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Clinical Trial Summary

The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) doses of QLM3003 compared to placebo. Also, pharmacokinetics (PK) of qlm3003 will be evaluated.


Clinical Trial Description

The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) doses of QLM3003 compared to placebo. Also, pharmacokinetics (PK) of qlm3003 will be evaluated.Eligible subjects will be assigned to a sequential treatment cohort and randomized to each treatment group (active/placebo ). Subject enrollment will continue into the next cohort after review of the dose safety from the previous dose cohort. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05932888
Study type Interventional
Source Qilu Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date June 25, 2023
Completion date August 30, 2023

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