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NCT00699777 · ClinicalTrials.gov registry record · Phase 1

Assess Bioequivalence of One 150 mg Risedronate Tablet Versus Two 75 mg Risedronate Tablets in Healthy Subjects

A Phase 1 study of Osteoporosis, sponsored by Warner Chilcott.

Completed
Registry status
Phase 1
Development phase
96
Enrollment target
4
Study locations

NCT00699777 is a Phase 1 study of Osteoporosis that has completed, run by Warner Chilcott. The registered enrollment target is 96 participants, below the 1,545-participant average among 84 other Osteoporosis trials with a reported enrollment target (94% lower). The trial reports 4 study locations across 2 states.

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The verdict

NCT00699777, a Phase 1 study of Osteoporosis, has completed, sponsored by Warner Chilcott.

COMPLETED
Registry status
Phase 1
Development phase
96 participants
Enrollment target
4
Study locations

Study Summary

This study is a randomized, open-label, crossover study to assess the bioequivalence of 1 risedronate 150 mg tablet versus 2 risedronate 75 mg tablets administered as a single oral dose. Approximately 320 subjects will be enrolled from 4 study centers in the U.S.

Conditions Studied

Interventions

  • DRUG Risedronate

Study Locations (4)

Florida

  • Research Site - Gainesville
  • Research Facility - Miramar

Texas

  • Research Facility - Austin
  • Research Facility - Dallas

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2008-01
Est. Completion 2008-04
Phase Phase 1

Sponsor

Warner Chilcott

53 total trials

What the Registry Record Tells You About NCT00699777

The ClinicalTrials.gov registry entry for NCT00699777 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 96 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,545-participant average among 84 other Osteoporosis trials with a reported enrollment target (94% lower). The listed sponsor is Warner Chilcott, which has 53 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Osteoporosis appearing as the primary indexed condition, and to 1 intervention - of which Risedronate is the first listed.

NCT00699777 reports 4 study locations spanning 2 distinct geographic areas - top geographies include Florida, Texas.

Frequently Asked Questions

What is clinical trial NCT00699777 about?

NCT00699777 is a clinical study titled "Assess Bioequivalence of One 150 mg Risedronate Tablet Versus Two 75 mg Risedronate Tablets in Healthy Subjects". This study is a randomized, open-label, crossover study to assess the bioequivalence of 1 risedronate 150 mg tablet versus 2 risedronate 75 mg tablets administered as a single oral dose. Approximately 320 subjects will be enrolled from 4 study centers in the U.S.

What is the current status of trial NCT00699777?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 96 participants. The study started on 2008-01. Estimated completion is 2008-04.

What conditions does trial NCT00699777 study?

This clinical trial studies the following conditions: Osteoporosis.

What interventions are being tested in trial NCT00699777?

The interventions under investigation include: Risedronate (DRUG).

Who is sponsoring clinical trial NCT00699777?

This trial is sponsored by Warner Chilcott, which has 53 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00699777 being conducted?

This trial has 4 study locations across Florida, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.