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NCT00651534 · ClinicalTrials.gov registry record · Phase 1

To Estimate Relative Bioavailability of 5 Formulations of Ronacaleret Given to Healthy Postmenopausal Females

A Phase 1 study, sponsored by GlaxoSmithKline.

Completed
Registry status
Phase 1
Development phase
32
Enrollment target

NCT00651534 is a Phase 1 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 32 participants.

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The verdict

NCT00651534, a Phase 1 study, has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
Phase 1
Development phase
32 participants
Enrollment target

Study Summary

This study will examine the effects of formulation on the relative bioavailability of SB-751689 (400 mg) administered to healthy postmenopausal women. Subjects will receive a single oral dose of each formulation, with five formulations of SB-751689 tested in total. Blood samples will be taken up to 24 hours postdose after each dose administration. This study will provide information for future possible formulation development of SB-751689 for Phase III.

Interventions

  • DRUG Ronacaleret

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2008-02
Phase Phase 1

Sponsor

GlaxoSmithKline

1,345 total trials

What the Registry Record Tells You About NCT00651534

The ClinicalTrials.gov registry entry for NCT00651534 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.

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

NCT00651534 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00651534 about?

NCT00651534 is a clinical study titled "To Estimate Relative Bioavailability of 5 Formulations of Ronacaleret Given to Healthy Postmenopausal Females". This study will examine the effects of formulation on the relative bioavailability of SB-751689 (400 mg) administered to healthy postmenopausal women. Subjects will receive a single oral dose of each formulation, with five formulations of SB-751689 tested in total. Blood samples will be taken up to ...

What is the current status of trial NCT00651534?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2008-02.

What interventions are being tested in trial NCT00651534?

The interventions under investigation include: Ronacaleret (DRUG).

Who is sponsoring clinical trial NCT00651534?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

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

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.