BioLineRx Announces Oral Presentation On Data From Phase 1 Clinical Trial Evaluating Motixafortide For CD34+ Hematopoietic Stem Cell Mobilization For Gene Therapies In Sickle Cell Disease At ASH 2024
BioLineRx Announces Oral Presentation On Data From Phase 1 Clinical Trial Evaluating Motixafortide For CD34+ Hematopoietic Stem Cell Mobilization For Gene Therapies In Sickle Cell Disease At ASH 2024
- Findings suggest motixafortide alone, and in combination with natalizumab, could support the collection of the large number of stem cells required by gene therapies for sickle cell disease within a single apheresis cycle -
- 研究結果表明,單獨使用motixafortide或與納利麥昔單抗結合,可以在單個間隔採集所需數量的幹細胞,用於鐮狀細胞病的基因治療 -
- Data from proof-of-concept study shows that motixafortide was safe and well tolerated -
- 概念證明研究數據顯示,motixafortide安全耐受性良好 -
- Oral presentation at ASH 2024 on Saturday, December 7, 2024 in San Diego, California -
- 2024年12月7日(星期六)在加利福尼亞州聖迭戈舉行的ASH 2024口頭報告 -
TEL AVIV, Israel and WALTHAM, Mass., Nov. 5, 2024 /PRNewswire/ -- BioLineRx Ltd. (NASDAQ: BLRX) (TASE: BLRX), a commercial stage biopharmaceutical company pursuing life-changing therapies in oncology and rare diseases, today announced that an abstract including the initial results from a Phase 1 clinical trial evaluating motixafortide as monotherapy and in combination with natalizumab for CD34+ hematopoietic stem cell (HSC) mobilization for gene therapies in sickle cell disease (SCD) was accepted for oral presentation at the 66th American Society of Hematology (ASH) Annual Meeting & Exposition taking place December 7-10, 2024 in San Diego, California. The proof-of-concept study, conducted in collaboration with Washington University School of Medicine in St. Louis, is exploring alternative HSC mobilization strategies that could significantly improve the treatment journey of patients with sickle cell disease seeking gene therapy.
以色列特拉維夫和馬薩諸塞沃爾瑟姆,2024年11月5日/美通社/ - BioLineRx Ltd.(納斯達克:BLRX)(以色列證券交易所:BLRX)是一家在腫瘤學和罕見疾病領域追求改變生命的商業階段生物製藥公司,今天宣佈接受了一份摘要,其中包括評估motixafortide作爲單藥物治療和與納利麥昔單抗結合用於鐮狀細胞病(SCD)基因治療的CD34+造血幹細胞(HSC)動員的1期臨床試驗初步結果,該研究被接受在2024年12月7日至10日加利福尼亞州聖迭戈舉行的第66屆美國血液學會年會及展覽會上進行口頭報告。與聖路易斯華盛頓大學醫學院合作進行的概念證明研究正在探索替代HSC動員策略,可能顯著改善尋求基因治療的鐮狀細胞病患者的治療旅程。
譯文內容由第三人軟體翻譯。