drugset / Trial / NCT00350831

Study of XL820 Given Orally Daily to Subjects With Solid Tumors

NCT00350831 ↗

Phase 1 Completed 30 enrolled Exelixis
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and tolerability of the KIT inhibitor XL820 when given orally daily to adults with advanced solid tumors.

Timeline

Start
2006-07
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject XL820 Unknown — Oral

Indications