Study identifier:1839IL/0128
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised phase II study: Treatment with daily p.o. Iressa™ (ZD1839) or placebo in combination with weekly IV infusion of docetaxel in patients with metastatic breast cancer
Metastatic Breast Cancer
Phase 2
No
Gefitinib, Docetaxel
Female
66
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
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