Qeybta: kansarka kaadi mareenka

Bogga Hore / Sanad La Aasaasay

Nivolumab oo ay weheliso cisplatin iyo gemcitabine waxa ay USFDA u ansixisay kansarka kaadi mareenka ee aan la dabar goyn ama metastatic.
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Nivolumab oo ay weheliso cisplatin iyo gemcitabine waxa ay USFDA u ansixisay kansarka kaadi mareenka ee aan la dabar goyn ama metastatic.

Maarso 2024: Maamulka Cuntada iyo Dawooyinka ayaa oggolaaday isticmaalka nivolumab (Opdivo, Bristol-Myers Squibb Company) iyada oo lala kaashanayo cisplatin iyo gemcitabine oo ah daawaynta ugu horreysa ee bukaannada qaangaarka ah ee qaba cillad la'aan.

Padcev oo loogu talagalay daawaynta kansarka kaadi mareenka
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Enfortumab vedotin-ejfv oo leh pembrolizumab waxa u ansixisay USFDA kansarka urothelial urothelial ee horumarsan ama metastatic

Feb 2024: Maamulka Cuntada iyo Dawooyinka ayaa dadajiyay nidaamka oggolaanshaha ee laba daawo, enfortumab vedotin-ejfv (Padcev, Astellas Pharma) iyo pembrolizumab (Keytruda, Merck). Daawooyinkan waxaa loogu talagalay in lagu daweeyo dadka deegaanka ..

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Nivolumab waxaa ansixiyay FDA si loogu isticmaalo sidii daaweyn wax ku ool ah kansarka urothelial

Ogosto 2021: Nivolumab (Opdivo, Bristol-Myers Squibb Co.) waxaa ansixiyay Maamulka Cuntada iyo Dawooyinka si loogu daweeyo bukaanada qaba kansarka kaadi mareenka (UC) kuwaas oo qatar weyn ugu jira soo noqnoqoshada rad.

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FDA waxay siisay enfortumab vedotin-ejfv oggolaanshaha daaweynta kansarka urothelial maxalliga ah ama metastatic

Ogosto 2021: Enfortumab vedotin-ejfv (Padcev, Astellas Pharma US, Inc.), Nectin-4-antibody-antibody iyo microtubule inhibitor inhibitor, waxaa ansixiyay Maamulka Cuntada iyo Dawooyinka bukaanada qaangaarka ah

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Govitecan Sacituzumab wuxuu oggolaansho deg deg ah ka helaa FDA kansarka kaadi mareenka ee horumarsan

Ogosto 2021: Sacituzumab govitecan (Trodelvy, Immunomedics Inc.) ayaa Maamulka Cuntada iyo Dawooyinka siisay oggolaansho degdeg ah bukaannada qaba kansarka urothelial -ka maxalliga ah ama metastatic urothelial (mUC) oo hore u qaatay.

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