drugset / Trial / NCT00215605

Study of XL184 (Cabozantinib) in Adults With Advanced Malignancies

NCT00215605

Phase 1 Completed 85 enrolled Exelixis
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the best and safest dose of XL184 administered orally. XL184 is a new chemical entity that inhibits VEGFR2, MET and RET, kinases implicated in tumor formation, growth and migration. To determine the highest safe dose, subjects will receive different amounts of the drug. The first group of subjects will receive the lowest dose of XL184. As long as no medically unacceptable side effects are noted, the dose will be increased for the next group. When the maximum tolerated dose (MTD) is reached, at least 20 subjects with Medullary Thyroid Cancer (MTC) will be enrolled to evaluate the effect of XL184 in this population.

Timeline

Start
2005-09
Primary completion
2011-04
Completion
2012-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabozantinib Small molecule 175 mg Oral