To investigate the ability of 600 mg of Glivec®, given once daily by mouth to patients with rising PSA following radical prostatectomy, to produce a sustained biochemical response during the first 6 months of treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
51
Novartis Investigative Site
Aachen, Germany
Novarts Investigative Site
Berlin, Germany
Novartis Investigative Site
Bonn, Germany
Novartis Investigative Site
Borken, Germany
Novartis Investigative Site
Cologne, Germany
Novartis Investigative Site
Darmstadt, Germany
Novartis Investigative Site
Fürth, Germany
Novartis Investigative Site
Gardelegen, Germany
Novarts Investigative Site
Hamburg, Germany
Novartis Investigative Site
Marburg, Germany
...and 3 more locations
investigate the ability of 600 mg of Glivec®, given once daily by mouth to patients with rising PSA following radical prostatectomy, to produce a sustained biochemical response during the first 6 months of treatment.
Time frame: 2 - 4 weeks
investigate the time to sustained biochemical response under the treatment of Glivec® in this patient population
Time frame: continuous
investigate duration of biochemical sustained response under the treatment with Glivec® in this patient population.
Time frame: continuous
To assess the response rates: number of patients with complete, partial and minor biochemical response and stable PSA
Time frame: continuous
To assess the time to clinical progression of this patient population treated with Glivec® at this dose and schedule.
Time frame: continuous
To descriptively characterize the safety and tolerability of Glivec® administered at this dose and schedule to this patient population.
Time frame: continuous
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