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一项针对酒精使用障碍患者的开放标签、单剂量研究

2026年5月21日 更新者:Beckley Psytech Limited

一项针对酒精使用障碍患者的开放标签、2a 期单剂量研究

一项开放标签的 2a 期研究,旨在评估单次鼻内剂量 BPL-003 结合预防复发心理支持的安全性、耐受性和药效学效应,以探索对酒精使用患者的酒精使用和相关症状的潜在影响紊乱。

研究概览

地位

完全的

干预/治疗

详细说明

大约 12 名符合条件的参与者将接受单剂 BPL-003,鼻内给药,并进行 12 周的随访评估。 将在给药前、给药期间和给药后给予心理支持

研究类型

介入性

注册 (实际的)

13

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • London、英国
        • King's College London
      • London、英国、W1G 8DR
        • Clerkenwell Health

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 64年 (成人)

接受健康志愿者

不

描述

纳入标准:

  1. 愿意并能够给予知情同意。
  2. 筛选时年龄在 18 至 64 岁之间。
  3. 诊断为严重程度可能受益于药物治疗的 AUD,即中度至重度 AUD。
  4. 筛选前 28 天内至少有 10 天大量饮酒。
  5. 自上次 HDD 或完成解毒后不超过 14 天。
  6. 可以在给药前 72 小时内戒除任何酒精物质的消耗。
  7. 从筛选到研究结束愿意放弃使用消遣性药物
  8. 愿意在给药当天在诊所期间戒烟。
  9. 从筛选到研究结束,愿意避免使用迷幻药。
  10. 住在社区稳定/安全的住处。
  11. 拥有个人手机并能够指定至少一名定位人员(例如,家庭成员、朋友或康复导师),并提供可验证的地址和电话号码,以协助安排后续预约。

排除标准:

  1. 精神分裂症、双相情感障碍、精神障碍、妄想障碍、偏执障碍或分裂情感障碍的个人或一级家族史。
  2. 除轻度或中度焦虑和/或抑郁之外的任何主要精神疾病。
  3. 创伤后应激障碍的临床诊断。
  4. 筛选时有自杀意念或行为。
  5. 经常使用或依赖咖啡因或尼古丁以外的其他药物。
  6. 在过去 6 个月内任何自我报告的迷幻化合物的使用。
  7. 癫痫发作史。
  8. 在给药日表现出任何酒精戒断迹象的患者。
  9. 给药日酒精呈阳性。
  10. 非法药物或滥用药物的阳性尿液药物筛查。
  11. 任何鼻塞、堵塞或充血症状。
  12. 恶性高热的任何个人或家族史。
  13. 患有不受控制的心血管疾病的患者,研究者认为,如果他/她参加研究,可能会干扰研究结果的解释或对患者构成健康风险。
  14. 不受控制或依赖胰岛素​​的糖尿病。

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:BPL-003手臂
单剂量鼻内给药

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Percentage of Participants With Treatment Emergent Adverse Events
大体时间:Up to 12 weeks
The number (%) of participants with at least one treatment-emergent adverse event is presented. More detailed information is provided in the dedicated 'Adverse Events' section
Up to 12 weeks
Percentage of Participants With Clinically Significant Abnormal Laboratory Tests
大体时间:Up to 12 weeks
The number (%) of participants with any clinically significant abnormal laboratory tests (routine haematology, clinical chemistry and coagulation) is presented
Up to 12 weeks
Percentage of Participants With Clinically Significant Abnormal Vital Signs
大体时间:Up to 12 weeks
The number (%) of participants with any clinically significant abnormal vital signs (blood pressure, heart rate and temperature) result is presented
Up to 12 weeks
Number of Participants With Post-baseline Suicidal Ideation or Behaviour Based on C-SSRS Score
大体时间:Up to 12 weeks
The C-SSRS was performed at screening, on Day 0 (dosing day), and on Days 1, 7, and 84 post-dose. Participants were counted if they answered 'yes' to any question. At baseline, the C-SSRS assessed the worst-point suicidal ideation experienced during the participant's lifetime. Beyond baseline, suicidal ideation and behaviour since last visit was assessed.
Up to 12 weeks
Time to Readiness for Discharge Post-dose Using the Readiness for Discharge Questionnaire (RDQ)
大体时间:1 Day

The RDQ was a brief assessment scale to ensure that ahead of discharge after BPL-003 dosing, participants:

  • Were fully responsive, aware of their surroundings, and reacted adequately
  • The acute psychedelic effects of the drug had completely subsided
  • Were fully orientated (name, location, time)
  • Had normal (or only slightly elevated) blood pressure and pulse rate, and normal breathing frequency and body temperature
  • Had a stable gate, normal muscle coordination, and could walk safely
  • Had only mild to moderate potential side affects that did not need to be medically monitored
  • Had no acute suicidal ideations or suicidal intentions
  • Possible distress or feelings of overwhelm had sufficiently subsided and the participant felt safe to be discharged.

Readiness for discharge was assessed at 90 minutes post-dose and then every 30 minutes until the participant was deemed ready for discharge (eg, the answer was 'yes' to all of the above items).

1 Day
Percentage of Participants With Occurrence of Reactivation Using the Reactivation Questionnaire (ReAQ)
大体时间:Up to 12 weeks
The occurrence and (if applicable) frequency, emotional valence, and functional impact of any reactivation events was determined. To determine if reactivation had occurred, participants were asked if they had any flashbacks or recurrence of any effects of the study drug experience.
Up to 12 weeks

次要结果测量

结果测量
措施说明
大体时间
Effects on the Mystical Experience Questionnaire (MEQ-30)
大体时间:1 Day
The MEQ-30 was performed to assess the extent of a participant's mystical experience after receiving BPL-003 on Day 0 (dosing day). The questionnaire comprises a list of 30 phenomena, with subscales to measure mystical, positive mood, transcendence of space and time, and ineffability factors, measured on a 0 to 5 scale (0=none; not at all to 5=extreme). A 'total MEQ-30 score' was calculated for each participant as the average of all their responses. The total MEQ-30 score is presented. The higher the score, the greater the mystical experience. A total score of ≥3 was considered to be a significant mystical experience.
1 Day
Effects on the Ego Dissolution Inventory (EDI)
大体时间:1 Day
The EDI was performed to assess the extent of a participant's dissolution of ego after receiving BPL-003 on Day 0 (dosing day). The inventory comprises 8 statements. Participants rated their agreement to each statement by marking on a visual analogue scale from 0 ("no, not more than usually") to 100 ("yes, entirely or completely"). Higher scores are indicative of more intense ego dissolution. In practice, this means participants with higher scores could have a reduced sense of having a distinct, separate self; greater feelings of unity with the environment or universe; a loss of self-referential thoughts or identity; or altered boundaries between 'self' and 'other'. A 'total EDI score' was calculated for each participant as the average of their individual-item scores. The total EDI score is presented.
1 Day
Percentage of Participants With a Complete Mystical Experience Using the MEQ-30
大体时间:1 Day

The MEQ-30 was performed to assess the extent of a participant's mystical experience after receiving BPL-003 on Day 0 (dosing day). The questionnaire comprises a list of 30 phenomena, with subscales to measure mystical, positive mood, transcendence, and ineffability factors, measured on a 0 to 5 scale (0=none; not at all to 5=extreme). A 'total MEQ-30 score' was calculated for each participant as the average of all their responses.

A complete mystical experience was defined as reaching or exceeding a score of 3 on all four sub-domains (mystical, positive mood, transcendence of time and space, and ineffability) of the MEQ-30 scale.

1 Day
Percentage of Participants Experiencing an Ego Dissolution Using the EDI
大体时间:1 Day
The EDI was performed to assess the extent of a participant's dissolution of ego after receiving BPL-003 on Day 0 (dosing day). The inventory comprises 8 statements. Participants rated their agreement to each statement by marking on a visual analogue scale from 0 ("no, not more than usually") to 100 ("yes, entirely or completely"). Participants were classed as experiencing an ego dissolution if they had a total score of >50.0 out of 100 on the EDI scale.
1 Day
Description of the BPL-003 Subjective Experience Data, From a Qualitative Interview
大体时间:Interviews were conducted approximately 2 hours after dosing
After BPL-003 dosing, participants had the option to participate in a one-to-one guided interview with independent researchers trained in microphenomenology methods to describe their psychedelic experience. Temporal aspects of drug effects (e.g., sensory, cognitive, metacognitive, and sense of self/other/connectedness) were elicited through open-ended interview questions.
Interviews were conducted approximately 2 hours after dosing
Feedback From Therapists on the Frequency and Duration of Psychotherapy Sessions, Therapy Manual and Overall Therapy Model
大体时间:1 Day
Key themes from qualitative feedback on the treatment model was sought from therapists on frequency and duration of psychotherapy sessions, implementation of therapy manual, and overall therapy model. Feedback was obtained in a qualitative interview with each therapist after each participant's last integration session (between Day 15 and Day 42).
1 Day
Semi-structured Interview to Assess Psychological Changes Following BPL-003 Treatment
大体时间:Up to 12 weeks
After BPL-003 dosing, participants had the option to participate in a semi-structured interview. The interviews were topic-guided, qualitative interviews to understand psychological changes shortly after dosing on Day 1, and on Day 84.
Up to 12 weeks

其他结果措施

结果测量
措施说明
大体时间
Timeline Follow-Back (TLFB) Interview to Assess the Percentage of Abstinent Days (PAD)
大体时间:Up to 12 weeks
Using the TLFB interview, the PAD in the 85 days before Day -3 (or start of detox) vs the PAD post-dosing measured on Days 14, 28, 56, and 84 were determined to assess alcohol use.
Up to 12 weeks
TLFB Interview to Assess the Percentage of Heavy Drinking Days (PHDD)
大体时间:Up to 12 weeks
Using the TLFB interview, the PHDD in the 85 days before Day -3 (or start of detox) vs PHDD post-dosing measured on Days 14, 28, 56, and 84 were determined to assess alcohol use.
Up to 12 weeks
TLFB Interview to Assess the Percentage of Drinking Days (PDD)
大体时间:Up to 12 weeks
Using the TLFB interview, the PDD in the 85 days before Day -3 (or start of detox) vs PDD post-dosing measured on Days 14, 28, 56, and 84 were determined to assess alcohol use.
Up to 12 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Kevin Craig, M.D.、Beckley Psytech Ltd

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2023年5月30日

初级完成 (实际的)

2024年10月2日

研究完成 (实际的)

2024年10月2日

研究注册日期

首次提交

2022年12月13日

首先提交符合 QC 标准的

2022年12月21日

首次发布 (实际的)

2023年1月9日

研究记录更新

最后更新发布 (实际的)

2026年5月22日

上次提交的符合 QC 标准的更新

2026年5月21日

最后验证

2025年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • BPL-003-203

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

IPD 计划说明

根据英国 GDPR,个人参与者数据将不会公开共享。 小组数据将在研究完成后发表。

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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