This protocol endeavors to determine the safety and efficacy of these two noted chemotherapy agents when administered in combination with each other. Thus, we will be assessing toxicity as well as response to treatment or time of progression free survival, depending on the histology of the patient. GCRC expertise with clinical trials will be helpful with the following study procedures: 1) administration and documentation that study medications were received at the proper doses and with the correct timing relative to each other. 2) consistant and thorough assessment and monitoring of toxicity while patient is receiving drug.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000079-36S1
Application #
6264380
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
36
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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