This study is to assess the safety and tolerability of Cediranib (RECENTIN™, AZD2171)in combination with etoposide and cisplatin (EP) as first line treatment for lung cancer patients with extensive stage or metastatic disease for whom EP would be a standard therapy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
62
Research Site
Sacramento, California, United States
Research Site
Denver, Colorado, United States
Research Site
Kansas City, Kansas, United States
Research Site
Houston, Texas, United States
Assess the safety and tolerability of Cediranib (RECENTIN™, AZD2171) in combination with etoposide and cisplatin (EP).
Time frame: From date of consent through to data cut-off, 7th August 2009.
Preliminary efficacy assessment of Cediranib in combination with etoposide & cisplatin using available tumor assessment data to assess response rate,duration of response,change in tumor size(only those with measurable disease)& progression free survival
Time frame: From date of randomisation through to data cut-off, 7th August 2009.
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