drugset / Trial / NCT00430781

Pazopanib Plus Lapatinib Compared to Lapatinib Alone and Pazopanib Alone In Subjects With Metastatic Cervical Cancer

NCT00430781

Phase 2 Completed 228 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is being conducted to compare the efficacy and safety of pazopanib in combination with lapatinib with that of lapatinib alone or pazopanib alone in subjects with metastatic cervical cancer

Timeline

Start
2006-11
Primary completion
2008-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Lapatinib Small molecule 1000 mg Oral
Subject Lapatinib Small molecule 1500 mg Oral
Comparator Pazopanib Small molecule 400 mg Oral
Comparator Pazopanib Small molecule 800 mg Oral

Indications