{"id":7540,"date":"2021-10-27T18:02:58","date_gmt":"2021-10-28T01:02:58","guid":{"rendered":"https:\/\/rakuten-med.com\/us\/?post_type=press_releases&#038;p=7540"},"modified":"2022-04-19T21:26:17","modified_gmt":"2022-04-20T04:26:17","slug":"data-from-phase-1-2a-study-of-rm-1929-photoimmunotherapy-in-patients-with-recurrent-head-and-neck-squamous-cell-carcinoma-was-published-in-head-and-neck","status":"publish","type":"press_releases","link":"https:\/\/rakuten-med.com\/us\/news\/press-releases\/2021\/10\/27\/7540\/","title":{"rendered":"Data from Phase 1\/2a study of RM-1929 Photoimmunotherapy in Patients with Recurrent Head and Neck Squamous Cell Carcinoma was Published in Head and Neck"},"content":{"rendered":"<p>SAN MATEO, California \u2013 (PRNewswire) \u2013 Rakuten Medical, Inc. (Rakuten Medical) announced that data from a phase 1\/2a, open-label, multicenter study of RM-1929 photoimmunotherapy in patients with locoregional, recurrent head and neck squamous cell carcinoma (rHNSCC) (RM-1929-101 study, ClinicalTrials.gov Identifier: <a href=\"https:\/\/clinicaltrials.gov\/ct2\/show\/NCT02422979\">NCT02422979<\/a>) was accepted for publication in <em>Head and Neck<\/em> and published online on October 9<sup>th<\/sup>, 2021.<\/p>\n<p>&nbsp;<\/p>\n<p>The manuscript describes the design and results of the 2-part study, which was aimed to elucidate the recommended dose, safety, pharmacokinetics, immunogenicity, and preliminary efficacy of RM-1929 photoimmunotherapy in patients with locoregional rHNSCC.\u00a0 Part 1* of the study (dose-escalation) determined the recommended drug dose of RM-1929 to be 640 mg\/m<sup>2<\/sup> with a fixed light dose of 50 J\/cm<sup>2<\/sup> for superficial tumors and 100 J\/cm fiber diffuser length for interstitial tumors.<\/p>\n<p>&nbsp;<\/p>\n<p>Among Part 2* participants, 30 patients received RM-1929 photoimmunotherapy, and were included in the safety and treated population. Among Part 2* study participants, 13 (43.3%) patients reported a serious TEAE wherein 3 were considered to be treatment related (tumor pain, oral pain, and airway obstruction).\u00a0 Also, for patients enrolled in Part 2* of the study, the median OS was 9.30 months (95% CI 5.16\u201316.92 months). \u00a0Confirmed and unconfirmed objective responses were achieved in 13 (43.3%, 95% CI 25.46%\u201362.57%) patients, with 4 (13%) patients achieving a complete response (CR) and 9 (30.0%) patients demonstrating a partial response (PR). \u00a0Disease control [defined as CR, PR, or stable disease (SD)] was observed in 24 (80%, 95% CI 61.43%\u201392.29%) patients.<\/p>\n<p>&nbsp;<\/p>\n<p>The full text article is available at <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/hed.26885\">https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/hed.26885<\/a><\/p>\n<p>&nbsp;<\/p>\n<p>*Part 1: Phase 1 study part (safety and dose-finding) \/ Part 2: Phase 2a study part (safety and preliminary anticancer activity; patients were treated with up to 4 cycles of RM-1929 photoimmunotherapy)<\/p>\n<p>&nbsp;<\/p>\n<p>**RM-1929 and ASP-1929 are analogous. Extensive physiochemical studies show that they have comparable physical and chemical properties.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>About Rakuten Medical, Inc.\u00a0<\/strong><\/p>\n<p>Rakuten Medical, Inc. is a global biotechnology company developing and commercializing precision, cell-targeting investigational therapies on its\u00a0Illuminox<sup>TM\u00a0<\/sup>platform, which, in pre-clinical studies have been shown to induce rapid and selective cell killing and tumor necrosis. Outside of Japan, Illuminox\u2122\u00a0therapies have not yet been approved as safe or effective by any regulatory authority. The company\u2019s\u00a0first drug developed on the Illuminox\u2122 platform, ASP-1929, has received approval from the Japanese Ministry of Health,\u00a0Labour, and Welfare, and is currently the subject of a global phase 3 clinical trial for recurrent head and neck cancer. Rakuten Medical is committed to its mission to conquer cancer and aims to realize a society where cancer patients can lead fulfilling lives. The company has\u00a06 locations in 5 countries,\u00a0including the United States, where it is headquartered, Japan, the Netherlands, Taiwan, and Switzerland. For more information, visit www.rakuten-med.com.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>About ASP-1929**\u00a0<\/strong><\/p>\n<p>Since 2013, Rakuten Medical, Inc. has been using an exclusively licensed antibody complex to develop new cancer therapies based on its\u00a0Illuminox<sup>TM<\/sup>\u00a0technology platform. Rakuten Medical&#8217;s first pipeline drug developed using its Illuminox\u2122 platform is ASP-1929, an antibody-dye conjugate comprised of the antibody cetuximab and\u00a0IRDye\u00ae\u00a0700DX, a light activatable dye. ASP-1929 binds to epidermal growth factor receptors (EGFR), a cancer antigen expressed in multiple types of solid tumors, including head and neck, cutaneous, esophageal, lung, colon and pancreatic cancers. After binding to cancer cells, ASP-1929 is locally activated by non-thermal red light (690 nm) illumination emitted by a laser device system.\u00a0 Pre-clinical data indicates that Illuminox\u2122 technology induces a biophysical process that compromises cell membrane integrity, leading to cancer cell death and tumor necrosis. ASP-1929 received conditional early approval from the Japanese Ministry of Health, Labor, and Welfare in\u00a0September 2020, and is currently under investigation in a global phase 3 clinical trial for recurrent head and neck cancer. Rakuten Medical, Inc. is moving forward with product development by conducting clinical trials of monotherapy and combination therapy with other drugs. Outside of\u00a0Japan, ASP-1929 and the laser device system have not yet been approved by any regulatory authority.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>About Illuminox\u2122\u00a0platform\u00a0<\/strong><\/p>\n<p>The Illuminox\u2122 platform is an investigational platform based on a cancer therapy called photoimmunotherapy, which was developed by Dr.\u202fHisataka\u00a0Kobayashi\u202fand team from the National Cancer Institute in\u202fthe United States. Rakuten Medical is developing the Illuminox\u2122 platform as a technology consisting of a drug, device, and other related components. The drug component of the platform consists of a targeting moiety conjugated with one or more dyes leading to selective cell surface binding.\u202fThe device component consists of a light source that locally illuminates the targeted cells with non-thermal light to transiently activate the drug.\u202f Pre-clinical data have shown that this activation elicits rapid and selective necrosis of targeted cells through a biophysical process that compromises the membrane integrity of the targeted cells. Therapies developed on Illuminox\u2122 may also result in local and systemic innate and adaptive immune activation due to immunogenic cell death of the targeted cells and\/or the removal of immunosuppressive elements within the microenvironment. Outside of\u202fJapan,\u00a0Illuminox\u2122 therapies have not yet been approved as safe or effective by any regulatory authority.<\/p>\n<p>&nbsp;<\/p>\n<p>&nbsp;<\/p>\n<p><strong>Forward Looking Statements\u00a0<\/strong><\/p>\n<p>This press release contains forward looking statements that correspond to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements include various risks, uncertainties, and assumptions that may cause Rakuten Medical&#8217;s business plans and results to differ from the anticipated results and expectations expressed in these statements. These &#8220;forward looking statements&#8221; contain information about the status and development of our products, including ASP-1929, the Illuminox\u2122 platform and IRDye\u00ae\u202f700DX, as well as other regulatory and marketing authorization efforts, the potential benefits, efficacy, and safety of ASP-1929 and other therapies created using the Illuminox\u2122 platform, and the status of regulatory filings. The approval and commercial success of such therapies may not be achieved, and the results and effects shown in pre-clinical studies and data may not be replicated in clinical trials. Such statements may include words such as &#8220;expect,&#8221; &#8220;believe,&#8221; &#8220;hope,&#8221; &#8220;estimate,&#8221; &#8220;looks as though,&#8221; &#8220;anticipate,&#8221; &#8220;intend,&#8221; &#8220;may,&#8221; &#8220;suggest,&#8221; &#8220;plan,&#8221; &#8220;strategy,&#8221; &#8220;will,&#8221; \u201chopeful,\u201d \u201cexcited,\u201d &#8220;do,&#8221; \u201caims,\u201d \u201cdevelop\u201d and similar expressions. Forward-looking statements are neither historical facts nor assurances of future performance.\u00a0 Such forward-looking statements are based upon Rakuten Medical&#8217;s current beliefs, expectations, and assumptions regarding the future of its business, future plans and strategies, projections, anticipated events and trends, the economy and other future conditions. Because forward-looking statements relate to the future, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of Rakuten Medical\u2019s control. Rakuten Medical\u2019s actual results and financial condition may differ materially from those indicated in the forward-looking statements. Therefore, you should not rely on any of these forward-looking statements. In addition, this press release uses terms such as \u201ctolerable and manageable safety profile\u201d and \u201cclinically meaningful\u201d to express opinions about clinical trial data. Ongoing clinical trial studies include various risks and uncertainties, in particular, problems that arise during the manufacturing stage of ASP-1929 or other product candidates, the occurrence of adverse safety events, situations in failure to demonstrate therapeutic benefits, and other various risks and uncertainties, both reasonable and unreasonable. For this reason, actual results, including regulatory approvals and uncertainties in the commercialization process of ASP-1929 or other product candidates, may differ from published information. Except to the extent required by applicable law, we undertake no obligation to publicly update this or any other forward-looking statement, whether because of new information, future developments or events, changes in assumptions, changes in the factors affecting forward-looking statements. If one or more forward-looking statement(s) is updated, no inference should be drawn that additional updates will be made to those or other forward-looking statements.<\/p>\n<p>&nbsp;<\/p>\n<p>Rakuten Medical Public Relations:\u202f <a href=\"https:\/\/rakuten-med.com\/us\/contact\/\">https:\/\/rakuten-med.com\/us\/contact\/<\/a><\/p>\n<p>SOURCE\u00a0Rakuten Medical, Inc.<\/p>\n<p>Related Links:\u00a0 <a href=\"https:\/\/rakuten-med.com\/us\">https:\/\/rakuten-med.com\/us<\/a><\/p>\n<p>Release <a href=\"https:\/\/www.prnewswire.com\/news-releases\/data-from-phase-12a-study-of-rm-1929-photoimmunotherapy-in-patients-with-recurrent-head-and-neck-squamous-cell-carcinoma-was-published-in-head-and-neck-301410368.html?tc=eml_cleartime\">HERE<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>SAN MATEO, California \u2013 (PRNewswire) \u2013 Rakuten Medical, Inc. (Rakuten Medical) announced that data from a phase 1\/2a, open-label, multicenter [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"template":"","meta":{"_acf_changed":false,"_genesis_hide_title":false,"_genesis_hide_breadcrumbs":false,"_genesis_hide_singular_image":false,"_genesis_hide_footer_widgets":false,"_genesis_custom_body_class":"","_genesis_custom_post_class":"","_genesis_layout":""},"class_list":{"0":"post-7540","1":"press_releases","2":"type-press_releases","3":"status-publish","5":"entry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.7 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Data from Phase 1\/2a study of RM-1929 Photoimmunotherapy in Patients with Recurrent Head and Neck Squamous Cell Carcinoma was Published in Head and Neck - Rakuten Medical - To conquer cancer.<\/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:\/\/rakuten-med.com\/us\/news\/press-releases\/2021\/10\/27\/7540\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Data from Phase 1\/2a study of RM-1929 Photoimmunotherapy in Patients with Recurrent Head and Neck Squamous Cell Carcinoma was Published in Head and Neck - Rakuten Medical - To conquer cancer.\" \/>\n<meta property=\"og:description\" content=\"SAN MATEO, California \u2013 (PRNewswire) \u2013 Rakuten Medical, Inc. 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