Finkel Julia C, Goldberg Jutta, Rosenburg Ronald, Ariyawansa Jay, Sun Tao, Ochs-Ross Rachel, Zannikos Peter, Zhang Liping, Etropolski Mila
Children's National Medical Center, Washington, DC, USA.
Grünenthal GmbH, Aachen, Germany.
J Pain Res. 2019 Jun 28;12:1925-1936. doi: 10.2147/JPR.S197348. eCollection 2019.
This is the first clinical trial in the global pediatric clinical development program for the use of the analgesic tapentadol in children and adolescents.
This multicenter, open-label clinical trial investigated pharmacokinetics, safety and tolerability, and efficacy of tapentadol and its major metabolite tapentadol-O-glucuronide after administration of a single dose of tapentadol oral solution (OS) in pediatric patients aged 6 to <18 years experiencing moderate to severe acute pain after surgery. Efficacy (change in pain intensity after tapentadol intake) was assessed in an exploratory manner using the McGrath Color Analog Scale and Faces Pain Scale-Revised. Adverse events were monitored throughout the trial.
Forty-four patients who received a single dose of 1 mg/kg tapentadol OS were included in this investigation. Maximum serum concentrations of tapentadol (111 ng/mL) and tapentadol-O-glucuronide (2,400 ng/mL) observed in this trial were within the range of individual maximum concentrations observed in healthy adults administered a comparable dose (range for tapentadol 23.2-129 ng/mL, for tapentadol-O-glucuronide 1,040-4,070 ng/mL). Following tapentadol administration, pain intensity scores improved from baseline at all timepoints. Treatment-emergent adverse events, none of which were serious, were experienced by 45.5% of the patients; the most commonly reported were vomiting (29.5%) and nausea (9.1%).
Tapentadol OS administered as a single dose of 1 mg/kg in children aged 6 to <18 years was generally well tolerated and produced similar serum concentrations as administration of 50-100 mg tapentadol immediate-release tablets in adults. A decrease in postsurgical pain was observed using exploratory subject-reported pain assessments. Tapentadol OS may provide a new treatment option in the management of moderate to severe acute pain in children and adolescents.
这是全球儿科临床开发项目中首次针对儿童和青少年使用镇痛药曲马多的临床试验。
这项多中心、开放标签的临床试验研究了6至<18岁经历中度至重度术后急性疼痛的儿科患者单次服用曲马多口服溶液(OS)后曲马多及其主要代谢产物曲马多-O-葡萄糖醛酸苷的药代动力学、安全性和耐受性以及疗效。使用麦格拉思彩色模拟量表和面部疼痛量表修订版以探索性方式评估疗效(服用曲马多后疼痛强度的变化)。在整个试验过程中监测不良事件。
本研究纳入了44例接受单次1mg/kg曲马多OS的患者。本试验中观察到的曲马多(111ng/mL)和曲马多-O-葡萄糖醛酸苷(2400ng/mL)的最大血清浓度在给予可比剂量的健康成年人中观察到的个体最大浓度范围内(曲马多范围为23.2-129ng/mL,曲马多-O-葡萄糖醛酸苷范围为1040-4070ng/mL)。服用曲马多后,所有时间点的疼痛强度评分均从基线有所改善。45.5%的患者出现了治疗中出现的不良事件,均不严重;最常报告的是呕吐(29.5%)和恶心(9.1%)。
在6至<18岁儿童中单次服用1mg/kg的曲马多OS总体耐受性良好,产生的血清浓度与成人服用50-100mg曲马多速释片相似。使用探索性的受试者报告的疼痛评估观察到术后疼痛有所减轻。曲马多OS可能为儿童和青少年中度至重度急性疼痛的管理提供一种新的治疗选择。