Efficacy of Orally Disintegrating Selegiline in Parkinson's Patients Experiencing Adverse Effects With Dopamine Agonists

PHASE4CompletedINTERVENTIONAL
Enrollment

77

Participants

Timeline

Start Date

March 31, 2007

Primary Completion Date

September 30, 2008

Study Completion Date

December 31, 2008

Conditions
Parkinson's Disease
Interventions
DRUG

orally disintegrating selegiline (Zelapar)

1.25 mg once daily orally disintegrating selegiline for 6 weeks with an increase to 2.5 mg once daily orally disintegrating selegiline for remaining 6 weeks if tolerated

Trial Locations (17)

33486

Parkinson's Disease and Movement Disorder Center of Boca Raton, Boca Raton

33606

University of South Florida, Tampa

43614

University of Toledo, Toledo

48034

Henry Ford Health Center - Franklin Pointe, Southfield

50309

Methodist Plaza Speciality Clinic, Des Moines

55427

Struthers Parkinson's Center, Golden Valley

66160

University of Kansas Medical Center, Kansas City

70121

Ochsner Clinic Foundation, New Orleans

75231

Neurology Specialists Dallas, Dallas

75701

ETMC Neurological Institute, Tyler

90093

University of Southern California, Los Angeles

92037

Coastal Neurological Medical Group, Inc, La Jolla

92697

University of California - Irvine, Irvine

94085

The Parkinson's Institute, Sunnyvale

02215

Beth Israel Deaconess Medical Center, Boston

Harvard Vanguard Medical Associates, Boston

02886

NeuroHealth Parkinson Disease and Movement Disorder Center, Warwick

All Listed Sponsors
collaborator

Bausch Health Americas, Inc.

INDUSTRY

lead

Parkinson's Disease and Movement Disorder Center of Boca Raton

OTHER

NCT00443872 - Efficacy of Orally Disintegrating Selegiline in Parkinson's Patients Experiencing Adverse Effects With Dopamine Agonists | Biotech Hunter | Biotech Hunter