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Clinical Trials associated with HS-10390 / Not yet recruitingPhase 2 A Randomized, Multicenter, Double-blind, Parallel Active-control Study of the Efficacy and Safety of HS-10390 for the Treatment of Participants With Chronic Kidney Disease
The purpose of the study was to evaluate the efficacy and safety of HS-10390 in participants with chronic kidney disease (CKD) with estimated glomerular filtration rate (eGFR) ≥ 30 and <90 mL/min/1.73 m^2, and urinary albumin to creatinine ratio (UACR) ≥ 150 mg/g and < 3000 mg/g
/ Not yet recruitingPhase 2 A Randomized, Multicenter, Open-label, Active-control Study of the Efficacy and Safety of HS-10390 for the Treatment of Immunoglobulin a Nephropathy
This study will evaluate the efficacy and safety of HS-10390 in subjects with primary IgA nephropathy, and explore the optimal dose for the treatment.
/ Active, not recruitingPhase 1 [Translation] Study on the effect of standard meal on the pharmacokinetics of HS-10390
主要研究目的:在健康受试者中评价标准餐对HS-10390药代动力学的影响。
次要研究目的:在空腹和标准餐后状态下,评价健康受试者单次口服HS-10390片后的安全性和耐受性。
探索性研究目的:可能对健康受试者空腹状态单次口服HS-10390片后尿液和粪便 中 的 HS-10390进行浓度定量分析,以及对血样、尿样、粪便中 HS-10390代谢产物进行鉴定或特定代谢产物定量分析。
[Translation] Primary study objective: To evaluate the effect of a standard meal on the pharmacokinetics of HS-10390 in healthy subjects.
Secondary study objective: To evaluate the safety and tolerability of a single oral dose of HS-10390 tablets in healthy subjects in the fasting and standard meal state.
Exploratory study objective: To quantitatively analyze the concentration of HS-10390 in urine and feces after a single oral dose of HS-10390 tablets in healthy subjects in the fasting state, and to identify HS-10390 metabolites in blood samples, urine samples, and feces or quantitatively analyze specific metabolites.
100 Clinical Results associated with HS-10390
100 Translational Medicine associated with HS-10390
100 Patents (Medical) associated with HS-10390
100 Deals associated with HS-10390