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COMPLETED Phase 4

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

NCT01049984 · View on ClinicalTrials.gov ↗

Study Summary

To assess the efficacy of rasagiline 1 mg as a first add-on treatment to dopamine agonist therapy in early Parkinson Disease (PD) patients, , not optimally controlled on dopamine agonists as compared to placebo.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Rasagiline

Study Locations (20)

California

  • Teva Investigational Site 15 — Fountain Valley
  • Teva Investigational Site 19 — Fresno
  • Teva Investigational Site 36 — Fresno
  • Teva Investigational Site 04 — La Jolla
  • Teva Investigational Site 29 — Reseda
  • Teva Investigational Site 69 — San Francisco
  • Teva Investigational Site 02 — Sunnyvale
  • Teva Investigational Site 43 — Ventura

Florida

  • Teva Investigative Site 63 — Atlantis
  • Teva Investigational Site 30 — Boca Raton
  • Teva Investigational Site 13 — Clearwater
  • Teva Investigational Site 70 — Sunrise
  • Teva Investigational Site 41 — Tampa
  • Teva Investigational Site 61 — Vero Beach

Arizona

  • Teva Investigational Site 34 — Phoenix
  • Teva Investigational Site 42 — Sun City

Connecticut

  • Teva Investigational Site 44 — Fairfield
  • Teva Investigational Site 07 — Manchester

Delaware

  • Teva Investigational Site 25 — Newark

Georgia

  • Teva Investigational Site 01 — Decatur

Trial Details

FieldValue
Enrollment Target 328 participants
Start Date 2009-12
Est. Completion 2012-10
Phase Phase 4

Sponsor

Teva Neuroscience

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01049984

The ClinicalTrials.gov registry entry for NCT01049984 describes a study currently listed as completed. It is categorized as Phase 4, 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 328 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Neuroscience, which has 2 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 2 interventions — of which Placebo 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: NCT01049984 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT01049984 about?

NCT01049984 is a clinical study titled "Rasagiline as Add on to Dopamine Agonists in the Treatment of Parkinson's Disease". To assess the efficacy of rasagiline 1 mg as a first add-on treatment to dopamine agonist therapy in early Parkinson Disease (PD) patients, , not optimally controlled on dopamine agonists as compared to placebo.

What is the current status of trial NCT01049984?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 328 participants. The study started on 2009-12. Estimated completion is 2012-10.

What conditions does trial NCT01049984 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 NCT01049984?

The interventions under investigation include: Placebo (DRUG), Rasagiline (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01049984?

This trial is sponsored by Teva Neuroscience, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01049984 being conducted?

This trial has 20 study locations across Arizona, California, Connecticut, Delaware, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial