Stephanie Knatz Peck, Samantha Shao, Tessa Gruen, Kevin Yang, Alexandra Babakanian, Julie Trim, Daphna M Finn, Walter H Kaye
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The primary aim was to assess safety, tolerability and feasibility at post-treatment by incidences and occurrences of adverse events (AEs) and clinically significant changes in electrocardiogram (ECG), laboratory tests, vital signs and suicidality. No clinically significant changes were observed in ECG, vital signs or suicidality. Two participants developed asymptomatic hypoglycemia at post-treatment, which resolved within 24 h. No other clinically significant changes were observed in laboratory values. All AEs were mild and transient in nature. Participants' qualitative perceptions suggest that the treatment was acceptable for most participants. Results suggest that psilocybin therapy is safe, tolerable and acceptable for female AN, which is a promising finding given physiological dangers and problems with treatment engagement. ClinicalTrials.gov identifier NCT04661514. 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引用次数: 0
摘要
神经性厌食症(AN)是一种致命的疾病,目前尚无行之有效的治疗方法来逆转其核心症状,也没有任何药物获得美国食品和药物管理局的批准。目前迫切需要新的治疗方法来改善临床疗效。在这项开放标签可行性研究中,一家学术临床研究机构招募了10名符合《精神疾病诊断与统计手册》第五版(DSM-5)标准的成年女性参与者(平均体重指数为19.7 kg m-2;标准差为3.7),她们均为AN或pAN(部分缓解)患者。参与者在接受心理支持的同时,单次服用 25 毫克合成西洛赛宾。研究的主要目的是评估治疗后的安全性、耐受性和可行性,包括不良事件(AEs)的发生率和发生率,以及心电图(ECG)、实验室检查、生命体征和自杀倾向的临床显著变化。在心电图、生命体征和自杀方面未观察到明显的临床变化。两名患者在治疗后出现无症状性低血糖,在 24 小时内缓解。所有不良反应均为轻微且短暂的。参与者的定性看法表明,大多数参与者都能接受治疗。结果表明,对于女性自闭症患者来说,迷幻药治疗是安全、可耐受和可接受的,考虑到生理上的危险性和治疗参与性问题,这是一个很有希望的发现。ClinicalTrials.gov 标识符 NCT04661514。最初发表于《Nat Med 2023; 29:1947-1953》。
Psilocybin Therapy for Females With Anorexia Nervosa: A Phase 1, Open-Label Feasibility Study.
Anorexia nervosa (AN) is a deadly illness with no proven treatments to reverse core symptoms and no medications approved by the US Food and Drug Administration. Novel treatments are urgently needed to improve clinical outcomes. In this open-label feasibility study, 10 adult female participants (mean body mass index 19.7 kg m-2; s.d. 3.7) who met Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5) criteria for AN or pAN (partial remission) were recruited to a study conducted at an academic clinical research institute. Participants received a single 25-mg dose of synthetic psilocybin in conjunction with psychological support. The primary aim was to assess safety, tolerability and feasibility at post-treatment by incidences and occurrences of adverse events (AEs) and clinically significant changes in electrocardiogram (ECG), laboratory tests, vital signs and suicidality. No clinically significant changes were observed in ECG, vital signs or suicidality. Two participants developed asymptomatic hypoglycemia at post-treatment, which resolved within 24 h. No other clinically significant changes were observed in laboratory values. All AEs were mild and transient in nature. Participants' qualitative perceptions suggest that the treatment was acceptable for most participants. Results suggest that psilocybin therapy is safe, tolerable and acceptable for female AN, which is a promising finding given physiological dangers and problems with treatment engagement. ClinicalTrials.gov identifier NCT04661514. Appeared originally in Nat Med 2023; 29:1947-1953.