Target- |
MechanismNeuroprotectants |
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Drug Highest PhaseApproved |
First Approval Ctry. / Loc.CN |
First Approval Date29 Jul 2020 |
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Inactive Indication- |
Drug Highest PhasePhase 2 |
First Approval Ctry. / Loc.- |
First Approval Date- |
/ Active, not recruitingPhase 3 Y-2舌下片治疗急性缺血性卒中III期临床试验——多中心、随机、双盲、平行、安慰剂对照III期临床研究
[Translation] Phase III clinical trial of Y-2 sublingual tablets in the treatment of acute ischemic stroke: a multicenter, randomized, double-blind, parallel, placebo-controlled phase III clinical study
评价Y-2舌下片治疗急性缺血性卒中患者的有效性和安全性
[Translation] To evaluate the efficacy and safety of Y-2 sublingual tablets in the treatment of patients with acute ischemic stroke
/ Active, not recruitingPhase 1 评价Y-2舌下片单/多次给药在健康成年受试者中的安全性、耐受性和药代动力学临床研究
[Translation] A clinical study to evaluate the safety, tolerability and pharmacokinetics of single/multiple administration of Y-2 sublingual tablets in healthy adult subjects
主要目的: 评估单/多次递增剂量下的Y-2舌下片在健康成年男性和女性受试者中的安全性和耐受性。 次要目的: 研究单/多次给药后依达拉奉和右旋莰醇在健康成年男性和女性受试者体内的药代动力学(PK)特征。
[Translation] Primary objective: To evaluate the safety and tolerability of Y-2 sublingual tablets in healthy adult male and female subjects at single/multiple ascending doses. Secondary objective: To study the pharmacokinetic (PK) characteristics of edaravone and dextrorotatory borneol in healthy adult male and female subjects after single/multiple administrations.
Sublingual Y-2(Edaravone And Borneol) Tablet For Acute Ischemic And Hemorrhagic Patients-the SALVAGE Trial
The primary objective is to evaluate the safety and tolerability of single ascending dose of Y-2 sublingual tablets in healthy male and female adult subjects. The secondary objective is to characterize the single-dose pharmacokinetics of Y-2 sublingual tablets in healthy male and female adult subjects.
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