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A Clinical Trial to Evaluate the Efficacy and Safety of YMC026 in Respiratory Disease Patients

Respiratory Disease Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial to Evaluate the Efficacy and Safety of YMC026 in Respiratory Disease Patients With Cough and Sputum as the Main Symptoms

Clinical Trial Summary

This is a phase 4, randomized, double-blind, multicenter clinical trial to evaluate the efficacy and safety of YMC026 in respiratory disease patients with cough and sputum as the main symptoms

Clinical Trial Description

The study has planned 4 visits during 2 weeks period (1 week of screening period, 1 week of treatment period). All subjects who agree to participate in the study and voluntarily give written informed consent are assessed by inclusion and exclusion criteria at the screening visit. After the screening period, the final eligibility of the subjects will be assessed at the randomization visit. Subjects who are determined to be appropriate for this study will be allocated to experimental group(YMC026) or control group(placebo) randomly in a 1:1 ratio. Subject will be administered the investigational product daily for 6 days. The safety for the subjects will be assessed at Day 3 and Day 6 visit, and the efficacy evaluation will be assessed at Day 6 visit. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03334916
Study type Interventional
Source Yuhan Corporation
Contact
Status Completed
Phase Phase 4
Start date October 27, 2017
Completion date October 30, 2018
View Details
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