Study identifier:9238IL/0048
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Double Blind, Multicenter Study to Compare the Efficacy and Tolerability of Fulvestrant (FASLODEX™) vs. Exemestane (AROMASIN™) in Postmenopausal Women with Hormone Receptor Positive Advanced Breast Cancer with Disease Progression after Prior Non-Steroidal Aromatase Inhibitor (AI) Therapy
Locally advanced breast cancer
Phase 3
No
Fulvestrant, Exemestane
Female
694
Interventional
32 Years - 91 Years
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Feb 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of this study is to compare the efficacy of Faslodex (fulvestrant) to Aromasin (exemestane) in hormone receptor positive postmenopausal women with advanced breast cancer. Patients will be treated until disease progression or until the investigator has determined that treatment is not in the best interest of the patient, whichever occurs first.
Location
Location
BUENOS AIRES, Buenos Aires, Argentina
Location
CIUDAD DE BUENOS AIRES, Buenos Aires, Argentina
Location
MAR DEL PLATA, Buenos Aires, Argentina
Location
ROSARIO, SANTA FE, Argentina
Location
BRUSSELS, BELGIUM, Belgium
Location
LEUVEN, BELGIUM, Belgium
Location
OTTIGNIES, BELGIUM, Belgium
Location
WILRIJK, BELGIUM, Belgium
Arms | Assigned Interventions |
---|---|
Active Comparator: 1 Exemestane | Drug: Exemestane oral capsule Other Name: AROMASIN™ |
Experimental: 2 Fulvestrant | Drug: Fulvestrant intramuscular injection Other Name: Faslodex Other Name: ZD9238 |
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