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Clinical Trials associated with NBL-012A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of NBL-012 in Healthy Chinese Subjects
This is a phase 1, randomized, double-blind, placebo-controlled, sequential cohort study to evaluate the safety, tolerability and pharmacokinetics (PK) of NBL-012 as single ascending doses (SAD) administered subcutaneously to healthy Chinese subjects.
评价NBL-012在中国健康受试者中的安全性、耐受性和药代动力学特征的Ⅰ期临床试验
[Translation] Phase I clinical trial to evaluate the safety, tolerability and pharmacokinetic characteristics of NBL-012 in healthy Chinese subjects
主要目的:评价NBL-012在中国健康受试者中单次皮下注射给药的安全性和耐受性。
次要目的:
1.评价NBL-012在中国健康受试者中单次皮下注射给药的药代动力学(PK)特征。
2.评价NBL-012在中国健康受试者中单次皮下注射给药的免疫原性。
3.评价NBL-012在中国健康受试者中单次皮下注射给药的药效动力学(PD)特征。
[Translation] Primary objective: To evaluate the safety and tolerability of a single subcutaneous injection of NBL-012 in healthy Chinese subjects.
Secondary objectives:
1. To evaluate the pharmacokinetic (PK) characteristics of a single subcutaneous injection of NBL-012 in healthy Chinese subjects.
2. To evaluate the immunogenicity of a single subcutaneous injection of NBL-012 in healthy Chinese subjects.
3. To evaluate the pharmacodynamic (PD) characteristics of a single subcutaneous injection of NBL-012 in healthy Chinese subjects.
100 Clinical Results associated with NBL-012
100 Translational Medicine associated with NBL-012
100 Patents (Medical) associated with NBL-012
100 Deals associated with NBL-012