Takeda Development Center Americas, Inc. (TDCA), 35 Landsdowne Street, Cambridge, Massachusetts, 02139, USA.
AAPS J. 2022 Jan 31;24(1):31. doi: 10.1208/s12248-021-00678-7.
Given the recent success of gene therapy modalities and the growing number of cell and gene-based therapies in clinical development across many different therapeutic areas, it is evident that this evolving field holds great promise for the unmet medical needs of patients. The recent approvals of Luxturna® and Zolgensma® prove that recombinant adeno-associated virus (rAAV)-based gene therapy is a transformative modality that enables curative treatment for genetic disorders. Over the last decade, Takeda has accumulated significant experience with rAAV-based gene therapies, especially in the early stage of development. In this review, based on the learnings from Takeda and publicly available information, we aim to provide a guiding perspective on Drug Metabolism and Pharmacokinetics (DMPK) substantial role in advancing therapeutic gene therapy modalities from nonclinical research to clinical development, in particular the characterization of gene therapy product biodistribution, elimination (shedding), immunogenicity assessment, multiple platform bioanalytical assays, and first-in-human (FIH) dose projection strategies. Graphical abstract.
鉴于基因治疗模式的近期成功,以及越来越多的细胞和基因治疗药物在许多不同治疗领域的临床开发中,很明显,这个不断发展的领域为满足患者的未满足的医疗需求带来了巨大的希望。最近 Luxturna® 和 Zolgensma® 的批准证明,基于重组腺相关病毒(rAAV)的基因治疗是一种变革性的治疗方式,可为遗传疾病提供治愈疗法。在过去十年中,武田积累了大量基于 rAAV 的基因治疗经验,特别是在早期开发阶段。在这篇综述中,基于武田和公开信息的经验,我们旨在提供一个指导性的观点,即药物代谢动力学(DMPK)在将治疗性基因治疗模式从非临床研究推进到临床开发中的重要作用,特别是对基因治疗产品的生物分布、消除(脱落)、免疫原性评估、多平台生物分析测定和首次人体(FIH)剂量预测策略的特征。图表摘要。