drugset / Trial / NCT01981941

Post-marketing Study of Gabapentin Enacarbil to Evaluate the Effect in Restless Leg Syndrome (RLS) Patients With Moderate Renal Impairment

NCT01981941

Phase 4 Completed 19 enrolled Astellas Pharma Inc
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the safety, efficacy and pharmacokinetics of gabapentin enacarbil in moderate to severe primary RLS patients with moderate renal impairment and to confirm dosage and administration in such population.

Timeline

Start
2013-11-05
Primary completion
2015-05-13
Completion
2015-05-13

Drugs

EvaluationDrugModalityDoseRoute
Subject gabapentin enacarbil Small molecule Oral