drugset / Trial / NCT06328400

A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Oral Deuremidevir Hydrobromide for Suspension

NCT06328400

Phase 1 Completed 24 enrolled Vigonvita Life Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial is a multi dose, randomized, double-blind, placebo-controlled, single center Phase I clinical study. The purpose of this study is to evaluate the safety, tolerability, and PK characteristics of Deuteromide Hydrobromide for Suspension administered multiple times in healthy volunteers.

Timeline

Start
2024-03-27
Primary completion
2024-05-06
Completion
2024-05-06

Drugs

EvaluationDrugModalityDoseRoute
Subject REMIDEVIR Small molecule 900 mg Oral
Subject REMIDEVIR Small molecule 1200 mg Oral