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A Randomized, Open-label Study of the Effect of Herceptin Plus Arimidex Compared With Arimidex Alone on Progression-free Survival in Patients With HER2-positive and Hormone-receptor Positive Metastatic Breast Cancer
This 2 arm study assessed the safety and efficacy of adding intravenous trastuzumab (Herceptin®) to daily oral anastrozole (Arimidex®) tablets as first- and second-line treatment in postmenopausal patients with human epidermal growth factor receptor-2 (HER2) overexpressing metastatic breast cancer (ER+ve and/or PR+ve). Patients were randomized to receive either anastrazole 1 mg per os (po) daily, or anastrazole 1 mg po daily + a loading dose of Herceptin® 4 mg/kg intravenous (iv) followed by weekly doses of Herceptin® 2 mg/kg iv. The anticipated time on study treatment was until disease progression, and the target sample size was 100-500 individuals.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
No
Phoenix, Arizona, United States
Little Rock, Arkansas, United States
Los Angeles, California, United States
Vallejo, California, United States
Gainsville, Florida, United States
Miami, Florida, United States
Plantation, Florida, United States
Chicago, Illinois, United States
Chicago, Illinois, United States
Kansas City, Kansas, United States
Start Date
January 1, 2001
Primary Completion Date
October 1, 2009
Completion Date
October 1, 2009
Last Updated
June 13, 2013
208
ACTUAL participants
trastuzumab (Herceptin®)
DRUG
anastrazole (Arimidex®)
DRUG
Lead Sponsor
Hoffmann-La Roche
Collaborators
NCT04550494
NCT05673200
Data Source & Attribution
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