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

NCT00440427 · ClinicalTrials.gov registry record · Phase 1

Study Evalutating the Pharmacokinetics (PK) and Safety of a Single Dose of Desvenlafaxine Sustained Release (DVS SR)

A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Completed
Registry status
Phase 1
Development phase
12
Enrollment target

NCT00440427 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 12 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00440427, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
12 participants
Enrollment target

Study Summary

To assess the initial pharmacokinetic profile of single doses of 25mg and 50 mg of DVS SR to healthy subjects.

Interventions

  • DRUG Desvenlafaxine Sustained Release (DVS SR)

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2007-02
Est. Completion 2007-02
Phase Phase 1

What the Registry Record Tells You About NCT00440427

The ClinicalTrials.gov registry entry for NCT00440427 describes a study currently listed as completed, categorized as Phase 1. 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 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 (DVS SR) is the first listed.

NCT00440427 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00440427 about?

NCT00440427 is a clinical study titled "Study Evalutating the Pharmacokinetics (PK) and Safety of a Single Dose of Desvenlafaxine Sustained Release (DVS SR)". To assess the initial pharmacokinetic profile of single doses of 25mg and 50 mg of DVS SR to healthy subjects.

What is the current status of trial NCT00440427?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2007-02. Estimated completion is 2007-02.

What interventions are being tested in trial NCT00440427?

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

Who is sponsoring clinical trial NCT00440427?

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.