drugset / Trial / NCT00104117

Study of XL999 in Adults With Solid Tumors

NCT00104117 ↗

Phase 1 Completed 52 enrolled Symphony Evolution, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and tolerability of XL999 in adults with advanced solid tumors.

Timeline

Start
2004-11
Primary completion
2008-09
Completion
2008-10

Drugs

EvaluationDrugModalityDoseRoute
Subject XL999 Small molecule 0.2 mg/kg Intravenous
Subject XL999 Small molecule 200 mg Intravenous

Indications