{"id":10394,"date":"2020-07-28T16:05:47","date_gmt":"2020-07-28T10:35:47","guid":{"rendered":"https:\/\/www.delveinsight.com\/blog\/?p=10394"},"modified":"2022-08-16T10:00:07","modified_gmt":"2022-08-16T04:30:07","slug":"pharma-happenings-for-az-daiichi-moderna-solid","status":"publish","type":"post","link":"https:\/\/www.delveinsight.com\/blog\/pharma-happenings-for-az-daiichi-moderna-solid","title":{"rendered":"AZ, Daiichi inks an oncology deal; Moderna begins Phase III trial of its COVID-19 vaccine; No good news for Solid&#8217;s DMD gene therapy trial"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\" id=\"h-az-daiichi-put-their-trust-into-trop2-based-drugs-inks-an-oncology-deal-to-together-develop-and-commercialize-ds-1062\"><strong>AZ, Daiichi put their trust into TROP2-based drugs, inks an oncology deal to together develop and commercialize DS-1062<\/strong><\/h2>\n\n\n\n<div class=\"wp-block-media-text alignwide is-stacked-on-mobile\" style=\"grid-template-columns:22% auto\"><figure class=\"wp-block-media-text__media\"><img decoding=\"async\" width=\"341\" height=\"148\" src=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130349\/Astrazeneca-1.png\" alt=\"AZ, Daiichi inks an oncology deal \" class=\"wp-image-10397 size-full\" srcset=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130349\/Astrazeneca-1.png 341w, https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130349\/Astrazeneca-1-300x130.png 300w\" sizes=\"(max-width: 341px) 100vw, 341px\" \/><\/figure><div class=\"wp-block-media-text__content\">\n<p class=\"has-text-align-right\">AstraZeneca has inked an oncology deal with Daiichi Sankyo to jointly develop and commercialize an antibody-drug conjugate DS-1062 (trastuzumab deruxtecan), worldwide except in Japan. Daiichi holds exclusive rights to the drug in Japan.<\/p>\n<\/div><\/div>\n\n\n\n<div class=\"wp-block-media-text alignwide has-media-on-the-right is-stacked-on-mobile is-vertically-aligned-center\" style=\"grid-template-columns:auto 15%\"><figure class=\"wp-block-media-text__media\"><img decoding=\"async\" width=\"300\" height=\"269\" src=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130428\/daiichi-sankyo-logo-300x269-1.jpg\" alt=\"AZ, Daiichi inks an oncology deal \" class=\"wp-image-10398 size-full\"\/><\/figure><div class=\"wp-block-media-text__content\">\n<p>Daiichi\u2019s <strong>DS-1062<\/strong>, a trophoblast cell-surface antigen 2 (TROP2) directed DXd antibody-drug conjugate (ADC) is currently in Phase I clinical trial for multiple cancer types including the majority of <a href=\"https:\/\/www.delveinsight.com\/blog\/non-small-cell-lung-cancer-market-2\" target=\"_blank\" rel=\"noreferrer noopener\">non-small cell lung cancer<\/a> (NSCLC) and <a aria-label=\"undefined (opens in a new tab)\" href=\"https:\/\/www.delveinsight.com\/report-store\/triple-negative-breast-cancer-tnbc-market\" target=\"_blank\" rel=\"noreferrer noopener\">triple-negative breast cancer<\/a> (TNBC).<\/p>\n<\/div><\/div>\n\n\n\n<p>Under the term of the deal, AZ will pay Daiichi an upfront sum of USD 1 Billion in staged payments. Daiichi will also be eligible to receive up to USD 1 Billion upon receiving regulatory recommendations and milestone sale-related payments of up to USD 4 Billion. In return, AZ gets to be an equal shareholder of the profits on the sale of the drug conjugate. The duo had entered into a similar kind of collaboration last year to develop and commercialize Daiichi\u2019s Enhertu; a HER2 directed DXd ADC.<\/p>\n\n\n\n<p>However, companies are not the only ones who believe in the potential of TROP2-based drugs. Immunomedics has recently won the FDA recommendation for its anti-TROP2 ADC, <strong>Trodelvy<\/strong> (sacituzumab govitecan-hziy) indicated for metastatic triple-negative breast cancer (TNBC).<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-with-an-additional-aid-of-usd-472-million-moderna-begins-phase-iii-study-of-its-covid-19-vaccine-mrna-1273\"><strong>With an additional aid of USD 472 Million, Moderna begins Phase III study of its COVID-19 vaccine, mRNA-1273<\/strong><\/h2>\n\n\n\n<div class=\"wp-block-media-text alignwide is-stacked-on-mobile\" style=\"grid-template-columns:23% auto\"><figure class=\"wp-block-media-text__media\"><img decoding=\"async\" width=\"1024\" height=\"512\" src=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130633\/Moderna.jpg\" alt=\"Moderna COVID-19 vaccine trial \" class=\"wp-image-10399 size-full\" srcset=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130633\/Moderna.jpg 1024w, https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130633\/Moderna-300x150.jpg 300w, https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130633\/Moderna-768x384.jpg 768w\" sizes=\"(max-width: 1024px) 100vw, 1024px\" \/><\/figure><div class=\"wp-block-media-text__content\">\n<p class=\"has-text-align-right\"><a aria-label=\"undefined (opens in a new tab)\" href=\"https:\/\/www.delveinsight.com\/blog\/recent-pharma-happenings-for-moderna-quidel-neurotrope-clovis\/\" target=\"_blank\" rel=\"noreferrer noopener\">Moderna<\/a> has initiated the first large-scale Phase III clinical trial of its <a href=\"https:\/\/www.delveinsight.com\/report-store\/covid-19-therapeutic-pipeline-vaccines\" target=\"_blank\" rel=\"noreferrer noopener\">COVID-19 vaccine<\/a>, <strong>mRNA-1273<\/strong> after an expanded contract with the Biomedical Advanced Research and Development Authority (BARDA).<\/p>\n<\/div><\/div>\n\n\n\n<div class=\"wp-block-media-text alignwide has-media-on-the-right is-stacked-on-mobile\" style=\"grid-template-columns:auto 16%\"><figure class=\"wp-block-media-text__media\"><img decoding=\"async\" width=\"225\" height=\"225\" src=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130734\/BARDA.png\" alt=\"BARDA\" class=\"wp-image-10400 size-full\" srcset=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130734\/BARDA.png 225w, https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130734\/BARDA-150x150.png 150w, https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130734\/BARDA-100x100.png 100w\" sizes=\"(max-width: 225px) 100vw, 225px\" \/><\/figure><div class=\"wp-block-media-text__content\">\n<p>The company also received additional funding from the BARDA worth USD 472 Million to support the Phase III clinical development of the vaccine. Earlier, the company had received up to USD 483 Million from the BARDA, making the total grant of up to USD 955 Million to the company.<\/p>\n<\/div><\/div>\n\n\n\n<p>The Phase III COVE (Coronavirus Efficacy) trial will include about 30,000 participants from the US. The randomized, placebo-controlled trial will evaluate 100 micrograms of doses of the vaccine. The primary endpoint of the study will be the prevention of symptomatic COVID-19. Key secondary endpoints of the study are prevention of severe COVID-19, defined as the need for hospitalization, and prevention of SARS-CoV-2 infection regardless of symptoms.<\/p>\n\n\n\n<p>At present, more than <a href=\"https:\/\/www.delveinsight.com\/blog\/coronavirus-vaccine-candidates\" target=\"_blank\" rel=\"noreferrer noopener\">150 vaccine candidates<\/a> are in various stage of clinical development against SARS-CoV-2.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-no-relief-to-solid-biosciences-as-fda-demands-more-data-to-lift-the-hold-on-the-company-s-dmd-gene-therapy-trial\"><strong>No relief to Solid Biosciences as FDA demands more data to lift the hold on the company\u2019s DMD gene therapy trial<\/strong><\/h2>\n\n\n\n<div class=\"wp-block-media-text alignwide is-stacked-on-mobile\" style=\"grid-template-columns:25% auto\"><figure class=\"wp-block-media-text__media\"><img decoding=\"async\" width=\"364\" height=\"138\" src=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130901\/Solid-Bio.jpg\" alt=\"Solid Biosciences DMD gene therapy trial \" class=\"wp-image-10401 size-full\" srcset=\"https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130901\/Solid-Bio.jpg 364w, https:\/\/assets.delveinsight.com\/blog\/wp-content\/uploads\/2020\/07\/28130901\/Solid-Bio-300x114.jpg 300w\" sizes=\"(max-width: 364px) 100vw, 364px\" \/><\/figure><div class=\"wp-block-media-text__content\">\n<p class=\"has-text-align-right\">Solid Biosciences announced the decision of the US FDA to maintain a clinical hold on Solid\u2019s Phase I\/II clinical trial, IGNITE, for DMD.<\/p>\n<\/div><\/div>\n\n\n\n<p>The trial is evaluating <strong>SGT-001, <\/strong>which is a novel adeno-associated viral vector-mediated gene transfer indicated for <a href=\"https:\/\/www.delveinsight.com\/report-store\/duchenne-muscular-dystrophy-market\" target=\"_blank\" rel=\"noreferrer noopener\">Duchenne muscular dystrophy<\/a>. The drug delivers a synthetic dystrophin gene, called micro-dystrophin, in order to address the genetic aberrations in <a aria-label=\"undefined (opens in a new tab)\" href=\"https:\/\/www.delveinsight.com\/blog\/duchene-muscular-dystrophy-market\/\" target=\"_blank\" rel=\"noreferrer noopener\">DMD<\/a> patients. However, last year due to adverse side effects such as complement activation, a decrease in red blood cell count, acute kidney injury and cardio-pulmonary insufficiency, the drug caused, the US FDA decided to put the trial on a clinical hold.<\/p>\n\n\n\n<p>In April 2020, Solid submitted the information and measures taken to improve the patient experience and safety of the drug; however, the regulatory authority does not seem to be impressed with the information provided and requests for more information on the manufacturing process, updated safety and efficacy data for all patients dosed, and additional direction on total viral load to be administered per patient.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>AZ, Daiichi put their trust into TROP2-based drugs, inks an oncology deal to together develop and commercialize DS-1062 AstraZeneca has inked an oncology deal with Daiichi Sankyo to jointly develop and commercialize an antibody-drug conjugate DS-1062 (trastuzumab deruxtecan), worldwide except in Japan. Daiichi holds exclusive rights to the drug in Japan. Daiichi\u2019s DS-1062, a trophoblast [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":10408,"comment_status":"open","ping_status":"open","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":[18594,18596,18595,18598,348,349,16972,6733,1111,639,18597,2014,2012],"industry":[17225],"therapeutic_areas":[17228,17234,17411],"class_list":["post-10394","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-notizia","tag-az","tag-covid19-vaccine","tag-daiichi","tag-dmd-gene-therapy","tag-latest-business-news","tag-latest-pharma-news","tag-moderna","tag-non-small-cell-lung-cancer","tag-nsclc","tag-pharma-news","tag-solid-biosciences","tag-tnbc","tag-triple-negative-breast-cancer","industry-pharmaceutical","therapeutic_areas-oncology","therapeutic_areas-rare-diseases","therapeutic_areas-womens-health"],"acf":[],"yoast_head":"<!-- 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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\">AZ<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">COVID19 Vaccine<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">Daiichi<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">DMD Gene Therapy<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">latest business news<\/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\">Moderna<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">Non-small cell lung cancer<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">NSCLC<\/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\">Solid Biosciences<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">TNBC<\/a>","<a href=\"https:\/\/www.delveinsight.com\/blog\/notizia\/\" class=\"advgb-post-tax-term\">TRIPLE NEGATIVE BREAST CANCER<\/a>"],"unlinked":["<span class=\"advgb-post-tax-term\">AZ<\/span>","<span class=\"advgb-post-tax-term\">COVID19 Vaccine<\/span>","<span class=\"advgb-post-tax-term\">Daiichi<\/span>","<span class=\"advgb-post-tax-term\">DMD 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