Isigaba: Umdlavuza we-Urethral

Ikhaya / Unyaka Omisiwe

I-Nivolumab ihlanganiswe ne-cisplatin ne-gemcitabine igunyazwe yi-USFDA nge-carcinoma ye-urothelial engasahlekiyo noma ye-metastatic.
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I-Nivolumab ihlanganiswe ne-cisplatin ne-gemcitabine igunyazwe yi-USFDA nge-carcinoma ye-urothelial engasahlekiyo noma ye-metastatic.

March 2024: The Food and Drug Administration has granted approval for the use of nivolumab (Opdivo, Bristol-Myers Squibb Company) in conjunction with cisplatin and gemcitabine as the initial treatment for adult patients with unres..

I-Padcev yokwelashwa komdlavuza we-urothelial
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I-Enfortumab vedotin-ejfv ene-pembrolizumab igunyazwe yi-USFDA nge-carcinoma ye-urothelial ethuthukisiwe endaweni noma e-metastatic.

Feb 2024: The Food and Drug Administration has sped up the approval process for two drugs, enfortumab vedotin-ejfv (Padcev, Astellas Pharma) and pembrolizumab (Keytruda, Merck). These drugs are meant to treat people with locally ..

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INivolumab ivunyelwe yi-FDA ukuthi isetshenziswe njengokwelashwa okunciphisayo kwe-urothelial carcinoma

Agasti 2021: I-Nivolumab (Opdivo, Bristol-Myers Squibb Co.) igunyazwe yi-Food and Drug Administration ukuze zelashwe i-adjuvant yeziguli ezine-urothelial carcinoma (UC) ezisengozini enkulu yokuphinda iphinde iphinde ilandele i-rad.

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I-FDA inikeze imvume ye-enfortumab vedotin-ejfv yokwelashwa kwe-carcinoma esezingeni eliphakeme noma yasendaweni.

Agasti 2021: I-Enfortumab vedotin-ejfv (Padcev, Astellas Pharma US, Inc.), inhlanganisela ye-antibody eqondiswe ku-Nectin-4 kanye ne-microtubule inhibitor, igunyazwe i-Food and Drug Administration ezigulini ezikhulile ezine-adv yasendaweni.

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ISacituzumab govitecan ithola imvume esheshayo evela kwi-FDA yomdlavuza we-urothelial osezingeni eliphakeme

Agasti 2021: I-Sacituzumab govitecan (Trodelvy, Immunomedics Inc.) yanikezwa ukugunyazwa okusheshayo yi-Food and Drug Administration ezigulini ezinomdlavuza wendawo othuthukile noma we-metastatic urothelial (mUC) owake wathola ngaphambilini.

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