Trial to Evaluate The Efficacy Of Rotigotine on Parkinson's Disease-Associated Motor Symptoms And Apathy

PHASE4CompletedINTERVENTIONAL
Enrollment

122

Participants

Timeline

Start Date

February 28, 2013

Primary Completion Date

January 31, 2014

Study Completion Date

March 31, 2014

Conditions
Idiopathic Parkinson's Disease
Interventions
DRUG

Rotigotine

"Rotigotine, transdermal patches:~10 cm\^2 (2 mg / 24 hours); 20 cm\^2 (4 mg / 24 hours); 30 cm\^2 (6 mg / 24 hours); 40 cm\^2 (8 mg / 24 hours)~The maximum Rotigotine dose allowed is 8 mg / 24 hours or 16 mg / 24 hours for patients with advanced Parkinson's Disease and 6 mg / 24 hours or 8 mg / 24 hours for those with early Parkinson's Disease Duration: up to 21 weeks (including de-escalation)"

OTHER

Placebo

"Placebo, matching transdermal patches~Duration: up to 21 weeks (including de-escalation)"

Trial Locations (42)

Unknown

4320, Birmingham

4309, Oxnard

4306, Ormond Beach

4311, Palm Beach Gardens

4313, Tampa

4314, Decatur

4318, Chicago

4316, Winfield

4322, Des Moines

4304, Kansas City

4326, Springfield

4330, Ocean Springs

4302, Las Vegas

4303, Commack

4317, New York

4323, New York

4319, Asheville

4325, Charlotte

4329, Akron

4312, Cincinnati

4324, Beaufort

4332, Charleston

4305, San Antonio

4307, Salt Lake City

4333, Virginia Beach

3001, Innsbruck

3003, Linz

3301, Budapest

3302, Debrecen

3509, Gdansk

3506, Gdynia

3504, Poznan

3801, Banská Bystrica

3805, Bratislava

3806, Krompachy

3807, Žilina

3901, Ljubljana

4001, Barcelona

4006, Barcelona

4009, Oviedo

4005, Seville

4010, Seville

All Listed Sponsors
lead

UCB BIOSCIENCES GmbH

INDUSTRY

NCT01782222 - Trial to Evaluate The Efficacy Of Rotigotine on Parkinson's Disease-Associated Motor Symptoms And Apathy | Biotech Hunter | Biotech Hunter