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Clinical Trials associated with TAB014 / Active, not recruitingPhase 3 A Phase III, Randomized, Multicenter, Doubled-blind Clinical Trial Comparing the Efficacy and Safety of TAB014 and Lucentis in Neovascular Age-related Macular Degeneration (nAMD) Patients
This study is a randomized, multi-center, double blind, Lucentis controlled non-inferiority study in neovascular age-related macular degeneration patients. The objective of this study is to compare the efficacy and safety of TAB014 and ranibizumab (Lucentis).
TAB014治疗湿性(新生血管性)年龄相关性黄斑变性(AMD)的I期临床研究
[Translation] Phase I clinical study of TAB014 for the treatment of wet (neovascular) age-related macular degeneration (AMD)
要目的: 评估TAB014单抗注射液玻璃体单次和多次注射给药的安全性和耐受性; 评估TAB014单抗注射液玻璃体单次和多次注射给药后血药代动力学参数。 次要目的: 评估TAB014单抗注射液剂量限制性毒性及不良反应; 评估TAB014单抗注射液治疗湿性(新生血管性)年龄相关性黄斑变性(AMD)的有效性; 评估TAB014单抗注射液的免疫原性; 为II期确定给药剂量提供依据。
[Translation] Primary objectives: To evaluate the safety and tolerability of single and multiple intravitreal injections of TAB014 monoclonal antibody injection; To evaluate the blood pharmacokinetic parameters after single and multiple intravitreal injections of TAB014 monoclonal antibody injection. Secondary objectives: To evaluate the dose-limiting toxicity and adverse reactions of TAB014 monoclonal antibody injection; To evaluate the efficacy of TAB014 monoclonal antibody injection in the treatment of wet (neovascular) age-related macular degeneration (AMD); To evaluate the immunogenicity of TAB014 monoclonal antibody injection; To provide a basis for determining the dosage in Phase II.
A Phase Ⅰ Clinical Study of TAB014 in Wet( Neovascular)Age-related Macular Degeneration(AMD) Subjects
Subjects with secondary wet age-related macular degeneration(AMD) or recurrent subfoveal choroidal neovascularization (CNV) in only one study eye will be enrolled into the study.
100 Clinical Results associated with TAB014
100 Translational Medicine associated with TAB014
100 Patents (Medical) associated with TAB014
100 Deals associated with TAB014