Clinical Trials Directory

Trials / Completed

CompletedNCT06005714

Effect of Pharmacokinetics in Healthy Chinese Subjects

Effect of Clarithromycin or Cyclosporine on Pharmacokinetics of Deuterium Hydrobromide Ramidvir Tablets in Healthy Chinese Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Shanghai Vinnerna Biosciences Co., Ltd. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This study is a single-center, open label, self-controlled phase I clinical study, to evaluate the effects of clarithromycin or cyclosporine on pharmacokinetics of deuterium hydrobromide ramidvir tablets in healthy Chinese subjects.

Conditions

Interventions

TypeNameDescription
DRUGMindeudesivir hydrobromide tablets and Clarithromycin tabletsMindeudesivir hydrobromide tablets are administered once at D1 and D4, and clarithromycin tablets are administered twice from D1 to D10.
DRUGMindeudesivir hydrobromide tablets and Cyclosporine softgelsMindeudesivir hydrobromide tablets are administered once at D1 and D4, and cyclosporine sofgels are administered once at D4.

Timeline

Start date
2023-08-15
Primary completion
2023-10-31
Completion
2023-10-31
First posted
2023-08-22
Last updated
2025-06-29

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06005714. Inclusion in this directory is not an endorsement.