Guo Jie, Hu Xiaolei, Wang Jing, Yu Bin, Li Juan, Chen Jianting, Nie Xiaoli, Zheng Zhijian, Wang Shixuan, Qin Qun
National Institution of Drug Clinical Trial, Xiangya Hospital, Central South University, Changsha, China.
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
Front Pharmacol. 2022 Oct 21;13:1015941. doi: 10.3389/fphar.2022.1015941. eCollection 2022.
Compound methyl salicylate liniment (Ammeltz) is composed of various components, such as methyl salicylate, menthol, camphor, chlorpheniramine maleate, and thymol. It was approved for listing in China in 2011. The purpose of this phase Ⅳ clinical trial was to evaluate the safety and efficacy of Ammeltz in a real-life environment in China. Adverse events and adverse drug reactions were used to assess the safety of the monitored drugs. Visual analog scale (VAS) scores were evaluated to assess the severity of pain and the pain relief rate was used to evaluate the efficacy of the study drug. Of 3,600 subjects enrolled, 3,515 (97.64%) subjects completed the study and 85 (2.36%) terminated the study prematurely. A total of 277 adverse events occurred in 258 subjects (7.28%). The most common adverse events included upper respiratory infections (130 cases, 3.67%), local pruritus (17 cases, 0.48%), and diarrhea (12 cases, 0.34%). A total of 50 (1.41%) subjects experienced 58 adverse drug reactions. The most common adverse drug reactions included local pruritus (17 cases, 0.48%), a burning sensation at the application site (10 cases, 0.28%), and irritation at the application site (local) (7 cases, 0.2%). No adverse reactions were identified as new adverse drug reactions. The majority of adverse drug reactions were mild (48 cases, 1.36%), and no severe adverse drug reactions occurred. The subjects experienced significant pain relief after using Ammeltz (mean VAS scores: 5.34 . 2.79; Day 7 ± 1 . Baseline; < 0.0001). The pain relief rate was 47.11% ± 23.13%, and in 2,769 cases (78.31%) the drug was effective in pain relief. After excluding subjects who used drugs that could affect the efficacy of the study drug, the subgroups of subjects experienced significant pain relief after using Ammeltz (mean VAS scores: 5.31 vs 2.77; Day 7 ± 1 vs Baseline; < 0.0001). The pain relief rate was 47.34% ± 23.00%, and 2,612 subjects (78.75%) experienced effective pain relief. In conclusion, Ammeltz is safe and effective in real-life use. It can significantly relieve soft tissue pain caused by shoulder and neck pain, back pain, or muscle pain. No new adverse drug reactions were found in our multicenter real-world study. https://clinicaltrials.gov/ct2/show/NCT05489939?cond=Safety+and+efficacy+of+compound+methyl+salicylate+liniment+for+topical+pain%3A+A+multicenter+real-world+study+in+China&draw=2&rank=1, identifier NCT05489939.
复方水杨酸甲酯搽剂(Ammeltz)由多种成分组成,如水杨酸甲酯、薄荷脑、樟脑、马来酸氯苯那敏和麝香草酚。它于2011年在中国获批上市。这项Ⅳ期临床试验的目的是在中国的实际应用环境中评估Ammeltz的安全性和有效性。通过不良事件和药物不良反应来评估所监测药物的安全性。采用视觉模拟评分法(VAS)评估疼痛严重程度,并使用疼痛缓解率来评估研究药物的疗效。在纳入的3600名受试者中,3515名(97.64%)受试者完成了研究,85名(2.36%)受试者提前终止了研究。258名受试者(7.28%)共发生277起不良事件。最常见的不良事件包括上呼吸道感染(130例,3.67%)、局部瘙痒(17例,0.48%)和腹泻(12例,0.34%)。共有50名(1.41%)受试者发生58起药物不良反应。最常见的药物不良反应包括局部瘙痒(17例,0.48%)应用部位烧灼感(10例,0.28%)和应用部位(局部)刺激(7例,0.2%)。未发现有不良反应为新的药物不良反应。大多数药物不良反应为轻度(48例,1.36%),未发生严重药物不良反应。受试者使用Ammeltz后疼痛明显缓解(平均VAS评分:5.34对2.79;第7天±1天对基线;P<0.0001)。疼痛缓解率为47.11%±23.13%,2769例(78.31%)患者用药后疼痛缓解有效。在排除使用可能影响研究药物疗效的药物的受试者后,各亚组受试者使用Ammeltz后疼痛明显缓解(平均VAS评分:5.