Treatment of Prostate Cancer With Adjuvant Bevacizumab Plus Erlotinib
Part of paid clinical trials in Alhambra, California.
- Sponsor
- Translational Oncology Research International
- Study ID
- NCT00203424
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Erlotinib + Bevacizumab — DRUGErlotinib every day for 24 weeks and Bevacizumab every 3 weeks for a total of 8 doses
Study Details
The purpose of this study is to evaluate the safety and effectiveness of bevacizumab plus erlotinib following radical prostatectomy.
Key Dates
- First listed
- Sep 20, 2005
- Start date
- Jan 31, 2006
- Status verified
- Feb 2016
- Primary completion
- Feb 28, 2009
- Completion
- Jun 30, 2010
Study Design
- Enrollment
- 23 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Erlotinib + BevacizumabParticipants received Erlotinib every day for 24 weeks and Bevacizumab every 3 weeks for a total of 8 doses
Primary Outcome Measure
To Evaluate the Efficacy of Bevacizumab Plus Erlotinib [ Time Frame: Determined by time to tumor recurrence, as measured by rising prostate specific antigen (PSA) after radical prostatectomy. ]
Locations (16)
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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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