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Terminated Phase 3 Interventional

A Study to Assess the Efficacy of Intravenous Bondronat (Ibandronate) in Patients With Malignant and Painful Bone Disease

ClinicalTrials.gov ID: NCT00099203

Public ClinicalTrials.gov record NCT00099203. 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 Jul 21, 2026, 4:51 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

A Randomized, Placebo-controlled, Double-blind Study of the Effect of Bondronat Compared With Zoledronic Acid on Pain in Patients With Malignant Bone Disease Experiencing Moderate to Severe Pain

Study identification

NCT ID
NCT00099203
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
163 participants

Conditions and interventions

Interventions

  • ibandronate [Bondronat] Drug
  • zoledronic acid Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jun 30, 2005
Primary completion
Nov 30, 2007
Completion
Nov 30, 2007
Last update posted
Aug 15, 2017

2005 – 2007

United States locations

U.S. sites
26
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Not listed Birmingham Alabama 35205
Not listed Sedona Arizona 86336
Not listed Ocoee Florida 34761
Not listed Macon Georgia 31201
Not listed Galesburg Illinois 61401
Not listed Indianapolis Indiana 46227
Not listed Kansas City Missouri 64131
Not listed Henderson Nevada 89052
Not listed Reno Nevada 89502
Not listed Albany New York 12208
Not listed Oklahoma City Oklahoma 73120
Not listed Eugene Oregon 97401-8122
Not listed Nashville Tennessee 37209
Not listed Abilene Texas 79606-5208
Not listed Arlington Texas 76014
Not listed Beaumont Texas 77702-1449
Not listed Dallas Texas 75230
Not listed Dallas Texas 75231
Not listed Fort Worth Texas 76177
Not listed Fredericksburg Texas 78624
Not listed Longview Texas 75601
Not listed Round Rock Texas 78681
Not listed Norfolk Virginia 23502
Not listed Seattle Washington 98104
Not listed Spokane Washington 99218
Not listed Vancouver Washington 98684

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 46 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00099203, 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 Aug 15, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00099203 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →