Magic Wand Research LLC, Philadelphia, Pennsylvania, USA.
Teva Branded Pharmaceutical Products Inc. Research and Development, Netanya, Israel.
Clin Pharmacol Drug Dev. 2022 Jul;11(7):865-877. doi: 10.1002/cpdd.1078. Epub 2022 Mar 4.
TV-46000 is a long-acting subcutaneous antipsychotic that uses a novel copolymer drug delivery technology in combination with a well-characterized molecule, risperidone, that is in clinical development as a treatment for schizophrenia. A population pharmacokinetic (PPK) modeling and simulation approach was implemented to identify TV-46000 doses and dosing schedules for clinical development that would provide the best balance between clinical efficacy and safety. The PPK model was created by applying pharmacokinetic data from a phase 1 study of 97 patients with a diagnosis of schizophrenia or schizoaffective disorder who received either single or repeated doses of TV-46000. The PPK model was used to characterize the complex release profile of the total active moiety (TAM; the sum of the risperidone and 9-OH risperidone concentrations) concentration following subcutaneous injections of TV-46000. The PK profile was best described by a double Weibull function of the in vivo release rate and by a 2-compartment disposition and elimination model. Simulations were performed to determine TV-46000 doses and dosing schedules that maintained a median profile of TAM concentrations similar to published TAM exposure following oral risperidone doses that have been correlated to a 40% to 80% dopamine-D2 receptor occupancy therapeutic window. The simulations showed that therapeutic dose ranges for TV-46000 are 50 to 125 mg for once-monthly and 100 to 250 mg for the once every 2 months regimens. This PPK model provided a basis for prediction of patient-specific exposure and dopamine-D2 receptor occupancy estimates to support further clinical development and dose selection for the phase 3 studies.
TV-46000 是一种长效皮下抗精神病药物,它采用了一种新型的共聚物药物输送技术,结合了一种经过充分研究的分子——利培酮,该分子正在开发中,用于治疗精神分裂症。采用群体药代动力学(PPK)建模和模拟方法,确定 TV-46000 的剂量和给药方案,以在临床疗效和安全性之间取得最佳平衡。该 PPK 模型是通过应用 97 例患有精神分裂症或分裂情感障碍的患者的 1 期研究中的药代动力学数据创建的,这些患者接受了 TV-46000 的单次或重复剂量。该 PPK 模型用于描述 TV-46000 皮下注射后总活性部分(TAM;利培酮和 9-OH 利培酮浓度之和)浓度的复杂释放曲线。PK 曲线最好由体内释放率的双 Weibull 函数和 2 隔室分布和消除模型来描述。进行模拟以确定 TV-46000 的剂量和给药方案,以维持类似于已发表的口服利培酮剂量后 TAM 暴露的中位数 TAM 浓度曲线,该暴露与 40%至 80%的多巴胺-D2 受体占有率治疗窗相关。模拟结果表明,TV-46000 的治疗剂量范围为每月一次 50 至 125 毫克和每两个月一次 100 至 250 毫克。该 PPK 模型为预测患者特异性暴露和多巴胺-D2 受体占有率估计值提供了基础,以支持进一步的临床开发和 3 期研究的剂量选择。