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Synaptogenix Joins Leading Neuroscientists and Academics as Speaker at USC-Sponsored Forum on Age-Related Diseases Including Alzheimer's

Synaptogenix Joins Leading Neuroscientists and Academics as Speaker at USC-Sponsored Forum on Age-Related Diseases Including Alzheimer's

Synaptogenix与领先的神经科学家和学者一起在南加州大学赞助的包括阿尔茨海默氏症在内的年龄相关疾病论坛上担任发言人
PR Newswire ·  2023/12/06 09:00

Presenters, including Nobel Laureate in Medicine, to discuss innovative treatments for neurodegeneration

包括诺贝尔医学奖得主在内的主持人将讨论神经变性的创新疗法

Company to feature lead therapeutic's statistically significant benefits, p < 0.007, for severe Alzheimer's disease (AD) patients

公司将介绍先导疗法对严重阿尔茨海默病(AD)患者的统计学显著益处,p

NEW YORK, Dec. 6, 2023 /PRNewswire/ -- Synaptogenix, Inc. (Nasdaq: SNPX) ("Synaptogenix" or the "Company"), an emerging biopharmaceutical company developing therapeutics for neurodegenerative disorders, today announced that its President and Chief Scientific Officer, Daniel Alkon, M.D., will join more than 30 leading neuroscientists and academics as a speaker at IABS Forum-2023, "New Concepts for the Treatment of Neurodegenerative Disorders." The distinguished scientific forum, to be held on December 7-8, 2023 in Irvine, CA, is co-sponsored by the University of Southern California School of Pharmacy and the International Association of Biomedical Sciences (IABS).

纽约,2023 年 12 月 6 日 /PRNewswire/ — 开发神经退行性疾病疗法的新兴生物制药公司 Synaptogenix, Inc.(纳斯达克股票代码:SNPX)(“Synaptogenix” 或 “公司”)今天宣布,其总裁兼首席科学官丹尼尔·阿尔康医学博士将与30多位领先的神经科学家和学者一起在IABS上发表演讲论坛2023,“神经退行性疾病治疗的新概念”。杰出科学论坛将于2023年12月7日至8日在加利福尼亚州尔湾举行,由南加州大学药学院和国际生物医学协会(IABS)共同赞助。

The forum's keynote address, entitled "Towards a Cell Biology of Alzheimer's Disease," will be delivered by Dr. Thomas Südhof, Nobel Laureate in Physiology or Medicine 2013. Dr. Südhof is known for his groundbreaking research on the mechanisms underlying synaptic transmission, which plays a vital role in learning, memory, and various neurological processes.

论坛的主题演讲题为 “迈向阿尔茨海默氏病的细胞生物学”,将由2013年诺贝尔生理学或医学奖得主托马斯·苏德霍夫博士主讲。苏德霍夫博士以其对突触传播机制的开创性研究而闻名,突触传递在学习、记忆和各种神经系统过程中起着至关重要的作用。

AD is also the topic of Dr. Alkon's presentation. He will speak about the latest clinical results for Bryostatin-1, which, as previously disclosed, met the secondary efficacy endpoints in the Phase 2 trial with statistical significance. In the Phase 2 trial, no significant cognitive decline was observed throughout the 10-month study, with Bryostatin-1 demonstrating safe, significant, and persistent benefits at least 16 weeks beyond the final dosing. A research article detailing the results was published earlier this year in the Journal of Alzheimer's Disease.

AD 也是阿尔康博士演讲的主题。他将介绍Bryostatin-1的最新临床结果,正如先前披露的那样,该结果在2期试验中达到了次要疗效终点,具有统计学意义。在2期试验中,在为期10个月的研究中,未观察到明显的认知能力下降,Bryostatin-1在最终给药后至少16周显示出安全、显著和持续的益处。今年早些时候,在《阿尔茨海默氏病杂志》上发表了一篇详细介绍研究结果的研究文章。

"I am honored to accept the invitation to speak at IABS Forum-2023, in the company of many of the world's greatest minds in neuroscience," said Dr. Alkon. "Renowned institutions, publishers, and symposiums continue to recognize the benefits of our novel therapy, developed to restore synaptic loss, and its potential for advanced stage Alzheimer's patients."

阿尔康博士说:“我很荣幸接受邀请,在2023年IABS论坛上发表演讲,届时有许多世界上神经科学领域的杰出人才。”“知名机构、出版商和研讨会继续认识到我们为恢复突触损失而开发的新疗法的益处,及其对晚期阿尔茨海默氏症患者的潜力。”

About Synaptogenix

关于 Synaptogenix

Synaptogenix is a clinical-stage biopharmaceutical company that has historically worked to develop novel therapies for neurodegenerative diseases. Synaptogenix has conducted clinical and preclinical studies of its lead therapeutic candidate, Bryostatin-1, in Alzheimer's disease. Preclinical studies have also demonstrated Bryostatin's regenerative mechanisms of action for the rare disease Fragile X syndrome, and for other neurodegenerative disorders such as multiple sclerosis, stroke, and traumatic brain injury. The U.S. Food and Drug Administration has granted Orphan Drug Designation to Synaptogenix for Bryostatin-1 as a treatment for Fragile X syndrome. Bryostatin-1 has already undergone testing in more than 1,500 people in cancer studies, thus creating a large safety data base that will further inform clinical trial designs.

Synaptogenix是一家处于临床阶段的生物制药公司,历来致力于开发治疗神经退行性疾病的新疗法。Synaptogenix已对其治疗阿尔茨海默病的主要候选药物Bryostatin-1进行了临床和临床前研究。临床前研究还表明,Bryostatin对罕见疾病Fragile X综合征以及多发性硬化、中风和创伤性脑损伤等其他神经退行性疾病具有再生作用机制。美国食品药品监督管理局已授予Synaptogenix孤儿药称号,用于治疗脆性X综合征的Bryostatin-1。Bryostatin-1已经在癌症研究中对1,500多人进行了测试,从而创建了一个庞大的安全数据库,可以进一步为临床试验设计提供信息。

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