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COMPLETED Phase 2

Comparison of IPX054 and Immediate-Release Carbidopa-Levodopa in Patients With Parkinson's Disease

NCT00253084 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare the clinical efficacy of IPX054 to immediate-release carbidopa-levodopa in subjects with Parkinson's disease.

Conditions Studied

Interventions

  • DRUG IPX054 200 mg
  • DRUG CD-LD IR
  • DRUG IPX054 Placebo
  • DRUG CD-LD IR Placebo

Study Locations (2)

Illinois

  • Site 1 — Chicago

South Carolina

  • Site 2 — Charleston

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2005-11
Est. Completion 2007-12
Phase Phase 2

Sponsor

Impax Laboratories

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00253084

The ClinicalTrials.gov registry entry for NCT00253084 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 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Impax Laboratories, which has 6 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 4 interventions — of which IPX054 200 mg 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: NCT00253084 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Illinois, South Carolina. 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 NCT00253084 about?

NCT00253084 is a clinical study titled "Comparison of IPX054 and Immediate-Release Carbidopa-Levodopa in Patients With Parkinson's Disease". The purpose of this study is to compare the clinical efficacy of IPX054 to immediate-release carbidopa-levodopa in subjects with Parkinson's disease.

What is the current status of trial NCT00253084?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 12 participants. The study started on 2005-11. Estimated completion is 2007-12.

What conditions does trial NCT00253084 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 NCT00253084?

The interventions under investigation include: IPX054 200 mg (DRUG), CD-LD IR (DRUG), IPX054 Placebo (DRUG), CD-LD IR Placebo (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00253084?

This trial is sponsored by Impax Laboratories, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00253084 being conducted?

This trial has 2 study locations across Illinois, South Carolina. 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