Study identifier:1839IL/0710
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A DOUBLE BLIND, PLACEBO CONTROLLED, PARALLEL GROUP, MULTICENTRE, RANDOMISED PHASE III STUDY OF DISEASE-RELATED SYMPTOMS COMPARING ZD1839 (IRESSA)(250MG TABLET) PLUS BEST SUPPORTIVE CARE (BSC) VERSUS PLACEBO PLUS BSC IN SYMPTOMATIC PATIENTS WITH ADVANCED NSCLC WHO HAVE RECEIVED ONE OR TWO PRIOR CHEMOTHERAPY REGIMENS AND ARE REFRACTORY OR INTOLERANT TO THEIR MOST RECENT REGIMENS
lung 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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