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Mechanismfungal CYP51A1 inhibitors |
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Drug Highest PhaseApproved |
First Approval Ctry. / Loc.United States |
First Approval Date03 Feb 1975 |
克霉唑含片治疗口咽部念珠菌病的有效性及安全性的多中心、随机、双盲、阳性对照临床研究
[Translation] A multicenter, randomized, double-blind, positive-controlled clinical study on the efficacy and safety of clotrimazole lozenges in the treatment of oropharyngeal candidiasis
评价克霉唑含片治疗口咽部念珠菌病的有效性和安全性。
[Translation] To evaluate the efficacy and safety of clotrimazole lozenges in the treatment of oropharyngeal candidiasis.
/ CompletedNot Applicable 头孢地尼片在中国健康受试者空腹和餐后状态下单中心、随机、开放、双周期、双交叉设计的生物等效性试验
[Translation] A single-center, randomized, open-label, two-period, double-crossover bioequivalence study of cefdinir tablets in Chinese healthy volunteers under fasting and fed conditions
主要目的:评价江苏亚邦强生药业有限公司的头孢地尼片(规格:0.1g/片)与持证商为LTL Pharma Co., Ltd.的头孢地尼胶囊(规格:0.1g/粒,广州白云山光华制药股份有限公司分包装)在健康成年受试者空腹和餐后状态下单次口服给药的人体生物等效性。次要目的:评价头孢地尼片在健康成年受试者中的安全性。
[Translation] Primary objective: To evaluate the bioequivalence of cefdinir tablets (specification: 0.1 g/tablet) from Jiangsu Yabang Johnson Pharmaceutical Co., Ltd. and cefdinir capsules (specification: 0.1 g/capsule, packaged by Guangzhou Baiyunshan Guanghua Pharmaceutical Co., Ltd.) from the licensee LTL Pharma Co., Ltd. in healthy adult subjects after single oral administration in fasting and fed state. Secondary objective: To evaluate the safety of cefdinir tablets in healthy adult subjects.
/ CompletedNot Applicable [Translation] Bioequivalence study of indapamide tablets in human body
本试验的目的是以江苏亚邦强生药业有限公司提供的吲达帕胺片(规格:2.5mg)为受试制剂,以法国施维雅药厂生产的吲达帕胺片(商品名:Natrilix® 规格:2.5mg)为参比制剂,按有关生物等效性试验的规定,评估二者作用于空腹状态下的健康受试者的生物等效性。
[Translation] The purpose of this study is to use indapamide tablets (specification: 2.5 mg) provided by Jiangsu Yabang Johnson Pharmaceutical Co., Ltd. as the test preparation and indapamide tablets (trade name: Natrilix® specification: 2.5 mg) produced by Servier Pharmaceuticals in France as the reference preparation, and to evaluate the bioequivalence of the two in healthy subjects in the fasting state in accordance with the relevant provisions of the bioequivalence test.
100 Clinical Results associated with Jiangsu Yabang Johnson & Johnson Pharmaceutical Co., Ltd.
0 Patents (Medical) associated with Jiangsu Yabang Johnson & Johnson Pharmaceutical Co., Ltd.
100 Deals associated with Jiangsu Yabang Johnson & Johnson Pharmaceutical Co., Ltd.
100 Translational Medicine associated with Jiangsu Yabang Johnson & Johnson Pharmaceutical Co., Ltd.