Clinical Trials Directory

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

TypeNameDescription
DRUGGS3-007 oral liquidThe 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.