drugset / Trial / NCT02250027

A Multicenter, Randomized, Double-blind, Parallel Group Study to Determine the Optimal Dose of HL301 After 7 Days Oral Administration in Acute Bronchitis or Acute Exacerbations of Chronic Bronchitis Patients (HL301: Mixed Extract of Rehmannia Glutinosa, Schisandra and so on)

NCT02250027 ↗

Phase 2 Completed 156 enrolled Hanlim Pharm. Co., Ltd.
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine the optimal dose of HL301 in patients with acute bronchitis or acute exacerbations of chronic bronchitis. \- BSS(Bronchitis Severity Score), BCSS(Breathlessness, Cough, and Sputum Scale), evaluation of symptoms of cough and sputum

Timeline

Start
2014-03
Primary completion
2014-07
Completion
2014-07

Drugs

EvaluationDrugModalityDoseRoute
Subject HL301 Unknown 0.6 g Oral
Subject HL301 Unknown 1.2 g Oral
Subject HL301 Unknown 1.8 g Oral

Indications