drugset / Trial / NCT06328400
A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Oral Deuremidevir Hydrobromide for Suspension
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | REMIDEVIR | Small molecule | 900 mg | Oral |
| Subject | REMIDEVIR | Small molecule | 1200 mg | Oral |