drugset / Trial / NCT00452673

Phase I Study of Dasatinib (BMS-354825) and Capecitabine for Women With Advanced Breast Cancer

NCT00452673

Phase 1 Completed 52 enrolled Bristol-Myers Squibb
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to learn about the safety and efficacy of Dasatinib in combination with Capecitabine for patients with advanced breast cancer, and who have received treatment with a taxane and an anthracycline

Timeline

Start
2007-06
Primary completion
2012-10
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule 825 mg/m2 Oral
Subject Capecitabine Small molecule 1000 mg/m2 Oral
Subject dasatinib anhydrous Small molecule 50 mg Oral
Subject dasatinib anhydrous Small molecule 70 mg Oral
Subject dasatinib anhydrous Small molecule 100 mg Oral

Indications