Clinical Trials Directory

Trials / Completed

CompletedNCT00837148

Sorafenib and Dacarbazine in Soft Tissue Sarcoma

Phase II Trial of Sorafenib and Dacarbazine in Soft Tissue Sarcoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
37 (actual)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to find out what effects, good and/or bad, the combination of sorafenib and dacarbazine has on sarcoma. Recurrent sarcoma is difficult to treat. Standard chemotherapy drugs can be toxic, and the length of benefit is usually short. As a result, we need new treatments for sarcoma. Sorafenib is a new type of "targeted" chemotherapy that attacks specific proteins (including "raf" and "VEGF receptor") in cells. We hope that by blocking these proteins we can cause the tumor to shrink. Sorafenib is also known as BAY 43-9006 and by the trade name Nexavar®. The FDA approved sorafenib in December of 2005 to treat patients with kidney cancer and in November of 2007 to treat patients with liver cancer. This drug is not approved by the U.S. Food and Drug Administration (FDA) or any other licensing authority for the treatment of sarcoma and is therefore considered to be experimental in this setting.

Conditions

Interventions

TypeNameDescription
DRUGSorafenib and DacarbazineTreatment will be administered on an outpatient basis. Sorafenib is supplied as 200-mg tablets. The starting dose of sorafenib will be 400 mg PO twice daily (every 12 hours) continuously. There is no planned treatment interruption between cycles. All patients will receive dacarbazine as an open-label dose of 850 mg/m2 by IV infusion over 60 minutes, starting on Week 1 and repeated every 3 weeks until disease progression or intolerance.

Timeline

Start date
2009-02-01
Primary completion
2013-11-01
Completion
2013-11-01
First posted
2009-02-05
Last updated
2015-11-20
Results posted
2015-11-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00837148. Inclusion in this directory is not an endorsement.