drugset / Trial / NCT06860282
A Study of CX2101A Enteric-Coated Tablets in Healthy Chinese Adult Subjects
RandomizedParallel-groupOpen-labelTreatment
Summary
This study is divided into two parts, including Part I: a randomized, open-label, positive drug-controlled, single ascending dose (SAD) study, a food effect (FE) study, and Part II: a randomized, double-blind, placebo-controlled, multiple ascending dose (MAD) study.
Timeline
- Start
- 2022-12-26
- Primary completion
- 2023-03-27
- Completion
- 2023-03-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CX2101A | Unknown | 20 mg | Oral |
| Subject | CX2101A | Unknown | 80 mg | Oral |
| Subject | CX2101A | Unknown | 100 mg | Oral |
| Subject | CX2101A | Unknown | 160 mg | Oral |
| Subject | CX2101A | Unknown | 300 mg | Oral |
| Subject | CX2101A | Unknown | 600 mg | Oral |
| Comparator | Remdesivir | Small molecule | 100 mg | Intravenous |