[Translation] A single-dose, fasting/postprandial, two-formulation, two-period, two-sequence, randomized, open-label, self-crossover average bioequivalence study of Olmesartan Medoxomil Tablets in Chinese healthy subjects
Main research purpose: This study uses Olmesartan Medoxomil Tablets (specification: 20 mg) produced by Chongqing Kerui Pharmaceutical (Group) Co., Ltd. as the test preparation and Olmesartan Medoxomil Tablets (trade name: Aotan®; specification: 20 mg) produced by Daiichi Sankyo Pharmaceutical (Shanghai) Co., Ltd. as the reference preparation to evaluate the bioequivalence of the test preparation and the reference preparation when administered under fasting/postprandial conditions.
Secondary research purpose: Observe the safety of the test preparation and the reference preparation in healthy subjects.
[Translation] A single-dose, randomized, open-label, two-period, two-sequence, double-crossover, fasting and fed bioequivalence study of pregabalin capsules in Chinese healthy subjects
主要目的:本研究以重庆科瑞制药(集团)有限公司生产的普瑞巴林胶囊为受试制剂,以Pfizer Manufacturing Deutschland GmbH,Betriebsstatte Freiburg生产、辉瑞制药有限公司进口分包装的普瑞巴林胶囊(Lyrica)为参比制剂,对比两制剂在空腹和餐后条件下,在健康人体内的吸收速度和吸收程度,评价两制剂间的生物等效性。
次要目的:观察受试制剂普瑞巴林胶囊和参比制剂普瑞巴林胶囊(Lyrica)在健康受试者中的安全性。
[Translation]
Main purpose: This study used pregabalin capsules produced by Chongqing Kerui Pharmaceutical (Group) Co., Ltd. as the test preparation, and pregabalin capsules (Lyrica) produced by Pfizer Manufacturing Deutschland GmbH, Betriebsstatte Freiburg and imported and packaged by Pfizer Pharmaceutical Co., Ltd. as the reference preparation. The absorption rate and degree of the two preparations in healthy people under fasting and postprandial conditions were compared to evaluate the bioequivalence between the two preparations.
Secondary purpose: To observe the safety of the test preparation pregabalin capsules and the reference preparation pregabalin capsules (Lyrica) in healthy subjects.
[Translation] This study adopted a single-center, randomized, open, single-dose, two-drug, four-period, two-sequence completely repeated crossover design, which was divided into two parts: fasting administration and postprandial administration human bioequivalence study.
The aim of this study was to investigate the pharmacokinetic characteristics of prasugrel hydrochloride tablets (5 mg) developed and produced by Chongqing Kerui Pharmaceutical (Group) Co., Ltd. after single fasting and postprandial oral administration; using prasugrel hydrochloride tablets (Efient®, 5 mg) produced by Daiichi Sankyo Co., Ltd. as the reference preparation, the pharmacokinetic parameters Cmax, AUC0-t, and AUC0-∞ of the two preparations were compared, and the bioequivalence of the two preparations in humans was evaluated.
AbstractC19H18N2O, orthorhombic, Pna21 (no. 33), a = 21.838(2) Å, b = 13.9663(11) Å, c = 4.9806(4) Å, V = 1519.1(2) Å3, Z = 4, Rgt(F) = 0.0702, wRref(F2) = 0.1948, T = 293 K.
15 Dec 2023·Zeitschrift für Kristallographie - New Crystal Structures
Crystal structure of dichlorido-bis[2-(2,4-difluorophenyl)pyridine-κ1N]platinum(II), C22H14Cl2F4N2Pt
The statistics for drugs in the Pipeline is the current organization and its subsidiaries are counted as organizations,Early Phase 1 is incorporated into Phase 1, Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3
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