Safety, tolerance, pharmacokinetic and pharmacodynamic properties of thrombopoietin mimetic peptide for injection in Chinese healthy volunteers: a randomized, placebo-controlled, double-blind study

被引:0
作者
Sheng, Xiao-Yan [1 ]
Liu, Zhi-Yan [1 ]
Zhao, Jing [2 ]
Song, Lei [3 ]
Zhao, Wen-Ming [3 ]
Zhao, Xia [1 ]
Cui, Yi-Min [1 ,4 ]
机构
[1] Peking Univ First Hosp, Dept Pharm, Beijing, Peoples R China
[2] Peking Univ First Hosp, Dept Cardiol, Beijing, Peoples R China
[3] Shandong Quangang Pharmaceut Co Ltd, Ctr Res & Dev, Jinan, Peoples R China
[4] Peking Univ, Inst Clin Pharmacol, Beijing, Peoples R China
关键词
China; Pharmacodynamics; pharmacokinetics; thrombopoietin mimetic peptide for injection; IMMUNE THROMBOCYTOPENIC PURPURA; LONG-TERM TREATMENT; ROMIPLOSTIM; EFFICACY; CHILDREN; AMG-531; ADULTS; EPIDEMIOLOGY; ELTROMBOPAG; MANAGEMENT;
D O I
10.1080/09537104.2022.2073344
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The thrombopoietin mimetic peptide for injection is a second-generation thrombopoietin receptor agonist (TPO-RA) used in the treatment of patients with immune thrombocytopenia. The aim of the present study was to assess the safety, tolerance, pharmacokinetic and pharmacodynamic properties of thrombopoietin mimetic peptide for injection in Chinese healthy volunteers. A randomized, placebo-controlled, double-blind, dose-escalation study was conducted in healthy Chinese subjects aged 18-50 years. Thirty subjects received single subcutaneous injection of 0.3 mu g/kg, 1.0 mu g/kg, 2.0 mu g/kg thrombopoietin mimetic peptide or placebo. Thrombopoietin mimetic peptide was safe and well tolerated at doses of 0.3-2.0 mu g/kg. There was no significant change in mean platelet count (PLT) from baseline at the 0.3 mu g/kg or placebo groups. The mean PLT of subjects in the 1.0 mu g/kg and 2.0 mu g/kg groups peaked at day 12 (+/- 1), began to decline around day 17, and returned to the baseline level at day 28 (+/- 1). Platelet aggregation rates of the three dose groups showed no significant change before and after administration. Serum concentrations of thrombopoietin mimetic peptide in all subjects were below the quantization limit. This was the first study to demonstrate that subcutaneous injection of thrombopoietin mimetic peptide at doses of 0.3-2.0 mu g/kg was safe and well tolerated in Chinese healthy subjects. As a second-generation TPO-RA, thrombopoietin mimetic peptide is effective at improving PLT after single subcutaneous injection at dose of >= 1 mu g/kg. Plain language summary What is the context? ? Immune thrombocytopenia (ITP) is a rare, serious autoimmune disorder characterized by low platelet count (PLT) without an alternate cause. The treatment goal of ITP is to increase the platelet count to a safe level that can stop active bleeding and reduce the risks of future bleeding. ? Thrombopoietin receptor agonists (TPO-RAs, e.g. eltrombopag, avatrombopag, hetrombopag, and romiplostim) have shown high response rates in stimulating platelet production and reducing the risk of bleeding. TPO-RAs provide ITP patients with well-tolerated, long-term treatment choices. What is new? ? The thrombopoietin mimetic peptide for injection is a new TPO-RAs developed by Shandong Quangang Pharmaceutical Co., Ltd. (China). ? This study showed that thrombopoietin mimetic peptide is effective at improving PLT after a single subcutaneous injection. ? The thrombopoietin mimetic peptide is safe and well-tolerated in Chinese healthy subjects. What is the impact? ? This study provides evidence for the further development potential of the thrombopoietin mimetic peptide.
引用
收藏
页码:1185 / 1191
页数:7
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