Treatment of HER2-Positive Metastatic Breast Cancer With Herceptin and Bevacizumab (Antibodies Against HER2 and VEGF)
Part of paid clinical trials in Alhambra, California.
- Sponsor
- Translational Oncology Research International
- Study ID
- NCT00095706
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
Study Details
The purpose of this study is to evaluate the safety and effectiveness of combined treatment with trastuzumab (Herceptin) and bevacizumab (anti-VEGF antibody) in patients with HER2-positive metastatic breast cancer.
Key Dates
- First listed
- Nov 8, 2004
- Start date
- Jun 30, 2003
- Status verified
- Sep 2015
- Primary completion
- Apr 30, 2007
- Completion
- Jan 31, 2012
Study Design
- Enrollment
- 50 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Primary Outcome Measure
To establish the maximum tolerated dose (MTD) or recommended phase II dose of rhuMAb VEGF (bevacizumab) administered intravenously every 14 days to patients with HER2-amplified relapsed or metastatic breast cancer receiving concomitant Herceptin therapy
Locations (18)
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Central Hematology Oncology Medical Group, Inc.· Alhambra, CAComprehensive Blood and Cancer Center· Bakersfield, CAVirginia K. Crosson Cancer Center· Fullerton, CAPacific Shores Medical Group· Long Beach, CAUCLA Medical Center· Los Angeles, CANorth Valley Hematology/Oncology Medical Group· Northridge, CA
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