RecruitingPhase 3NCT07583849

A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Phase III Study of HSK39004 Inhalation Powder for the Treatment of COPD

A Phase III Clinical Study to Evaluate the Efficacy and Safety of HSK39004 Inhalation Powder in the Treatment of Chronic Obstructive Pulmonary Disease (COPD): a Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Design


Sponsor

Haisco Pharmaceutical Group Co., Ltd.

Enrollment

376 participants

Start Date

May 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

To evaluate the efficacy and safety of a 12-week administration of HSK39004 inhalation powder in clinical trial participants with COPD


Eligibility

Min Age: 40 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called HSK39004 Dry Powder Inhaler Simulant and a drug called HSK39004 Dry Powder Inhaler-0.75mg for people with copd, chronic obstructive pulmonary disease. The study is currently recruiting participants at 1 location. People eligible for this study include aged 40 Years to 80 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGHSK39004 Dry Powder Inhaler Simulant

HSK39004 Dry Powder Inhaler Simulants, administered via oral inhalation, 1 tablet each time, twice daily

DRUGHSK39004 Dry Powder Inhaler-0.75mg

HSK39004 Dry Powder Inhaler: Inhale through the mouth, 0.75mg each time, twice a day


Locations(1)

Peking University People's Hospital

Beijing, Beijing Municipality, China

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NCT07583849


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