From the Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina (J.D.K., K.L.R.B.) Union University, Jackson, Tennessee (J.S.O.) Yale Medical School, New Haven, Connecticut (P.M.H.) Weill Cornell Medical College, New York, New York (C.A.L., J.J.S.) Nuventra Pharma Sciences, Durham, North Carolina (V.D.S.).
Anesthesiology. 2018 Jun;128(6):1107-1116. doi: 10.1097/ALN.0000000000002157.
CW002 is an investigational nondepolarizing, neuromuscular blocking agent with a rapid onset and intermediate duration of action in animals. This is a single ascending dose, healthy subject study exploring tolerability, pharmacokinetics, and potency.
Population pharmacokinetic and pharmacokinetic/pharmacodynamic models were developed using plasma drug concentration data from a previously published dose-response study in 28 healthy subjects receiving single doses of CW002 during sevoflurane anesthesia. Subjects included in the models were from five different dose cohorts (cohorts 3, 4, 5, 6, and 8 receiving 0.04, 0.06, 0.08, 0.10, and 0.14 mg/kg, respectively). Serial arterial plasma concentrations and muscle twitch heights were monitored.
A four-compartment model was fit to the concentration-time data, whereas a transit compartment with a sigmoid Emax model was fit to the pharmacokinetic/pharmacodynamic data. The population pharmacokinetics of CW002 was linear with very low interindividual variability in clearance (10.8%). Simulations were conducted to predict the onset and offset of effect at 2×, 3×, and 4× ED95. The time to 80% block was predicted to be 1.5, 0.8, and 0.7 min for 2×, 3×, and 4× ED95 doses, respectively. The simulated 25 to 75% recovery index was independent of dose.
CW002 has predictable pharmacokinetics and is likely to have a rapid onset with an intermediate duration of action at 3× ED95. This model provides information to inform critical decisions (e.g., dose, study design) for continued development of CW002.
CW002 是一种具有快速起效和中等作用持续时间的研究用非去极化神经肌肉阻滞剂,在动物中具有良好的效果。这是一项单递增剂量的健康受试者研究,旨在探索其耐受性、药代动力学和效力。
使用先前发表的一项在七氟醚麻醉下接受单剂量 CW002 的 28 名健康受试者的剂量反应研究中的血浆药物浓度数据,开发了群体药代动力学和药代动力学/药效动力学模型。模型中包含的受试者来自五个不同的剂量组(接受 0.04、0.06、0.08、0.10 和 0.14mg/kg 的第 3、4、5、6 和 8 组)。监测了动脉血浆浓度和肌肉抽搐高度的系列变化。
对浓度-时间数据进行了四室模型拟合,对药效动力学数据进行了具有 Emax 模型的转移室拟合。CW002 的群体药代动力学呈线性,清除率的个体间差异非常低(10.8%)。进行了模拟以预测 2×、3×和 4×ED95 时的作用开始和结束时间。预测 2×、3×和 4×ED95 剂量时,80%阻滞的时间分别为 1.5、0.8 和 0.7min。模拟的 25%至 75%恢复指数与剂量无关。
CW002 具有可预测的药代动力学特性,在 3×ED95 时可能具有快速起效和中等作用持续时间。该模型提供了信息,为 CW002 的持续开发提供了决策依据(例如剂量、研究设计)。