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COMPLETED Phase 2

A Study to Assess Safety and Tolerability of Oral AZD3241 in Patients With Parkinson's Disease

NCT01603069 · View on ClinicalTrials.gov ↗

Study Summary

This is a study where AZD3241 or placebo is given to patients with Parkinson's disease in a blinded and randomized assignment. The main objective is to see if safety and tolerability of the drug is acceptable.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG AZD3241 300 mg BID
  • DRUG AZD3241 600 mg BID

Study Locations (13)

Florida

  • Research Site — Atlantis
  • Research Site — Boca Raton
  • Research Site — Orlando
  • Research Site — Sunrise
  • Research Site — Tampa

New Jersey

  • Research Site — Lawrenceville
  • Research Site — Marlton

Alabama

  • Research Site — Birmingham

California

  • Research Site — Long Beach

Connecticut

  • Research Site — New Haven

Kansas

  • Research Site — Kansas City

Michigan

  • Research Site — Bingham Farms

Nebraska

  • Research Site — Omaha

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2012-10
Est. Completion 2013-06
Phase Phase 2

Sponsor

AstraZeneca

1,053 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01603069

The ClinicalTrials.gov registry entry for NCT01603069 describes a study currently listed as completed. It is categorized as Phase 2, 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 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,053 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 3 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: NCT01603069 reports 13 study locations spanning 8 distinct geographic areas — top geographies include Florida, New Jersey, Alabama. 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 NCT01603069 about?

NCT01603069 is a clinical study titled "A Study to Assess Safety and Tolerability of Oral AZD3241 in Patients With Parkinson's Disease". This is a study where AZD3241 or placebo is given to patients with Parkinson's disease in a blinded and randomized assignment. The main objective is to see if safety and tolerability of the drug is acceptable.

What is the current status of trial NCT01603069?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 51 participants. The study started on 2012-10. Estimated completion is 2013-06.

What conditions does trial NCT01603069 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 NCT01603069?

The interventions under investigation include: Placebo (DRUG), AZD3241 300 mg BID (DRUG), AZD3241 600 mg BID (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01603069?

This trial is sponsored by AstraZeneca, which has 1,053 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01603069 being conducted?

This trial has 13 study locations across Alabama, California, Connecticut, Florida, Kansas. 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