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| Monday, November 11, 2024 |
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云顶新耀宣布耐赋康(R)Ⅲ期试验开放标签第二疗程扩展研究积极结果 |
| 云顶新耀（HKEX 1952.HK）是一家专注于创新药研发、临床开发、制造和商业化的生物制药公司，今日宣布耐赋康(R)（布地奈德肠溶胶囊，NEFECON(R)）的全球III期临床试验NefIgArd研究开放标签扩展（OLE）研究的结果近日在2024美国肾脏病学会（American Society of Nephrology, ASN）上公布。 more info >> |
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| Friday, October 25, 2024 |
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Everest Medicines Announces the Launch of VELSIPITY(R) in the Guangdong-Hong Kong-Macau Greater Bay Area |
| Everest Medicines (HKEX 1952.HK, "Everest", or the "Company"), a biopharmaceutical company focused on the discovery, clinical development, manufacturing and commercialization of innovative therapeutics, today announced that, through the "Hong Kong and Macau Medicine and Equipment Connect" policy, VELSIPITY(R) has officially been approved for patients with moderately to severely active ulcerative colitis (UC) by the Guangdong Provincial Medical Products Administration and can first be used in the Foshan Fosun Chancheng Hospital and the First Affiliated Hospital of Sun Yat-sen University, two of the medical institutions designated by the "Hong Kong and Macau Medicine and Equipment Connect" policy in the Greater Bay Area. more info >> |
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云顶新耀宣布伊曲莫德（VELSIPITY）获批进入粤港澳大湾区 为溃疡性结肠炎患者带来新选择 |
| 云顶新耀（HKEX 1952.HK）是一家专注于创新药研发、临床开发、制造和商业化的生物制药公司，今日宣布，得益于“港澳药械通”政策，伊曲莫德（VELSIPITY®）正式获得“粤港澳大湾区内地临床急需进口港澳药品批件”批准，可以在佛山复星禅诚医院、中山大学附属第一医院两家大湾区药械通政策指定的医疗机构先行使用，后续该产品将在其他药械通资质医院陆续引入。 more info >> |
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雲頂新耀宣佈伊曲莫德（VELSIPITY(R)）獲批進入粵港澳大灣區 為潰瘍性結腸炎患者帶來新選擇 |
| 雲頂新耀（HKEX 1952.HK）是一家專注于創新藥研發、臨床開發、製造和商業化的生物製藥公司，今日宣佈，得益於「港澳藥械通」政策，伊曲莫德（VELSIPITY(R)）正式獲得「粵港澳大灣區內地臨床急需進口港澳藥品批件」批准，可以在佛山複星禪誠醫院、中山大學附屬第一醫院兩家大灣區藥械通政策指定的醫療機構先行使用，後續該產品將在其他藥械通資質醫院陸續引入。 more info >> |
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| Tuesday, October 22, 2024 |
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Everest Medicines Announces Positive Results of Complete Chinese Subpopulation Data from the NEFECON Global Phase 3 NefIgArd Clinical Trial |
| Everest Medicines (HKEX 1952.HK, "Everest", or the "Company"), a biopharmaceutical company focused on the discovery, clinical development, manufacturing and commercialization of innovative therapeutics, today announced that the "Kidney 360" magazine has published the complete two-year subpopulation data from Chinese patients in the Phase 3 NefIgArd clinical trial of NEFECON under the title "Efficacy and Safety of Nefecon in Patients With Immunoglobulin A Nephropathy From Mainland China: 2-Year NefIgArd Trial Results". more info >> |
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雲頂新耀宣佈耐賦康®NefIgArd III期全球臨床試驗完整中國亞組資料的積極結果 |
| 雲頂新耀（HKEX 1952.HK）是一家專注于創新藥研發、臨床開發、製造和商業化的生物製藥公司，今日宣佈《腎臟360》（Kidney 360）雜誌以「Efficacy and Safety of Nefecon in Patients With Immunoglobulin A Nephropathy From Mainland China: 2-Year NefIgArd Trial Results」《耐賦康®在中國大陸IgA腎病患者中的療效和安全性：2年NefIgArd試驗結果》為題，刊登了耐賦康®（布地奈德腸溶膠囊，NEFECON®）在NefIgArd III期研究中完整2年資料的中國亞組資料。 more info >> |
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云顶新耀宣布耐赋康(R) NefIgArd III期全球临床试验完整中国亚组数据的积极结果 |
| 云顶新耀（HKEX 1952.HK）是一家专注于创新药研发、临床开发、制造和商业化的生物制药公司，今日宣布《肾脏360》（Kidney 360）杂志以"Efficacy and Safety of Nefecon in Patients With Immunoglobulin A Nephropathy From Mainland China: 2-Year NefIgArd Trial Results"《耐赋康 在中国大陆IgA肾病患者中的疗效和安全性：2年NefIgArd试验结果》为题，刊登了耐赋康®（布地奈德肠溶胶囊，NEFECON® 在NefIgArd III期研究中完整2年数据的中国亚组数据。 more info >> |
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| Monday, October 21, 2024 |
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Everest Medicines Announces Taiwan TFDA Approval of NEFECON for the Treatment of Primary IgA Nephropathy |
| Everest Medicines (HKEX 1952.HK, "Everest", or the "Company"), a biopharmaceutical company focused on the discovery, clinical development, manufacturing and commercialization of innovative therapeutics, today announces that the Taiwan Food and Drug Administration (TFDA) has approved NEFECON indicated "to reduce the loss of kidney function in adult patients with primary immunoglobulin A nephropathy (IgAN) who are at risk for disease progression1". There are no restrictions on initial proteinuria levels in the approved indication. more info >> |
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云顶新耀宣布中国台湾地区药政部门批准全球首个对因治疗IgA肾病药物耐赋康®的新药上市许可申请 |
| 云顶新耀（HKEX 1952.HK）是一家专注于创新药研发、临床开发、制造和商业化的生物制药公司，今日宣布，中国台湾地区药政部门（TFDA）已批准耐赋康®（布地奈德肠溶胶囊，NEFECON®）用于治疗罹患原发性免疫球蛋白A肾病变(IgA nephropathy)且病情有进展风险的成人病人，用以延缓肾功能下降1 ，且无基线蛋白尿水平限制。 more info >> |
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雲頂新耀宣佈中國台灣地區藥政部門批准全球首個對因治療IgA腎病藥物耐賦康®的新藥上市許可申請 |
| 雲頂新耀（HKEX 1952.HK）是一家專注于創新藥研發、臨床開發、製造和商業化的生物製藥公司，今日宣佈，中國台灣地區藥政部門（TFDA）已批准耐賦康®（布地奈德腸溶膠囊，NEFECON®）用於治療罹患原發性免疫球蛋白A腎病變(IgA nephropathy)且病情有惡化風險的成人病人，用以減緩腎功能下降1，且無基線蛋白尿水平限製。 more info >> |
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