Efficacy and Safety of Everolimus in Combination Therapy, in Patients With HER2-overexpressing Metastatic Breast Cancer
Status: | Completed |
---|---|
Conditions: | Breast Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | July 2007 |
End Date: | March 2014 |
A Phase Ib/II Study Investigating the Combination of Everolimus With Trastuzumab and Paclitaxel in Patients With HER2-overexpressing Metastatic Breast Cancer
Phase I: will look at different dose levels and regimens of everolimus combined with weekly
trastuzumab and paclitaxel therapy in patients with HER-2 overexpressing metastatic breast
cancer.
Phase II: will assess the efficacy and safety of the 10mg daily dose of everolimus combined
with weekly trastuzumab and paclitaxel therapy in patients with HER-2 overexpressing
metastatic breast cancer.
trastuzumab and paclitaxel therapy in patients with HER-2 overexpressing metastatic breast
cancer.
Phase II: will assess the efficacy and safety of the 10mg daily dose of everolimus combined
with weekly trastuzumab and paclitaxel therapy in patients with HER-2 overexpressing
metastatic breast cancer.
Inclusion Criteria:
- Female or male patients ≥ 18 years old with WHO performance status ≤ 1
- HER-2 over-expressing metastatic breast cancer cells confirmed by histology
- Progressive disease on prior trastuzumab alone/or in combination with other
anticancer agents, or relapsed any time after completion of this therapy (phase l)
- Patient resistance to trastuzumab and taxanes (Phase ll)
- Measurable disease according to RECIST (Phase ll)
- Patients neurologically stable with adequate bone marrow, liver and renal function
Exclusion Criteria:
- Patients receiving endocrine therapy for breast cancer ≤ 2 weeks prior to study
treatment start
- Patients currently receiving chemotherapy, immunotherapy or radiotherapy or who have
received these ≤ 4 weeks prior to study treatment start or patients who have received
lapatinib ≤ 2 weeks prior to study treatment start
- Patients who have previously received mTOR inhibitors
Other protocol-defined inclusion/exclusion criteria may apply
We found this trial at
12
sites
St. Louis, Missouri 63110
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Atlanta, Georgia 30322
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