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Mechanism5-HT1A receptor agonists [+5] |
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Drug Highest PhaseApproved |
First Approval Ctry. / Loc.United States |
First Approval Date30 Sep 2013 |
Target- |
Mechanism- |
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Inactive Indication- |
Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
/ CompletedNot Applicable VHDT口崩片在健康人体空腹和餐后条件下的生物等效性试验
[Translation] Bioequivalence studies of VHDT orally disintegrating tablets in healthy subjects under fasting and postprandial conditions.
考察空腹及餐后条件下,健康研究参与者单次口服厦门恩成制药有限公司提供的受试制剂(VHDT口崩片,规格:10mg)和H.Lundbeck A/S持证的参比制剂(氢溴酸伏硫西汀片,商品名:心达悦®,规格:10mg)的药代动力学特征,评价两制剂间的生物等效性。
[Translation] The pharmacokinetic characteristics of the test formulation (VHDT orally disintegrating tablets, strength: 10 mg) provided by Xiamen Encheng Pharmaceutical Co., Ltd. and the reference formulation (vortioxetine hydrobromide tablets, trade name: Xindayue®, strength: 10 mg) certified by H. Lundbeck A/S were examined under fasting and postprandial conditions to evaluate the bioequivalence between the two formulations.
/ Not yet recruitingPhase 2 靖宫颗粒与安慰剂平行对照治疗气滞血瘀证型子宫肌瘤的随机、双盲、多中心Ⅱb期临床试验
[Translation] A randomized, double-blind, multicenter phase Ⅱb clinical trial of Jinggong granules versus placebo in the treatment of uterine fibroids of Qi stagnation and blood stasis syndrome
通过多中心、随机、双盲、安慰剂平行对照研究,评价靖宫颗粒治疗气滞血瘀证型子宫肌瘤患者的有效性和安全性。
[Translation] A multicenter, randomized, double-blind, placebo-controlled parallel study was conducted to evaluate the efficacy and safety of Jinggong Granule in the treatment of patients with uterine fibroids of Qi stagnation and blood stasis syndrome.
100 Clinical Results associated with Fuzhou Changfuxing New Drug Development Co., Ltd.
0 Patents (Medical) associated with Fuzhou Changfuxing New Drug Development Co., Ltd.
100 Deals associated with Fuzhou Changfuxing New Drug Development Co., Ltd.
100 Translational Medicine associated with Fuzhou Changfuxing New Drug Development Co., Ltd.