Overview

A Study of the Relative Bioavailability of ASC18 Tablets vs Reference Tablets in Healthy Volunteers

Status:
Completed
Trial end date:
2020-12-15
Target enrollment:
Participant gender:
Summary
The objective of this study is to evaluate potential drug interaction between RDV and SOF in ASC18 tablets (RDV/SOF compound tablets) and the influence of food effect on the pharmacokinetics of ASC18 tablets were evaluated in healthy subjects -and compare the pharmacokinetic parameters of ASC18 tablets(ravidasvir and sofosbuvir fixed dose combination)with ravidasvir tablets and sofosbuvir tablets in healthy subjects after single and multiple oral dosing.
Phase:
Phase 1
Details
Lead Sponsor:
Ascletis Pharmaceuticals Co., Ltd.
Treatments:
Sofosbuvir