drugset / Trial / NCT00375427

Safety and Efficacy of Zoledronic Acid in Patients With Breast Cancer With Metastatic Bone Lesions

NCT00375427

Phase 3 Completed 430 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The objective of this study is to assess the clinical benefit of two different dosing schedules of zoledronic acid in patients with metastatic bone lesions from breast cancer who have already been treated with zoledronic acid for about one year.

Timeline

Start
2006-02
Primary completion
2010-02
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Zoledronic acid Other / unclassified 3 mg Intravenous
Subject Zoledronic acid Other / unclassified 3.3 mg Intravenous
Subject Zoledronic acid Other / unclassified 3.5 mg Intravenous
Subject Zoledronic acid Other / unclassified 4 mg Intravenous

Indications