Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
ADAGIO Follow Up Study: Evaluation of the Long-Term Effects of Rasagiline in Parkinson's Disease Subjects
NCT00936676 · View on ClinicalTrials.gov ↗
Study Summary
Eligible participants, who participated in the ADAGIO trial and who sign an approved informed consent form, will be enrolled into the study at their original study locations. participants who have stopped rasagiline therapy and in the opinion of the investigator will gain clinical benefit from restarting treatment can also be considered for enrollment in the Core follow-up study period. Use of any other anti-PD treatment is permitted as deemed necessary by the treating physician (according to the participants clinical status).
Conditions Studied
Interventions
- DRUG rasagiline mesylate
Study Locations (20)
California
- Teva Investigational Site 7018 — Irvine
- Teva Investigational Site 7019 — La Jolla
- Teva Investigational Site 7039 — Loma Linda
- Teva Investigational Site 7023 — Los Angeles
- Teva Investigational Site 7022 — Sunnyvale
Florida
- Teva Investigational Site 7020 — Boca Raton
- Teva Investigational Site 7011 — Gainesville
- Teva Investigational Site 7045 — Miami
- Teva Investigational Site 7017 — Tampa
Illinois
- Teva Investigational Site 7013 — Chicago
- Teva Investigational Site 7052 — Chicago
- Teva Investigational Site 7001 — Northbrook
- Teva Investigational Site 7008 — Springfield
Connecticut
- Teva Investigational Site 7024 — Danbury
- Teva Investigational Site 7016 — Farmington
Georgia
- Teva Investigational Site 7055 — Atlanta
- Teva Investigational Site 7043 — Augusta
Alabama
- Teva Investigational Site 7054 — Birmingham
Arizona
- Teva Investigational Site 7006 — Tucson
Iowa
- Teva Investigational Site 7037 — Des Moines
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 684 participants |
| Start Date | 2009-07 |
| Est. Completion | 2013-03 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00936676
The ClinicalTrials.gov registry entry for NCT00936676 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 684 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 103 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Parkinson's Disease appearing as the primary indexed condition, and to 1 intervention — of which rasagiline mesylate is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00936676 reports 20 study locations spanning 8 distinct geographic areas — top geographies include California, Florida, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00936676 about?
NCT00936676 is a clinical study titled "ADAGIO Follow Up Study: Evaluation of the Long-Term Effects of Rasagiline in Parkinson's Disease Subjects". Eligible participants, who participated in the ADAGIO trial and who sign an approved informed consent form, will be enrolled into the study at their original study locations. participants who have stopped rasagiline therapy and in the opinion of the investigator will gain clinical benefit from resta...
What is the current status of trial NCT00936676?
This trial is currently completed. The enrollment target is 684 participants. The study started on 2009-07. Estimated completion is 2013-03.
What conditions does trial NCT00936676 study?
This clinical trial studies the following conditions: Parkinson's Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00936676?
The interventions under investigation include: rasagiline mesylate (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00936676?
This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 103 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00936676 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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