Burt Consultancy, LLC, Durham, North Carolina, USA.
Department of Anesthesiology, Duke University, Durham, North Carolina, USA.
Clin Transl Sci. 2017 Sep;10(5):351-359. doi: 10.1111/cts.12477. Epub 2017 Jul 8.
Intra-Target Microdosing (ITM) is a novel drug development approach aimed at increasing the efficiency of first-in-human (FIH) testing of new molecular entities (NMEs). ITM combines intra-target drug delivery and "microdosing," the subpharmacological systemic exposure. We hypothesized that when the target tissue is small (about 1/100th of total body mass), ITM can lead to target therapeutic-level exposure with minimal (microdose) systemic exposure. Each of five healthy male volunteers received insulin microdose into the radial artery or full therapeutic dose intravenously in separate visits. Insulin and glucose levels were similar between systemic administration and ITM administration in the ipsilateral hand, and glucose levels demonstrated a reduction in the ipsilateral hand but not in the contralateral hand. Positron emission tomography (PET) imaging of F-fluorodeoxyglucose (FDG) uptake demonstrated differences between the ipsilateral and contralateral arms. The procedures were safe and well-tolerated. Results are consistent with ITM proof-of-concept (POC) and demonstrate the ethical, regulatory, and logistical feasibility of the approach.
靶向内微量给药(ITM)是一种新型药物开发方法,旨在提高新分子实体(NME)的首次人体(FIH)测试效率。ITM 将靶向内药物输送和“微剂量”(低于药理学的全身暴露量)结合在一起。我们假设当靶组织较小时(约占总体重的 1/100),ITM 可以在最小的(微剂量)全身暴露量下导致靶组织治疗水平的暴露。五名健康男性志愿者分别在不同的访问中接受胰岛素微剂量桡动脉内给药或全治疗剂量静脉内给药。同侧手部的全身给药和 ITM 给药的胰岛素和血糖水平相似,而同侧手部的血糖水平降低,但对侧手部没有降低。正电子发射断层扫描(PET)成像显示 F-氟脱氧葡萄糖(FDG)摄取的差异。这些程序是安全且耐受良好的。结果与 ITM 概念验证(POC)一致,并证明了该方法在伦理、监管和后勤方面的可行性。