drugset / Trial / NCT06157918
Relative Bioavailability and Food Effect of SYHA1813 Oral Solution in Healthy Participants
RandomizedCrossoverOpen-labelTreatment
Summary
This is a three-period crossover phase I study designed to evaluate the relative bioavailability, food effect, safety and tolerability of SYHA1813 oral solution in healthy participants.
Timeline
- Start
- 2023-12-20
- Primary completion
- 2024-01-26
- Completion
- 2024-01-26
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SYHA1813 | Unknown | 25 mg | Oral |
| Subject | SYHA1813 | Unknown | 200 mg | Oral |
Indications
No indication recorded.