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A Prospective, Randomized, Double-blind, Stratified, Multi-center, 2-arm Trial of the Continued Efficacy and Safety of Zoledronic Acid (Every 4 Weeks vs. Every 12 Weeks) in in the 2nd Year of Treatment in Patients With Documented Bone Metastases From Breast Cancer
Clinical trial in breast cancer patients with bone metastases pretreated for approximately 1 year with a standard zoledronic acid regimen. Looking at the continued effectiveness and safety of giving zoledronic acid every 4 weeks versus every 12 weeks given over 1 year. This study is prospective, double-blind, stratified, multi-center, and two-arm.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Providence Alaska Medical Center Cancer Research
Anchorage, Alaska, United States
Heritage Physicians Group Oncology
Hot Springs, Arkansas, United States
The Center for Chest Care
Springdale, Arkansas, United States
Pacific Cancer Medical Center, Inc.
Anaheim, California, United States
South Bay Oncology Hematology Partners
Campbell, California, United States
Bay Area Cancer Research
Concord, California, United States
Pacific Coast Hem/Onc
Fountain Valley, California, United States
Wilshire Oncology Medical Group
La Verne, California, United States
Kenmar Research Institute
Los Angeles, California, United States
North Valley Hematology/Oncology Providence Holy Cross Medical
Northridge, California, United States
Start Date
February 1, 2006
Primary Completion Date
July 1, 2013
Completion Date
July 1, 2013
Last Updated
August 22, 2014
416
ACTUAL participants
Zoledronic acid
DRUG
Placebo
DRUG
Lead Sponsor
Novartis Pharmaceuticals
NCT04550494
NCT05673200
Data Source & Attribution
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