Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 2

Efficacy and Safety of TAK-583 in Subjects With Diabetic Peripheral Neuropathy

NCT00760955 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine the safety and effectiveness of TAK-583, once daily (QD), in the treatment of neuropathy caused by diabetes mellitus.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG TAK-583

Study Locations (20)

Florida

  • — Largo
  • — Miami
  • — New Port Richey
  • — Palm Beach Gardens
  • — Sunrise
  • — West Palm Beach

California

  • — Huntington Beach
  • — La Jolla
  • — Los Angeles
  • — Pasadena
  • — Tustin

Arizona

  • — Mesa
  • — Peoria
  • — Phoenix
  • — Tucson

Arkansas

  • — Jonesboro

Georgia

  • — Decatur

Idaho

  • — Idaho Falls

Illinois

  • — Chicago

Massachusetts

  • — Boston

Trial Details

FieldValue
Enrollment Target 338 participants
Start Date 2006-09
Est. Completion 2008-02
Phase Phase 2

Sponsor

Takeda

387 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00760955

The ClinicalTrials.gov registry entry for NCT00760955 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 338 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Takeda, which has 387 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 Neuropathies 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: NCT00760955 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, 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 NCT00760955 about?

NCT00760955 is a clinical study titled "Efficacy and Safety of TAK-583 in Subjects With Diabetic Peripheral Neuropathy". The purpose of this study is to determine the safety and effectiveness of TAK-583, once daily (QD), in the treatment of neuropathy caused by diabetes mellitus.

What is the current status of trial NCT00760955?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 338 participants. The study started on 2006-09. Estimated completion is 2008-02.

What conditions does trial NCT00760955 study?

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

What interventions are being tested in trial NCT00760955?

The interventions under investigation include: Placebo (DRUG), TAK-583 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00760955?

This trial is sponsored by Takeda, which has 387 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00760955 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, Florida, Georgia. 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