An Open-Label, Randomized Pilot Study Comparing the Safety of a Single Dose of TNX-1300 to Usual Care (UC) Alone for the Treatment of Signs and Symptoms of Acute Cocaine Intoxication in Male Emergency Department (ED) Subjects
2022年6月23日 更新者:Tonix Pharmaceuticals, Inc.
An Open-Label, Randomized Pilot Study Comparing the Safety of a Single Dose of TNX-1300 to Usual Care (UC) Alone for the Treatment of Signs and Symptoms of Acute Cocaine Intoxication in Male Emergency Department (ED) Subjects
研究概览
研究类型
介入性
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
-
-
Michigan
-
Detroit、Michigan、美国、48202
- Henry Ford Hospital
-
-
Missouri
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Saint Louis、Missouri、美国、63110
- Washington University School of Medicine
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-
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 50年 (成人)
接受健康志愿者
不
有资格学习的性别
男性
描述
Inclusion Criteria:
- Subject is male (sex assigned at birth).
- Subject is 18-50 years of age.
- Subject has the capacity to provide voluntary written informed consent.
- At Screening, subject presents with a SIS total score of ≥6 and a score >1 on at least 1 of the 3 cardiovascular items (HR, systolic and diastolic BP).
- At Screening, subject presents with cardiac symptoms not present prior to cocaine intoxication, with or without behavioral symptoms.
- Subject has a positive urine drug screen test at Screening to confirm cocaine use and detect polysubstance abuse (subject may test positive for cannabinoids or opiates).
- Subject is a suitable candidate for investigational treatment based on the opinion of the investigator.
Exclusion Criteria:
- Subject who has been admitted to the ED involuntarily.
- Subject who participated in this clinical study previously.
- Subject received naloxone (Narcan) within 3 hours prior to informed consent.
- Subject tests positive for 3,4-Methylenedioxymethamphetamine (MDMA) or amphetamine at Screening.
- Subject has a prior or current clinically significant untreated cardiac condition. Untreated hypertension may be allowed if not considered severe or life threatening.
- Subject incurred or is likely to incur a myocardial infarction or other life-threatening severe event or has acute ECG changes indicative of acute coronary syndrome according to investigator judgment.
- Subject has a clinically significant or unstable medical illness, condition, or disorder that would be anticipated to potentially compromise subject safety or adversely affect the evaluation of clinical outcome parameters.
- Subject requires physical restraints due to physiological and/or behavioral symptoms.
- Participation in another investigational drug study (current or within 30 days of Screening).
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:随机化
- 介入模型:并行分配
- 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:TNX-1300
TNX-1300 Intravenous injection 200 mg once over 2 mins
|
TNX 1300 200 mg Intravenous injection
|
|
其他:Usual Care
Usual Care per the Emergency Department protocol for treating Cocaine Intoxication
|
Usual Care per the Emergency Department protocol for Cocaine Intoxication
|
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 |
|---|---|---|
|
Incidence of Treatment Emergent Adverse Events, Adverse Events of Special Interests, and Adverse Drug Reactions
大体时间:Baseline to 12 Hours
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Incidence of Treatment Emergent Adverse Events, Adverse Events of Special Interests, and Adverse Drug Reactions
|
Baseline to 12 Hours
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Reduction of cardiovascular and other signs and symptoms associated with acute cocaine intoxication identified at Baseline on the Stimulant Intoxication Scale (SIS)
大体时间:Baseline to 6 Hours
|
Reduction of cardiovascular and other signs and symptoms associated with acute cocaine intoxication identified at Baseline on the Stimulant Intoxication Scale (SIS)
|
Baseline to 6 Hours
|
|
Reduction of circulating cocaine, cocaethylene, and EME levels after 15, 60, 120, 240, and 360 minutes in the TNX-1300 arm compared to Baseline
大体时间:Baseline to 6 Hours
|
Reduction of circulating cocaine, cocaethylene, and EME levels after 15, 60, 120, 240, and 360 minutes in the TNX-1300 arm compared to Baseline
|
Baseline to 6 Hours
|
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:Gregory Sullivan, MD、Medical Monitor
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)
2021年9月3日
初级完成 (实际的)
2022年6月16日
研究完成 (实际的)
2022年6月16日
研究注册日期
首次提交
2021年8月3日
首先提交符合 QC 标准的
2021年8月3日
首次发布 (实际的)
2021年8月9日
研究记录更新
最后更新发布 (实际的)
2022年6月29日
上次提交的符合 QC 标准的更新
2022年6月23日
最后验证
2022年6月1日
更多信息
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.