|
Friday, August 15, 2025 |
|
Etrasimod Receives Strong Recommendation in the ACG Clinical Guideline Update: Ulcerative Colitis in Adults for Induction and Maintenance Phase of Moderately to Severely Active UC |
Everest Medicines today announced that etrasimod (VELSIPITY(R)) has been included in the ACG Clinical Guideline Update: Ulcerative Colitis in Adults (the 'Updated Guidelines'). Etrasimod, an S1P receptor modulator, is recommended for the induction of remission in patients with moderately to severely active UC and for continuation in the maintenance of remission, compared with no treatment after induction of remission. Both recommendations are strong, with a moderate quality of evidence. more info >> |
|
艾曲莫德入選《2025 ACG臨床指南:成人潰瘍性結腸炎》,獲強烈推薦用於中重度潰瘍性結腸炎的誘導緩解及維持緩解治療 |
雲頂新耀今日宣布,旗下創新藥艾曲莫德(VELSIPITY(R),etrasimod)被納入《2025 ACG 臨床指南:成人潰瘍性結腸炎》(下稱「新版指南」),並獲得強烈推薦用於中重度活動性潰瘍性潰瘍性結腸炎(UC)患者的誘導緩解及維持緩解治療(中等質量證據)。 more info >> |
|
艾曲莫德入选《2025 ACG临床指南:成人溃疡性结肠炎》,获强烈推荐用于中重度溃疡性结肠炎的诱导缓解及维持缓解治疗 |
云顶新耀今日宣布,旗下创新药艾曲莫德(VELSIPITY(R),etrasimod)被纳入《2025 ACG 临床指南:成人溃疡性结肠炎》(下称"新版指南"),并获得强烈推荐用于中重度活动性溃疡性溃疡性结肠炎(UC)患者的诱导缓解及维持缓解治疗(中等质量证据)。 more info >> |
|
Everest Medicines' New Drug Application for Etrasimod Accepted in Taiwan, Marking Another Milestone in Asia Market Access |
Everest Medicines (HKEX 1952.HK, 'Everest') today announced that the Taiwan Food and Drug Administration (TFDA) has officially accepted the New Drug Application (NDA) for VELSIPITY' (etrasimod) for the treatment of patients with moderately to severely active ulcerative colitis (UC). more info >> |
|
Thursday, August 14, 2025 |
|
雲頂新耀維長寧(艾曲莫德)在中國台灣新藥上市申請獲受理 亞洲市場准入再迎里程碑 |
雲頂新耀今日宣布,中國台灣地區藥政主管部門(TFDA)已正式受理維長寧(艾曲莫德,中國台灣地區商品名:「維長寧」)用於治療中重度活動性潰瘍性結腸炎(UC)患者的新藥上市許可申請(NDA)。 more info >> |
|
云顶新耀维长宁(艾曲莫德)在中国台湾新药上市申请获受理 亚洲市场准入再迎里程碑 |
云顶新耀今日宣布,中国台湾地区药政主管部门(TFDA)已正式受理维长宁(艾曲莫德,中国台湾地区商品名:"維長寧")用于治疗中重度活动性溃疡性结肠炎(UC)患者的新药上市许可申请(NDA)。 more info >> |
|
Friday, August 8, 2025 |
|
Everest Medicines Announces Full Approval of NEFECON(R) in Taiwan |
Everest Medicines (HKEX 1952.HK) recently announced the Taiwan Food and Drug Administration (TFDA) has approved the supplementary application for NEFECON'. more info >> |
|
雲頂新耀耐賦康(R)擴產獲批 亞洲全域完全批准雙突破 加速邁向50億銷售峰值 |
近日,雲頂新耀(HKEX: 1952.HK)宣布在擴產補充申請獲國家藥監局批准後,其旗下全球首個且唯一獲得完全批准的IgA腎病對因治療藥物耐賦康(R)(布地奈德腸溶膠囊)又取得突破性進展。 more info >> |
|
云顶新耀耐赋康(R)扩产获批 亚洲全域完全批准双突破 加速迈向50亿销售峰值 |
近日,云顶新耀(HKEX: 1952.HK)宣布在扩产补充申请获国家药监局批准后,其旗下全球首个且唯一获得完全批准的IgA肾病对因治疗药物耐赋康(R)(布地奈德肠溶胶囊)又取得突破性进展。 more info >> |
|
Tuesday, August 5, 2025 |
|
NEFECON(R) Receives NMPA Approval for Production Expansion in China, as Everest Medicines Accelerates Accessibility and Capacity Efforts |
Everest Medicines (HKEX 1952.HK) today announced that the supplemental application for the production expansion of NEFECON has been officially approved by China's National Medical Products Administration (NMPA). more info >> |
|
|
|