Study identifier:1839US/0713
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Phase II Multicenter, Double-Blind, Randomized Trial Comparing Anastrozole (ZD1033, Arimidex™)-Placebo to the Combination Anastrozole-ZD1839 (gefitinib, IRESSA™) in Postmenopausal Patients with Estrogen Receptor (ER) and/or Progesterone Receptor (PgR) Metastatic Breast Cancer
Breast Cancer
Phase 2
No
Gefitinib, Anastrozole
Female
174
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Jul 2014 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Active Comparator: Anastrozole-placebo Anastrozole (ZD1033, Arimidex)-Placebo | Drug: Anastrozole 1 mg Anastrozole (ZD1033, Arimidex) + PLACEBO 1 TABLET/DAY PO Other Name: Arimidex |
Active Comparator: Anastrozole-ZD1839 Anastrozole (ZD1033, Arimidex)-ZD1839 (gefitinib, IRESSA) | Drug: Gefitinib ZD1839 (gefitinib, IRESSA) 250 mg/DAY PO + 1 mg Anastrozole (ZD1033, Arimidex) Other Name: IRESSA |