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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 06:17

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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.
临床阶段制药公司SciSparc Ltd.宣布向美国食品药品监督管理局(FDA)提交了SCI-110的Phase IIb临床试验的Investigational New Drug (IND)申请,旨在治疗"跳跃症"(TS)。该试验计划在美国医学院耶鲁大学儿童研究中心,德国汉诺威医学院和以色列特拉维夫Sourasky医疗中心进行。所有机构已获得研究伦理委员会批准,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在18至65岁成年人中的疗效,安全性和耐受性,并将药物与安慰剂进行比较。SciSparc的首席执行官Oz Adler对SCI-110改变TS治疗领域的潜力表示信心。该公司还有其他基于大麻素药物的药物开发计划,用于治疗不同疾病。
临床阶段制药公司SciSparc Ltd.宣布向美国食品药品监督管理局(FDA)提交了SCI-110的Phase IIb临床试验的Investigational New Drug (IND)申请,旨在治疗"跳跃症"(TS)。该试验计划在美国医学院耶鲁大学儿童研究中心,德国汉诺威医学院和以色列特拉维夫Sourasky医疗中心进行。所有机构已获得研究伦理委员会批准,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在18至65岁成年人中的疗效,安全性和耐受性,并将药物与安慰剂进行比较。SciSparc的首席执行官Oz Adler对SCI-110改变TS治疗领域的潜力表示信心。该公司还有其他基于大麻素药物的药物开发计划,用于治疗不同疾病。
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