drugset / Trial / NCT00088114

STA-4783 and Paclitaxel for Treatment of Solid Tumors

NCT00088114 ↗

Phase 1 Completed 50 enrolled Synta Pharmaceuticals Corp.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safety, toxicity and maximum tolerated dose of single doses of STA-4783/paclitaxel in combination when administered intravenously to patients with refractory cancer. To determine the pharmacokinetics of STA-4783 and paclitaxel when co-administered. To assess the anti-tumor activity of STA-4783 and paclitaxel when co-administered.

Timeline

Start
2003-01
Primary completion
2004-10
Completion
2004-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Elesclomol Small molecule — Intravenous
Subject Paclitaxel Small molecule — Intravenous

Indications