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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:外國發行人報告
美股SEC公告 ·  08/26 06:17

Moomoo AI 已提取核心訊息

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.
臨床階段藥品公司SciSparc Ltd.宣佈向美國食品藥品監督管理局(FDA)提交了SCI-110的階段IIb臨床試驗的IND(Investigational New Drug)申請,該藥旨在治療圖雷特綜合徵(TS)。該試驗將在三個知名機構進行:美國耶魯大學醫學院的耶魯兒童研究中心、德國漢諾威醫學院和以色列特拉維夫索拉斯基醫療中心。所有機構都已獲得倫理審查委員會和以色列衛生部以及德國聯邦藥品和醫療器械研究所的批准。該試驗將評估SCI-110對18至65歲成年人的療效、安全性和耐受性,使用耶魯全球抽動嚴重度量表將藥物與安慰劑進行比較。SciSparc的首席執行官奧茲·阿德勒對SCI-110改變TS治療格局的潛力表達了信心。該公司還有其他以大麻爲基礎的藥品開發計劃,針對不同的疾病。
臨床階段藥品公司SciSparc Ltd.宣佈向美國食品藥品監督管理局(FDA)提交了SCI-110的階段IIb臨床試驗的IND(Investigational New Drug)申請,該藥旨在治療圖雷特綜合徵(TS)。該試驗將在三個知名機構進行:美國耶魯大學醫學院的耶魯兒童研究中心、德國漢諾威醫學院和以色列特拉維夫索拉斯基醫療中心。所有機構都已獲得倫理審查委員會和以色列衛生部以及德國聯邦藥品和醫療器械研究所的批准。該試驗將評估SCI-110對18至65歲成年人的療效、安全性和耐受性,使用耶魯全球抽動嚴重度量表將藥物與安慰劑進行比較。SciSparc的首席執行官奧茲·阿德勒對SCI-110改變TS治療格局的潛力表達了信心。該公司還有其他以大麻爲基礎的藥品開發計劃,針對不同的疾病。
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