drugset / Trial / NCT00706030

Study Evaluating Neratinib (HKI-272) In Combination With Vinorelbine In Subjects With Solid Tumors And Metastatic Breast Cancer

NCT00706030

Phase 1/2 Completed 92 enrolled Puma Biotechnology, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to identify the highest tolerable dose of neratinib (HKI-272) in combination with vinorelbine and to assess the safety of the combination of the two drugs as well as to obtain preliminary information on whether the combination of the two drugs has any effect on solid tumors. The study will be conducted in two parts. In the first part, testing will be done on up to 12 subjects to determine the highest tolerable dose of HKI-272 and vinorelbine in patients with advanced solid tumors. In the second part of the study, approximately 60 additional subjects with metastatic ErbB-2-positive breast cancer, with no prior exposure to lapatinib, are planned to be added to better define the tolerability and preliminary activity of HKI-272 in combination with vinorelbine. Up to 20 additional subjects with ErbB-2-positive breast cancer with prior lapatinib exposure are also planned to be enrolled in part 2 for exploratory analyses.

Timeline

Start
2008-04-29
Primary completion
2009-10
Completion
2018-06-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Neratinib Small molecule 160 mg Oral
Subject Neratinib Small molecule 240 mg Oral
Subject Vinorelbine Small molecule 25 mg/m2 Intravenous

Indications