drugset / Trial / NCT03138421
Central Pain Study for ABX-1431
RandomizedCrossoverTriple-blindTreatment
Summary
This study will determine the safety and tolerability of ABX-1431 in patients with central pain when added on to background pain therapy. During the course of this study, each participant will take a daily dose of 20 mg of ABX-1431 or a matching placebo for approximately 7 to 9 weeks.
Timeline
- Start
- 2017-08-01
- Primary completion
- 2018-07-23
- Completion
- 2018-07-24
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ABX-1431 | Small molecule | 20 mg | — |