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Clinical Trial Summary

This is a first-in-human,randomized, double-blind, placebo-controlled, single dose escalation, phase 1 study to evaluate the safety, tolerability, PK/PD and immunogenicity of AK102 administered subcutaneously in healthy subjects. Subjects will be randomized into 4 planned single dose escalation cohorts or placebo cohort.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04169386
Study type Interventional
Source Akeso
Contact
Status Completed
Phase Phase 1
Start date May 9, 2018
Completion date June 30, 2019

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