drugset / Trial / NCT03138421

Central Pain Study for ABX-1431

NCT03138421 ↗

Phase 1 Completed 9 enrolled Abide Therapeutics
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

EvaluationDrugModalityDoseRoute
Subject ABX-1431 Small molecule 20 mg —