The objective of this phase I multicenter study is to evaluate the safety profile of dose-limiting toxicity/maximum tolerated dose (DLT/MTD) & the pharmacokinetics of SCH52365 given orally once a day for 5 consecutive days (days 1-5) in combination with a single dose of cisplatin administered as a 1-hour IV infusion on day 1 of a 28-day cycle to adult patients with advanced cancers. This study will determine if the MTD of this combination regimen is lower than MTD dose of SCH52365 & the standard dose of cisplatin when given individually.

Project Start
1997-03-18
Project End
1997-11-30
Budget Start
1996-10-01
Budget End
1997-09-30
Support Year
36
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Pittsburgh
Department
Type
DUNS #
053785812
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
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