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Clinical Trial Summary

This study will evaluate the safety/efficacy of zoledronic acid when given by intravenous infusion every 4 weeks in addition to letrozole as endocrine therapy in postmenopausal patients with hormone responsive breast cancer


Clinical Trial Description

Open-label, multicenter, randomized phase II trial over approx 6.5 months of neoadjuvant treatment with letrozole with or without zoledronic acid in postmenopausal patients with primary breast cancer. A total of approximately 850 patients were originally planned to be enrolled; primary study endpoint was the objective response rate (according to modified RECIST criteria) after 6 months of treatment. After the core study, patients willing to participate were followed-up for further 5 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00375752
Study type Interventional
Source Novartis
Contact
Status Terminated
Phase Phase 4
Start date June 1, 2006
Completion date December 16, 2010

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