A Sleep Laboratory Study to Investigate the Safety and Efficacy of the Rotigotine Skin Patch in Subjects With Restless Legs Syndrome and End-Stage Renal Disease Requiring Hemodialysis

Completed · Phase 3 · Has a placebo group

Conditions studied: Restless Legs Syndrome, End-Stage Renal Disease

In brief

This is a sleep laboratory study to evaluate the efficacy and safety of Rotigotine in subjects with Restless Legs Syndrome and End-Stage Renal Disease requiring hemodialysis. The objectives are to demonstrate superiority of Rotigotine against Placebo as well as to investigate the effect of Rotigotine on quality of life and sleep.

Key facts

Study ID: NCT01537042
Run by: UCB BIOSCIENCES GmbH
People needed: 30
Starts: 2012-04-01
Expected to finish: 2013-10-01
Last updated by the study team: 2014-11-03

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

End-Stage Renal Disease (ESRD) requiring hemodialysis and regular dialysis schedule
Fulfillment of pre-defined criteria of hematology parameters
Diagnosis of Restless Legs (RLS) based on the 4 cardinal diagnostic clinical features according to the International Restless Legs Syndrome Study Group
Initial response to previous dopaminergic treatment for RLS, or has had no previous dopaminergic treatment (ie, de novo)
Score of ≥ 15 points on the IRLS (indicating moderate to severe RLS) at Baseline
Score of ≥ 11 points on the RLS-DI (Diagnostic Index) at Baseline
Score of ≥ 4 points on the Clinical Global Impressions (CGI) Item 1 assessment (indicating moderately ill) at Baseline
Scores ≥ 15 Periodic Limb Movements (PLMs) per hour on the Periodic Limb Movement Index (PLMI) based on Polysomnography (PSG) (recorded during the second night) as assessed by the investigator at Baseline

You may not qualify if…

Clinically relevant Polyneuropathy or Varicosis which cannot be clearly differentiated from RLS symptoms in the opinion of the investigator
Clinically relevant concomitant diseases, such as Attention Deficit Hyperactivity Disorder, Painful Legs, and Moving Toes
Other central nervous system diseases
Evidence of an impulse control disorder according to the modified Minnesota Impulsive Disorders Interview (mMIDI)
Lifetime history of suicide attempt (including an active attempt, interrupted attempt, or aborted attempt), or has suicidal ideation in the past 6 months as indicated by a positive response ('yes') to either Question 4 or Question 5 of the Columbia-Suicidality Severity Rating Scale (C-SSRS) at Screening (Visit 1) or Baseline (Visit 2)
Prior history of psychotic episodes
History of symptomatic (not asymptomatic) Orthostatic Hypotension
Clinically relevant Cardiovascular Disease
Clinically relevant Venous or Arterial Peripheral Vascular Disease
Malignant Neoplastic Disease requiring therapy within 12 months prior to Screening (Visit 1)
Treatment with any of the following drug classes: neuroleptics, norepinephrine and dopamine reuptake inhibitors (bupropion), gabapentin, budipine, dopamine antagonist antiemetics (except domperidone), opioids, monoamine oxidase (MAO) inhibitors, catechol-O-methyltransferase (COMT) inhibitors, or psychostimulants (eg, amphetamines)
Subject is pregnant, nursing, or is a woman of childbearing potential who is not surgically sterile, 2 years postmenopausal, or does not consistently use 2 combined effective methods of contraception (including at least 1 barrier method), unless sexually abstinent
Previous treatment with dopamine agonists within a period of 14 days prior to Baseline (Visit 2), or L-dopa within 7 days prior to Baseline (Visit 2)
Medical history indicating intolerability to dopaminergic therapy (if pretreated) or has experienced Augmentation (Garcia-Borreguero and Williams, 2010) when previously treated with any dopaminergic agent
Subject has received previous treatment with Rotigotine
Known hypersensitivity to any of the components of the study medication, such as a history of significant Skin Hypersensitivity to adhesives, known Hypersensitivity to other transdermal medications, or unresolved Contact Dermatitis

Where it is running

606 — Brandon, Florida, United States
604 — Newton, Massachusetts, United States
603 — West Seneca, New York, United States
607 — Dublin, Ohio, United States
605 — West Chester, Pennsylvania, United States
601 — Austin, Texas, United States
101 — Innsbruck, Austria
201 — Helsinki, Finland
203 — Tampere, Finland
302 — Bordeaux, France
301 — Montpellier Cédex 5, France
404 — Berlin, Germany
401 — Marburg, Germany
402 — Schwerin, Germany
502 — Pisa, Italy

Full record on ClinicalTrials.gov

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