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  • 3rd PARP inhibitor Talzenna readies for Korean market
  • by Eo, Yun-Ho | translator Byun Kyung A | Dec 6, 2019 09:39am
Following Lynparza and Zejula to the competition in breast cancer treatments
EMBRACA study confirms efficacy, patients to get more treatment option
A pharmaceutical industry source reported on Dec. 6 that Pfizer Korea has recently submitted an application to Ministry of Food and Drug Safety (MFDS) for an approval on PARP inhibitor Talzenna (talazoparib).

When it gets the green light from the ministry, it would be the third PARP inhibitor medicine in Korea to enter the market, following AstraZeneca¡¯s Lynparza (olaparib) and Takeda Pharmaceutical¡¯s Zejula (niraparib).

The application is for an approval on a single therapy indication to treat locally advanced or metastatic human epidermal growth factor receptor 2 (HER2)-negative breast cancer in women with an inherited BRCA mutation. The treatment has been approved in Europe last June and the U.S. in Octob
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