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NCT00543790 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating PRA-027 Multiple Ascending Doses In Cycling And Postmenopausal Women

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

Completed
Registry status
Phase 1
Development phase
48
Enrollment target

NCT00543790 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 48 participants.

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The verdict

NCT00543790, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
48 participants
Enrollment target

Study Summary

This is the first multiple-dose study in humans with PRA-027. This study will provide an assessment of the safety, tolerability, pharmacokinetics (how the drug is absorbed, metabolized and excreted by the body) and pharmacodynamics (a measure of whether the drug is active in the body) of PRA-027 after administration of 28 days of oral doses in women of childbearing potential (cycling) or postmenopausal women.

Interventions

  • DRUG PRA-027

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2007-11
Est. Completion 2008-12
Phase Phase 1

What the Registry Record Tells You About NCT00543790

The ClinicalTrials.gov registry entry for NCT00543790 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 48 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 PRA-027 is the first listed.

NCT00543790 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00543790 about?

NCT00543790 is a clinical study titled "Study Evaluating PRA-027 Multiple Ascending Doses In Cycling And Postmenopausal Women". This is the first multiple-dose study in humans with PRA-027. This study will provide an assessment of the safety, tolerability, pharmacokinetics (how the drug is absorbed, metabolized and excreted by the body) and pharmacodynamics (a measure of whether the drug is active in the body) of PRA-027 aft...

What is the current status of trial NCT00543790?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2007-11. Estimated completion is 2008-12.

What interventions are being tested in trial NCT00543790?

The interventions under investigation include: PRA-027 (DRUG).

Who is sponsoring clinical trial NCT00543790?

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.