drugset / Trial / NCT01332305

Dose-Response and Pharmacokinetics of Gabapentin Enacarbil (GEn [XP13512 / GSK1838262]) in Restless Legs Syndrome

NCT01332305

Phase 2 Completed 217 enrolled XenoPort, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The objective of the study was to generate the data necessary to determine the gabapentin exposure produced by 4 dose levels of GEn (600 mg, 1200 mg, 1800 mg, and 2400 mg) or placebo, and the corresponding relief of symptoms in subjects with Restless Legs Syndrome (RLS).

Timeline

Start
2007-01
Primary completion
2008-01
Completion
2008-01

Drugs

EvaluationDrugModalityDoseRoute
Subject gabapentin enacarbil Small molecule 600 mg Oral
Subject gabapentin enacarbil Small molecule 1200 mg Oral
Subject gabapentin enacarbil Small molecule 1800 mg Oral
Subject gabapentin enacarbil Small molecule 2400 mg Oral