Rare Disease Research Unit, Pfizer Inc., Cambridge, MA, USA.
Pfizer Clinical Research Unit, Brussels, Belgium.
J Thromb Haemost. 2018 Sep;16(9):1722-1731. doi: 10.1111/jth.14207. Epub 2018 Jul 20.
Essentials Tissue factor pathway inhibitor (TFPI) is an antagonist of FXa and the TF-FVIIa complex. PF-06741086 is an IgG monoclonal antibody that targets the Kunitz-2 domain of TFPI. Single doses of PF-06741086 were evaluated in a phase 1 study in healthy volunteers. Data from this study support further investigation of PF-06741086 in individuals with hemophilia.
Background Tissue factor pathway inhibitor (TFPI) is a protease inhibitor of the tissue factor-activated factor VII complex and activated FX. PF-06741086 is a mAb that targets TFPI to increase clotting activity. Objectives This study was a randomized, double-blind, sponsor-open, placebo-controlled, single intravenous or subcutaneous dose escalation study to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of PF-06741086. Patients/Methods Volunteers who provided written informed consent were assigned to cohorts with escalating dose levels. Safety endpoints included treatment-emergent adverse events (TEAEs), infusion/injection site reactions, vital signs, electrocardiogram, and coagulation and hematology laboratory parameters. Pharmacokinetic (PK) and pharmacodynamic (PD) endpoints included exposures of PF-06741086 in plasma and measures of PF-06741086 pharmacology, respectively. Results Forty-one male volunteers were recruited overall. Thirty-two were dosed with PF-06741086 from 30 mg subcutaneously to 440 mg intravenously. All doses were safe and well tolerated. TEAEs were mild or moderate in severity, laboratory abnormalities were transient, there were no serious adverse events, there were no infusion/injection site reactions, and no dose escalation stopping criteria were met. Plasma exposures of PF-06741086 increased greater than proportionally with dose under the same dosing route. Coagulation pharmacology was demonstrated via total TFPI, dilute prothrombin time, D-dimer, prothrombin fragment 1 + 2 and thrombin generation assay parameters. Conclusions Single doses of PF-06741086 at multiple dose levels were safe and well tolerated in a healthy adult male population. The safety, PK and PD data from this study support progression to a multiple-dose study in hemophilic patients.
组织因子途径抑制剂(TFPI)是组织因子激活的因子 VII 复合物和激活的 FX 的蛋白酶抑制剂。PF-06741086 是一种针对 TFPI 的 mAb,可增加凝血活性。
这是一项随机、双盲、研究者开放、安慰剂对照、单次静脉或皮下递增剂量的研究,旨在评估 PF-06741086 的安全性、耐受性、药代动力学和药效学。
志愿者在提供书面知情同意后被分配到递增剂量水平的队列中。安全性终点包括治疗期间出现的不良事件(TEAEs)、输注/注射部位反应、生命体征、心电图以及凝血和血液学实验室参数。药代动力学(PK)和药效学(PD)终点分别包括 PF-06741086 在血浆中的暴露和 PF-06741086 药效学的测量。
共有 41 名男性志愿者被招募。32 名志愿者接受了 30 毫克至 440 毫克的 PF-06741086 皮下或静脉注射。所有剂量均安全且耐受良好。TEAEs 为轻度或中度,实验室异常为一过性,无严重不良事件,无输注/注射部位反应,也未达到剂量递增的停药标准。相同给药途径下,PF-06741086 的血浆暴露量呈超比例增加。通过总 TFPI、稀释性凝血酶原时间、D-二聚体、凝血酶原片段 1+2 和血栓生成试验参数来证明凝血药效学。
在健康成年男性人群中,PF-06741086 单次剂量在多个剂量水平下均安全且耐受良好。本研究的安全性、PK 和 PD 数据支持在血友病患者中进行多剂量研究。