Overview

A Study to Investigate the Biomarkers of Hemay005 in Adult Participants With Moderate to Severe COPD

Status:
NOT_YET_RECRUITING
Trial end date:
2027-12-31
Target enrollment:
Participant gender:
Summary
A Multicenter, Randomized, Double-blind, Single-dummy, positive drug and placebo-controlled, Parallel Group, Phase 2a Study to Evaluate the Efficacy and Safety of Hemay005 in Adults with Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD).
Phase:
PHASE2
Details
Lead Sponsor:
Ganzhou Hemay Pharmaceutical Co., Ltd
Treatments:
Hemay005
Roflumilast