DOXIL &TAXOTERE IN PATIENTS W/ ADVANCED MALIGNANCIES

$21,006M01FY2000RRNIH

New York University School Of Medicine, New York NY

Investigators

Linked publications & trials

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Abstract

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.

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