{"id":413748,"date":"2021-01-13T04:42:28","date_gmt":"2021-01-13T09:42:28","guid":{"rendered":"http:\/\/www.marketnewsdesk.com\/?p=413748"},"modified":"2021-01-13T04:42:28","modified_gmt":"2021-01-13T09:42:28","slug":"celltrion-group-announces-positive-top-line-efficacy-and-safety-data-from-global-phase-ii-iii-clinical-trial-of-covid-19-treatment-candidate-ct-p59","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/celltrion-group-announces-positive-top-line-efficacy-and-safety-data-from-global-phase-ii-iii-clinical-trial-of-covid-19-treatment-candidate-ct-p59\/","title":{"rendered":"Celltrion Group announces positive top-line efficacy and safety data from global Phase II\/III clinical trial of COVID-19 treatment candidate CT-P59"},"content":{"rendered":"<p>        <!--.bwalignc { text-align: center; list-style-position: inside }\n.bwlistdisc { list-style-type: disc }body {font:normal small Arial,Helvetica,sans-serif;color:#000;background-color:#fff;padding:24px;margin:0;} a img {border:0;} h3 {font-size:medium;color:#000;margin:0 0 1em 0; text-align:center;}-->  <\/p>\n<p class=\"bwalignc\"><b>Celltrion Group announces positive top-line efficacy and safety data from global Phase II\/III clinical trial of COVID-19 treatment candidate CT-P59<\/b><\/p>\n<ul class=\"bwlistdisc\">\n<li><i>CT-P59 (40mg\/kg) treated patients reported reduced progression rates to severe COVID-19 by 54% for patients with mild-to-moderate symptoms and 68% for moderate patients aged 50 years and over<\/i><\/li>\n<li><i>CT-P59 (40mg\/kg) treated patients reported a significantly shortened time to clinical recovery ranging from 3.4 to 6.4 days quicker compared to placebo<\/i><\/li>\n<li><i>A significant reduction of viral load compared to placebo was reported at Day 7 in patients treated with CT-P59; with CT-P59 receiving a positive safety profile and no drug-related serious adverse events reported<\/i><\/li>\n<li><i>The preclinical data of CT-P59 against SARS-CoV-2, demonstrating a 100-fold reduction in viral load of SARS-CoV-2 and improved recovery time in animal models has been published in Nature Communications journal<\/i><\/li>\n<\/ul>\n<p>INCHEON, South Korea&#8211;(<a href=\"http:\/\/www.businesswire.com\">BUSINESS WIRE<\/a>)&#8211;<br \/>\nCelltrion Group today announced top-line results from its randomised, double-blind, and placebo controlled global Phase II\/III clinical trial of CT-P59, an anti-COVID-19 monoclonal antibody treatment candidate. The Part I of the trial enrolled 327 patients with mild-to-moderate symptoms of COVID-19 across three treatment groups (40mg\/kg, 80mg\/kg and placebo), in which approximately 60% of patients with moderate symptoms suffered from COVID-19 related pneumonia.\n<\/p>\n<p>\nThis data analysis has demonstrated that at Day 28, CT-P59 treated patients presented with a significantly reduced risk of COVID-19 related hospitalisation and oxygenation without mortality. When compared to placebo, CT-P59 (40mg\/kg) treated patients reported reduced progression rates to severe COVID-19 by 54% for mild-to-moderate<i \/>patients and 68% for moderate patients aged 50 years and over.\n<\/p>\n<p>\nCT-P59 treatment groups also reported with significantly shortened time to clinical recovery ranging from 3.4 to 6.4 days quicker compared to placebo. Patients treated with CT-P59 (40mg\/kg) recovered 3.4 days earlier than those in the placebo group [5.4 vs. 8.8 days; 95% C.I, 5.35(3.97, 6.78) to 8.77 (6.72, 11.73), log-rank p-value= 0.0097]. Patients with pneumonia treated with CT-P59 (40mg\/kg) reported shortened recovery time by 5.1 days compared to placebo [5.7 vs. 10.8 days; 95% C.I, 5.73 (4.13, 7.33) to 10.81 (6.81, N.C.)]. Moderate patients aged 50 years and over treated with CT-P59 (40mg\/kg) reported a shortened recovery time by 6.4 days compared to placebo [6.6 vs. 13.0 days; 95% C.I, 6.64 (4.13, 11.94) to 12.97 (6.81, N.C.)].\n<\/p>\n<p>\nIn addition, CT-P59 treated patients rapidly and significantly reduced viral load through Day 7 compared to placebo. Top-line results from the trial shows CT-P59 to have a positive safety profile, comparable to that of the placebo group, with no serious adverse advents reported. Infusion related reactions were mild and transient, with the CT-P59 treatment group having reported 0.5%, compared to 1.8% reported with placebo.\n<\/p>\n<p>\n\u201cThe data demonstrate that CT-P59 could contribute to both a reduced time to clinical recovery, as well as a reduced proportion of patients who progress to severe disease.\u201d said Professor Joong-Sik Eom, Infectious Disease Division at Gil Medical Center of Gachon University, \u201cThe treatment\u2019s safety profile was comparable to that of placebo and generally well-tolerated. Therefore, it is anticipated that CT-P59 would positively contribute to the management and control of the current COVID-19 pandemic across the world.\u201d\n<\/p>\n<p><i>Nature Communications<\/i> has published the preclinical data of CT-P59 against SARS-CoV-2, demonstrating a 100-fold reduction in the viral load of SARS-CoV-2 and improved recovery time in animal models. Additionally, the data showed encouraging results meeting several criteria from its studies; in-vitro plaque reduction neutralization test (PRNT) against SARS-CoV-2 and SARS-CoV-2 D614G variant to assess the neutralization potency of CT-P59, in-vivo efficacy in animal models to demonstrate in vivo antiviral efficacy of CT-P59, as well as in vitro antibody-dependent enhancement (ADE) assay to investigate the possible adverse effects of a COVID-19 treatment.<sup>1<\/sup><\/p>\n<p>\n\u201cOur top-line data from the global Phase II\/III clinical trial have demonstrated that CT-P59 is effective for the treatment of COVID-19 in mild-to-moderate patients and especially in moderate patients aged 50 years and over. We are encouraged by the robust and consistent nature of the top-line clinical profile of CT-P59 and our clinical studies are on track in more than 10 countries.\u201d said Dr. HoUng Kim, Ph.D., Head of Medical and Marketing Division at Celltrion Healthcare. \u201cWe are planning to manufacture doses for around two million patients in 2021 and hope to improve access to this treatment option for those that require.\u201d\n<\/p>\n<p class=\"bwalignc\">\n&#8211; <b>ENDS &#8211;<\/b><\/p>\n<p><b>Notes to Editors:<\/b><\/p>\n<p><b>About Celltrion Healthcare <\/b><\/p>\n<p>\nCelltrion Healthcare is committed to delivering innovative and affordable medications to promote patients\u2019 access to advanced therapies. Its products are manufactured at state-of-the-art mammalian cell culture facilities, designed and built to comply with the US FDA cGMP and the EU GMP guidelines. Celltrion Healthcare endeavours to offer high-quality cost-effective solutions through an extensive global network that spans more than 110 different countries. For more information please visit: <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fwww.celltrionhealthcare.com%2Fen-us&amp;esheet=52360714&amp;newsitemid=20210113005355&amp;lan=en-US&amp;anchor=https%3A%2F%2Fwww.celltrionhealthcare.com%2Fen-us&amp;index=1&amp;md5=8511a2c0233807522c75e29d60e123c7\">https:\/\/www.celltrionhealthcare.com\/en-us<\/a>.\n<\/p>\n<p><b>About CT-P59 (Regdanvimab)<\/b><\/p>\n<p>\nCT-P59 was identified as a potential treatment for COVID-19 through screening of antibody candidates and selecting those that showed the highest potency in neutralising the SARS-CoV-2 virus including the mutated G-variant strain (D614G variant). In pre-clinical data the treatment candidate demonstrated a 100-fold reduction in viral load of SARS-CoV-2, as well as a reduction in lung inflammation. Results from the global Phase I clinical trial of CT-P59 demonstrated promising safety, tolerability, antiviral effect and efficacy profile in patients with mild symptoms of COVID-19.<sup>2<\/sup><\/p>\n<p><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\/Celltrion Healthcare that may constitute forward-looking statements, under pertinent securities laws.\n<\/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.\n<\/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\/Celltrion Healthcare&#8217;s management, of which many are beyond its control.\n<\/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.\n<\/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.\n<\/p>\n<p>\nAlthough forward-looking statements contained in this presentation are based upon what management of Celltrion\/Celltrion Healthcare 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\/Celltrion Healthcare undertakes 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.\n<\/p>\n<p><b>References <\/b><\/p>\n<hr \/>\n<p><sup>1<\/sup> Kim, C., Ryu, DK., Lee, J. et al. A therapeutic neutralizing antibody targeting receptor binding domain of SARS-CoV-2 spike protein. Nat Commun 12, 288 (2021). <a rel=\"nofollow\" href=\"https:\/\/cts.businesswire.com\/ct\/CT?id=smartlink&amp;url=https%3A%2F%2Fdoi.org%2F10.1038%2Fs41467-020-20602-5&amp;esheet=52360714&amp;newsitemid=20210113005355&amp;lan=en-US&amp;anchor=https%3A%2F%2Fdoi.org%2F10.1038%2Fs41467-020-20602-5&amp;index=2&amp;md5=91845af8fadda438569b54390b5ee4f4\">https:\/\/doi.org\/10.1038\/s41467-020-20602-5<\/a> [Last accessed January 2021<br \/>\n<br \/><sup>2<\/sup> Celltrion Data on file\n<\/p>\n<p><img decoding=\"async\" alt=\"\" src=\"https:\/\/cts.businesswire.com\/ct\/CT?id=bwnews&amp;sty=20210113005355r1&amp;sid=flmnd&amp;distro=nx&amp;lang=en\" style=\"width:0;height:0\" \/><span class=\"bwct31415\" \/><\/p>\n<p id=\"mmgallerylink\"><span id=\"mmgallerylink-phrase\">View source version on businesswire.com: <\/span><span id=\"mmgallerylink-link\"><a href=\"https:\/\/www.businesswire.com\/news\/home\/20210113005355\/en\/\" rel=\"nofollow\">https:\/\/www.businesswire.com\/news\/home\/20210113005355\/en\/<\/a><\/span><\/p>\n<p>\nSophia Eminson<br \/>\n<br \/><a rel=\"nofollow\" href=\"mailto:seminson@hanovercomms.com\">seminson@hanovercomms.com<\/a>\u202f<br \/>\n<br \/>+44 (0) 7751 116252<\/p>\n<p>Donna Curran<br \/>\n<br \/><a rel=\"nofollow\" href=\"mailto:dcurran@hanovercomms.com\">dcurran@hanovercomms.com<br \/>\n<\/a><br \/>+44 (0) 7984 550312\n<\/p>\n<p><b>KEYWORDS:<\/b> Europe South Korea Asia Pacific<\/p>\n<p><b>INDUSTRY KEYWORDS:<\/b> Health Infectious Diseases Clinical Trials Research Science Pharmaceutical Biotechnology<\/p>\n<p><b>MEDIA:<\/b><\/p>\n<table cellpadding=\"3\" cellspacing=\"3\">\n<tr>\n<td><font face=\"Arial\" size=\"2\"><b>Logo<\/b><\/font><\/td>\n<\/tr>\n<tr>\n<td><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20210113005355\/en\/558284\/3\/Celltrionhealthcare_500px.jpg\" alt=\"Logo\" \/><\/td>\n<\/tr>\n<tr>\n<td><font face=\"Arial\" size=\"2\"><\/font><\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"<p>Celltrion Group announces positive top-line efficacy and safety data from global Phase II\/III clinical trial of COVID-19 treatment candidate CT-P59 CT-P59 (40mg\/kg) treated patients reported reduced progression rates to severe COVID-19 by 54% for patients with mild-to-moderate symptoms and 68% for moderate patients aged 50 years and over CT-P59 (40mg\/kg) treated patients reported a significantly shortened time to clinical recovery ranging from 3.4 to 6.4 days quicker compared to placebo A significant reduction of viral load compared to placebo was reported at Day 7 in patients treated with CT-P59; with CT-P59 receiving a positive safety profile and no drug-related serious adverse events reported The preclinical data of CT-P59 against SARS-CoV-2, demonstrating a 100-fold reduction in viral load of SARS-CoV-2 and &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/www.marketnewsdesk.com\/index.php\/celltrion-group-announces-positive-top-line-efficacy-and-safety-data-from-global-phase-ii-iii-clinical-trial-of-covid-19-treatment-candidate-ct-p59\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Celltrion Group announces positive top-line efficacy and safety data from global Phase II\/III clinical trial of COVID-19 treatment candidate CT-P59&#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-413748","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>Celltrion Group announces positive top-line efficacy and safety data from global Phase II\/III clinical trial 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treated patients reported reduced progression rates to severe COVID-19 by 54% for patients with mild-to-moderate symptoms and 68% for moderate patients aged 50 years and over CT-P59 (40mg\/kg) treated patients reported a significantly shortened time to clinical recovery ranging from 3.4 to 6.4 days quicker compared to placebo A significant reduction of viral load compared to placebo was reported at Day 7 in patients treated with CT-P59; with CT-P59 receiving a positive safety profile and no drug-related serious adverse events reported The preclinical data of CT-P59 against SARS-CoV-2, demonstrating a 100-fold reduction in viral load of SARS-CoV-2 and &hellip; Continue reading \"Celltrion Group announces positive top-line efficacy and safety data from global Phase II\/III clinical trial of COVID-19 treatment candidate 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