <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=wnkBtNf0WdWnQ-j83Z8oUODRGjAnXs7g8lMVDE2FVUD2Gs5mo40vp3wfdvQq3-0J7gL73jE6QBDtk8BXkvI7Ypu854twzZuxs5xRYSp2JV1wJFDEryU-v7lmhAWpWj5BMP86DCkB950gLTpn9iiRMJtOINBZbn3mvgU1c_k3Eelj0IcX8QObk1w1rTlvlxvlF-nG-C7yrSP9CbA78bSK76LHQ_G4XkB7nCxdVzMleDM=\" rel=\"nofollow noopener\" target=\"_blank\">16 countries in Europe<\/a>.<\/p>\n<p>In <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=Xh43SL7JIDoKO0iUVTshdnFWNl9G9mJirY5l7_kBwbHWSeaZtZpisjceLhmBNlF_nJ___9XVJfbt1P1A8bMjPFD_k9AQoRY30v1PsM5y0a9JtSuuYIVJ-z2_6rxn-ocs8ZqpndupIV0WGUf1nt7b6xngQiES05tK_6JL5LK1fVz8LWWAarASdxgPhzoMNSyADbw4TdYSV5-R3S35a2phCw==\" rel=\"nofollow noopener\" target=\"_blank\">May 2022<\/a>, Alvotech announced that a confirmatory clinical, safety and efficacy study for AVT04 had met its primary endpoint, in demonstrating therapeutic equivalence between Alvotech\u2019s biosimilar candidate and the reference product in patients with moderate to severe chronic plaque-type psoriasis. <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=99R5xtmy3rmIlDkxO8nmf1qYJvzeHKAw-hNCvioHUWGPybwku6uCoe0RguIKcPyQw41H_anrAAmJHsUeEjCfFxl9QzdhLAKj9FBwr0pgdKbpoinA5cr8E6B87WCMSv-sC2G9kY7bE5OVH4DHUqb8yxABiDAznCeIQzAlGqy6cpGlvtKyXMVkibJDuOO4MeBfWCjC0aUfO9CCnTvqAWyMH5Be5tfBdii-q1IBmeHJ45E=\" rel=\"nofollow noopener\" target=\"_blank\">Earlier in May 2022<\/a>, Alvotech also announced positive top-line results from a pharmacokinetic (PK) similarity study for AVT04. <\/p>\n<p>* Stelara<sup>\u00ae<\/sup> is a registered trademark of Johnson &amp; Johnson<\/p>\n<p>\n        <strong>About AVT04 (ustekinumab)<\/strong><br \/>\n        <br \/>AVT04 is a monoclonal antibody and a biosimilar candidate to Stelara<sup>\u00ae<\/sup> (ustekinumab). Ustekinumab binds to two cytokines, IL-12 and IL-23, that are involved in inflammatory and immune responses <sup>[1]<\/sup>. AVT04 is an investigational product and has not received regulatory approval in any country. Biosimilarity has not been established by regulatory authorities and is not claimed.<\/p>\n<p>\n        <sup>[1]<\/sup> https:\/\/www.janssenlabels.com\/package-insert\/product-monograph\/prescribing-information\/STELARA-pi.pdf<\/p>\n<p><strong>About STADA Arzneimittel AG <\/strong><br \/>STADA Arzneimittel AG is headquartered in Bad Vilbel, Germany. The company focuses on a three-pillar strategy consisting of generics, specialty pharma and non-prescription consumer healthcare products. Worldwide, STADA Arzneimittel AG sells its products in approximately 120 countries. In financial year 2021, STADA achieved group sales of EUR 3,249.5 million and reported earnings before interest, taxes, depreciation and amortization (EBITDA) of EUR 776.5 million. As of 31 December 2021, STADA employed 12,520 people worldwide.<\/p>\n<p><strong>About Alvotech <\/strong><br \/>Alvotech is a biotech company, founded by Robert Wessman, focused solely on the development and manufacture of biosimilar medicines for patients worldwide. Alvotech seeks to be a global leader in the biosimilar space by delivering high quality, cost-effective products, and services, enabled by a fully integrated approach and broad in-house capabilities. Alvotech\u2019s current pipeline contains eight biosimilar candidates aimed at treating autoimmune disorders, eye disorders, osteoporosis, respiratory disease, and cancer. Alvotech has formed a network of strategic commercial partnerships to provide global reach and leverage local expertise in markets that include the United States, Europe, Japan, China, and other Asian countries and large parts of South America, Africa and the Middle East. Alvotech\u2019s commercial partners include Teva Pharmaceuticals, a US affiliate of Teva Pharmaceutical Industries Ltd. (US), STADA Arzneimittel AG (EU), Fuji Pharma Co., Ltd (Japan), Cipla\/Cipla Gulf\/Cipla Med Pro (Australia, New Zealand, South Africa\/Africa), JAMP Pharma Corporation (Canada), Yangtze River Pharmaceutical (Group) Co., Ltd. (China), DKSH (Taiwan, Hong Kong, Cambodia, Malaysia, Singapore, Indonesia, India, Bangladesh and Pakistan), YAS Holding LLC (Middle East and North Africa), Abdi Ibrahim (Turkey), Kamada Ltd. (Israel), Mega Labs, Stein, Libbs, Tuteur and Saval (Latin America) and Lotus Pharmaceuticals Co., Ltd. (Thailand, Vietnam, Philippines, and South Korea). Each commercial partnership covers a unique set of product(s) and territories. Except as specifically set forth therein, Alvotech disclaims responsibility for the content of periodic filings, disclosures and other reports made available by its partners. For more information, please visit <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=sfRCxIpGpbdSOxyjNMZSM8BcEHATOumfx9tQHPNIIhG_Pl3qzEo0_dmCp6gBVIk63_nk3zRs__U-_AWBCQ7xlA==\" rel=\"nofollow noopener\" target=\"_blank\"><u>www.alvotech.com<\/u><\/a>. None of the information on the Alvotech website shall be deemed part of this press release.<\/p>\n<p>\n        <strong>Forward Looking Statements<\/strong><br \/>\n        <br \/>Certain statements in this communication may be considered \u201cforward-looking statements\u201d within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements generally relate to future events or the future financial operating performance of Alvotech and may include, for example, Alvotech\u2019s expectations regarding competitive advantages, business prospects and opportunities including pipeline product development, future plans and intentions, results, level of activities, performance, goals or achievements or other future events, regulatory review and interactions, the success of its commercial partnerships, including its partnership with STADA, potential milestone and royalty payments, the potential approval and commercial launch of its product candidates, the timing of regulatory approvals and market launches, including in Europe, and the estimated size of the total addressable market of Alvotech\u2019s pipeline products, and the commercial success of AVT04, in Europe and other parts of the world, Alvotech\u2019s ability to improve global access to affordable biologics, and the effect of biosimilars on inflationary pressures for healthcare systems. In some cases, you can identify forward-looking statements by terminology such as \u201cmay\u201d, \u201cshould\u201d, \u201cexpect\u201d, \u201cintend\u201d, \u201cwill\u201d, \u201cestimate\u201d, \u201canticipate\u201d, \u201cbelieve\u201d, \u201cpredict\u201d, \u201cpotential\u201d, \u201caim\u201d or \u201ccontinue\u201d, or the negatives of these terms or variations of them or similar terminology. Such forward-looking statements are subject to risks, uncertainties, and other factors which could cause actual results to differ materially from those expressed or implied by such forward-looking statements. These forward-looking statements are based upon estimates and assumptions that, while considered reasonable by Alvotech and its management, are inherently uncertain and are inherently subject to risks, variability, and contingencies, many of which are beyond Alvotech\u2019s control. Factors that may cause actual results to differ materially from current expectations include, but are not limited to: (1) the outcome of any legal proceedings that may be instituted against Alvotech or others following the business combination between Alvotech Holdings S.A., Oaktree Acquisition Corp. II and Alvotech; (2) changes in applicable laws or regulations; (3) the possibility that Alvotech may be adversely affected by other economic, business, and\/or competitive factors; (4) Alvotech\u2019s estimates of expenses and profitability; (5) Alvotech\u2019s ability to develop, manufacture and commercialize the products and product candidates in its pipeline, including AVT04; (6) actions of regulatory authorities, which may affect the initiation, timing and progress of clinical studies or future regulatory approvals or marketing authorizations; (7) the ability of Alvotech or its partners to respond to inspection findings and resolve deficiencies to the satisfaction of the regulators; (8) the ability of Alvotech or its partners to enroll and retain patients in clinical studies; (9) the ability of Alvotech or its partners to gain approval from regulators for planned clinical studies, study plans or sites; (10) the ability of Alvotech\u2019s partners to conduct, supervise and monitor existing and potential future clinical studies, which may impact development timelines and plans; (11) Alvotech\u2019s ability to obtain and maintain regulatory approval or authorizations of its products, including AVT04, including the timing or likelihood of expansion into additional markets or geographies; (12) the success of Alvotech\u2019s current and future collaborations, joint ventures, partnerships or licensing arrangements, including the partnership with STADA; (13) Alvotech\u2019s ability, and that of its commercial partners, to execute their commercialization strategy for approved products, including AVT04; (14) Alvotech\u2019s ability to manufacture sufficient commercial supply of its approved products, including AVT04; (15) the outcome of ongoing and future litigation regarding Alvotech\u2019s products and product candidates; (16) the potential impact of the ongoing COVID-19 pandemic on the FDA\u2019s review timelines, including its ability to complete timely inspection of manufacturing sites; and (17) other risks and uncertainties set forth in the sections entitled \u201cRisk Factors\u201d and \u201cCautionary Note Regarding Forward-Looking Statements\u201d in documents that Alvotech may from time to time file or furnish with the SEC. There may be additional risks that Alvotech does not presently know or that Alvotech currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements. Nothing in this communication should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements, which speak only as of the date they are made. Alvotech does not undertake any duty to update these forward-looking statements or to inform the recipient of any matters of which any of them becomes aware of which may affect any matter referred to in this communication. Alvotech disclaims any and all liability for any loss or damage (whether foreseeable or not) suffered or incurred by any person or entity as a result of anything contained or omitted from this communication and such liability is expressly disclaimed. The recipient agrees that it shall not seek to sue or otherwise hold Alvotech or any of its directors, officers, employees, affiliates, agents, advisors, or representatives liable in any respect for the provision of this communication, the information contained in this communication, or the omission of any information from this communication.<\/p>\n<p>\n        <strong>CONTACTS<\/strong><\/p>\n<p>        <strong><br \/>\n          <em>Alvotech Investor Relations and Global Communications:<\/em><br \/>\n        <\/strong><br \/>\n        <br \/>Benedikt Stefansson, Director<br \/>E-Mail: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=fvbciXXx0tNsehVpQSvaRAdzkj80mZvHJqlLmfeX6Dbtuqw8FFzmqk-rpvXr-WvAQx5RaO0vz7xs_c6YrPYdugBkDTtB95d2osvqFqXdSfHBg21h9uLCQdOKcMHg0fUM\" rel=\"nofollow noopener\" target=\"_blank\"><u>alvotech.ir[at]alvotech.com<\/u><\/a><br \/>Web: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=HBG9-a1cC1GG9NM7plGFOgqKE7hMsXXWrUI2LjyicsRvEMsH9vJlz3gY-zy4cbQxuiBjw6S-ycuxKBW2BL2e2e-nDp9a2yMKdg5mwjSaBQp9t40jYjKiA7IpEnHIrnQr\" rel=\"nofollow noopener\" target=\"_blank\">https:\/\/investors.alvotech.com<\/a><br \/>LinkedIn: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=HBG9-a1cC1GG9NM7plGFOqElT8imNvOIrVnl-nfFVE9n60PRXEwQdnpgkx7TJhlqyJcMbcVPuX4Z0IeknN3Mzvj9W6R6maPK1oWOqXc0Aak0gg3qlTn788QnRI37WZHVLcjCxcuuwKBjVpp3_qmrEQ==\" rel=\"nofollow noopener\" target=\"_blank\">https:\/\/www.linkedin.com\/company\/alvotechpr\/<\/a><\/p>\n<p><strong><em>STADA information for journalists:<\/em><\/strong><br \/>STADA Arzneimittel AG &#8211; Media Relations<br \/>Stadastrasse 2-18<br \/>61118 Bad Vilbel &#8211; Germany <br \/>Phone: +49 (0) 6101 603-165<br \/>Fax: +49 (0) 6101 603-215<br \/>E-Mail: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=cukLCNW4ppKp4EhDiXJL0pbQYhDPA2S56I1FekGlAn7L1ZJ2XTCLF2RtZRj0xnWzvTCxts4rMmHnoOQ5gKYjMw==\" rel=\"nofollow noopener\" target=\"_blank\">press@stada.de<\/a><br \/>Or visit us on the Internet at <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=sfRCxIpGpbdSOxyjNMZSMzc9zXvpPPAMlqTAUA3nI2Vc2gayaehUQfYG5rynK1hx5hKbdnUUOuLv7LWQB09smERQs-8HxX6D71vPgjj7VgE=\" rel=\"nofollow noopener\" target=\"_blank\">www.stada.com\/press<\/a><br \/>Follow STADA on <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=CuxmbYRR4Xq6bhEfr_uPDzy9_j5kR5mSSoVvAIFb2BWOQP2Ruj3KV38eU0Z9LZeVStl0ZIorR-YSEtpr0uUKdMsbMzG7Vi0DglJy0TKRWu5v0Zjzzuc_BBgPapocJTUj\" rel=\"nofollow noopener\" target=\"_blank\">LinkedIn<\/a><\/p>\n<p><strong><em>STADA information for capital market participants:<\/em><\/strong><br \/>STADA Arzneimittel AG &#8211; Investor &amp; Creditor Relations <br \/>Stadastrasse 2-18<br \/>61118 Bad Vilbel \u2013 Germany<br \/>Phone: +49 (0) 6101 603-4689<br \/>Fax: +49 (0) 6101 603-215<br \/>E-mail: <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=y57JZNiV25dMVhPFAb6JmrDTLNA1O_UTF8oRshGXdMdpAb3PrQSRV-U_BPslDK7GZt1RKei3UYRpF8Q4sGn94Q==\" rel=\"nofollow noopener\" target=\"_blank\">ir@stada.de<\/a><br \/>Or visit us on the Internet at <a href=\"https:\/\/www.globenewswire.com\/Tracker?data=sfRCxIpGpbdSOxyjNMZSM8f7kSgVi_ZiWxOnpfBekPMOvtblzWG-XfSHtj9mN0Ri-2eiVPGXPtsMIlHjMzTRjgXbpMX5EJbHAs5tAR1GbsXNIKYjf575r657b-gwMd6l\" rel=\"nofollow noopener\" target=\"_blank\">www.stada.com\/investor-relations<\/a><\/p>\n<p>      <img decoding=\"async\" class=\"__GNW8366DE3E__IMG\" src=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=MTAwMDc4MTYzOCM0MDE0ODA4MzUjMjIzMzgzMw==\" \/><br \/>\n      <br \/>\n      <img decoding=\"async\" src=\"https:\/\/ml-eu.globenewswire.com\/media\/MWVjMDA3YmUtNjg4NC00ZTljLWIxNDgtYWY3ODc5NmI2NzIxLTEyNDUzODY=\/tiny\/Alvotech.png\" \/>\n    <\/div>\n<div class=\"mw_contactinfo\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Partners Alvotech and STADA have marketing authorization application (MAA) for ustekinumab accepted for filing by the European Medicines Agency (EMA) EMA opinion on AVT04 could come as soon as the second half of 2023 Reference product Stelara\u00ae\u00a0(ustekinumab) is prescribed to treat a variety of inflammatory conditions REYKJAVIK, Iceland and BAD VILBEL, Germany, Feb. 09, 2023 (GLOBE NEWSWIRE) &#8212; Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, and global pharmaceutical company STADA Arzneimittel (STADA) today announced that the European Medicines Agency (EMA) has accepted a Marketing Authorization Application for AVT04, Alvotech\u2019s proposed biosimilar to Stelara\u00ae (ustekinumab). The companies anticipate that the EMA could recommend approving a marketing authorization for AVT04 &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab)&#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-730000","post","type-post","status-publish","format-standard","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.5 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab) - 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\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab) - Market Newsdesk\" \/>\n<meta property=\"og:description\" content=\"Partners Alvotech and STADA have marketing authorization application (MAA) for ustekinumab accepted for filing by the European Medicines Agency (EMA) EMA opinion on AVT04 could come as soon as the second half of 2023 Reference product Stelara\u00ae\u00a0(ustekinumab) is prescribed to treat a variety of inflammatory conditions REYKJAVIK, Iceland and BAD VILBEL, Germany, Feb. 09, 2023 (GLOBE NEWSWIRE) &#8212; Alvotech (NASDAQ: ALVO), a global biotech company specializing in the development and manufacture of biosimilar medicines for patients worldwide, and global pharmaceutical company STADA Arzneimittel (STADA) today announced that the European Medicines Agency (EMA) has accepted a Marketing Authorization Application for AVT04, Alvotech\u2019s proposed biosimilar to Stelara\u00ae (ustekinumab). The companies anticipate that the EMA could recommend approving a marketing authorization for AVT04 &hellip; Continue reading &quot;EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab)&quot;\" \/>\n<meta property=\"og:url\" content=\"https:\/\/www.marketnewsdesk.com\/index.php\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\/\" \/>\n<meta property=\"og:site_name\" content=\"Market Newsdesk\" \/>\n<meta property=\"article:published_time\" content=\"2023-02-09T07:33:10+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/www.globenewswire.com\/newsroom\/ti?nf=MTAwMDc4MTYzOCM0MDE0ODA4MzUjMjIzMzgzMw==\" \/>\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=\"8 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\\\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\\\/\"},\"author\":{\"name\":\"Newsdesk\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/#\\\/schema\\\/person\\\/482f27a394d4fda80ecb5499e519d979\"},\"headline\":\"EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab)\",\"datePublished\":\"2023-02-09T07:33:10+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\\\/\"},\"wordCount\":1718,\"image\":{\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/www.globenewswire.com\\\/newsroom\\\/ti?nf=MTAwMDc4MTYzOCM0MDE0ODA4MzUjMjIzMzgzMw==\",\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\\\/\",\"url\":\"https:\\\/\\\/www.marketnewsdesk.com\\\/index.php\\\/ema-confirms-acceptance-of-application-for-avt04-a-proposed-biosimilar-to-stelara-ustekinumab\\\/\",\"name\":\"EMA Confirms Acceptance of Application for AVT04, a Proposed Biosimilar to Stelara\u00ae (ustekinumab) - 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