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Kabazitaksel

Kabazitaksel, doğal bir taksoidin yarı sentetik bir türevidir.[1] Bir mikrotübül inhibitörü ve kanser tedavisi olarak onaylanacak dördüncü taksandır.

Kabazitaksel, Sanofi-Aventis tarafından geliştirilmiş ve Haziran 2010'da ABD Gıda ve İlaç Dairesi (FDA) tarafından hormona dirençli prostat kanserinin tedavisi için onaylanmıştır.[2] Jenerik ilaç olarak mevcuttur.[3][4]

Kaynakça

[değiştir | kaynağı değiştir]
  1. ^ "Cabazitaxel". NCI Drug Dictionary. U.S. Department of Health and Human Services, National Institutes of Health, National Cancer Institute. 2 Şubat 2011. 25 Nisan 2015 tarihinde kaynağından arşivlendi. Erişim tarihi: 30 Aralık 2022. 
  2. ^ "Drug Approval Package: Jevtana (Cabazitaxel) NDA #201023". U.S. Food and Drug Administration (FDA). 8 Temmuz 2013. 30 Aralık 2022 tarihinde kaynağından arşivlendi. Erişim tarihi: 30 Aralık 2021. 
  3. ^ "Cabazitaxel: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). 30 Aralık 2022 tarihinde kaynağından arşivlendi. Erişim tarihi: 30 Aralık 2021. 
  4. ^ "First Generic Drug Approvals". U.S. Food and Drug Administration. 17 Ekim 2022. 26 Ocak 2021 tarihinde kaynağından arşivlendi. Erişim tarihi: 28 Kasım 2022. 
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Kabazitaksel
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