drugset / Trial / NCT00880009

Study Evaluating Bosutinib-Letrozole Combination Versus Letrozole Alone In Post Menopausal Women With Breast Cancer

NCT00880009

Phase 2 Terminated 16 enrolled Pfizer
RandomizedOpen-labelTreatment

Summary

This is a phase 2 study of bosutinib administered in combination with letrozole versus letrozole alone in post-menopausal women with breast cancer. This is a 2-part study. Subjects in part 1 will receive bosutinib and letrozole daily, and will be closely monitored for 28 days. The second part will proceed with subjects receiving a dose that is determined to be safe based on the safety evaluation of the first part. Eligible subjects will be randomly assigned to receive either bosutinib daily combined with daily letrozole, or daily letrozole alone for a specified period of time. Subjects will be followed up for survival after study drug discontinuation.

Timeline

Start
2009-07-30
Primary completion
2010-05-31
Completion
2010-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Bosutinib Small molecule 400 mg Oral
Comparator Letrozole Other / unclassified 2.5 mg Oral

Indications