Thursday, May 7, 2020

中央大學(徐國鎧教授)+聯新醫院(吳清平副院長) 開發 “智慧呼吸器”

中大攜手聯新醫院研發「呼吸器警報系統」提升醫療新能量 桃園電子報 記者謝宜芳2020-04-27 加護病房裏,插管的重症患者生死交關,為讓患者能獲得有效的監測照顧,並減輕醫護人員的工作負擔,由中央大學電機系徐國鎧講座教授和聯新國際醫院吳清平副院長團隊共同研發的智慧型「呼吸器警報系統」,可以精準地提供患者最佳每分鐘通氣量,還有當呼吸參數異常時,可立即作警報提醒,成果獲美中台三項專利之肯定。中央大學表示,新冠肺炎疫情席捲全球,呼吸器日益難求,中央大學與聯新國際醫院共同研發的新一代呼吸器受到醫界矚目。因為病人在呼吸方面的問題通常都非常緊急,在幾分鐘以內若不作出處置,可能會造成極大傷害。然而,由於醫護人員有限,無法全天候地留在每個病人旁觀察呼吸參數,且當呼吸參數發生異常時,通常並不是調整呼吸器的操作設定就能解決。 中央大學表示,該發明提供一種智慧型之呼吸器和警報系統,透過各項生理呼吸異常數據所觸發的警報訊號,以提供醫護人員有效的警報及即時作業管理,如一旦偵測痰音時,影響呼吸時,會發出提醒;另有管路脫離或漏氣等各項條件之警報。徐國鎧表示,根據聯新國際醫院提供的20-30年臨床治療經驗,發現病患最佳每分鐘通氣量都因人而異,而現況醫療使用的呼吸器都是固定無法適應不同病患狀況。以往都是靠呼吸治療師的經驗手動調整,但為更有效監測,該團隊想出了建置自動化控制系統,將臨床的治療經驗結合理論分析,再透過精密的演算法設計,將呼吸器進一步改造,以精準地自動提供患者最佳每分鐘通氣量,讓患者呼吸更加順暢,並提供即時的警報系統。研究專長在伺服馬達控制的徐國鎧,早期曾開發出「智慧型看護系統」,幫助長期卧床的重症病患,找回自主與自尊,在研究中注入更多人性關懷。近年來則專注在呼吸器控制平台的研發上,希望讓病患得到更好的治療,也減輕第一線醫護人員的工作負荷,並讓世界看見台灣的醫療研發能量。

(新冠病毒篩檢)TFDA專案輸入已核准9件

檢驗產業未受關愛 台灣的快篩試劑在那裡? 2020-05-02 10:06聯合報 記者陳雨鑫/台北即時報導 想像歐、美等國解封、恢復航線後,我們該如與之恢復往來?在疫苗問世前,許多人把希望放在「快篩檢驗試劑」的研發,誰能先研發出靈敏度、專一性高的快篩試劑,能夠讓新冠肺炎像流感一樣可以透過快篩檢測,就能搶下先機。不過,新冠病毒快篩試劑的研發,仍面臨許多障礙。目前各國使用的檢驗試劑皆以核酸檢測為主,檢驗新冠病毒基因序列片段來確定是否被感染,靈敏度高,缺點是需耗費三到四小時,寶齡富錦生技發言人丁爾昆說明,雖然已有一小時就有結果的產品上市,大家仍寄望只需十五分鐘就明結果的抗原檢測試劑。但目前全球都還沒有找到靈敏度、專一性都高的抗原檢測試劑。永加利醫學科技董事長瞿志豪說,各界雖對快篩試劑寄與厚望,但抗原檢測必須體內病毒量每西西血液達到十的六次方以上,患者於潛伏期就會呈現偽陰性。目前各國面臨的挑戰大同小異,到底COVID-19產生出的抗體蛋白質是哪一款,全世界都抓不準,但中研院三月中旬發表的COVID-19抗原,被學界認為極具代表性,若是臨床試驗成功,將有機會量產,可望率先開發高靈敏度、專一性高的抗原試劑,讓台灣有機會在快篩檢驗試劑的戰爭中脫穎而出。食藥署醫粧組研究員王兆儀說,設置綠色通道後,食藥署成立專案輔導團隊,提供即時諮詢,截至昨天為止,我國已輔導案件達五十件,有八件提出申請,今天也通過首件國產核酸檢驗試劑。王兆儀表示,該款核酸檢驗試劑,從採檢到結果為85分鐘,業者已完成臨床試驗,檢驗試劑的敏感度與特異性都超過95%,今通過後,即起可以專案製造;另外針對專案輸入的案件,目前已經核准9件。王兆儀說,目前業界最困擾的應是台灣確診者少,檢體取得相對困難,國衛院成立「病毒技術分析平台」之後,可媒合業界與醫院,盼能協助開發試劑。食藥署則開放綠色通道,在臨床前試驗開放使用模擬檢體,但業者仍須與收治確診病患的醫院合作,產品必須要交替檢測,通過五陰五陽的確效,才能通過許可。瞿志豪說,食藥署的綠色通道比照美國食藥局,現階段台灣檢驗試劑面臨的挑戰,仍是民間的檢驗量能本身才有機會突破。我國檢驗產業長年以來並未受政府大力扶植,現在要補足民間的檢驗產業能力,除了政府要給足資源,也要看產業多久以後能把技術學起來,展開研發。

異體MSC (Remestemcel-L)治療新冠病毒引發肺部ARDS臨床試驗 (~300 patients)

Clinical Trials Of Mesoblast's Stem Cell Treatment For COVID-19 Set To Begin Soon

Alex Knapp Forbes Staff, May 2, 2020  Mesoblast's stem cells replicating during the manufacturing process. Melbourne-based biotech company Mesoblast announced earlier this week that it's begun enrolling up to 300 patients for a randomized, controlled study of its stem cell therapy remestemcel-L in the treatment of COVID-19 patients experiencing acute respiratory distress syndrome. Over 20 hospitals will participate in the study, which is anticipated to last 3-4 months. The announcement came about a week after the company reported that treatment with remestemcel-L in a group of 12 COVID-19 patients with ARDS at Mt. Sinai hospital in New York had a survival rate of 83%. The purpose of the randomized, controlled clinical trial is to test that survival rate on a larger scale."We were very pleased with preliminary data demonstrating the cells seem to have benefitted some of these patients," says CEO Silviu Itescu. "If the cells work in COVID-19 ARDS, we're in a position to provide products to as many patients as possible." For coronavirus patients, ARDS is one of the deadliest complications of the disease, and often ends up requiring the use of ventilators in order to ensure they're getting sufficient oxygen. It's caused by what's known as a "cytokine storm" - an overreaction of the immune system in which the body ends up damaging the lungs in an attempt to destroy the coronavirus and the lung cells that it has infected."The cytokines these cells make destroy lung tissue," says Itescu. "It's a trade-off being trying to get rid of the virus and trying to limit destruction to your own lung tissue." According to the CDC, between 20-42% of hospitalized COVID-19 patients develop ARDS, with as many as 85% of patients admitted to intensive care having this complication. Among those ICU patients who develop ARDS, over 40% die (some studies show that number as high as 72%) and those who survive spend an average of 10-13 days in the hospital. Mesoblast's remestemcel-L treatment is derived from allogenic mesenchymal stem cells, which when infused into the body can slow down an immune response and prevent the body from damaging itself. Its technology originally spun out of a research collaboration between Columbia University and Australian scientists, leading to the founding of the company in 2004. One of the diseases the company has been working to treat is graft-vs-host disease, a condition that arises in patients who receive bone marrow transplants. In that disease, the donated bone marrow begins to see its new host as "foreign" and directs the immune system to attack it in a manner similar to that of the cytokine storm seen in ARDS. The company is one of several biotech firms aiming to use mesenchymal stem cells as a potential COVID-19 treatment. Cleveland-based Athersys, which is working on stem cell therapies for strokes, heart disease and other conditions, is also expected to begin clinical trials soon. Haifa, Israel-based Pluristem, which is developing stem cell treatments as well, secured 50 million Euro (about $55.4 million) in financing this week from the European Investment Bank to support its COVID-19 trials. So far, says Itescu, Mesoblast's treatment has been tested in clinical trials in over 1,100 graft-vs-host patients. On April 1, the FDA accepted a priority review filing for use of the treatment against graft-vs-host disease. On April 6, the FDA gave clearance for an investigational new drug application for remestemcel-L in COVID-19 patients, which paved the way for this clinical trial. Using Mesoblast's treatment for coronavirus patients with ARDS "has a rationale behind it" says Dr. Wayne Marasco, who's studied a number of coronavirus diseases and is currently researching potential antibody treatments for COVID-19. "That would be in line with how it works with graft-versus-host disease." Itesecu says that his company is focused on the next phase of its clinical research in the midst of this pandemic, and hopes it proves to be part of a number of effective therapies against the disease."We're going to do our best to provide a solution to those patients in greatest need: those who are in intensive care on ventilators, where I think a safe and effective way to reduce severe inflammation is needed," says Itescu. "We hope that what we're doing is complementary to what folks who are developing vaccines and antivirals are doing."

 

Wednesday, May 6, 2020

新冠篩檢CE認證: 普生 出貨 法國/中東/東南亞

肺炎快篩國家隊線上秀實力 全球買主洽單 2020/04/29 時報資訊 沈培華 為將台灣防疫產品向國際傳播,以解國際防疫之急,外貿協會號召普生、金萬林、偉喬、奎克、大江、工研院生醫所,以及22日才宣布成軍,由台康、寶齡富錦及安(月太)共同組成的AEP快篩聯盟等7家專業團隊,舉辦了一場「COVID-19快篩檢測線上發表會」。為方便受疫情重創的歐美國家,這場發表會安排在27日晚上9點進行直播,共有37國的300位全球買主上線與會,包含保加利亞最大國立醫院Pirogov Hospital、拉丁美洲最大的免疫生物學和生物製藥生產商Butantan、新加坡國家傳染病中心National Centre for Infectious Diseases等。外貿協會秘書長葉明水在致詞時表示,台灣擁有卓越的生技研發能量,自2003年經歷SARS風暴,我國持續保持警戒並致力於傳染性疾病的預防及防護。AEP快篩聯盟的COVID-19 Antigen Rapid Test(Vstrip),可用於病毒量尚不大的早期感染者篩檢,最快10分鐘即可獲得快篩結果,線上遠在法國、加拿大、印度、波蘭、保加利亞的外商詢問不斷,會後收到近60件詢問。偉喬生醫的產品涵蓋抗原及抗體檢測兩種,在不同情境下操作活用性大且快速,獲巴西買主積極詢問,期能爭取代理。此次準確率高的PCR核酸檢測特別受買主青睞,包含甫於上週取得CE認證的普生,準確率超過9成,已出貨到法國、中東、東南亞;奎克生技光電的雙功能(Digital/Quantitative)dqPCR,專用於檢測微量病毒,靈敏度比標準PCR高出10倍,90分鐘可完成6個檢體;也已取得CE認證的金萬林,高靈敏度、高專一性的PCR有望於近期取得美國FDA認證;工研院推出的「疫開罐」標榜高精準、高靈敏、高輕巧和高效率等四大特色;大江基因推出的24小時全自動檢測設備,每天可檢測近900個檢體,會後吸引大型美商洽詢合作機會。

興櫃價格熔斷: 普生/敏成/清淨海

生技熱燒到興櫃 今年熔斷四次 2020-04-27 22:44經濟日報 記者王奐敏/台北即時報導 新冠肺炎疫情帶動防疫概念股續夯,上櫃股票包括高端疫苗、寶齡富錦、台康生技今(27)日都高掛漲停,連帶興櫃股票的普生也連二日大漲,且都啟動熔斷機制。而今年來興櫃啟動過四次冷卻機制,都是防疫相關個股。櫃買中心表示,普生在明(28)日即恢復正常交易,明天若又達暫停標準,則會有規定再暫停交易,沒有特別的處置。普生昨日均價為40.55元,高於24日均價27.03元達50%,因此暫停交易至收盤。這是今年第四次發生,第三次也是普生,24日均價27.03元高於23日均價18.02元達50%。前兩次則是敏成及清淨海,在1月30日發生,也同樣都是均價飆漲到熔斷。敏成是生產靜電濾材/熔噴不織布廠商;清淨海是生產高生物分解環保家用清潔用品、高生物分解環保個人清潔化妝產品,以及防疫性產品廠商;普生則是精準醫療廠,23日甫宣布研發生產的新冠肺炎核酸檢測試劑,獲得歐盟認證。櫃買中心表示,由於興櫃股票為議價交易,並未設漲跌幅度的限制,但為了保護投資人,特別新增興櫃股票個股價格異常之冷卻機制,當股票成交均價較前一營業日的價格漲跌逾50%以上,即暫停該檔興櫃股票之交易直到當日交易時間結束,以達到對價格異常波動的特定股票適時冷卻的效果。

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