一项I期随机、双盲、安慰剂对照研究:舌下给药大麻二酚/ δ 9-四氢大麻二酚(10:1)方案治疗2型糖尿病患者的疗效和安全性

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Shima Afshar, Shayesteh Khalili, Gholamreza Amin, Mohammad Abbasinazari
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引用次数: 1

摘要

目前的研究旨在评估一种基于大麻的舌下喷雾剂CBDEX10®(含100微克大麻二酚和10微克Δ9-tetrahydrocannabinol)的安全性和有效性;CBD/Δ9-THC 10:1)在改善糖尿病患者血脂和血糖状态方面的作用。50例糖尿病患者随机分配到治疗组(n = 25;接受两剂CBDEX10®,每日两次)或对照组(n = 25;接受两剂安慰剂)。该研究的主要终点是评估CBDEX10®辅助治疗在改善糖尿病患者血脂和血糖状态方面的疗效;次要终点是评估喷雾的安全性和耐受性。总胆固醇有统计学意义的下降[估计治疗差异(ETD) = -19.73 mg/dL;P < 0.05],甘油三酯(ETD = -27.84 mg/dL;P < 0.01), LDL-C (ETD = -5.37 mg/dL;P < 0.01),胎牛血清(ETD = -12 mg/dL;P < 0.01),血红蛋白A1C (ETD = -0.21 mg/dL;P < 0.01)和胰岛素分泌(ETD = -5.21 mIU/L;CBDEX10治疗组在8周治疗期结束时P < 0.01)。在安全性方面,上述辅助方案效果良好,无严重不良反应。综上所述,CBDEX1®舌下喷雾剂可能成为糖尿病患者血脂和血糖控制的新药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Phase I Randomized, Double-blind, Placebo-controlled Study on Efficacy and Safety Profile of a Sublingually Administered Cannabidiol /Delta 9-tetrahydrocannabidiol (10: 1) Regimen in Diabetes Type 2 Patients.

A Phase I Randomized, Double-blind, Placebo-controlled Study on Efficacy and Safety Profile of a Sublingually Administered Cannabidiol /Delta 9-tetrahydrocannabidiol (10: 1) Regimen in Diabetes Type 2 Patients.

The current study aimed to evaluate the safety profile and efficacy of a cannabis-based sublingual spray, CBDEX10® (containing 100 µg cannabidiol and 10 µg Δ9-tetrahydrocannabinol per puff; CBD/Δ9-THC 10:1), in improving lipid profile and glycemic state of the diabetic patients. Fifty diabetic patients were randomly allocated to the treatment (n = 25; receiving two puffs of CBDEX10® twice daily) or the control groups (n = 25; receiving two puffs of placebo). The primary endpoint of the study was to evaluate the efficacy of the CBDEX10® adjunctive therapy in improving the lipid profile and glycemic state of diabetic patients; the secondary endpoint was to assess the safety profile and tolerability of the spray. A statistically significant decline in total cholesterol [estimated treatment difference (ETD) = -19.73 mg/dL; P < 0.05], triglyceride (ETD = -27.84 mg/dL; P < 0.01), LDL-C (ETD = -5.37 mg/dL; P < 0.01), FBS (ETD = -12 mg/dL; P < 0.01), Hb A1C (ETD = -0.21 mg/dL; P < 0.01) and insulin secretion (ETD = -5.21 mIU/L; P < 0.01) was observable in the patients treated with CBDEX10® at the end of the 8-week treatment period. Regarding safety, the mentioned adjunctive regimen was well, and there were no serious or severe adverse effects. Overall, CBDEX1® sublingual spray could be a new therapeutic agent for lipid and glycemic control in diabetic patients.

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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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