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

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

SciSparc | 6-K:外国发行人报告
美股SEC公告 ·  08/26 18:17

牛牛AI助手已提取核心信息

SciSparc Ltd., a clinical-stage pharmaceutical company, announced the submission of an Investigational New Drug (IND) application to the U.S. Food and Drug Administration (FDA) for a Phase IIb clinical trial of SCI-110, aimed at treating Tourette Syndrome (TS). The trial is set to take place at three renowned institutions: Yale Child Study Center at Yale School of Medicine in the USA, Hannover Medical School in Germany, and Tel Aviv Sourasky Medical Center in Israel. Institutional Review Board approvals have been obtained from all sites, along with necessary approvals from the Israeli Ministry of Health and the Federal Institute for Drugs and Medical Devices in Germany. The trial will assess the efficacy, safety, and tolerability of SCI-110 in adults aged 18 to 65, comparing the drug to a placebo using the Yale Global Tic Severity Scale. SciSparc's CEO, Oz Adler, expressed confidence in SCI-110's potential to change the treatment landscape for TS. The company also has other drug development programs based on cannabinoid pharmaceuticals for various conditions.
SciSparc Ltd., a clinical-stage pharmaceutical company, announced the submission of an Investigational New Drug (IND) application to the U.S. Food and Drug Administration (FDA) for a Phase IIb clinical trial of SCI-110, aimed at treating Tourette Syndrome (TS). The trial is set to take place at three renowned institutions: Yale Child Study Center at Yale School of Medicine in the USA, Hannover Medical School in Germany, and Tel Aviv Sourasky Medical Center in Israel. Institutional Review Board approvals have been obtained from all sites, along with necessary approvals from the Israeli Ministry of Health and the Federal Institute for Drugs and Medical Devices in Germany. The trial will assess the efficacy, safety, and tolerability of SCI-110 in adults aged 18 to 65, comparing the drug to a placebo using the Yale Global Tic Severity Scale. SciSparc's CEO, Oz Adler, expressed confidence in SCI-110's potential to change the treatment landscape for TS. The company also has other drug development programs based on cannabinoid pharmaceuticals for various conditions.
临床药物公司SciSparc Ltd.宣布向美国食品药品监督管理局(FDA)提交了SCI-110的新药研究申请(IND),旨在治疗Tourette综合症(TS)的IIb期临床试验。该试验将在美国的耶鲁大学医学院耶鲁儿童研究中心,德国的汉诺威医学院和以色列的特拉维夫索拉斯基医疗中心三个著名机构进行。已从所有试验地点获得机构审查委员会的批准,并获得以色列卫生部和德国联邦药品和医疗器械研究所的必要批准。该试验将使用耶鲁全球抽动严重度量表评估SCI-110对18至65岁成年人的疗效、安全性和耐受性,与安慰剂进行比较。SciSparc的CEO奥兹·阿德勒对SCI-110改变TS治疗格局的潜力表示了信心。该公司还根据大麻药物制剂开发了其他针对不同疾病的药物研发项目。
临床药物公司SciSparc Ltd.宣布向美国食品药品监督管理局(FDA)提交了SCI-110的新药研究申请(IND),旨在治疗Tourette综合症(TS)的IIb期临床试验。该试验将在美国的耶鲁大学医学院耶鲁儿童研究中心,德国的汉诺威医学院和以色列的特拉维夫索拉斯基医疗中心三个著名机构进行。已从所有试验地点获得机构审查委员会的批准,并获得以色列卫生部和德国联邦药品和医疗器械研究所的必要批准。该试验将使用耶鲁全球抽动严重度量表评估SCI-110对18至65岁成年人的疗效、安全性和耐受性,与安慰剂进行比较。SciSparc的CEO奥兹·阿德勒对SCI-110改变TS治疗格局的潜力表示了信心。该公司还根据大麻药物制剂开发了其他针对不同疾病的药物研发项目。

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