Lung Cancer Clinical Trial
This Study is to Assess the Efficacy and Safety of ZD6474 in Subjects With Non-small Cell Lung Cancer.
Summary
The purpose of this study is to assess the efficacy and safety of ZD6474 in patients with NSCLC after Failure of Prior Platinum-based Chemotherapy.
Eligibility Criteria
Inclusion Criteria:
Histologic or cytologic confirmation of NSCLC (locally advanced or metastatic, IB-IV)
Failure of first-line platinum-based chemotherapy
Exclusion Criteria:
Mixed small cell or non-small-cell histology
Bronchoalveolar carcinoma
Prior chemotherapy or herbal preparations must be discontinued more than 4 weeks before the start of study therapy (6 weeks for nitrosoureas, mitomycin and suramin)
Prior treatment with docetaxel
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There is 1 Location for this study
Los Angeles California, , United States
Jacksonville Florida, , United States
Atlanta Georgia, , United States
New Orleans Louisiana, , United States
Boston Massachusetts, , United States
Pittsfield Massachusetts, , United States
Ann Arbor Michigan, , United States
Detroit Michigan, , United States
Billings Montana, , United States
Great Neck New York, , United States
New York New York, , United States
Durham North Carolina, , United States
Coos Bay Oregon, , United States
Philadelphia Pennsylvania, , United States
Pittsburgh Pennsylvania, , United States
Houston Texas, , United States
Brno , , Czech Republic
Chomutov , , Czech Republic
Hradec , , Czech Republic
Ostrava , , Czech Republic
Plzen , , Czech Republic
Praha , , Czech Republic
Budapest , , Hungary
Debrecen , , Hungary
Deszk , , Hungary
Torokbalint , , Hungary
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