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项与 Hepatitis B surface antigen targeting antibody(Yangshengtang/Syneos Health) 相关的临床试验A Multi-center, Randomized, Double-blind, Placebo-controlled Phase Ib Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of 162 With a Single Ascending Dose in Subjects With Chronic Hepatitis B Virus Infection
The goal of this intervention research is to learn about the safety and tolerability of 162 with a single ascending dose in subjects with chronic hepatitis B virus (HBV) infection.
A Randomized, Double-blind, Placebo-controlled Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics of 162 With a Single Ascending Dose in Healthy Adult Subjects
This is the first in human study of 162, and the primary objective is to evaluate the safety and tolerability of 162 with a single ascending dose in healthy adult subjects.
The dose-escalation stage will be conducted sequentially at 5 dose levels, which are 100 mg in the pre-test, and 200 mg, 400 mg, 800 mg and 1200 mg in the formal test.
Two healthy adult subjects will be enrolled at 100 mg dose level and all given 162. Eight healthy adult subjects will be enrolled at each remaining dose levels (200 mg, 400 mg, 800 mg and 1200 mg), respectively.
100 项与 Hepatitis B surface antigen targeting antibody(Yangshengtang/Syneos Health) 相关的临床结果
100 项与 Hepatitis B surface antigen targeting antibody(Yangshengtang/Syneos Health) 相关的转化医学
100 项与 Hepatitis B surface antigen targeting antibody(Yangshengtang/Syneos Health) 相关的专利(医药)
100 项与 Hepatitis B surface antigen targeting antibody(Yangshengtang/Syneos Health) 相关的药物交易