drugset / Trial / NCT01998672
Multiple 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 7 days multiple oral dosing.
Timeline
- Start
- 2012-02
- Primary completion
- 2012-10
- Completion
- 2012-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Px-102 | Small molecule | 0.5 mg/kg | Oral |
| Comparator | Px-102 | Small molecule | 1 mg/kg | Oral |
| Comparator | Px-102 | Small molecule | 1.5 mg/kg | Oral |
Indications
No indication recorded.