BrainStorm Cell Therapeutics to Host KOL Webinar on Current Developments in the Treatment of Amyotrophic Lateral Sclerosis (ALS) on December 11, 2024
BrainStorm Cell Therapeutics to Host KOL Webinar on Current Developments in the Treatment of Amyotrophic Lateral Sclerosis (ALS) on December 11, 2024
NEW YORK, Dec. 2, 2024 /PRNewswire/ -- BrainStorm Cell Therapeutics Inc. (NASDAQ: BCLI), a leading developer of adult stem cell therapeutics for neurodegenerative diseases, today announced that it will host a key opinion leader (KOL) webinar on Wednesday, December 11, 2024 at 10:00 AM ET. To register, click here.
纽约,2024年12月2日 /新华社/ -- BrainStorm细胞治疗公司(纳斯达克:BCLI)是成年干细胞治疗神经退行性疾病的领先开发商,今天宣布将于2024年12月11日周三上午10:00在ET举办一场关键意见领袖(KOL)网络研讨会。要注册, 点击这里。
The webinar will feature Dr. Terry Heiman-Patterson, a KOL from the Lewis Katz School of Medicine at Temple University, who will discuss the current treatment landscape and advances for patients with amyotrophic lateral sclerosis (ALS). Dr. Heiman-Patterson will be joined by BrainStorm's management team, who will share updates on the company's planned Phase 3b registrational clinical trial, NurOwn (autologous MSC-NTF cells), and future development plans.
这次网络研讨会将邀请来自Temple University Lewis Katz医学院的KOL,Terry Heiman-Patterson博士,他将讨论患有肌萎缩侧索硬化症(ALS)患者目前治疗局势和进展。Heiman-Patterson博士将与BrainStorm的管理团队一同参与,他们将分享公司计划中的第30亿阶段注册临床试验NurOwn(自体MSC-NTF细胞)以及未来的发展计划。
Successful completion of the randomized portion (Part A) of the Phase 3b trial is expected to support a Biologic License Application (BLA) for NurOwn.
预计成功完成第30亿阶段(A部分)的随机试验将有助于支持NurOwn的生物许可申请(BLA)。
A live Q&A session will follow the formal presentations.
正式介绍结束后将进行现场问答环节。
About Terry Heiman-Patterson, MD
关于Terry Heiman-Patterson,MD
Dr. Terry Heiman-Patterson is a pioneering figure in ALS care and research, with a career spanning decades of groundbreaking contributions to neurology. She is the Director of the Center for Neurodegenerative Disorders and a Professor in the Department of Neurology at the Lewis Katz School of Medicine at Temple University. Previously, she held esteemed roles as Vice Chair of the Department of Neurology, Director of the Division of Neuromuscular Disease, and Professor of Neurology at Drexel University College of Medicine in Philadelphia, PA.
Terry Heiman-Patterson博士是ALS护理和研究领域的开拓者,她在神经病学领域做出了数十年的创新贡献。她是Temple University Lewis Katz医学院神经退行性疾病中心主任,神经病学系教授。此前,她担任Philadelphia Drexel大学医学院神经病学系副主任,神经肌肉病专科主任,以及神经病学教授。
For over 20 years, Dr. Heiman-Patterson directed the MDA/ALS Center of Hope at Drexel, and for more than 30 years, she led the outpatient Muscular Dystrophy Clinic at Good Shepherd Rehabilitation Center in Allentown. She co-founded and serves as President of the ALS Hope Foundation and has been a driving force as Co-chair of the Northeast Amyotrophic Lateral Sclerosis Consortium (NEALS) Executive Committee.
在过去的20多年中,Heiman-Patterson博士领导了Drexel的MDA/ALS希望中心,30多年来,她主导了Allentown的Good Shepherd康复中心门诊肌肉营养不良诊所。她是ALS Hope基金会的联合创办人兼主席,并担任东北部肌萎缩侧索硬化联盟(NEALS)执行委员会联合主席。
Dr. Terry Heiman-Patterson has spearheaded 24 clinical trials, establishing key standards in ALS care. She has authored more than 50 groundbreaking papers on motor neuron diseases and published hundreds of papers, abstracts, and book chapters on ALS and related disorders. Her work has earned national and international acclaim, including the prestigious Forbes Norris Award for her dedication to improving ALS patient care and advancing research
Terry Heiman-Patterson博士领导了24项临床试验,在ALS护理方面确立了关键标准。她撰写了50多篇开创性论文,涉及运动神经元疾病,并在ALS及相关疾病上发表了数百篇论文、摘要和书章。她的工作获得了国家和国际认可,包括因致力于改进ALS患者护理和推动研究而荣获备受推崇的Forbes Norris奖。
Dr. Heiman-Patterson earned her medical degree at Albany Medical College in Albany, NY. She completed her Neurology Residency at Albany Medical College and specialized in Muscular Dystrophy through fellowships at the University of Pennsylvania in Philadelphia, PA. Her profound expertise and relentless dedication to advancing ALS research and care make her a cornerstone in the field of neurology.
Heiman-Patterson博士在纽约州奥尔巴尼市的奥尔巴尼医学院获得了医学学位。她在奥尔巴尼医学院完成了神经内科住院医师培训,并通过在宾夕法尼亚大学的肌肉萎缩症专科研究生课程专攻肌肉萎缩症。她深厚的专业知识和对推动ALS研究和护理的不懈奉献使她成为神经病学领域的重要人物。
About BrainStorm Cell Therapeutics Inc.
关于brainstorm cell therapeutics公司
BrainStorm Cell Therapeutics Inc. is a leading developer of innovative autologous adult stem cell therapeutics for debilitating neurodegenerative diseases. BrainStorm holds the rights to clinical development and commercialization of the NurOwn technology platform used to produce autologous MSC-NTF cells through an exclusive, worldwide licensing agreement. Autologous MSC-NTF cells have received Orphan Drug designation status from the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of amyotrophic lateral sclerosis (ALS). BrainStorm has completed a Phase 3 trial in ALS (NCT03280056); this trial investigated the safety and efficacy of repeat-administration of autologous MSC-NTF cells and was supported by a grant from the California Institute for Regenerative Medicine (CIRM CLIN2-0989), and another grant from the ALS Association and I AM ALS. BrainStorm completed under an investigational new drug application a Phase 2 open-label multicenter trial (NCT03799718) of autologous MSC-NTF cells in progressive MS and was supported by a grant from the National MS Society (NMSS).
brainstorm cell therapeutics公司是创新自体成体干细胞治疗方案的领先开发商,用于治疗令人痛苦的神经退行性疾病。brainstorm拥有临床开发和商业化NurOwn技术平台的权利,通过独家的全球许可协议使用来生产自体msc-ntf细胞。自体msc-ntf细胞已获得美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)颁发的孤儿药物认定,用于治疗肌萎缩性侧索硬化(ALS)。brainstorm已完成了一项ALS的3期试验(NCT03280056);该试验调查了重复注射自体msc-ntf细胞的安全性和疗效,并获得了加利福尼亚再生医学研究所(CIRm CLIN2-0989)的资助,以及ALS协会和I am ALS的另一笔资助。brainstorm在一项自体msc-ntf细胞进行进行性MS的2期开放标签多中心试验(NCT03799718)中完成,该试验得到了国家多发性硬化症协会(NMSS)的资助。
Notice Regarding Forward-Looking Statements
关于前瞻性陈述的通知
This press release contains "forward-looking statements" that are subject to substantial risks and uncertainties, including statements regarding meetings with the probability of NurOwn demonstrating a treatment effect in ALS, the patient enrollment and dosing in the Phase 3b trial for NurOwn, and the clinical development of NurOwn as a therapy for the treatment of ALS, the future availability of NurOwn to patients, and the future success of BrainStorm. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as "anticipate," "believe," "contemplate," "could," "estimate," "expect," "intend," "seek," "may," "might," "plan," "potential," "predict," "project," "target," "aim," "should," "will" "would," or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on BrainStorm's current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict. These potential risks and uncertainties include, without limitation, management's ability to successfully achieve its goals, BrainStorm's ability to raise additional capital, BrainStorm's ability to continue as a going concern, prospects for future regulatory approval of NurOwn, whether BrainStorm's future interactions with the FDA will have productive outcomes, and other factors detailed in BrainStorm's annual report on Form 10-K and quarterly reports on Form 10-Q available at http://www.sec.gov. These factors should be considered carefully, and readers should not place undue reliance on BrainStorm's forward-looking statements. The forward-looking statements contained in this press release are based on the beliefs, expectations, and opinions of management as of the date of this press release. We do not assume any obligation to update forward-looking statements to reflect actual results or assumptions if circumstances or management's beliefs, expectations or opinions should change, unless otherwise required by law. Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity, performance, or achievements.
本新闻稿包含可能涉及重大风险和不确定性的“前瞻性陈述”,包括关于 NurOwn 在ALS症状表现治疗作用的会议、NurOwn 第3期试验中的患者入组和用药概率、NurOwn 作为ALS治疗疗法的临床研发、NurOwn 未来对患者的可用性以及BrainStorm 未来成功的陈述。除本新闻稿中所含历史事实陈述外,所有其他未来展望均为前瞻性陈述。本新闻稿中的前瞻性陈述可能通过诸如“预期”、“相信”、“考虑”、“可能”、“估计”、“期望”、“打算”、“寻求”、“或许”、“可以”、“计划”、“潜在”、“预测”、“项目”、“目标”、“瞄准”、“应该”、“将”、“愿意”等词语进行识别,或这些词语的否定形式或其他类似表达,尽管并非所有前瞻性陈述均包含这些词语。前瞻性陈述基于BrainStorm目前的预期,并且受到难以预测的固有不确定性、风险和假设的影响。这些潜在的风险和不确定性包括但不限于:管理层成功实现其目标的能力、BrainStorm筹集额外资本的能力、BrainStorm持续作为一个持续经营实体的能力、NurOwn未来获得监管批准的前景、BrainStorm未来与FDA的互动是否会产生积极成果,以及BrainStorm年度10-k表格和季度10-Q表格中详细列出的其他因素在内的各种因素。这些因素应仔细考虑,读者不应过度依赖BrainStorm的前瞻性陈述。本新闻稿中的前瞻性陈述基于管理层截至本新闻稿日期的信念、预期和意见。除非法律另有规定,我们不承担更新前瞻性陈述以反映实际结果或假设的义务,即使情况或管理层的信念、预期或意见发生变化。尽管我们认为前瞻性陈述中所反映的期望是合理的,但我们无法保证未来结果、活动水平、表现或成就。
CONTACTS
联系人
IR:
Michael Wood
Phone: +1 646-597-6983
[email protected]
IR:
Michael Wood
电话:+1 646-597-6983
[email protected]
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SOURCE BrainStorm Cell Therapeutics Inc.
来源:BrainStorm Cell Therapeutics Inc.