Trials / Completed
CompletedNCT05622864
Study on Single and Multiple Atomization Inhalation of HRS-9821 Suspension for Inhalation in Healthy Subjects and COPD Patients
Phase I Study on the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of a Single Dose Escalation of Nebulized Inhalation of HRS-9821 Suspension in Healthy Individuals and Multiple Doses in COPD Patients
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 106 (actual)
- Sponsor
- Guangdong Hengrui Pharmaceutical Co., Ltd · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
The increased safety and tolerance of single and multiple atomized inhalation of HRS-9821 suspension for inhalation doses in healthy subjects and COPD patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | HRS-9821 | HRS-9821 |
| DRUG | HRS-9821 | HRS-9821 |
Timeline
- Start date
- 2023-01-12
- Primary completion
- 2025-05-07
- Completion
- 2025-06-16
- First posted
- 2022-11-21
- Last updated
- 2025-07-24
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05622864. Inclusion in this directory is not an endorsement.