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NCT00499629 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating the Safety of FXR-450 in Healthy Subjects

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

Completed
Registry status
Phase 1
Development phase
64
Enrollment target

NCT00499629 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 64 participants.

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The verdict

NCT00499629, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
64 participants
Enrollment target

Study Summary

The primary purpose of the study is to evaluate the safety of FXR-450 in healthy subjects. This study will also evaluate pharmacokinetics (PK) of FXR-450 in healthy subjects.

Interventions

  • DRUG placebo
  • DRUG FXR 450

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2007-10
Est. Completion 2008-02
Phase Phase 1

What the Registry Record Tells You About NCT00499629

The ClinicalTrials.gov registry entry for NCT00499629 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 64 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 2 interventions - of which placebo is the first listed.

NCT00499629 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00499629 about?

NCT00499629 is a clinical study titled "Study Evaluating the Safety of FXR-450 in Healthy Subjects". The primary purpose of the study is to evaluate the safety of FXR-450 in healthy subjects. This study will also evaluate pharmacokinetics (PK) of FXR-450 in healthy subjects.

What is the current status of trial NCT00499629?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 64 participants. The study started on 2007-10. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00499629?

The interventions under investigation include: placebo (DRUG), FXR 450 (DRUG).

Who is sponsoring clinical trial NCT00499629?

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.