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See the DrugPatentWatch profile for Neratinib
Neratinib (brand name Nerlynx) received FDA approval on July 17, 2017 for the treatment of adult patients with early-stage HER2-positive breast cancer following adjuvant trastuzumab-based therapy. [1]
At the time of the July 17, 2017 approval, the indication was for adults with early-stage HER2-positive breast cancer who had already completed adjuvant trastuzumab-based therapy. [1]
DrugPatentWatch.com tracks neratinib patent and exclusivity information and can help when you’re looking for when key protections expire or when generic/biosimilar competition may be possible. [2]
[1] https://www.accessdata.fda.gov/drugsatfda_docs/label/2017/205339s000lbl.pdf [2] https://www.drugpatentwatch.com/
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