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临床试验/NCT04461756
NCT04461756已完成1 期

A Phase I Exploratory Study to Assess the Pharmacokinetics of Single Inhaled Dose of Cannabis (Delta-9-Tetrahydrocannabinol / Cannabidiol) Administered by Vaporization Using a 4-Day Dose Titration In Healthy Male And Female Volunteers

Tetra Bio-Pharma1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2018年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
12
试验地点
1
主要终点
Assessment of adverse events [Safety and Tolerability]

研究概览

简要总结

The primary objective of this study was to evaluate the pharmacokinetics (PK) of THC, 11-OH-THC and CBD following a single inhaled dose of PPP001 administered by vaporization.

The secondary objective of this study was to determine the safety and tolerability of THC and CBD after a single inhaled dose of PPP001 administered by vaporization in healthy volunteers.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Body mass index within 21.0 to 32.0 kg/m2, inclusively
  • A light-, non- or ex-smoker of nicotine
  • A history of recreational cannabis use (at least 10 times in the last 5 years)
  • Consumed cannabis in the last 3 months before Day 1 of the study, but not within 1 month before Day 1 of the study
  • Presence of intact oral mucosa
  • Able to follow instructions at the training vaporizing session
  • Clinical laboratory values within the laboratory's stated normal range; if not within this range, they must have been without clinical significance, as determined by an investigator
  • No clinically significant diseases captured in the medical history or evidence of clinically significant findings on the physical examination (including vital signs), or ECG, as determined by an investigator

排除标准

  • 未提供

研究组 & 干预措施

inhaled THC/CBD (PPP001)

Experimental

干预措施: PPP001 (Drug)

结局指标

主要结局

Assessment of adverse events [Safety and Tolerability]

时间窗: over 5 days

To evaluate treatment-related adverse events of PPP001

Biochemistry test results [Safety and Tolerability]

时间窗: over 5 days

Number of subjects with alkaline phosphatase and alanine aminotransferase (ALT) increase

Temperature [Safety and Tolerability]

时间窗: over 5 days

Oral temperature in Celsius

Pulse rate [Safety and Tolerability]

时间窗: over 5 days

Pulse rate (in beats per minute)

Blood pressure [Safety and Tolerability]

时间窗: over 5 days

Blood pressure (systolic/diastolic blood pressure in mm Hg)

Clinically significant ECG abnormalities [Safety and Tolerability]

时间窗: over 5 days

Number of subjects with clinically significant ECG abnormalities (measured with a 12-lead ECG)

Plasma concentrations of delta-9-tetrahydrocannabinol produced by PPP001 were determined. (pharmacokinetics)

时间窗: over 5 days

Plasma concentrations of 11-OH-delta-9-tetrahydrocannabinol produced by PPP001 were determined. (pharmacokinetics)

时间窗: over 5 days

Plasma concentrations of cannabidiol produced by PPP001 were determined. (pharmacokinetics)

时间窗: over 5 days

次要结局

未报告次要终点

研究者

发起方
Tetra Bio-Pharma
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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