drugset / Trial / NCT00434317

Assessment of Pain and Quality of Life in Breast and Prostate Cancer Patients With Bone Metastases

NCT00434317

Phase 4 Completed 80 enrolled Novartis
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety, tolerability and efficacy of zoledronic acid administered intravenously every 3-4 weeks in patients with bone metastases from either breast cancer or prostate cancer.

Timeline

Start
2005-08
Primary completion
2008-04
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Zoledronic acid Other / unclassified Intravenous

Indications