Neratinib was approved in July 2017 for use as an extended adjuvant therapy in Human Epidermal Growth Factor Receptor 2 (HER2) positive breast cancer. Approval was granted to Puma Biotechnology Inc. for the tradename Nerlynx. Neratinib is currently under investigation for use in many other forms of cancer.
For use as an extended adjuvant treatment in adult patients with early stage HER2-overexpressed/amplified breast cancer, to follow adjuvant trastuzumab-based therapy [FDA Label].
Massachusetts General Hospital, Boston, Massachusetts, United States
Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
Institut Gustave Roussy, Villejuif, France
The Medical Oncology Centre of Rosebank, Johannesburg, Gauteng, South Africa
Division of Medical Oncology, Department of Medicine, Bangkok-noi, Bangkok, Thailand
Broomfield Hospital, Chelmsford, Essex, United Kingdom
Investigational Site, Tokyo, Japan
Border Medical Oncology, Wodonga, Victoria, Australia
University Hospital Center Zagreb Department of Oncology, Zagreb, Croatia
Saint-Petersburg State Medical University n.a. acad. I.P. Pavlov, Laboratory of Thoracic Oncology of Pulmonology Research Institute, Saint Petersburg, Russian Federation
Albert Einstein Cancer Center, Bronx, New York, United States
Centre Paul Papin, Angers, France
Centro Oncologico de Galicia, A Coruña, Spain
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