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NCT00424892 · ClinicalTrials.gov registry record · Phase 2

Study Evaluating DVS SR in Patients With Fibromyalgia Syndrome

A Phase 2 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Completed
Registry status
Phase 2
Development phase
600
Enrollment target

NCT00424892 is a Phase 2 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 600 participants.

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The verdict

NCT00424892, a Phase 2 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
600 participants
Enrollment target

Study Summary

The primary objective is to evaluate the long-term safety of desvenlafaxine succinate sustained-release (DVS SR) during open-label treatment in adult outpatients with fibromyalgia syndrome.

Interventions

  • DRUG Desvenlafaxine Sustained Release

Trial Details

FieldValue
Enrollment Target 600 participants
Est. Completion 2007-06
Phase Phase 2

What the Registry Record Tells You About NCT00424892

The ClinicalTrials.gov registry entry for NCT00424892 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Desvenlafaxine Sustained Release is the first listed.

NCT00424892 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00424892 about?

NCT00424892 is a clinical study titled "Study Evaluating DVS SR in Patients With Fibromyalgia Syndrome". The primary objective is to evaluate the long-term safety of desvenlafaxine succinate sustained-release (DVS SR) during open-label treatment in adult outpatients with fibromyalgia syndrome.

What is the current status of trial NCT00424892?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 600 participants. Estimated completion is 2007-06.

What interventions are being tested in trial NCT00424892?

The interventions under investigation include: Desvenlafaxine Sustained Release (DRUG).

Who is sponsoring clinical trial NCT00424892?

This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.