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Inactive Indication- |
Drug Highest PhaseApproved |
First Approval Ctry. / Loc.United States |
First Approval Date26 Aug 2020 |
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Mechanism- |
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Inactive Indication- |
Drug Highest PhaseApproved |
First Approval Ctry. / Loc.China |
First Approval Date12 Nov 2018 |
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Inactive Indication- |
Drug Highest PhaseApproved |
First Approval Ctry. / Loc.China |
First Approval Date01 Jan 1996 |
/ Not yet recruitingPhase 3 A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study to Evaluate the Efficacy and Safety of 1% Clascoterone Cream in the Treatment of Acne Vulgaris
This is a multicenter, randomized, double-blind, parallel, placebo-controlled Phase III clinical study to evaluate the efficacy and safety of 1% Clascoterone Cream in the treatment of acne vulgaris.
Target population: Participants aged ≥12 years with moderate to severe acne vulgaris who meet the inclusion criteria and none of the exclusion criteria.
Treatment: The investigational group will receive 1% Clascoterone Cream, and the control group will receive placebo. Approximately 1 g of the cream will be applied evenly to the entire face twice daily (morning and evening) for 12 weeks.
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Study on the Efficacy and Safety of 5% Minoxidil Foam in the Treatment of Female Androgenetic Alopecia
The primary objective of this study is to evaluate the efficacy of once-daily 5% minoxidil foam versus placebo in female androgenetic alopecia, using the Target Area Terminal Hair Count (TAHC) as the primary endpoint.
/ CompletedNot Applicable [Translation] Bioequivalence study of metformin hydrochloride sustained-release tablets in humans
主要目的:比较空腹及餐后给药条件下,浙江三生蔓迪药业有限公司提供的盐酸二甲双胍缓释片(规格:0.5 g)与Merck Serono Limited持证的盐酸二甲双胍缓释片(商品名:Glucophage XR®/格华止®;规格:0.5 g)在健康人群中吸收程度和速度的差异。
次要目的:评价空腹及餐后给药条件下,浙江三生蔓迪药业有限公司提供的盐酸二甲双胍缓释片(规格:0.5 g)与Merck Serono Limited持证的盐酸二甲双胍缓释片(商品名:Glucophage XR®/格华止®;规格:0.5 g)的安全性。
[Translation] Primary objective: To compare the differences in absorption degree and speed of metformin hydrochloride sustained-release tablets (specification: 0.5 g) provided by Zhejiang Sansheng Mandi Pharmaceutical Co., Ltd. and metformin hydrochloride sustained-release tablets (trade name: Glucophage XR®/Glucophage®; specification: 0.5 g) certified by Merck Serono Limited in healthy people under fasting and postprandial administration conditions.
Secondary objective: To evaluate the safety of metformin hydrochloride sustained-release tablets (specification: 0.5 g) provided by Zhejiang Sansheng Mandi Pharmaceutical Co., Ltd. and metformin hydrochloride sustained-release tablets (trade name: Glucophage XR®/Glucophage®; specification: 0.5 g) certified by Merck Serono Limited under fasting and postprandial administration conditions.
100 Clinical Results associated with Zhejiang Sunshine Mandi Pharmaceutical Co.,Ltd.
0 Patents (Medical) associated with Zhejiang Sunshine Mandi Pharmaceutical Co.,Ltd.
100 Deals associated with Zhejiang Sunshine Mandi Pharmaceutical Co.,Ltd.
100 Translational Medicine associated with Zhejiang Sunshine Mandi Pharmaceutical Co.,Ltd.