[Translation] A single-center, randomized, open-label, two-dose, fasting and postprandial, single-dose, two-period, double-crossover bioequivalence study of dapoxetine hydrochloride tablets developed by Guoyuan Sinopharm (Guangdong) Pharmaceutical Group Co., Ltd. and the original reference preparation in healthy Chinese subjects
以国源国药(广东)制药集团有限公司研制的盐酸达泊西汀片(规格:60 mg)为受试制剂,持证商为Berlin-Chemie AG的盐酸达泊西汀片(商品名:Priligy®,规格:60 mg)为参比制剂,考察两制剂在空腹及餐后状态下单次给药的药代动力学参数及相对生物利用度,评价两制剂是否具有生物等效性。同时评价两种制剂在健康人体中的安全性和耐受性。
[Translation] Dapoxetine hydrochloride tablets (specification: 60 mg) developed by Guoyuan Guoyao (Guangdong) Pharmaceutical Group Co., Ltd. were used as the test preparation, and dapoxetine hydrochloride tablets (trade name: Priligy®, specification: 60 mg) from Berlin-Chemie AG were used as the reference preparation. The pharmacokinetic parameters and relative bioavailability of the two preparations after single administration in the fasting and postprandial states were investigated to evaluate whether the two preparations were bioequivalent. At the same time, the safety and tolerability of the two preparations in healthy humans were evaluated.