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COMPLETED Phase 2

Safety and Efficacy Study of QR-333 in Patient's With Symptomatic Diabetic Neuropathy

NCT00568035 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine whether QR-333 is safe and effective in the treatment of diabetic neuropathy as compared to placebo.

Conditions Studied

Interventions

  • DRUG QR-333

Study Locations (19)

Florida

  • Renstar Medical Research — Ocala
  • Baptist Clinical Research — Pensacola
  • Stedman Clinical Trails — Tampa
  • Metabolic Research Institute, Inc. — West Palm Beach

California

  • Pacific Sleep Medicine Services, Inc — Fountain Valley
  • Advanced Medical Research, LLC — Lakewood
  • Diablo Clinical Research, Inc. — Walnut Creek

Texas

  • UT Southwestern Medical Center at Dallas — Dallas
  • dgd Research — San Antonio
  • Endeavor Clinical Trials, PA — San Antonio

Alabama

  • Parkway Medical Center — Birmingham
  • Seale Harris Clinic / Alliance Clinical Research — Birmingham

New Jersey

  • Rwjms/Umdnj — New Brunswick
  • Land Clinical Studies — West Caldwell

Missouri

  • A&A Pain Institute — St Louis

New York

  • Kaleida Health, Diabetes Center of WNY — Buffalo

North Carolina

  • ECU Diabetes Research Center, Brody School of Medicine — Greenville

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2006-12
Est. Completion 2008-11
Phase Phase 2

Sponsor

Quigley Pharma

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00568035

The ClinicalTrials.gov registry entry for NCT00568035 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 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Quigley Pharma, which has 1 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 Diabetic Neuropathy appearing as the primary indexed condition, and to 1 intervention — of which QR-333 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: NCT00568035 reports 19 study locations spanning 10 distinct geographic areas — top geographies include Florida, California, Texas. 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 NCT00568035 about?

NCT00568035 is a clinical study titled "Safety and Efficacy Study of QR-333 in Patient's With Symptomatic Diabetic Neuropathy". The purpose of this study is to determine whether QR-333 is safe and effective in the treatment of diabetic neuropathy as compared to placebo.

What is the current status of trial NCT00568035?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 140 participants. The study started on 2006-12. Estimated completion is 2008-11.

What conditions does trial NCT00568035 study?

This clinical trial studies the following conditions: Diabetic Neuropathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00568035?

The interventions under investigation include: QR-333 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00568035?

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

Where is trial NCT00568035 being conducted?

This trial has 19 study locations across Alabama, California, Florida, Missouri, New Jersey. 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