Novel Epothilone Plus Capecitabine Versus Capecitabine Alone in Patients With Advanced Breast Cancer
Status: | Completed |
---|---|
Conditions: | Breast Cancer, Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | September 2003 |
End Date: | March 2008 |
A Phase III Trial of Novel Epothilone BMS-247550 Plus Capecitabine Versus Capecitabine Alone in Patients With Advanced Breast Cancer Previously Treated With or Resistant to an Anthracycline and Who Are Taxane Resistant
The purpose of this clinical research study is to learn if BMS-247550 added to the approved
therapy of capecitabine is better than capecitabine alone in shrinking or slowing the growth
of the cancer in women with metastatic breast cancer who are resistant to taxane and
received anthracycline chemotherapy. The safety of this treatment will also be studied.
therapy of capecitabine is better than capecitabine alone in shrinking or slowing the growth
of the cancer in women with metastatic breast cancer who are resistant to taxane and
received anthracycline chemotherapy. The safety of this treatment will also be studied.
- Patients must have received either 2 or 3 prior chemotherapy regimens including
adjuvant or neoadjuvant therapy.
- Prior treatment must have included both an anthracycline (i.e., doxorubicin or
epirubicin) and a taxane (i.e., paclitaxel or docetaxel).
- Patients must have received a minimum cumulative dose of anthracycline or must be
resistant to an anthracycline.
- Patients must be resistant to taxane therapy.
- Patients may not have any history of brain and/or leptomeningeal metastases.
- Patients may not have CTC Grade 2 or greater neuropathy (motor or sensory).
- Patients may have not have had prior treatment with an epothilone and/or capecitabine
(i.e., Xeloda)
We found this trial at
33
sites
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