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A Clinical Trial to Evaluate the Efficacy and Safety of HRS-9821 Inhalation Suspension in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
Sponsor: Guangdong Hengrui Pharmaceutical Co., Ltd
Summary
The study is being conducted to evaluate the efficacy and safety of HRS-9821 for patients with COPD, and to explore the reasonable dosage of HRS-9821 for patients with COPD.
Official title: A Multicenter, Randomized, Double-blind, Placebo-controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of HRS-9821 Inhalation Suspension in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
Key Details
Gender
All
Age Range
40 Years - 80 Years
Study Type
INTERVENTIONAL
Enrollment
90
Start Date
2026-06
Completion Date
2026-11
Last Updated
2026-06-10
Healthy Volunteers
No
Conditions
Interventions
HRS-9821 Inhalation Suspension
HRS-9821 Inhalation Suspension.
HRS-9821 Placebo Inhalation Suspension
HRS-9821 Placebo Inhalation Suspension.
Locations (1)
Shanghai Tongji Hospital
Shanghai, Shanghai Municipality, China