drugset / Trial / NCT02633683

An Extension Study to Evaluate the Efficacy and Safety of HORIZANT in Adolescents With Moderate-to-Severe Primary RLS

NCT02633683

Phase 4 Unknown 144 enrolled XenoPort, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The objectives of the trial are to evaluate the long-term efficacy and safety of HORIZANT (Gabapentin Enacarbil) 600 mg daily, for the treatment of RLS in adolescents (13 to 17 years of age) diagnosed with moderate-to-severe primary RLS.

Timeline

Start
2016-01
Primary completion
2024-05
Completion
2024-07

Drugs

EvaluationDrugModalityDoseRoute
Subject gabapentin enacarbil Small molecule 600 mg