Status:
COMPLETED
Bevacizumab, Erlotinib, and Imatinib in the Treatment of Advanced Renal Cell Carcinoma
Lead Sponsor:
SCRI Development Innovations, LLC
Collaborating Sponsors:
Genentech, Inc.
Novartis
Conditions:
Clear Cell Renal Cell Carcinoma
Eligibility:
All Genders
18+ years
Phase:
PHASE1
PHASE2
Brief Summary
This phase I/II trial will evaluate the bevacizumab/erlotinib combination with the addition of imatinib (Gleevec). The combined inhibition greatly enhances the anti-tumor effects. Although the safety ...
Detailed Description
Upon determination of eligibility, patients will be receive: Bevacizumab + Erlotinib + Imatinib A brief phase I dose escalation study will be performed to define the imatinib dose that will be used.
Eligibility Criteria
Inclusion
- To be included in this study, you must meet the following criteria:
- Metastatic or unresectable clear cell renal carcinoma confirmed by biopsy
- Previous nephrectomy is required
- Maximum of 1 previous systemic regimen for metastatic disease.
- Able to perform activities of daily living with minimal assistance
- Measurable disease
- Adequate bone marrow, liver and kidney
- Written informed consent.
Exclusion
- Age \< 18 years
- Treatment with more than 1 previous systemic regimen
- History of heart attack within 6 months
- Clinically significant cardiovascular disease
- Moderate to severe vascular disease.
- Active brain metastases.
- History or evidence by physical examination of brain tumor
- Seizures not controlled with standard medical therapy
- history of stroke or other serious disorders of the nervous system
- Clinical history of coughing or vomiting blood within the past 3 months.
- PEG tubes or G tubes
- Chronic therapy with NSAIDS or other platelet inhibitors
- Proteinuria
- Nonhealing wound, ulcer, or long bone fracture
- Clinical evidence or history of a bleeding disorder
- Requiring full dose anticoagulation with coumadin
- Receiving chronic steroid therapy
- Significant medical conditions.
- Tumors other than clear cell
- History of stroke within 6 months.
- History of abdominal fistula,perforation,or abscess within 6 months.
- Please note: There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Key Trial Info
Start Date :
June 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2011
Estimated Enrollment :
94 Patients enrolled
Trial Details
Trial ID
NCT00193258
Start Date
June 1 2004
End Date
August 1 2011
Last Update
January 31 2013
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