Study identifier:7054IL/0009
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A multicentre, randomised, comparative trial to assess the tolerance (maximum well-tolerated dose), efficacy and pharmacokinetics of escalating doses of CASODEX (300 mg po daily, increasing by 150 mg intervals) versus castration (medical or surgical) in the treatment of advanced carcinoma of the prostate
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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