Trials / Completed
CompletedNCT05921890
To Evaluate the Safety and Tolerability of Multiple Doses of GS3-007a Oral Solution in Healthy Subjects.
To Evaluate the Safety and Tolerability of GS3-007a Oral Solution in a Multi-dose, Randomized, Open, Single-center Study in Healthy Chinese Adult Subjects.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 36 (actual)
- Sponsor
- Changchun GeneScience Pharmaceutical Co., Ltd. · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
To evaluate the safety and tolerability of GS3-007a oral solution after multiple oral administration in Chinese healthy adult subjects.
Detailed description
To evaluate the pharmacodynamic (PD) and pharmacokinetics(PK) characteristics of GS3-007a oral solution after multiple oral administration in Chinese healthy adult subjects
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | GS3-007 oral liquid | The dosage was calculated according to body weight, once a day or twice a day. |
Timeline
- Start date
- 2023-06-19
- Primary completion
- 2023-10-28
- Completion
- 2023-10-28
- First posted
- 2023-06-27
- Last updated
- 2023-11-09
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05921890. Inclusion in this directory is not an endorsement.