drugset / Trial / NCT00128297

Pamidronate Administration in Breast Cancer Patients With Bone Metastases

NCT00128297

RandomizedParallel-groupOpen-labelOther

Summary

The study objective is to evaluate the differences, in terms of first occurrence of a skeletal event, in patients with breast cancer and symptomatic bone metastases, when pamidronate is administered during 2 years, or when it is administered during 6 months, followed by a six month rest period, and again a 6 month treatment period.

Timeline

Start
2000-10-18
Primary completion
2004-06-04
Completion
2004-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Pamidronate Small molecule 90 mg/m2 Intravenous