drugset / Trial / NCT04406415
Oral Nafamostat in Healthy Volunteers (NAF-101)
RandomizedSequentialSingle-blindTreatment
Summary
This is a randomized, double-blind, placebo-controlled Multiple Ascending Dose (MAD) study to evaluate the safety, tolerability and pharmacokinetics of oral nafamostat solution administered t.i.d.. for up to 5 days in healthy volunteer adult subjects
Timeline
- Start
- 2020-09-21
- Primary completion
- 2020-11-11
- Completion
- 2021-05-14
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nafamostat | Small molecule | 10 mg | Oral |
| Subject | Nafamostat | Small molecule | 50 mg | Oral |
| Subject | Nafamostat | Small molecule | 100 mg | Oral |
| Subject | Nafamostat | Small molecule | 200 mg | Oral |
Indications
No indication recorded.