Study identifier:9238IL/0042
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A double blind, double-dummy, randomised, parallel groupmulticentre trial to compare the efficacy, tolerability, endometrial and bone effects of FASLODEX (fulvestrant) 250 mg monthly with NOLVADEX (tamoxifen) 20 mg daily when given as neoadjuvant treatment in post menopausal women with primary breast cancer
Breast Cancer
Phase 2
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Interventional
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Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
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No locations available
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