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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 Oct 21, 2026, 1:54 AM 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

Brief summary

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

This 2 arm study will compare the efficacy of intravenous Bondronat with that of zoledronic acid in patients with malignant bone disease experiencing moderate to severe pain. Patients will be randomized to receive either Bondronat (6mg iv on days 1, 2 and 3 and then every 3-4 weeks) or zoledronic acid (4mg iv on day 1 and then every 3-4 weeks). The anticipated time of study treatment is 6-12 months, and the target sample size is 100-500 individuals.

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

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
Jul 2005 (Type not available)
Primary completion
Dec 2007 (Actual)
Completion
Dec 2007 (Actual)
Last update posted
Aug 16, 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 16, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00099203 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →