PHASE I TRIAL OF DOXIL, PACLITAXEL AND VALSPODAR PSC 833

$0M01FY2001RRNIH

Stanford University, Stanford CA

Investigators

Linked publications & trials

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Abstract

Valspodar (PSC 833) is a potent inhibitor of the multidrug resistance transporter P-glycoprotein. This drug is being evaluated along with Doxil and Paclitaxel (both of which are MDR substrates) in refractory solid tumors to determine the maximum tolerated dose of the drug alone and in combination with PSC.

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