Longardner Katherine, Shen Qian, Castellanos Francisco X, Tang Bin, Gandhi Rhea, Wright Brenton A, Momper Jeremiah D, Nahab Fatta B
University of California San Diego, Department of Neurosciences, La Jolla, CA, USA.
University of California San Diego, Department of Radiology, La Jolla, CA, USA.
Tremor Other Hyperkinet Mov (N Y). 2025 Apr 14;15:14. doi: 10.5334/tohm.1005. eCollection 2025.
Essential tremor (ET) is characterized by often disabling action tremors. No pharmacological agent has been developed specifically for symptomatic treatment. Anecdotal reports describe tremor improvement with cannabis, but no evidence exists to support these claims. We conducted a phase Ib/II double-blind, placebo-controlled, crossover pilot trial in participants with ET to investigate tolerability, safety, and efficacy of Tilray TN-CT120 LM, an oral pharmaceutical-grade formulation containing tetrahydrocannabinol (THC) 5 mg and cannabidiol (CBD) 100 mg. Our objectives were to determine if short-term THC/CBD exposure improved tremor amplitude and was tolerated.
Participants with ET were randomized (1:1) to receive either TN-CT120 LM or placebo. Dose titration, driven by tolerability, was attempted every 2-3 days to three capsules daily maximum. Participants remained on the highest tolerated dose for two weeks before returning to complete assessments. After completing the first arm, participants titrated off the agent, underwent a three-week washout, and then returned for the same procedures with the alternate compound. The primary endpoint was tremor amplitude change from baseline using digital spiral assessment. Secondary endpoints explored safety and tolerability.
Among thirteen participants screened, seven were eligible and enrolled. Five completed all visits; one withdrew following a serious adverse event, and another did not tolerate the lowest dose. Intent-to-treat analyses performed for six participants did not reveal significant effects on primary or secondary endpoints.
This pilot trial did not detect any signals of efficacy of THC/CBD in ET. Although preliminary due to the small sample size, our data do not support anecdotal reports of cannabinoid effectiveness for ET.
This double-blind, randomized, placebo-controlled efficacy and tolerability pilot trial did not detect any signals of efficacy of oral cannabidiol and tetrahydrocannabinol in reducing essential tremor amplitude using either digital outcome measures or clinical rating scales. The oral cannabinoids were well-tolerated by most (five out of seven) participants.
特发性震颤(ET)的特征是常常导致功能障碍的动作性震颤。目前尚未开发出专门用于对症治疗的药物。有轶事报道称大麻可改善震颤,但尚无证据支持这些说法。我们对特发性震颤患者进行了一项Ib/II期双盲、安慰剂对照、交叉试点试验,以研究Tilray TN-CT120 LM(一种含有5毫克四氢大麻酚(THC)和100毫克大麻二酚(CBD)的口服药用级制剂)的耐受性、安全性和疗效。我们的目标是确定短期接触THC/CBD是否能改善震颤幅度以及是否具有耐受性。
将特发性震颤患者随机(1:1)分为两组,分别接受TN-CT120 LM或安慰剂。根据耐受性情况,每2 - 3天尝试进行剂量滴定,最大剂量为每日三粒胶囊。参与者在维持最高耐受剂量两周后返回进行全面评估。完成第一组治疗后,参与者逐渐停用该药物,经过三周的洗脱期,然后返回使用另一种化合物进行相同的程序。主要终点是使用数字螺旋评估法测量的震颤幅度相对于基线的变化。次要终点包括安全性和耐受性。
在筛选的13名参与者中,7名符合条件并被纳入研究。5名完成了所有访视;1名因严重不良事件退出,另1名无法耐受最低剂量。对6名参与者进行的意向性分析未发现对主要或次要终点有显著影响。
这项试点试验未发现THC/CBD对特发性震颤有任何疗效信号。尽管由于样本量小,结果具有初步性,但我们的数据不支持大麻素对特发性震颤有效的轶事报道。
这项双盲、随机、安慰剂对照的疗效和耐受性试点试验,无论是使用数字评估指标还是临床评分量表,均未发现口服大麻二酚和四氢大麻酚在降低特发性震颤幅度方面有任何疗效信号。大多数(7名中的5名)参与者对口服大麻素耐受性良好。