drugset / Trial / NCT01998659
Single Ascending Oral Dose Phase I Study With Px-102
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this study is to assess the safety and tolerability of the FXR agonist Px-102 in healthy subjects after single oral dosing.
Timeline
- Start
- 2011-09
- Primary completion
- 2011-12
- Completion
- 2011-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Px-102 | Small molecule | 0.15 mg/kg | Oral |
| Comparator | Px-102 | Small molecule | 4.5 mg/kg | Oral |
Indications
No indication recorded.