Long-Term Study of Gabapentin Enacarbil (GEn, XP13512) vs. Placebo in Patients With Restless Legs Syndrome.
Completed
XenoPort, Inc.
Phase 3
2006-04-01
The primary objective of this trial is to assess the maintenance of efficacy of gabapentin
enacarbil (GEn, XP13512) taken once daily in the long-term treatment of patients suffering
from Restless Legs Syndrome (RLS).
XP13512 (Gabapentin Enacarbil) Extension Study in Patients With Restless Legs Syndrome.
Completed
XenoPort, Inc.
Phase 3
2006-06-01
The primary objective of this trial is to assess the long-term safety and efficacy of XP13512
(Gabapentin Enacarbil) taken once daily for the treatment of patients suffering from Restless
Legs Syndrome (RLS).
XP13512 vs. Placebo in Patients With Restless Legs Syndrome.
Completed
XenoPort, Inc.
Phase 3
2006-08-01
The primary objective of this trial is to assess the efficacy of XP13512 taken once daily
compared to placebo for the treatment of patients suffering from Restless Legs Syndrome
(RLS).
A Clinical Study in Subjects With Neuropathic Pain From PHN Who Have Had an Inadequate Response to Gabapentin Treatment
Completed
XenoPort, Inc.
Phase 2
2008-03-01
The purpose of this study is evaluate the difference between two doses of gabapentin
enacarbil (XP13512/GSK1838262), hereafter referred to as GEn, on pain associated with
post-herpetic neuralgia.
A Study In Patients With Neuropathic Pain From Post-Herpetic Neuralgia (PHN)
Completed
XenoPort, Inc.
Phase 2
2008-02-01
The purpose of this study is to determine whether gabapentin enacarbil (XP13512/GSK1838262),
hereafter referred to as GEn is effective in the treatment of neuropathic pain associated
with post-herpetic neuralgia (PHN).
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