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

SciSparc | 6-K:外國發行人報告

SEC announcement ·  01/30 05:06
牛牛AI助理已提取核心訊息
SciSparc Ltd., a specialty clinical-stage pharmaceutical company, has announced the commencement of patient recruitment for its clinical trial of SCI-210 in children with Autism Spectrum Disorder (ASD). The trial is set to take place at Soroka Medical Center in Israel, with the aim of enrolling 60 subjects aged between five and 18 over a 20-week period. The study is a double-blind, randomized, and placebo-controlled trial designed to evaluate the efficacy of SCI-210—a combination of cannabidiol (CBD) and CannAmide™—compared to standard CBD treatment in managing ASD symptoms. The company's CEO, Oz Adler, expressed optimism about the trial's potential to meet an unmet medical need and the company's goal to commercialize SCI-210 in Israel, followed by...Show More
SciSparc Ltd., a specialty clinical-stage pharmaceutical company, has announced the commencement of patient recruitment for its clinical trial of SCI-210 in children with Autism Spectrum Disorder (ASD). The trial is set to take place at Soroka Medical Center in Israel, with the aim of enrolling 60 subjects aged between five and 18 over a 20-week period. The study is a double-blind, randomized, and placebo-controlled trial designed to evaluate the efficacy of SCI-210—a combination of cannabidiol (CBD) and CannAmide™—compared to standard CBD treatment in managing ASD symptoms. The company's CEO, Oz Adler, expressed optimism about the trial's potential to meet an unmet medical need and the company's goal to commercialize SCI-210 in Israel, followed by other markets pending regulatory approval. The trial will measure efficacy using the Aberrant Behavior Checklist-Community (ABC-C) parent questionnaire, the Clinical Global Impressions-Improvement (CGI-I) scale, and the determination of an effective therapeutic dose. SciSparc has consulted with the National Autism Research Center in Israel for the trial's design. The announcement was made on January 29, 2024, and is part of SciSparc's broader focus on developing cannabinoid-based pharmaceuticals for central nervous system disorders.
ScisPARC Ltd. 是一家處於臨床階段的專業製藥公司,已宣佈開始爲其針對自閉症譜系障礙(ASD)兒童的 SCI-210 臨床試驗招募患者。該試驗將在以色列的索羅卡醫療中心進行,目標是在20周內招收60名年齡在5至18歲之間的受試者。該研究是一項雙盲、隨機和安慰劑對照試驗,旨在評估sci-210(大麻二酚(CBD)和CannaMide™ 的組合)與標準CBD治療相比在控制自閉症症狀方面的療效。該公司首席執行官奧茲·阿德勒對該試驗有可能滿足未滿足的醫療需求以及該公司在以色列和其他市場商業化 SCI-210 的目標表示樂觀,該目標尚待監管部門批准。該試驗將使用異常行爲清單社區(ABC-C)家長問卷、臨床全球印象改善(CGI-I)量表以及有效治療劑量的確定來衡量療效。ScisPARC已就該試驗的設計諮詢了以色列國家自閉症研究中心。該公告於2024年1月29日發佈,是ScisPARC更廣泛地關注開發治療中樞神經系統疾病的大麻素藥物的一部分。
ScisPARC Ltd. 是一家處於臨床階段的專業製藥公司,已宣佈開始爲其針對自閉症譜系障礙(ASD)兒童的 SCI-210 臨床試驗招募患者。該試驗將在以色列的索羅卡醫療中心進行,目標是在20周內招收60名年齡在5至18歲之間的受試者。該研究是一項雙盲、隨機和安慰劑對照試驗,旨在評估sci-210(大麻二酚(CBD)和CannaMide™ 的組合)與標準CBD治療相比在控制自閉症症狀方面的療效。該公司首席執行官奧茲·阿德勒對該試驗有可能滿足未滿足的醫療需求以及該公司在以色列和其他市場商業化 SCI-210 的目標表示樂觀,該目標尚待監管部門批准。該試驗將使用異常行爲清單社區(ABC-C)家長問卷、臨床全球印象改善(CGI-I)量表以及有效治療劑量的確定來衡量療效。ScisPARC已就該試驗的設計諮詢了以色列國家自閉症研究中心。該公告於2024年1月29日發佈,是ScisPARC更廣泛地關注開發治療中樞神經系統疾病的大麻素藥物的一部分。

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