The purpose of this study is to determine if this epothilone leads to a response in patients with recurrent ovarian cancer that has progressed during, or in the last six months since a treatment of platinum-based chemotherapy. We also aim to look at the safety of the study drug and assess the impact of the infusion duration on tolerability.
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
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
63
10.5 mg lyophilized sagopilone per vial
Proportion of responders
Time frame: 18 weeks
Duration of response
Time frame: up to 1 year after LPLTV
Time to disease progression
Time frame: up to 1 year after LPLTV
Number of participants with adverse events
Time frame: Approximately 30 weeks
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