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Completed Phase 4 Interventional Results available

Rasagiline as Add on to Dopamine Agonists in the Treatment of Parkinson's Disease

ClinicalTrials.gov ID: NCT01049984

Public ClinicalTrials.gov record NCT01049984. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 3:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-blind, Placebo Controlled, Randomized, Multicenter Study to Assess the Safety and Clinical Benefit of Rasagiline as an Add on Therapy to Stable Dose of Dopamine Agonists in the Treatment of Early Parkinson's Disease

Study identification

NCT ID
NCT01049984
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Teva Neuroscience, Inc.
Industry
Enrollment
328 participants

Conditions and interventions

Interventions

  • Rasagiline Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
30 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2009
Primary completion
Sep 30, 2012
Completion
Sep 30, 2012
Last update posted
May 19, 2016

2009 – 2012

United States locations

U.S. sites
58
U.S. states
30
U.S. cities
54
Facility City State ZIP Site status
Teva Investigational Site 34 Phoenix Arizona
Teva Investigational Site 42 Sun City Arizona
Teva Investigational Site 15 Fountain Valley California
Teva Investigational Site 19 Fresno California
Teva Investigational Site 36 Fresno California
Teva Investigational Site 04 La Jolla California
Teva Investigational Site 29 Reseda California
Teva Investigational Site 69 San Francisco California
Teva Investigational Site 02 Sunnyvale California
Teva Investigational Site 43 Ventura California
Teva Investigational Site 44 Fairfield Connecticut
Teva Investigational Site 07 Manchester Connecticut
Teva Investigational Site 25 Newark Delaware
Teva Investigative Site 63 Atlantis Florida
Teva Investigational Site 30 Boca Raton Florida
Teva Investigational Site 13 Clearwater Florida
Teva Investigational Site 70 Sunrise Florida
Teva Investigational Site 41 Tampa Florida
Teva Investigational Site 61 Vero Beach Florida
Teva Investigational Site 01 Decatur Georgia
Teva Investigational Site 58 Boise Idaho
Teva Investigational Site 49 Glenview Illinois
Teva Investigational Site 23 Peoria Illinois
Teva Investigational Site 47 Indianapolis Indiana
Teva Investigational Site 67 Indianapolis Indiana
Teva Investigational Site 76 Indianapolis Indiana
Teva Investigational Site 55 Des Moines Iowa
Teva Investigational Site 17 Lexington Kentucky
Teva Investigational Site 27 Paducah Kentucky
Teva Investigational Site 56 Scarborough Maine
Teva Investigational Site 62 Elkridge Maryland
Teva Investigational Site 51 Springfield Massachusetts
Teva Investigational Site 11 Detroit Michigan
Teva Investigational Site 33 West Bloomfield Michigan
Teva Investigational Site 39 Golden Valley Minnesota
Teva Investigational Site 22 St Louis Missouri
Teva Investigational Site 08 Great Falls Montana
Teva Investigational Site 59 Missoula Montana
Teva Investigational Site 60 Las Vegas Nevada
Teva Investigational Site 14 Somerset New Jersey
Teva Investigational Site 03 Commack New York
Teva Investigational Site 38 Plainview New York
Teva Investigational Site 05 Asheville North Carolina
Teva Investigational Site 31 Charlotte North Carolina
Teva Investigational Site 28 Raleigh North Carolina
Teva Investigational Site 26 Fargo North Dakota
Teva Investigational Site 35 Cincinnati Ohio
Teva Investigational Site 68 Cincinnati Ohio
Teva Investigational Site 64 Tulsa Oklahoma
Teva Investigational Site 21 Medford Oregon
Teva Investigational Site 40 Portland Oregon
Teva Investigative Site 65 Cordova Tennessee
Teva Investigational Site 71 Brownwood Texas
Teva Investigational Site 18 San Antonio Texas
Teva Investigational Site 32 Temple Texas
Teva Investigational Site 09 Richmond Virginia
Teva Investigational Site 46 Virginia Beach Virginia
Teva Investigational Site 77 Madison Wisconsin

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01049984, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 19, 2016 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01049984 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →