A Study to Assess the Efficacy of Intravenous/Oral Bondronat (Ibandronate) in Patients With Metastatic Bone Disease Experiencing Moderate to Severe Pain

Roche

Status and phase: Terminated; Phase 3

Conditions: Bone Neoplasm; Neoplasm Metastasis; Pain

Treatments: Drug: zoledronic acid; Drug: ibandronate [Bondronat]

Study type: Interventional

Funder types: Industry

Identifiers

NCT00099177

BO18039

Details and patient eligibility

About

This 2 arm study will compare the efficacy of a regimen of intravenous (iv) and oral 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 followed by Bondronat 5Omg po daily from day 22 to week 24) 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.

Enrollment: 96 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients with malignant bone disease;
• patients with moderate to severe pain.

Exclusion criteria

• patients who have received a bisphosphonate within 3 weeks from the signing of informed consent;
• patients receiving concurrent investigational therapy, or who have received investigational therapy within 30 days of the first scheduled day of dosing;
• untreated esophagitis or gastric ulcers;
• recent or pre-scheduled radiotherapy to bone;
• patients who are pregnant or breast-feeding.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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96 participants in 2 patient groups

1

Experimental group

Treatment:

Drug: ibandronate [Bondronat]

2

Active Comparator group

Treatment:

Drug: zoledronic acid