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Clinical Trials associated with YH2201 / Not yet recruitingPhase 1 评价YH2201干混悬剂在中国健康受试者中单次给药后药代动力学、药效动力学的Ia期临床研究
[Translation] A Phase Ia clinical study evaluating the pharmacokinetics and pharmacodynamics of YH2201 dry suspension in healthy Chinese subjects after a single dose
主要研究目的:比较空腹状态下单次给药后YH2201干混悬剂(规格:每袋含艾司奥美拉唑镁(按C17H19N3O3S计)20mg与碳酸氢钠1680mg)和对照药艾司奥美拉唑镁碳酸氢钠胶囊(商品名:海悦护偎®,规格:每粒含艾司奥美拉唑镁(按C17H19N3O3S计)20mg与碳酸氢钠1100mg)在中国健康受试者中药代动力学和药效动力学特征。
次要研究目的:评价单次给药后YH2201干混悬剂和对照药艾司奥美拉唑镁碳酸氢钠胶囊在中国健康受试者中的安全性。
[Translation] The primary study objective was to compare the pharmacokinetic and pharmacodynamic characteristics of a single-dose YH2201 dry suspension (specification: each bag contains 20 mg of esomeprazole magnesium (calculated as C₁₇H₁₇N₃O₃S) and 1680 mg of sodium bicarbonate) with a control drug, esomeprazole magnesium sodium bicarbonate capsules (trade name: Haiyue Huwei®, specification: each capsule contains 20 mg of esomeprazole magnesium (calculated as C₁₇H₁₇N₃O₃S) and 1100 mg of sodium bicarbonate) in healthy Chinese volunteers.
The secondary study objective was to evaluate the safety of a single-dose YH2201 dry suspension and a control drug, esomeprazole magnesium sodium bicarbonate capsules, in healthy Chinese volunteers.
100 Clinical Results associated with YH2201
100 Translational Medicine associated with YH2201
100 Patents (Medical) associated with YH2201
100 Deals associated with YH2201