drugset / Trial / NCT00451880

Study of XL281 in Adults With Solid Tumors

NCT00451880

Phase 1 Completed 180 enrolled Exelixis
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the safest dose of the multiple Raf kinase inhibitor (including c-Raf, B-Raf, and the activated mutant B-RafV600E) XL281, how often it should be taken, and how well subjects with cancer tolerate XL281. This study will also determine how the body reacts to XL281 when it is taken with and without food, and with and without Pepcid (famotidine), a drug that inhibits stomach acid production.

Timeline

Start
2007-02
Primary completion
2011-10
Completion
2011-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Famotidine Other / unclassified 20 mg
Subject Famotidine Other / unclassified 40 mg
Subject XL281 Small molecule 5 mg Oral
Subject XL281 Small molecule 25 mg Oral
Subject XL281 Small molecule 100 mg Oral