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Brief Title: ZD6474 Phase IIa Dose Finding Multicentre Study
Official Title: A Randomised, Double-blind, Parallel-group, Dose Finding Study to Assess the Efficacy and Safety of ZD6474 in Patients With Advanced, Metastatic, or Recurrent NSCLC Who Have Failed Previous Chemotherapy Regimens, at Least One of Which Contained Platinum [Title Abbreviated]
Study ID: NCT00252746
Brief Summary: To assess the objective response rates (by RECIST) to ZD6474 100, 200 and 300 mg/day respectively
Detailed Description:
Minimum Age: 20 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, Matsuyama, Ehime, Japan
Research Site, Isehara, Kanagawa, Japan
Research Site, Osakasayama, Osaka, Japan
Research Site, Toyonaka, Osaka, Japan
Research Site, Sunto-gun, Shizuoka, Japan
Research Site, Okayama, , Japan
Research Site, Tokyo, , Japan
Name: Clinical Sciences & Operations
Affiliation: Sanofi
Role: STUDY_DIRECTOR