Viewing Study NCT03992196



Ignite Creation Date: 2024-05-06 @ 1:21 PM
Last Modification Date: 2024-10-26 @ 1:12 PM
Study NCT ID: NCT03992196
Status: TERMINATED
Last Update Posted: 2023-10-30
First Post: 2019-06-17

Brief Title: A Follow-up Study of Rotigotine Patch in Adolescent Subjects With Restless Legs Syndrome
Sponsor: UCB Biopharma SRL
Organization: UCB Pharma

Study Overview

Official Title: A Remote Open-Label Long-Term Follow-up Study to Determine the Safety Tolerability and Efficacy of Rotigotine Transdermal System as Monotherapy in Adolescents With Restless Legs Syndrome
Status: TERMINATED
Status Verified Date: 2023-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Sponsor decision Not a safety decision
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the long-term safety tolerability and the long-term efficacy of rotigotine treatment in adolescents with idiopathic Restless Legs Syndrome RLS
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None