drugset / Trial / NCT05201690

Safety and Pharmacokinetics Study of Multiple Ascending Doses of VV116 in Healthy Volunteers

NCT05201690

Phase 1 Completed 36 enrolled Vigonvita Life Sciences
RandomizedSequentialTriple-blindTreatment

Summary

This is a randomized, double-blinded, placebo-controlled, single-center phase I clinical trial. The objective of this study is to evaluate the safety, tolerability, pharmacokinetic profiles of VV116 tablets after multiple ascending doses administered orally to Chinese healthy volunteers.

Timeline

Start
2021-12-14
Primary completion
2022-01-19
Completion
2022-01-23

Drugs

EvaluationDrugModalityDoseRoute
Subject REMIDEVIR Small molecule 200 mg Oral
Subject REMIDEVIR Small molecule 400 mg Oral
Subject REMIDEVIR Small molecule 600 mg Oral

Indications

No indication recorded.