drugset / Trial / NCT00522145

Study of XL647 in Subjects With NSCLC Who Have Progressed After Responding to Treatment With Gefitinib or Erlotinib

NCT00522145

Phase 2 Completed 41 enrolled Kadmon Corporation, LLC
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the best confirmed response rate of daily administration of the multiple receptor tyrosine kinase (RTK) inhibitor (including EGFR and VEGFR2) XL647 in subjects with NSCLC who have progressed after responding to treatment with either erlotinib or gefitinib.

Timeline

Start
2007-05
Primary completion
2009-10
Completion
2010-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Tesevatinib Small molecule 300 mg Oral