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A Study of Single Ascending Dose of LEM-S401 in Healthy Participants

Cicatrix Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Phase I Clinical Trial to Evaluate the Characteristics of the Safety, Tolerability and Pharmacokinetics of LEM-S401 in Healthy Adult Subjects

Clinical Trial Summary

The primary objective of the study is to assess the safety and tolerability of single dose of LEM-S401 in healthy adult subjects.

Clinical Trial Description

This study is designed to evaluate the safety and tolerability of LEM-S401 administered as subcutaneous injection in healthy adult subjects. Overall, 18 subjects will be studied in 3 groups. Each subject will receive LEM-S401 or placebo subcutaneously. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04707131
Study type Interventional
Source Lemonex
Contact
Status Completed
Phase Phase 1
Start date July 11, 2022
Completion date February 3, 2023
View Details
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