Overview

Dose Escalating Study of Rotigotine in Pediatric Subjects With Restless Legs Syndrome

Status:
Completed
Trial end date:
2014-05-01
Target enrollment:
Participant gender:
Summary
This was a multicenter, open-label, dose-escalation, Phase 2A study with multiple administrations of the rotigotine transdermal system. The study was conducted in adolescent subjects (13 to <18 years of age) with idiopathic Restless Legs Syndrome (RLS).
Phase:
Phase 2
Details
Lead Sponsor:
UCB BIOSCIENCES, Inc.
Treatments:
N 0437
Rotigotine