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hk_prnasia info@prnasia.com (美通社)
雲頂新耀宣布耐賦康®獲得中國國家藥品監督管理局完全批准
上海2025年5月7日 /美通社/ -- 雲頂新耀(HKEX 1952.HK)是一家專注於創新藥研發、臨床開發、制造和商業化的生物製藥公司,今日宣布耐賦康®(布地奈德腸溶膠囊,NEFECON®)正式獲得國家藥品監督管理局(NMPA)同意,由附條件批准轉為完全批准, 取消了對蛋白尿水平的限制,使更多患者獲益。【適應症】:NEFECON用於治療具有疾病進展風險的原發性免疫球蛋白A腎病(IgAN)成人患者,以減少腎功能損失。 2023年11月,耐賦康®通過優先審評程序獲得國家藥品監督管理局附條件上市批准,用於治療具有進展風險的原發性IgA腎病(IgAN)成人患者,是中國唯一獲得IgA腎病適應症的治療藥物。此次完全批准,意味著耐賦康®臨床研究的完整數據已獲通過,成為國內首個且唯一獲得NMPA完全批准的IgA腎病對因治療藥物。 雲頂新耀首席執行官羅永慶表示:「此次完全批准取消了對蛋白尿水平的限制,這將推動耐賦康®從改變治療格局走向重塑治療標準,延緩IgA腎病患者腎功能衰退,更好地滿足長期未被滿足的臨床需求,使更多患者獲益。新適應症的獲批充分驗證了耐賦康®的臨床療效與安全性,為醫生提供了更加堅實的治療決策依據,使其成為了中國首個且目前唯一獲得NMPA完全批准的IgA腎病對因治療藥物。 目前,中國約有500萬的IgA腎病患者,每年新增確診患者超過10萬人。耐賦康®已被納入國家醫保藥品目錄,截止今年3月底,全國26個省市的醫療機構已開始按醫保價格執行。未來,我們將繼續提高耐賦康®的可及性和可負擔性,為更多IgA腎病患者帶來福音。」 此次獲批是基於NefIgArd III期臨床研究的完整數據。NefIgArd III期臨床試驗是一項隨機、雙盲、全球多中心研究,在接受RAS抑制劑優化支持治療的原發性IgA腎病成人患者中評估了耐賦康®(16mg,每日一次)與安慰劑相比的療效和安全性。這項研究為期2年,包括9個月的耐賦康®或安慰劑治療期,隨後是15個月的停藥隨訪期。全球研究結果顯示:與安慰劑相比,耐賦康®不僅帶來了持久的蛋白尿下降,減少鏡下血尿風險,更重要的是在估算腎小球濾過率(eGFR)上顯示出臨床意義且統計學差異(p。 作為全球首個獲得美國食品藥品監督管理局(FDA)和歐洲藥品管理局(EMA)完全批准的IgA腎病治療藥物, 耐賦康®已相繼在雲頂新耀所有授權區域(中國澳門、中國大陸、新加坡、中國香港、中國台灣以及韓國)獲得批准,其中,中國澳門、中國大陸、新加坡和中國香港已商業化上市,韓國和中國台灣預計於年內上市。 關於耐賦康®(NEFECON®) 耐賦康®(NEFECON®)是布地奈德腸溶膠囊,作為全球首個對因治療IgA腎病的藥物,是靶向腸道黏膜B細胞的免疫調節劑,能減少50%腎功能下降1,在中國人群中能延緩腎功能衰退達66%2,預計將疾病進展至透析或腎移植的時間延緩12.8年3。同時布地奈德首過代謝程度達90%4,具有良好的安全性。耐賦康®專為IgA腎病患者研制,每顆膠囊含布地奈德4mg,通過特殊的遲釋及緩釋雙重制劑工藝,將布地奈德靶向釋放於回腸末端的黏膜B細胞(包括派爾集合淋巴結),膠囊溶解後,三層包衣微丸持續穩定釋放布地奈德,高濃度覆蓋整個靶區域,從而減少誘發IgA腎病的半乳糖缺陷的IgA1抗體(Gd-IgA1)產生,進而干預發病機制上游階段,達到治療IgA腎病的作用。 2019年6月,雲頂新耀與Calliditas Therapeutics 簽訂獨家授權許可協議,獲得在大中華地區和新加坡開發以及商業化耐賦康®的權利。該協議於2022年3月擴展,將韓國納入雲頂新耀的授權許可范圍。 關於雲頂新耀 雲頂新耀是一家專注於創新藥和疫苗研發、臨床開發、制造和商業化的生物製藥公司,致力於滿足亞洲市場尚未滿足的醫療需求。雲頂新耀的管理團隊在中國及全球領先製藥企業從事過高質量研發、臨床開發、藥政事務、化學制造與控制(CMC)、業務發展和商業化運營,擁有深厚的專長和豐富的經驗。雲頂新耀已打造多款疾病首創或者同類最佳的藥物組合,公司的治療領域包括腎科疾病、感染性和傳染性疾病、自身免疫性疾病。有關更多信息,請訪問公司網站:www.everestmedicines.com。 前瞻性聲明 本新聞稿所發布的信息中可能會包含某些前瞻性表述,乃基於本公司或管理層在做出表述時對公司業務運營情況及財務狀況的現有看法、相信、和現有預期,可能會使用「將」、「預期」、「預測」、「期望」、「打算」、「計劃」、「相信」、「預估」、「確信」及其他類似詞語進行表述。這些前瞻性表述並非對未來業績的保證,會受到風險、不確定性及其他因素的影響,有些乃超出本公司的控制范圍,難以預計。因此,受我們的業務、競爭環境、政治、經濟、法律和社會情況的未來變化及發展等各種因素及假設的影響,實際結果可能會與前瞻性表述所含資料有較大差別。本公司及各附屬公司、各位董事、管理人員、顧問及代理未曾且概不承擔更新該稿件所載前瞻性表述以反映在本新聞稿發布日後最新信息、未來項目或情形的任何義務,除非法律要求。 參考文獻 1.Lafayette R,et al. Lancet. 2023 Sep 9;402(10405):859-870. 2.2023ASN. Oral presentation. 3.Jonathan Barratt,et al. 2023 ASN. Poster no. SA-PO886. 4.Edsbäcker S,et al. Aliment Pharmacol Ther. 1999 Feb;13(2):219-24.
Sports 2025-05-06 23:30:00 (1 month before)
Formosa Pharmaceuticals Announces Licensing Agreement with Apotex Inc., for Commercialization of Clobetasol Propionate Ophthalmic Suspension for Post-Ocular Surgery Inflammation and Pain for MexicoFormosa Pharmaceuticals Announces Licensing Agreement with Apotex Inc., for Commercialization of Clobetasol Propionate Ophthalmic Suspension for Post-Ocular Surgery Inflammation and Pain for Mexico
en_prnasisa
Formosa Pharmaceuticals Announces Licensing Agreement with Apotex Inc., for Commercialization of Clobetasol Propionate Ophthalmic Suspension for Post-Ocular Surgery Inflammation and Pain for Mexico
Top 2025-05-06 22:30:00 (1 month before)
【C.S】集團:以樟芝酸A新藥啟動兩岸動物藥證申請【C.S】集團:以樟芝酸A新藥啟動兩岸動物藥證申請
hk_prnasia info@prnasia.com (美通社)
【C.S】集團:以樟芝酸A新藥啟動兩岸動物藥證申請
Business 2025-04-29 22:30:00 (1 month before)
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FDA Grants Authorisation for Minder®, the First and Only Implantable Continuous EEG Monitor Approved in US
The Australian-developed Minder system is an implantable device for continuous monitoring of brain activity in patients with epilepsy, developed to address the shortcomings in current electroencephalogram technologies The FDA has granted authorisation for Minder under its De Novo pathway creating a new classification of device, allowing for marketing and sale of the device in the US for patients with drug resistant epilepsy Epiminder intends to launch Minder in the US during H2 2025 MELBOURNE, Australia and DALLAS, April 23, 2025 /PRNewswire/ -- Epiminder, a pioneering medical device and information solutions company, today announced that it has been granted FDA authorisation via the De Novo classification for Minder, its proprietary implantable continuous electroencephalogram monitoring system (iCEMTM) for patients with epilepsy. Minder has also been designated as a Breakthrough Technology by the FDA, recognising its potential to provide more effective diagnosis and management for people living with epilepsy. This De Novo authorization is significant as it creates a new classification of device which underscores both the innovation and the clinical validation behind Minder. Without accurate diagnosis and monitoring, sustained and effective management of epilepsy can be challenging. Minder has been developed to address the shortcomings in current electroencephalogram (EEG) technologies, providing reliable and actionable diagnostic data for more patients and therefore better enabling their prospects for successful epilepsy treatment. Rohan Hoare PhD, CEO of Epiminder, said: " By extending the monitoring window of an EEG from days using current technologies to months or even years with Minder, we can deliver unprecedented access to a high-fidelity stream of continuous EEG data to health care professionals and their patients. The FDA's clearance of Minder is a significant milestone for Epiminder and more importantly for the 52 million people around the world who have epilepsy. As the first and only implantable continuous EEG monitor approved in US, Minder can provide health care professionals and their patients with more accurate and timely diagnoses, enhanced therapeutic drug monitoring, and can better inform decisions on non-drug treatments like surgery. Looking ahead, Epiminder plans to develop a suite of integrated software solutions that will extend the clinical impact of the Minder device, for example by providing patients with advance notice of seizures through AI-enabled forecasting." Epiminder intends to formally launch Minder in the US during H2 2025 undertaking a phased commercial roll out into leading epilepsy centres as part of a program to demonstrate the clinical utility of the system. Professor Robert Fisher MD, PhD, Director of the Stanford Epilepsy Center, past-President of the American Epilepsy Society, and Chair of the Data Safety Monitoring Board for the UMPIRE trial, said: "One of the greatest difficulties in caring for people with epilepsy is the lack of accurate information about a patient's seizures. Seizure diaries are of limited effectiveness. Minder can greatly improve seizure tracking and therefore seizure management. It will fill the significant gap in current EEG technologies, providing clinicians like me continuous and accurate data. By having a more complete picture, we can be more precise in our diagnoses, better able to rapidly adjust medication or neuromodulation regimens and identify patients for potential non-drug or surgical treatments. The result will be a reduction in the huge burden of drug resistant epilepsy." The safety and effectiveness of Minder was validated through Epiminder's UMPIRE clinical study, a multi-centre prospective, open design, case-controlled comparator trial that was undertaken in leading Australian hospitals between 2019 and 2023. The results of UMPIRE were used to support Epiminder's successful FDA application. Professor Mark Cook MD MBBS FRACP FRCP (London), Epiminder's Founder and Chief Medical Officer, said: "The results from UMPIRE exceeded our expectations and demonstrated Minder's ability to capture high-quality EEG data continuously for extended periods, including a groundbreaking five-year continuous recording in one participant. Minder delivered actionable clinical insights for nearly 90 percent of study participants, highlighting the real-life benefits that Epiminder's best-in-class iCEM can deliver relative to the current standard of care." Epilepsy is one of the most common serious chronic neurological disorders, affecting approximately 52 million people worldwide including 250,000 Australians and 3.4 million Americans. It is a neurological condition where a person experiences recurrent seizures caused by abnormal electrical activity in the brain. Seizures can present with a variety of clinical manifestations; some involve motor symptoms, such as intense muscle contractions, while others, such as absence or focal impaired awareness seizures, may present with subtle or no outward physical signs. The occurrence of seizures varies in frequency among patients, from less than one a year to several a day. Follow Epiminder on LinkedIn and explore www.epiminder.com for more information. About Minder Minder is a minimally invasive device for continuous monitoring of electrographic activity of the brain, providing epilepsy patients and their doctors with detailed data on brain activity over an extended period. Patients can wear the device as they go about their normal daily activities. Minder's long-term monitoring of patients outside of a controlled clinical environment provides data needed for better understanding and more effective treatment of underlying conditions, including determining the effectiveness of drug therapies and other potential interventions. About Epiminder Founded in 2017 by Professor Mark Cook together with the Bionics Institute, St Vincent's Hospital, the University of Melbourne and Cochlear Limited. Epiminder is a medical device and information solutions company focused on developing diagnostic and treatment tools for epilepsy and other seizure disorders where continuous monitoring is required. Epiminder is headquartered in Melbourne, Australia and has offices in the United States. Contact: Matt Wright, matt@nwrcommunications.com.au
Top 2025-04-22 22:15:00 (1 month before)
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