Study identifier:7054IL/0038
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised, double-blind, parallel-group trial to investigate the efficacy and tolerability of radiotherapy as prophylactic treatment against the development of CASODEX monotherapy induced gynaecomastia and breast pain in prostate cancer patients.
prostate cancer
Phase 3
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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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