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Safety, Tolerability and Pharmacokinetic Study of KL1333 in Healthy Male Volunteers

MELAS Syndrome Clinical Trial

Official title:
A Dose Block-randomized, Double-blind, Placebo-controlled, Single-dose, Dose-escalation, Phase I Clinical Study

Clinical Trial Summary

The purpose of this First In Human study is to investigate the safety and tolerability of KL1333 after a single oral dose and to investigate the pharmacokinetic characteristics of KL1333 after a single oral dose.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03056209
Study type Interventional
Source Yungjin Pharm. Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date June 26, 2017
Completion date April 16, 2018
View Details
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