The purpose of this study is to determine whether the study drug is effective and safe in the treatment of patients with non small cell lung cancer who have already received one platinum based chemotherapy.
The study has previously been posted by Schering AG, Germany. Schering AG, Germany has been renamed to Bayer Schering Pharma AG, Germany.Bayer Schering Pharma AG, Germany is the sponsor of the trial.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
112
1250 mg experimental drug od
1250 mg experimental drug bid (500mg + 750mg)
Unnamed facility
Paris, France
Unnamed facility
Paris, France
Unnamed facility
Villejuif, France
Unnamed facility
Göttingen, Lower Saxony, Germany
Unnamed facility
Tumor response rate (complete or partial response according to RECIST).
Time frame: At baseline and every 8 weeks afterwards
Time to disease progression.
Time frame: At baseline and every 8 weeks afterwards
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Essen, North Rhine-Westphalia, Germany
Unnamed facility
Mainz, Rhineland-Palatinate, Germany