This phase I investigator-initiated trial is for patients who have confirmed malignancy for which an effective therapy is unavailable or was already used with disease recurrence in < one year. The objectives are to determine the maximal tolerated dose of Taxotere that can be administered in combination with Doxil at a fixed dose of 30 mg/m2 every 21 days. Dose-limiting toxicity, antitumor activity and pharmacokinetics will be also be determined.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
New York University
Department
Type
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10016
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