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Clinical Trial Summary

This study is only for the first in human phase 1a study designed to investigate the safety and tolerability of LIV001 in healthy participants. LIV001 will be investigated for the safety and efficacy in participants with Ulcerative Colitis (UC) in a phase 1b study.


Clinical Trial Description

The study will be conducted in 2 parts. Approximately 36 subjects are planned to be enrolled into the study. - In Part A (SAD), approximately 18 healthy subjects will be enrolled in 2 sequential cohorts (Cohorts SAD1 and SAD2) and randomized 2:1 to receive a single dose of investigational product (IP) (LIV001 or placebo) - In Part B (MAD), approximately 18 healthy subjects will be enrolled into 2 sequential cohorts (Cohorts MAD1 and MAD2) and randomized 2:1 to receive LIV001 or placebo for 14 days. Oversight of the study will be provided by a Safety review committee (SRC) comprising the Principal Investigator (PI), the local Medical Monitor (MM), and a representative of the Sponsor, at a minimum. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05975047
Study type Interventional
Source Liveome Inc.
Contact Sophie Hyun-Ja-Ko
Phone +82-31-8065-8216
Email sophieko@liveome.co.kr
Status Recruiting
Phase Phase 1
Start date October 24, 2023
Completion date July 30, 2024

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