{"id":125558,"date":"2026-09-30T18:46:46","date_gmt":"2026-09-30T09:46:46","guid":{"rendered":"https:\/\/japanir.jp\/en\/ir\/4891-20260930-01_wp_executive_change\/"},"modified":"2026-09-30T18:46:46","modified_gmt":"2026-09-30T09:46:46","slug":"4891-20260930-01_wp_executive_change","status":"publish","type":"ir_release","link":"https:\/\/japanir.jp\/en\/company\/company-4891\/ir\/4891-20260930-01_wp_executive_change\/","title":{"rendered":"Notification of Submission of Clinical Trial Notification for Early Phase II Clinical Trial of TMS-008 for Acute Kidney Injury"},"content":{"rendered":"<p>Submitted a clinical trial notification to PMDA to initiate the domestic early Phase II clinical trial of TMS-008. The target population is patients at risk of acute kidney injury after cardiac surgery. The trial is double-blind, randomized, placebo-controlled, dose-escalation, and multicenter. Impact on this fiscal period&#8217;s results is unknown.<\/p>\n","protected":false},"comment_status":"open","ping_status":"closed","template":"","meta":{"Ticker":"","DATE":"","longName":"","company_name_ja":"","fullTimeEmployees":0,"address":"","phone":"","website":"","industry":"","sector":"","regularMarketPrice":0,"financialCurrency":"","marketCap":0,"fiftyTwoWeekLow":0,"fiftyTwoWeekHigh":0,"epsTrailingTwelveMonths":0,"epsForward":0,"bookValue":0,"totalRevenue":0,"OperatingIncome":0,"operatingMargins":0,"NetIncome":0,"profitMargins":0,"ebitda":0,"trailingPE":0,"forwardPE":0,"priceToBook":0,"returnOnEquity":0,"recommendationMean":0,"recommendationKey":"","targetMeanPrice":0,"numberOfAnalystOpinions":0,"analyst_earnings_data":"","dividendRate":0,"dividendYield":0,"payoutRatio":0,"totalEsg":0,"environmentScore":0,"socialScore":0,"governanceScore":0,"title":"","providerPublishTime":"","link":"","longBusinessSummary":"","longBusinessSummary_ja":"","quarterly_revenue":0,"quarterly_net_income":0,"quarterly_operating_profit":0,"enterprise_value":0,"price_fetched_at":"","company_officer_1_name":"","company_officer_1_title":"","company_officer_2_name":"","company_officer_2_title":"","company_officer_3_name":"","company_officer_3_title":"","company_officer_4_name":"","company_officer_4_title":"","company_officer_5_name":"","company_officer_5_title":"","company_officers_update_time":"","get_dividend_history_year1":0,"get_dividend_history_year2":0,"get_dividend_history_year3":0,"get_dividend_history_year4":0,"get_dividend_history_year5":0,"get_dividend_history_year6":0,"get_dividend_history_year7":0,"get_dividend_history_year8":0,"get_dividend_history_year9":0,"get_dividend_history_year10":0,"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-opacity":"","overlay-gradient":""}},"jir_stock_code":"4891","jir_company_name":"TMS Co., Ltd.","jir_importance":"\u2605\u2605\u2605\u2606\u2606","jir_publication_date":"2026-09-30","jir_source_link":"https:\/\/japanir.jp\/wp-content\/uploads\/2026\/09\/4891-20260930-01.pdf","jir_short_summary":"Submitted a clinical trial notification to PMDA to initiate the domestic early Phase II clinical trial of TMS-008. The target population is patients at risk of acute kidney injury after cardiac surgery. The trial is double-blind, randomized, placebo-controlled, dose-escalation, and multicenter. Impact on this fiscal period's results is unknown.","jir_summary":"### Business and R&D Developments\nTMS Co., Ltd. has submitted a clinical trial notification to the Pharmaceuticals and Medical Devices Agency (PMDA) to initiate the early Phase II clinical trial of TMS-008. This trial is a double-blind, randomized, placebo-controlled, dose-escalation, multicenter study targeting patients at risk of acute kidney injury following cardiovascular surgery, and aims to evaluate safety and efficacy. At this time, the impact of this trial on the current fiscal period's results is unknown.\n\n### Future Schedule and Risks\nCosts associated with initiating this trial are included in the R&D expense range disclosed on February 13, 2026, and no direct impact on the fiscal year ending December 2026 is expected at this time. The company will promptly disclose any new developments. Risk factors include future clinical trial progress, regulatory decisions, and uncertainties inherent in drug development.","jir_financial_highlights":"Unknown: Unknown (Unknown)","jir_category":"","jir_hashtags":"#TMSCoLtd, #ClinicalTrial, #ClinicalTrialNotification, #TMS-008","jir_key_figures":"Clinical trial notification submission date: Unknown\nTMS-008 trial type: Early Phase II clinical trial\nTarget indication: Patients at risk of acute kidney injury after cardiac surgery","jir_meta_title":"TMS Co., Ltd. \u2014 Submission of Clinical Trial Notification for Early Phase II Trial of TMS-008 for Acute Kidney Injury\uff5c2026\/09\/30","jir_meta_description":"TMS Co., Ltd. submitted a clinical trial notification to PMDA to initiate an early Phase II clinical trial of TMS-008 for patients at risk of acute kidney injury after cardiac surgery. The multicenter trial has been planned; cost impact is currently unknown.","jir_og_title":"TMS Co., Ltd.\uff5cClinical Trial Notification Submitted to Start Early Phase II Trial of TMS-008","jir_og_description":"TMS Co., Ltd. submitted a clinical trial notification to PMDA to initiate an early Phase II clinical trial of TMS-008 targeting patients at risk of acute kidney injury after cardiac surgery. Impact on this fiscal period's results is TBD.","jir_og_image_url":"\/assets\/og\/company-general_ir.jpg","jir_chart_data_collection":"[]","ir_related_company":59627,"ir_release_date":"","ir_type":"","ir_is_new":false,"ir_document_url":"","jir_ir_type":"executive_change","footnotes":""},"sector":[],"importance":[],"class_list":["post-125558","ir_release","type-ir_release","status-publish","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v24.7 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Notification of Submission of Clinical Trial Notification for Early Phase II Clinical Trial of TMS-008 for Acute Kidney Injury - Japan IR<\/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:\/\/japanir.jp\/en\/company\/company-4891\/ir\/4891-20260930-01_wp_executive_change\/\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/japanir.jp\/en\/company\/company-4891\/ir\/4891-20260930-01_wp_executive_change\/\",\"url\":\"https:\/\/japanir.jp\/en\/company\/company-4891\/ir\/4891-20260930-01_wp_executive_change\/\",\"name\":\"Notification of Submission of Clinical Trial Notification for Early Phase II Clinical Trial of TMS-008 for Acute Kidney Injury - 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