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Completed Phase 4 Interventional

PRIOR Study - A Study of Ibandronate (Boniva) in Postmenopausal Women With Osteoporosis or Osteopenia

ClinicalTrials.gov ID: NCT02598453

Public ClinicalTrials.gov record NCT02598453. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 23, 2026, 6:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label, Multi-Center Study to Determine Level of Adherence to Monthly Oral or Every Three Month Intravenous Ibandronate Treatment in Post-Menopausal Women With Osteoporosis or Osteopenia, Who Are GI Intolerant of Daily or Weekly Alendronate or Risendronate

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate treatment adherence to different regimens of ibandronate in postmenopausal women with osteoporosis or osteopenia who are intolerant to daily or weekly alendronate or risedronate therapy due to gastrointestinal (GI) side effects. The anticipated time on study treatment is 12 months, and the target sample size is 517 individuals.

Study identification

NCT ID
NCT02598453
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
545 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
Not listed
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2005 (Type not available)
Primary completion
Sep 2006 (Actual)
Completion
Sep 2006 (Actual)
Last update posted
Nov 2, 2016

2005 – 2006

United States locations

U.S. sites
60
U.S. states
30
U.S. cities
56
Facility City State ZIP Site status
Not listed Montgomery Alabama 36116 —
Not listed Lake Havasu City Arizona 86403 —
Not listed Paradise Valley Arizona 85253 —
Not listed Pine Bluff Arkansas 71603 —
Not listed San Diego California 92103 —
Not listed San Diego California 92108 —
Not listed Santa Monica California 90404 —
Not listed Tacoma California 98405 —
Not listed Vista California 92083 —
Not listed Beverly Hills Florida 34464 —
Not listed Fort Myers Florida 33901 —
Not listed Gainesville Florida 32605 —
Not listed Miami Florida 33186 —
Not listed Ocala Florida 34471 —
Not listed Palm Harbor Florida 34684 —
Not listed West Palm Beach Florida 33409 —
Not listed Augusta Georgia 30904 —
Not listed Coeur d'Alene Idaho 83814 —
Not listed Champaign Illinois 61820 —
Not listed Evansville Indiana 47714 —
Not listed Natchitoches Louisiana 71457 —
Not listed South Portland Maine 04106 —
Not listed Detroit Michigan 48202-2689 —
Not listed Detroit Michigan 48236 —
Not listed Chaska Minnesota 55318 —
Not listed Kansas City Missouri 64114 —
Not listed St Louis Missouri 63033 —
Not listed Billings Montana 59101 —
Not listed Broken Bow Nebraska 68822 —
Not listed Scottsbluff Nebraska 69361 —
Not listed Las Vegas Nevada 89104 —
Not listed Albuquerque New Mexico 87106 —
Not listed New York New York 10003 —
Not listed West Haverstraw New York 10993 —
Not listed Charlotte North Carolina 28209 —
Not listed Durham North Carolina 27704 —
Not listed Salisbury North Carolina 28144 —
Not listed Winston-Salem North Carolina 27103 —
Not listed Bismarck North Dakota 58501 —
Not listed Fargo North Dakota 58104 —
Not listed Canfield Ohio 44406 —
Not listed Columbus Ohio 43213 —
Not listed Mayfield Ohio 44143 —
Not listed Oklahoma City Oklahoma 73112 —
Not listed Wyomissing Pennsylvania 19610 —
Not listed Loris South Carolina 29569 —
Not listed Mt. Pleasant South Carolina 29464 —
Not listed Sioux Falls South Dakota 57105 —
Not listed Watertown South Dakota 57201 —
Not listed Bristol Tennessee 37620 —
Not listed Dallas Texas 75231 —
Not listed Denton Texas 76210 —
Not listed San Antonio Texas 78229 —
Not listed San Antonio Texas 78238 —
Not listed Seguin Texas 78155 —
Not listed Temple Texas 76508 —
Not listed Norfolk Virginia 23502 —
Not listed Richmond Virginia 23294 —
Not listed Richmond Virginia 23298 —
Not listed Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02598453, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 2, 2016 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02598453 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →