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Ltd.","value":-1.508362,"marketCap":81549592},{"symbol":"KAPA","name":"Kairos Pharma, Ltd.","value":-4.898329,"marketCap":13426320},{"symbol":"MURA","name":"Mural Oncology","value":-0.518803,"marketCap":66673486},{"symbol":"TRML","name":"Tourmaline Bio","value":-5.922279,"marketCap":433570041},{"symbol":"CTOR","name":"CITIUS ONCOLOGY INC","value":-1.891071,"marketCap":43646965},{"symbol":"INBX","name":"Inhibrx Biosciences","value":0.120949,"marketCap":204110246},{"symbol":"ORKA","name":"ORUKA THERAPEUTICS INC","value":-4.898591,"marketCap":447414094},{"symbol":"MTSR","name":"Metsera Inc.","value":-17.309229,"marketCap":2930192911},{"symbol":"NNNN","name":"Anbio Biotechnology","value":145.868472,"marketCap":328745088}]},"updateTime":1742750973898},"$inf$@#url:\"https://stock-news.skytigris.cn/v2/news/list\",params:#symbols:\"ARDS\",pageSize:16,pageCount:1,lang_content:\"en\",edition:\"fundamental\",,,undefined,":[{"items":[{"id":"2520458334","title":"Press Release: InflaRx Reports Full Year 2024 Results and Highlights Key Achievements and Expected Milestones","url":"https://stock-news.laohu8.com/highlight/detail?id=2520458334","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520458334?lang=en_us&edition=fundamental","pubTime":"2025-03-20 19:30","pubTimestamp":1742470200,"startTime":"0","endTime":"0","summary":"-- Received European Commission approval for GOHIBIC  for. the treatment of SARS-CoV-2-induced acute respiratory distress syndrome. pyoderma gangrenosum  to enable an expected interim analysis for. trial size adaptation or futility by the end of May 2025. -- Dosed first patient in Phase 2a trial for oral C5aR inhibitor, INF904,INF904 in CSU and HS -- Topline Phase 2a data expected in summer 2025. In December 2024, InflaRx announced that the first patient had been dosed in its Phase 2a basket study with INF904 in CSU and HS. This is a multi-center, open-label study evaluating multiple INF904 dosing regimens over 4 weeks of treatment in a total of 75 patients . The goal of the trial is to generate additional safety and pharmacokinetic  data and to provide signs of clinical benefit. After the 4-week treatment period, patients will be follow","market":"sg","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","LU0640476718.USD","PG","R","LU1868837300.USD","LU1868836757.USD","EC","LU1929549753.HKD","LU0323591593.USD","LU0689626769.HKD","BK4567","LU1162221912.USD","ARDS","BK4218","IE000M9KFDE8.USD","LU2552382132.HKD","LU0237698245.USD","IE00B1XK9C88.USD","BK4585","LU1430594728.SGD","PK","LU0234570918.USD","LU2129689431.USD","LU0320765646.SGD","LU0098860793.USD","LU1868837136.USD","LU1585245621.USD","SG9999002224.SGD","SG9999002232.USD","BK4022","LU0124676726.USD","BK4588","BK4201","LU2242652126.USD","IE00B3T34201.USD","BK4181","BK4559","LU0096364046.USD","LU1914381329.SGD","IE00BLSP4452.SGD","IE00BWXC8680.SGD","BK4018","SG9999014567.USD","LU0234572021.USD","LU0868494617.USD","LU0094547139.USD","IFRX","LU0061475181.USD","SG9999015341.SGD"],"gpt_icon":0},{"id":"2520297836","title":"Press Release: MiNK Therapeutics Reports Fourth Quarter & Full Year 2024 Results and Highlights Business Progress","url":"https://stock-news.laohu8.com/highlight/detail?id=2520297836","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2520297836?lang=en_us&edition=fundamental","pubTime":"2025-03-18 19:30","pubTimestamp":1742297400,"startTime":"0","endTime":"0","summary":"NEW YORK, March 18, 2025  -- MiNK Therapeutics, Inc. , a clinical-stage biopharmaceutical company pioneering the development of allogeneic, off-the-shelf invariant natural killer T  cell therapies, today announced its financial results for the fourth quarter and full year 2024, highlighting significant business progress and clinical advancements. The company will host a conference call and webcast at 8:30 a.m. ET.\"Throughout 2024, MiNK advanced its mission to bring off-the-shelf iNKT cell therapies to patients fighting hard-to-treat cancers and severe immune-related disorders,\" said Dr. Jennifer Buell, President and Chief Executive Officer of MiNK Therapeutics. \"We made significant clinical strides, strengthened our manufacturing foundation, and forged strategic alliances. Through disciplined capital management, we are positioned to scale efficiently and seize new collaboration opportunities for value creation. With our rapid AI-driven drug discovery platform generating a world-class l","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU2065732104.USD","ATS","PRGS","BK4139","BK4097","BK4161","INKT","LENZ","ARDS"],"gpt_icon":0},{"id":"2519270002","title":"Healios K.K Submits Approval Application for ARDS Treatment in Japan","url":"https://stock-news.laohu8.com/highlight/detail?id=2519270002","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2519270002?lang=en_us&edition=fundamental","pubTime":"2025-03-13 16:46","pubTimestamp":1741855580,"startTime":"0","endTime":"0","summary":"Healios K.K  plans to submit a conditional and time-limited approval application in Japan for HLCM051, following positive results from the Phase 2 ONE-BRIDGE study in Japan and the MUST-ARDS study in the US and UK.The upcoming global Phase 3 REVIVE-ARDS trial in the US will serve as a confirmatory study, according to its Thursday bourse filing.A portion of the data for this application, highlighting the efficacy of HLCM051 in extending ventilator-free days and reducing mortality, has been published in the journal Regenerative Therapy.This publication, led by Dr. Kazuya Ichikado, boosts the credibility of the submission.Price : $278.00, Change: $+2.0, Percent Change: +0.72%","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["ARDS","BK4139"],"gpt_icon":0},{"id":"2517480505","title":"InflaRx Showcases Vilobelimab’s Role in Immuno-Dermatology at the 2025 AAD Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2517480505","media":"GlobeNewswire","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517480505?lang=en_us&edition=fundamental","pubTime":"2025-03-07 21:00","pubTimestamp":1741352400,"startTime":"0","endTime":"0","summary":"JENA, Germany, March  07, 2025  (GLOBE NEWSWIRE) -- InflaRxN.V.(Nasdaq:IFRX), a biopharmaceutical company pioneering anti-inflammatory therapeutics targeting the complement system, today announced the","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2025/03/07/3038913/0/en/InflaRx-Showcases-Vilobelimab-s-Role-in-Immuno-Dermatology-at-the-2025-AAD-Annual-Meeting.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1868836914.USD","LU1929549753.HKD","LU1430594728.SGD","SG9999001440.SGD","LU1169589451.USD","LU1066053197.SGD","IE00BBT3K403.USD","LU2129689431.USD","SG9999015341.SGD","BK4568","LU1162221912.USD","LU0061475181.USD","LU0234572021.USD","BK4018","BNTX","LU0094547139.USD","BK4559","LU0868494617.USD","BK4567","SG9999002224.SGD","SG9999014542.SGD","USA","SG9999015358.SGD","BK4504","BK4139","LU0689626769.HKD","BK4558","IE00BWXC8680.SGD","ARDS","IE00BLSP4239.USD","LU1868836591.USD","SG9999002232.USD","SG9999014575.USD","BK4181","PK","IE00B3T34201.USD","LU2552382215.SGD","LU1585245621.USD","LU1868837136.USD","LU2129689514.USD","LU0234570918.USD","SG9999014567.USD","PG","BK4533","BK4581","BK4534","BK4535","PD","LU1868837300.USD","LU1066051498.USD"],"gpt_icon":0},{"id":"2514322448","title":"InflaRx to Showcase Vilobelimab’s Role in Immuno-Dermatology at the 2025 AAD Annual Meeting","url":"https://stock-news.laohu8.com/highlight/detail?id=2514322448","media":"GlobeNewswire","labels":["conferences"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2514322448?lang=en_us&edition=fundamental","pubTime":"2025-02-28 22:00","pubTimestamp":1740751200,"startTime":"0","endTime":"0","summary":"JENA, Germany, Feb. 28, 2025  -- InflaRxN.V., a biopharmaceutical company pioneering anti-inflammatory therapeutics targeting the complement system, today announced acceptance of all submitted abstracts, featuring the role of vilobelimab in pyoderma gangrenosum  and hidradenitis suppurativa , to be presented during the 2025 American Academy of Dermatology  Annual Meeting, March 7 - 11, in Orlando, FL.Camilla Chong, MD, Chief Medical Officer of InflaRx, commented: “We are proud to announce that all of our submitted abstracts have been accepted for presentation at the AAD Annual Meeting, reflecting the considerable scientific work that has gone into the clinical development of vilobelimab in pyoderma gangrenosum  and hidradenitis suppurativa . In HS, we are presenting for the first time the reduction in draining tunnels  with vilobelimab, and the relevance of our modified HiSCR which weighs the importance of these dTs which have a devastating impact on patients with HS.”About Vilobelimab","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/inflarx-showcase-vilobelimab-role-immuno-140000150.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"conferences","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["BNTX","BK4139","IFRX","LU1280957306.USD","SG9999002224.SGD","BK4588","SG9999001440.SGD","BK4581","BK4534","LU0689626769.HKD","LU2129689605.HKD","BK4551","LU0234572021.USD","LU1868837300.USD","BK4504","LU2129689431.USD","LU2129689514.USD","LU0320765646.SGD","LU0323591593.USD","BK4550","LU1430594728.SGD","PG","LU2552382132.HKD","LU1585245621.USD","LU2242646821.SGD","BK4535","BK4585","IE00BWXC8680.SGD","LU0237698245.USD","BK4018","IE00BLSP4239.USD","SG9999002232.USD","LU0124676726.USD","BK4568","USA","LU2242652126.USD","BK4533","LU1868836757.USD","LU2552382215.SGD","ARDS","IE00B3T34201.USD","IE00BLSP4452.SGD","LU0096364046.USD","LU0234570918.USD","LU1066053197.SGD","LU0098860793.USD","SG9999015358.SGD","IE00B1XK9C88.USD","LU2552382058.USD","SG9999015341.SGD"],"gpt_icon":0},{"id":"2512133223","title":"Bonus Biogroup Gains FDA Approval for Crucial Phase III ARDS Drug Trial","url":"https://stock-news.laohu8.com/highlight/detail?id=2512133223","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2512133223?lang=en_us&edition=fundamental","pubTime":"2025-02-18 15:58","pubTimestamp":1739865519,"startTime":"0","endTime":"0","summary":"The latest update is out from Bonus Biogroup ( ($IL:BONS) ). Bonus Biogroup has received FDA approval for an IND application to conduct a Phase III...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/bonus-biogroup-gains-fda-approval-for-crucial-phase-iii-ards-drug-trial?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/company-announcements/bonus-biogroup-gains-fda-approval-for-crucial-phase-iii-ards-drug-trial?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["III","ARDS","BK4139","BK4134"],"gpt_icon":0},{"id":"2511541311","title":"Edesa Biotech Announces $15.0 Million Private Placement Priced At-the-Market Under Nasdaq Rules","url":"https://stock-news.laohu8.com/highlight/detail?id=2511541311","media":"GlobeNewswire","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2511541311?lang=en_us&edition=fundamental","pubTime":"2025-02-13 20:00","pubTimestamp":1739448000,"startTime":"0","endTime":"0","summary":"Financing led by Velan Capital with participation from new and existing healthcare-focused institutional investors and insidersCapital raise to fund Edesa’s CXCL10 antibody program through the end of ","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.globenewswire.com/news-release/2025/02/13/3025767/0/en/Edesa-Biotech-Announces-15-0-Million-Private-Placement-Priced-At-the-Market-Under-Nasdaq-Rules.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["ARDS","EDSA",".IXIC","TQQQ","TSYW.SI","LU2210149790.SGD","BK4588","BK4112","BK4585","MNQmain","LU2210150020.SGD","LU2095319765.USD","PSQ","IE00BGHQF748.EUR","IE00B64PRP62.GBP","NVIW.SI","QLD","SQQQ","IE00BKPKM429.USD","NDAQ","NQmain","USJW.SI","BK4139","USAW.SI","IE00B3QW5Z07.USD","QID"],"gpt_icon":1},{"id":"2505784177","title":"EDSA: IND Expected in 2025 for EB06 for the Treatment of Vitiligo…","url":"https://stock-news.laohu8.com/highlight/detail?id=2505784177","media":"Zacks Small Cap Research","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2505784177?lang=en_us&edition=fundamental","pubTime":"2025-01-22 19:23","pubTimestamp":1737544980,"startTime":"0","endTime":"0","summary":"Edesa Biotech, Inc.  is planning for a Phase 2 study of its anti-CXCL10 monoclonal antibody for the treatment of moderate-to-severe non-segmental vitiligo patients. Vitiligo is a disease that causes areas of the skin to lose color, with non-segmental vitiligo being characterized by patches appearing on both sides of the body. It is caused when pigment-producing cells  die or stop producing melanin as a result of an autoimmune disease, genetics, or a triggering event .A 2022 publication reported that the estimated prevalence of vitiligo patients in the U.S. is between 1.9 million and 2.8 million . This corresponds to a vitiligo market is projected to reach approximately $1 billion by 2030 . In support of this, the following two transactions show the potential for vitiligo treatments in development:. The company is continuing IND-enabling work in 2025 and has already received approval from Health Canada to conduct a Phase 2 tr","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/edsa-ind-expected-2025-eb06-112300368.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["NVIW.SI","TSYW.SI","BK4588",".IXIC","SOC","BK4550","EDSA","QID","VYNE","MNQmain","ARDS","BK4139","USAW.SI","INCY","SIF","BK4532","SQQQ","BK4007","BK4187","PSQ","QLD","BK4213","BK4585","NQmain","TQQQ","USJW.SI"],"gpt_icon":1},{"id":"2504739413","title":"Healios Launches Medical Materials Division to Boost Culture Supernatant Supply","url":"https://stock-news.laohu8.com/highlight/detail?id=2504739413","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2504739413?lang=en_us&edition=fundamental","pubTime":"2025-01-20 07:10","pubTimestamp":1737328226,"startTime":"0","endTime":"0","summary":"Healios K.K  has launched a medical materials and equipment division to secure a steady supply of culture supernatant and expand its business, according to a Friday filing on the Tokyo Stock Exchange.The division will manage production, quality control, and regulatory compliance, and support market research and customer engagement.This follows Healios' partnership with AND medical group to supply culture supernatant for new treatments and cosmetics. Healios is also seeking conditional approval in Japan for its MultiStem therapy targeting acute respiratory distress syndrome .","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4588","BK4544","BK4139","BK4585","ARDS","ARKG"],"gpt_icon":0},{"id":"2504433569","title":"InflaRx Stock Rises 8% on Conditional EC Nod for COVID-19 Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2504433569","media":"Zacks","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2504433569?lang=en_us&edition=fundamental","pubTime":"2025-01-16 23:49","pubTimestamp":1737042540,"startTime":"0","endTime":"0","summary":"InflaRx N.V.IFRX shares gained 7.7% on Wednesday following the European Commission's  approval of marketing authorization, under exceptional circumstances, for Gohibic  to treat adult patients with acute respiratory distress syndrome  caused by SARS-CoV-2. The targeted patient population in the EU comprises individuals receiving systemic corticosteroids as standard-of-care therapy and undergoing invasive mechanical ventilation, with or without extracorporeal membrane oxygenation.The EC’s approval makes Gohibic the first and only approved treatment for SARS-CoV-2-induced ARDS in the EU. We remind the investors that in November 2024, the advisory committee to the European Medicines Agency had adopted a positive opinion recommending approval of the drug for the above indication, under exceptional circumstances. Gohibic is a first-in-class anti-C5a monoclonal antibody.More on the EC Nod for IFRX’s COVID-19-Induced ARDS Drug. The EU approval ofInflaRx’s Gohibic for the ADRS indication is ba","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.yahoo.com/news/inflarx-stock-rises-8-conditional-154900009.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"yahoofinance","symbols":["LU0098860793.USD","SG9999015358.SGD","LU0868494617.USD","IE000M9KFDE8.USD","BMRN","EC","ARDS","LU2552382215.SGD","BK4018","BK4568","LU2242652126.USD","BK4196","LU1430594728.SGD","LU1280957306.USD","BK4548","SG9999002232.USD","IE00BWXC8680.SGD","BK4551","LU0320765646.SGD","PG","LU1868836591.USD","LU0640476718.USD","SG9999014559.SGD","SG9999002224.SGD","IE00BLSP4452.SGD","SG9999014575.USD","IFRX","CSTL","LU0689626769.HKD","BK4504","LU1929549753.HKD","SG9999001440.SGD","LU1066051498.USD","BK4139","IE00B7SZLL34.SGD","IE00BBT3K403.USD","LU1066053197.SGD","LU1868837300.USD","BNTX","CTMX","LU0061475181.USD","BK4533","LU2242646821.SGD","LU1868837136.USD","BK4201","IE00BLSP4239.USD","LU0124676726.USD","LU2552382132.HKD","BK4581","LU0094547139.USD"],"gpt_icon":0},{"id":"2503606080","title":"Healios, Nobelpharma End Collaboration Talks for MultiStem ARDS Agreement","url":"https://stock-news.laohu8.com/highlight/detail?id=2503606080","media":"MT Newswires Live","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503606080?lang=en_us&edition=fundamental","pubTime":"2025-01-16 07:06","pubTimestamp":1736982409,"startTime":"0","endTime":"0","summary":"Healios K.K  and Nobelpharma terminated discussions regarding a development and commercialization agreement for MultiStem in Japan, according to a Wednesday filing on the Tokyo Stock Exchange.The decision follows unsuccessful renegotiations on the terms of the agreement after Healios opted not to proceed with a Phase 3 trial in Japan, as it was deemed unnecessary.Price : $200.00, Change: $-1.0, Percent Change: -0.50%","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4139","ARDS"],"gpt_icon":0},{"id":"2503606299","title":"Healios Reaches Agreement with PMDA on MultiStem ARDS Approval in Japan","url":"https://stock-news.laohu8.com/highlight/detail?id=2503606299","media":"MT Newswires Live","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503606299?lang=en_us&edition=fundamental","pubTime":"2025-01-16 07:03","pubTimestamp":1736982195,"startTime":"0","endTime":"0","summary":"Healios K.K  has agreed with Japan's Pharmaceuticals and Medical Devices Agency  on the clinical data package for conditional approval of MultiStem for Acute Respiratory Distress Syndrome, according to a Wednesday filing with the Tokyo Stock Exchange.The approval will be based on Phase 2 trial results, with future Phase 3 data from the US as confirmatory support.MultiStem is a regenerative medicine targeting ARDS, ischemic stroke, and trauma, and has received FDA Fast Track and RMAT designations.Price : $200.00, Change: $-1.0, Percent Change: -0.50%","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["ARDS","BK4139"],"gpt_icon":0},{"id":"2503760318","title":"InflaRx Secures EU Approval for GOHIBIC in Treating COVID-19-Induced ARDS","url":"https://stock-news.laohu8.com/highlight/detail?id=2503760318","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503760318?lang=en_us&edition=fundamental","pubTime":"2025-01-16 05:59","pubTimestamp":1736978398,"startTime":"0","endTime":"0","summary":"InflaRx ( ($IFRX) ) has provided an update. On January 15, 2025, InflaRx announced the European Commission’s marketing authorization for their drug...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/inflarx-secures-eu-approval-for-gohibic-in-treating-covid-19-induced-ards?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/company-announcements/inflarx-secures-eu-approval-for-gohibic-in-treating-covid-19-induced-ards?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["ARDS","BK4139","BK4548","BK4156","BK4588","BK4535","BK4568","BK4585","BNTX","BK4551"],"gpt_icon":0},{"id":"2503823678","title":"InflaRx announces EC grants marketing authorization to Gohibic for ARDS","url":"https://stock-news.laohu8.com/highlight/detail?id=2503823678","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503823678?lang=en_us&edition=fundamental","pubTime":"2025-01-16 01:35","pubTimestamp":1736962510,"startTime":"0","endTime":"0","summary":"InflaRx (IFRX) announced that the European Commission has granted marketing authorization under exceptional circumstances for Gohibic for the treat...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/inflarx-announces-ec-grants-marketing-authorization-to-gohibic-for-ards?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/inflarx-announces-ec-grants-marketing-authorization-to-gohibic-for-ards?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["BK4201","IFRX","ARDS","EC","BK4139"],"gpt_icon":0},{"id":"2503162032","title":"InflaRx Receives European Commission Approval for GOHIBIC® (vilobelimab) for the Treatment of SARS-CoV-2-Induced Acute Respiratory Distress Syndrome (ARDS)","url":"https://stock-news.laohu8.com/highlight/detail?id=2503162032","media":"GlobeNewswire","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503162032?lang=en_us&edition=fundamental","pubTime":"2025-01-16 01:30","pubTimestamp":1736962200,"startTime":"0","endTime":"0","summary":"JENA, Germany, Jan.  15, 2025  (GLOBE NEWSWIRE) -- InflaRxN.V.(Nasdaq:IFRX), a biopharmaceutical company pioneering anti-inflammatory therapeutics targeting the complement system, today announced 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Ends Collaboration Talks with Nobelpharma on ARDS Therapy","url":"https://stock-news.laohu8.com/highlight/detail?id=2503866041","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2503866041?lang=en_us&edition=fundamental","pubTime":"2025-01-15 15:30","pubTimestamp":1736926204,"startTime":"0","endTime":"0","summary":"Healios KK ( ($JP:4593) ) has shared an update. Healios K.K. announced the termination of its collaboration discussions with Nobelpharma for the de...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/healios-ends-collaboration-talks-with-nobelpharma-on-ards-therapy?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/company-announcements/healios-ends-collaboration-talks-with-nobelpharma-on-ards-therapy?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["ARDS","BK4139"],"gpt_icon":0}],"pageSize":16,"totalPage":3,"pageCount":1,"totalSize":44}]}}