RecruitingPhase 1NCT07567872

A Phase I Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of HRS-9821 Powder for Inhalation Administered as a Single Dose in Healthy Participants and Multiple Doses in Patients With COPD


Sponsor

Guangdong Hengrui Pharmaceutical Co., Ltd

Enrollment

48 participants

Start Date

Jul 9, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of this study was to evaluate the safety and tolerability of HRS-9821 Powder for Inhalation administered in a single dose in healthy individuals and multiple doses in patients with COPD。


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called HRS-9821 Powder for Inhalation and a drug called Placebo for people with copd. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 75 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

DRUGHRS-9821 Powder for Inhalation

HRS-9821 Powder for Inhalation

DRUGPlacebo

placebo for HRS-9821 Powder Inhalation


Locations(1)

West China Hospital, Sichuan University

Chengdu, Sichuan, China

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NCT07567872


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