Safety and Efficacy of AQW051 in L-dopa Induced Dyskinesias in Patients With Parkinson's Disease

PHASE2CompletedINTERVENTIONAL
Enrollment

71

Participants

Timeline

Start Date

September 15, 2011

Primary Completion Date

February 21, 2013

Study Completion Date

February 21, 2013

Conditions
DyskinesiasDrug-induced
Interventions
DRUG

AQW051

Patients will receive AQW051 in a high dose once daily orally for 28 days.

DRUG

AQW051

Patients will receive AQW051 in a low dose once daily orally for 28 days.

DRUG

Placebo

Patients will receive placebo once daily orally for 28 days.

Trial Locations (24)

10178

Novartis Investigative Site, Berlin

11030

Novartis Investigative Site, Manhasset

13385

Novartis Investigative Site, Marseille

31059

Novartis Investigative Site, Toulouse

33604

Novartis Investigative Site, Pessac

34128

Novartis Investigative Site, Kassel

34295

Novartis Investigative Site, Montpellier

35039

Novartis Investigative Site, Marburg

44093

Novartis Investigative Site, Nantes

44195

Novartis Investigative Site, Cleveland

45219

Novartis Investigative Site, Cincinnati

59037

Novartis Investigative Site, Lille

63003

Novartis Investigative Site, Clermont Fd

67098

Novartis Investigative Site, Strasbourg

69677

Novartis Investigative Site, Bron

72076

Novartis Investigative Site, Tübingen

75013

Novartis Investigative Site, Paris

80804

Novartis Investigative Site, München

83527

Novartis Investigative Site, Haag

86021

Novartis Investigative Site, Poitiers

95817

Novartis Investigative Site, Sacramento

01307

Novartis Investigative Site, Dresden

07551

Novartis Investigative Site, Gera

00163

Novartis Investigative Site, Roma

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY