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 -
-研究结果表明,单独使用motixafortide以及与那他珠单抗联合使用可以支持在单个血液分离周期内收集镰状细胞病基因疗法所需的大量干细胞-
- Data from proof-of-concept study shows that motixafortide was safe and well tolerated -
-概念验证研究的数据表明,motixafortide是安全的,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亚州圣地亚哥举行的 ASH 2024 上的口头演讲-
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.
以色列特拉维夫和马萨诸塞州沃尔瑟姆,2024年11月5日 /PRNewswire/ — BIOLinerX Ltd.(纳斯达克股票代码:BLRX)(TASE:BLRX)是一家致力于改变肿瘤学和罕见疾病生活疗法的商业阶段生物制药公司,今天宣布了一份摘要,其中包括评估莫替沙福肽作为单一疗法以及与那他珠莫联合疗法的1期临床试验的初步结果用于镰状细胞病 (SCD) 基因疗法的 CD34+ 造血干细胞 (HSC) 动员的 b 已获准在第 66 届美国血液学会作口头陈述 (ASH) 年会和博览会将于 2024 年 12 月 7-10 日在加利福尼亚州圣地亚哥举行。这项概念验证研究是与圣路易斯华盛顿大学医学院合作进行的,正在探索替代的HSC动员策略,这些策略可以显著改善寻求基因疗法的镰状细胞病患者的治疗过程。