Bevacizumab, Everolimus, and Erlotinib in Treating Patients With Advanced Solid Tumors
Part of paid clinical trials in Durham, North Carolina.
- Sponsor
- Herbert Hurwitz, MD
- Study ID
- NCT00276575
- Phase
- PHASE1
- Status
- Completed
Conditions
- Unspecified Adult Solid Tumor, Protocol Specific
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- bevacizumab — BIOLOGICAL
- erlotinib hydrochloride — DRUG
- everolimus — DRUG
Study Details
RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Erlotinib and everolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab and everolimus may also block blood flow to the tumor. Giving everolimus and erlotinib together with bevacizumab may kill more tumor cells. PURPOSE: This randomized phase I trial is studying the side effects and best dose of erlotinib and everolimus when given together with bevacizumab in treating patients with advanced solid tumors.
Key Dates
- First listed
- Jan 13, 2006
- Start date
- Mar 31, 2005
- Status verified
- Nov 2014
- Primary completion
- Oct 31, 2012
- Completion
- Sep 30, 2014
Study Design
- Enrollment
- 65 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Bevacizumab, Everolimus, and ErlotinibDose Level Dose Bevacizumab (mg/kg q2wks) Everolimus (mg daily) Erlotinib (mg daily) -1 5 5 --- 1. 10 5 --- 2. 10 10 --- 3. 10\* 10\* 75 4. 10\* 10\* 150
Primary Outcome Measure
Maximum Tolerated Dose [ Time Frame: Until study completion ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Duke Comprehensive Cancer Center | Durham | North Carolina | 27710 | - |
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