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NCT00760955 · ClinicalTrials.gov registry record · Phase 2
Efficacy and Safety of TAK-583 in Subjects With Diabetic Peripheral Neuropathy
A Phase 2 study of Diabetic Neuropathies, sponsored by Takeda.
- Completed
- Registry status
- Phase 2
- Development phase
- 338
- Enrollment target
- 20
- Study locations
NCT00760955 is a Phase 2 study of Diabetic Neuropathies that has completed, run by Takeda. The registered enrollment target is 338 participants, above the 286-participant average among 8 other Diabetic Neuropathies trials with a reported enrollment target (18% higher). The trial reports 20 study locations across 8 states.
The verdict
NCT00760955, a Phase 2 study of Diabetic Neuropathies, has completed, sponsored by Takeda.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 338 participants
- Enrollment target
- 20
- Study locations
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
| Field | Value |
|---|---|
| Enrollment Target | 338 participants |
| Start Date | 2006-09 |
| Est. Completion | 2008-02 |
| Phase | Phase 2 |
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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, categorized as Phase 2. The registered enrollment target is 338 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 286-participant average among 8 other Diabetic Neuropathies trials with a reported enrollment target (18% higher). The listed sponsor is Takeda, which has 408 total studies on file at ClinicalTrials.gov.
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.
NCT00760955 reports 20 study locations spanning 8 distinct geographic areas - top geographies include Florida, California, Arizona.
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.
What interventions are being tested in trial NCT00760955?
The interventions under investigation include: Placebo (DRUG), TAK-583 (DRUG).
Who is sponsoring clinical trial NCT00760955?
This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.
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.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.