L-377202 is a potent and effective antitumor treatment.
The specific aims of this protocol are to determine the maximally tolerated dose (MTD) of L-377202 administered once a week for 3 weeks, to evaluate the safety and tolerability of L-377202 including the dose-limiting adverse effects of treatment with L-377202, and to assess the pharmacokinetics of various doses of L-377202 and the plasma profile of liberated doxorubicin and leu-doxorubicin. Our secondary specific aims are to evaluate radiologic and/or prostate-specific antigen (PSA) responses to treatment with L-377202, and to evaluate the relationship between baseline serum PSA level and response to treatment with L-377202.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000585-29
Application #
6409695
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
1976-12-01
Project End
2004-11-30
Budget Start
Budget End
Support Year
29
Fiscal Year
2000
Total Cost
Indirect Cost
Name
Mayo Clinic, Rochester
Department
Type
DUNS #
City
Rochester
State
MN
Country
United States
Zip Code
55905
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