Protocol Specific Research Support is designed to provide research support for the conduct of Phase I, and pilot or feasibility clinical research trials approved by the Clinical Investigations Committee. The CIC functions administratively within the Clinical Investigation Support Office (CISO). Phase I protocols are reviewed by CIC and subsequently by CISO and the Cancer Center Executive Committee. Active trials are reviewed at six month intervals. The Cancer Center Executive Committee exercises full and sole authority in awarding funds to support the trial for a six month interval. This support element is composed of 2.0 FTE Research Nurses and 1.0 FTE Data Manager. Ninety-six patients were accrued to the intramural Phase I and feasibility or pilot protocols and supported by these personnel between July 1, 1998 and June 30, 1999. The application stresses the higher volume of work and the complexity of Phase I type studies. During this period, 28 protocols were recommended for support by this committee and awarded support by the Executive Committee. These included hematology (9), medical oncology (12), gynecologic oncology (3), radiation oncology (3) and pediatric oncology (1). There were a total 384 patients entered into these 28 protocols.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA014089-27S1
Application #
6577736
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2002-04-02
Project End
2002-11-30
Budget Start
Budget End
Support Year
27
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
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Sebio, A; Stintzing, S; Heinemann, V et al. (2018) A genetic variant in Rassf1a predicts outcome in mCRC patients treated with cetuximab plus chemotherapy: results from FIRE-3 and JACCRO 05 and 06 trials. Pharmacogenomics J 18:43-48
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