share_log

和黃醫藥:和黃醫藥宣佈武田獲得歐盟委員會批准FRUZAQLA (呋喹替尼)

HUTCHMED: HUTCHMED Announces European Commission Approval for FRUZAQLA (fruquintinib) Received by Takeda

Hong Kong Stock Exchange ·  Jun 24 08:00
Summary by Futu AI
和黃醫藥(HUTCHMED)宣布其合作夥伴武田藥品工業獲得歐盟委員會批准FRUZAQLA®(呋喹替尼)用於治療經治的轉移性結直腸癌患者。這是基於FRESCO-2全球III期臨床研究的積極結果,標誌著歐盟超過十年來首個批准的創新靶向療法。FRUZAQLA®是針對所有三種VEGFR亞型的選擇性抑制劑,為轉移性結直腸癌患者及臨床醫生提供了新的治療選擇。和黃醫藥首席執行官兼首席科學官蘇慰國博士表示,這是公司研發在歐洲獲批的首個產品,並通過與武田的合作在短時間內實現了這一目標。FRUZAQLA®已於2023年6月獲歐洲藥品管理局確認及受理上市許可申請,並在同年6月發表於《柳葉刀》的FRESCO-2研究數據支持了申請。結直腸癌是全球第三大常見癌症,歐洲為第二大常見癌症,治療選擇有限,FRUZAQLA®的批准為患者帶來新希望。
和黃醫藥(HUTCHMED)宣布其合作夥伴武田藥品工業獲得歐盟委員會批准FRUZAQLA®(呋喹替尼)用於治療經治的轉移性結直腸癌患者。這是基於FRESCO-2全球III期臨床研究的積極結果,標誌著歐盟超過十年來首個批准的創新靶向療法。FRUZAQLA®是針對所有三種VEGFR亞型的選擇性抑制劑,為轉移性結直腸癌患者及臨床醫生提供了新的治療選擇。和黃醫藥首席執行官兼首席科學官蘇慰國博士表示,這是公司研發在歐洲獲批的首個產品,並通過與武田的合作在短時間內實現了這一目標。FRUZAQLA®已於2023年6月獲歐洲藥品管理局確認及受理上市許可申請,並在同年6月發表於《柳葉刀》的FRESCO-2研究數據支持了申請。結直腸癌是全球第三大常見癌症,歐洲為第二大常見癌症,治療選擇有限,FRUZAQLA®的批准為患者帶來新希望。
Hutchmed (China) announced that its partner Takeda Pharmaceutical Company has received approval from the European Commission for FRUZAQLA® (fugui teni) to treat refractory metastatic colorectal cancer patients. This is based on the positive results of the global Phase III clinical trial FRESCO-2, marking the first approved innovative targeted therapy in the European Union in over a decade. FRUZAQLA® is a selective inhibitor of all three VEGFR subtypes, providing new treatment options for metastatic colorectal cancer patients and clinical physicians. Dr. Su Weiguo, CEO and Chief Scientific Officer of Hutchmed, stated that this is the company's first approved product in Europe, and this goal was achieved in a short period of time through cooperation with Takeda. FRUZAQLA® has been confirmed...Show More
Hutchmed (China) announced that its partner Takeda Pharmaceutical Company has received approval from the European Commission for FRUZAQLA® (fugui teni) to treat refractory metastatic colorectal cancer patients. This is based on the positive results of the global Phase III clinical trial FRESCO-2, marking the first approved innovative targeted therapy in the European Union in over a decade. FRUZAQLA® is a selective inhibitor of all three VEGFR subtypes, providing new treatment options for metastatic colorectal cancer patients and clinical physicians. Dr. Su Weiguo, CEO and Chief Scientific Officer of Hutchmed, stated that this is the company's first approved product in Europe, and this goal was achieved in a short period of time through cooperation with Takeda. FRUZAQLA® has been confirmed and accepted for market approval application by the European Medicines Agency in June 2023, and FRESCO-2 study data published in The Lancet in June of the same year supported the application. Colorectal cancer is the third most common cancer globally and the second most common cancer in Europe, with limited treatment options. The approval of FRUZAQLA® brings new hope to patients.

The translation is provided by third-party software.


The information provided by Futu AI is automatically generated by third-party artificial intelligence (AI) software based on news content. It is only available to users located outside of China mainland.


The above content is for informational or educational purposes only and does not constitute any investment advice related to Futu. Although we strive to ensure the truthfulness, accuracy, and originality of all such content, we cannot guarantee it.