Phase I Study of Vorinostat and Sorafenib in Advanced Cancer
Part of paid clinical trials in Aurora, Colorado.
- Sponsor
- University of Colorado, Denver
- Study ID
- NCT00635791
- Phase
- PHASE1
- Status
- Completed
Conditions
- Malignant Solid Tumour
- Non Small Cell Lung Carcinoma
- Renal Cell Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Sorafenib — DRUGGiven by mouth
- Vorinostat — DRUGGiven by mouth
Study Details
This phase I trial studies the side effects and best dose of giving vorinostat and sorafenib tosylate together in treating patients with kidney or non-small cell lung cancer. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Sorafenib tosylate may stop the growth of solid tumors by blocking blood flow to the tumor. Giving vorinostat together with sorafenib tosylate may kill more tumor cells.
Key Dates
- Start date
- Mar 31, 2008
- Status verified
- Jun 2013
- Primary completion
- Oct 31, 2011
- Completion
- Mar 31, 2012
Study Design
- Enrollment
- 36 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Sorafenib tosylate and vorinostatPatients receive sorafenib tosylate by mouth twice a day on days 1-21 and vorinostat by mouth every day on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.
Primary Outcome Measure
Maximum tolerated dose (MTD) [ Time Frame: Up to 21 days ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Colorado Cancer Center | Aurora | Colorado | 80045 | - |
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