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MechanismIL-4Rα inhibitors |
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Drug Highest PhaseApproved |
First Approval Ctry. / Loc.CN |
First Approval Date10 Sep 2024 |
一项评价司普奇拜单抗注射液用于结节性痒疹受试者的有效性和安全性的随机、双盲、安慰剂对照III期临床研究
[Translation] A randomized, double-blind, placebo-controlled phase III clinical study to evaluate the efficacy and safety of sepakinumab injection in subjects with nodular prurigo
主要目的:评价司普奇拜用于结节性痒疹(PN)受试者的有效性
次要目的: 评价司普奇拜用于PN受试者的安全性。
评价司普奇拜在PN受试者中的药代动力学(PK)特征。
评价司普奇拜在PN受试者中的药效学(PD)效应。
评价司普奇拜在PN受试者中的免疫原性。
[Translation] Primary objective: To evaluate the efficacy of sepkiba in subjects with prurigo nodularis (PN)
Secondary objectives: To evaluate the safety of sepkiba in subjects with PN.
To evaluate the pharmacokinetic (PK) characteristics of sepkiba in subjects with PN.
To evaluate the pharmacodynamic (PD) effects of sepkiba in subjects with PN.
To evaluate the immunogenicity of sepkiba in subjects with PN.
100 Clinical Results associated with Chengdu Kangnuoxing Biopharma,Inc.
0 Patents (Medical) associated with Chengdu Kangnuoxing Biopharma,Inc.
100 Deals associated with Chengdu Kangnuoxing Biopharma,Inc.
100 Translational Medicine associated with Chengdu Kangnuoxing Biopharma,Inc.