Trials / Completed
CompletedNCT06380153
To Evaluate the Pharmacokinetics of Hemay005 Tablets in Patients With Renal Impairment
To Evaluate the Pharmacokinetics of Hemay005 Tablets in Subjects With Mild and Moderate Renal Impairment and Normal Renal Function After a Single Oral Administration
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 26 (actual)
- Sponsor
- Ganzhou Hemay Pharmaceutical Co., Ltd · Industry
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
The aim of this study was to evaluate the pharmacokinetics of Hemay005 tablets in subjects with mild to moderate renal impairment and normal renal function, and to provide a basis for the formulation of clinical medication regimens for patients with renal impairment.
Detailed description
To evaluate the pharmacokinetics and safety of Hemay 005 tablets in subjects with mild to moderate renal impairment and normal renal function, and to provide a basis for the formulation of clinical medication regimens for patients with renal impairment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Hemay005 | 15mg/tablet,Four tablets (60mg) each time. Participants will receive a single dose of Hemay005 tablet in Day1 |
Timeline
- Start date
- 2024-05-07
- Primary completion
- 2025-04-16
- Completion
- 2025-04-16
- First posted
- 2024-04-23
- Last updated
- 2025-12-04
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06380153. Inclusion in this directory is not an endorsement.