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6-K: Report of foreign private issuer [Rules 13a-16 and 15d-16]

6-K: Report of foreign private issuer [Rules 13a-16 and 15d-16]

6-K:外国发行人报告
美股SEC公告 ·  10/24 20:34

牛牛AI助手已提取核心信息

NeuroSense Therapeutics Ltd., a biotechnology company, announced on October 24, 2024, significant findings from its PARADIGM clinical trial for PrimeC, a treatment for ALS (Amyotrophic Lateral Sclerosis). The trial results showed that PrimeC significantly regulates key microRNAs (miRNAs) involved in ALS progression, offering new hope for treating the disease. PrimeC, an extended-release oral formulation combining ciprofloxacin and celecoxib, targets multiple key mechanisms of ALS. The trial included 68 participants across Canada, Italy, and Israel, with 96% choosing to continue PrimeC treatment after the 6-month double-blind portion. The data indicated a 29% difference in efficacy in favor of PrimeC over placebo, with a 37.4% slowing of disease progression observed. PrimeC has been granted Orphan Drug Designation by the FDA and the European Medicines Agency. NeuroSense is dedicated to developing treatments that address the root causes of neurodegenerative diseases and believes PrimeC's ability to regulate miRNAs is a significant step toward providing more therapeutic options for ALS patients.
NeuroSense Therapeutics Ltd., a biotechnology company, announced on October 24, 2024, significant findings from its PARADIGM clinical trial for PrimeC, a treatment for ALS (Amyotrophic Lateral Sclerosis). The trial results showed that PrimeC significantly regulates key microRNAs (miRNAs) involved in ALS progression, offering new hope for treating the disease. PrimeC, an extended-release oral formulation combining ciprofloxacin and celecoxib, targets multiple key mechanisms of ALS. The trial included 68 participants across Canada, Italy, and Israel, with 96% choosing to continue PrimeC treatment after the 6-month double-blind portion. The data indicated a 29% difference in efficacy in favor of PrimeC over placebo, with a 37.4% slowing of disease progression observed. PrimeC has been granted Orphan Drug Designation by the FDA and the European Medicines Agency. NeuroSense is dedicated to developing treatments that address the root causes of neurodegenerative diseases and believes PrimeC's ability to regulate miRNAs is a significant step toward providing more therapeutic options for ALS patients.
NeuroSense Therapeutics Ltd.,一家生物技术公司,于2024年10月24日宣布了其PARADIGm临床试验关于PrimeC治疗ALS(肌萎缩侧索硬化症)的重大发现。试验结果显示PrimeC显著调节了与ALS进展相关的关键miRNAs,为治疗该疾病带来了新的希望。PrimeC是一种延时释放口服制剂,结合了环丙沙星和塞来考昔,针对ALS的多个关键机制。该试验包括了加拿大、意大利和以色列共68名参与者,其中96%选择在6个月的双盲部分结束后继续接受PrimeC治疗。数据显示,在PrimeC与安慰剂之间,疗效有利于PrimeC的差异为29%,疾病进展减缓37.4%。PrimeC已被美国FDA和欧洲药品管理局授予孤儿药品认定。NeuroSense致力于开发治疗方案,以解决神经退行性疾病的根本原因,并认为PrimeC对调节miRNAs的能力是为ALS患者提供更多治疗期权的重要一步。
NeuroSense Therapeutics Ltd.,一家生物技术公司,于2024年10月24日宣布了其PARADIGm临床试验关于PrimeC治疗ALS(肌萎缩侧索硬化症)的重大发现。试验结果显示PrimeC显著调节了与ALS进展相关的关键miRNAs,为治疗该疾病带来了新的希望。PrimeC是一种延时释放口服制剂,结合了环丙沙星和塞来考昔,针对ALS的多个关键机制。该试验包括了加拿大、意大利和以色列共68名参与者,其中96%选择在6个月的双盲部分结束后继续接受PrimeC治疗。数据显示,在PrimeC与安慰剂之间,疗效有利于PrimeC的差异为29%,疾病进展减缓37.4%。PrimeC已被美国FDA和欧洲药品管理局授予孤儿药品认定。NeuroSense致力于开发治疗方案,以解决神经退行性疾病的根本原因,并认为PrimeC对调节miRNAs的能力是为ALS患者提供更多治疗期权的重要一步。

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