Breast Cancer Clinical Trial
Official title:
Phase II Study of CT-2103 in Patients With Metastatic Breast Cancer
The purpose of this study is to collect information on what effects (good or bad) CT-2103 (Xyotax) has on breast cancer as well as any side effects the drug may cause.
- Patients will be given CT-2103 intravenously every 3 weeks. One week after the first
dose of CT-2103 a physical exam, blood work and assessment of any side effects will be
performed.
- Prior to each injection of CT-2103, a physical exam, blood work and assessment of any
side effects will be performed (every 3 weeks).
- Every 6 weeks the patient's cancer will be re-evaluated with either a CT scan or MRI to
determine whether the treatment is working.
- Additional blood work will be performed once per week after the first two doses of
CT-2103.
- The participation in this study will last at least 2 cycles (6 weeks), however patients
may remain on the study as long as there is no disease progression, and they are able
to tolerate the study drug without severe side effects.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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