drugset / Trial / NCT02272634

A Phase 2a Study to Assess Safety, Daily Symptoms, PK, and Biomarkers of YPL-001 in COPD Patients

NCT02272634 ↗

Phase 2 Completed 61 enrolled Yungjin Pharm. Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 2a, proof-of-concept, multicenter, randomized, double-blind, double dummy, 3-treatment, parallel study, with low and high YPL 001 doses (low dose and high dose twice daily \[BID\]) and a placebo control in moderate to severe Chronic Obstructive Pulmonary Disease (COPD) patients.

Timeline

Start
2015-06-04
Primary completion
2017-11-08
Completion
2017-11-08

Outcome

Met primary endpoint

release “이 시험에서 일차목표는 안전성과 내약성에 대한 평가였으며, YPL-001 투약군은 위약군에 비해 안전성 측면에서 부작용 발생 빈도를 50% 이상 감소시켰다.” yungjin.co.kr ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject YPL 001 Unknown 80 mg Oral
Subject YPL 001 Unknown 160 mg Oral