Maamulka Cuntada iyo Dawooyinka (FDA) waxay ansixiyeen Encorafenib (Braftovi, Array BioPharma Inc., oo ah shirkad hoos timaada Pfizer) iyo binimetinib (Mektovi, Array BioPharma Inc.) bishii Noofambar 2023 sida daawooyinka loo isticmaali karo ...
Noofambar 2023: Bukaannada carruurta ee da'doodu tahay hal sano iyo ka badan oo qaba marxaladda dabadheeraad (CP) Ph+ chronic myelogenous leukemia (CML), ha ahaato kuwa dhowaan la baaray (ND) ama adkaysi u leh ama u adkaysan la' (R/I) daawaynta hore, Maamulka Cuntada iyo Dawooyinka. .
July 2023: The Food and Drug Administration cleared talazoparib (Talzenna, Pfizer, Inc.) with enzalutamide for homologous recombination repair (HRR) gene mutations in metastatic castration-resistant prostate cancer (mCRPC). TALAP..
Julaay 2022: Crizotinib (Xalkori, Pfizer Inc.) waxa siisay ogolaanshaha Maamulka Cuntada iyo Dawooyinka (FDA) ee daawaynta dadka waaweyn iyo bukaanada carruurta 1 sano jir ah iyo kuwa ka wayn kuwaas oo laga helay cudurka aan la daabicin, soo noqnoqda.
Ogosto 2021: Lorlatinib (Lorbrena, Pfizer Inc.) waxay heshay oggolaansho joogto ah oo FDA ah oo loogu talagalay bukaannada qaba kansarka sanbabada ee unugyada yar-yar (NSCLC) oo burooyinkoodu yihiin lymphoma kinase anaplastic kinase (ALK), sida uu go'aamiyay FDA-app.
Ogosto 2021: Lorlatinib (Lorbrena, Pfizer Inc.) waxay heshay oggolaansho joogto ah oo FDA ah oo loogu talagalay bukaannada qaba kansarka sanbabada ee unugyada yar-yar (NSCLC) oo burooyinkoodu yihiin lymphoma kinase anaplastic kinase (ALK), sida uu go'aamiyay FDA-app.
Dr. Julie Gralow ayaa ka jawaabtay su'aalaha ku saabsan tallaalka COVID-19. Sideen ku hubin karnaa in tallaaladu badbaadsan yihiin haddii la soo saaray oo lagu ansixiyay muddo gaaban gudaheed?