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A Phase 1/2 Study Of HKI-272 In Combination With Vinorelbine In Subjects With Solid Tumors And Metastatic Breast Cancer
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Highlands Oncology Group
Fayetteville, Arkansas, United States
City of Hope National Medical Center
Duarte, California, United States
Norris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, United States
Columbia University Medical Center
New York, New York, United States
Hematology Oncology Associates of Rockland
Nyack, New York, United States
Albert Einstein Cancer Center
The Bronx, New York, United States
Carolinas Hematology-Oncology Associates
Charlotte, North Carolina, United States
Fox Chase Cancer Center
Philadelphia, Pennsylvania, United States
AZ Klina Brasschaat
Brasschaat, Belgium
Institut Jules Bordet
Brussels, Belgium
Start Date
April 29, 2008
Primary Completion Date
October 1, 2009
Completion Date
June 7, 2018
Last Updated
August 9, 2018
92
ACTUAL participants
neratinib
DRUG
vinorelbine
DRUG
Lead Sponsor
Puma Biotechnology, Inc.
NCT04704661
NCT05245812
Data Source & Attribution
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