[Translation] A randomized, open-label, single-dose, four-period, two-sequence complete repeated crossover postprandial bioequivalence study of Hebomib atorvastatin calcium tablets in healthy volunteers
本试验旨在研究餐后单次口服瀚晖制药有限公司研制、浙江海正药业股份有限公司生产的海博麦布阿托伐他汀钙片(20 mg/10 mg)的药代动力学特征;以浙江海正药业股份有限公司生产的海博麦布片(赛斯美®,20 mg)及辉瑞制药有限公司生产的阿托伐他汀钙片(立普妥®,10 mg)联用作为对照,比较海博麦布阿托伐他汀钙片与海博麦布片和阿托伐他汀钙片联用的药动学参数〔总海博麦布(海博麦布+海博麦布-葡萄糖醛酸结合物)、海博麦布、阿托伐他汀:Cmax、AUC0-t、AUC0-∞〕,评价海博麦布阿托伐他汀钙片与海博麦布片和阿托伐他汀钙片联用的人体生物等效性。次要目的:评价海博麦布阿托伐他汀钙片在健康成年受试者中的安全性。
[Translation] This study aims to study the pharmacokinetic characteristics of Hebomib Atorvastatin Calcium Tablets (20 mg/10 mg) developed by Hanhui Pharmaceutical Co., Ltd. and produced by Zhejiang Hisun Pharmaceutical Co., Ltd. after a single oral administration after a meal; using Hebomib Tablets (Cesme®, 20 mg) produced by Zhejiang Hisun Pharmaceutical Co., Ltd. and Atorvastatin Calcium Tablets (Lipitor®, 10 mg) produced by Pfizer Pharmaceuticals Co., Ltd. as controls, to compare the pharmacokinetic parameters of Hebomib Atorvastatin Calcium Tablets and Hebomib Tablets and Atorvastatin Calcium Tablets in combination [total Hebomib (Hebomib + Hebomib-glucuronic acid conjugate), Hebomib, Atorvastatin: Cmax, AUC0-t, AUC0-∞], and to evaluate the bioequivalence of Hebomib Atorvastatin Calcium Tablets and Hebomib Tablets and Atorvastatin Calcium Tablets in humans. Secondary objective: To evaluate the safety of Hebomib Atorvastatin Calcium Tablets in healthy adult subjects.