drugset / Trial / NCT05718518

Study to Evaluate Safety, Tolerability, PK and the Food Effect on PK of ASC11/RTV Tablets in Healthy Subjects

NCT05718518 ↗

Phase 1 Completed 72 enrolled Ascletis Pharmaceuticals Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled phase I clinical study evaluating the safety, tolerability, and pharmacokinetics of ASC11 plus ritonavir tablets in healthy subjects and an open-label, cross-over study evaluating the effect of food on the pharmacokinetics of ASC11 plus ritonavir tablets

Timeline

Start
2023-01-13
Primary completion
2023-04-14
Completion
2023-04-14

Drugs

EvaluationDrugModalityDoseRoute
Subject ASC11 Unknown 100 mg —
Subject ASC11 Unknown 200 mg —
Subject ASC11 Unknown 300 mg —
Subject ASC11 Unknown 400 mg —
Subject ASC11 Unknown 800 mg —
Subject RTV Unknown 100 mg —

Indications