I-Tag: Pfizer

Ikhaya / Unyaka Omisiwe

I-FDA igunyaza i-enorafenib ene-binimetinib yomdlavuza wamaphaphu we-metastatic ongewona omncane ngokuguqulwa kwe-BRAF V600E
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I-Encorafenib ene-binimetinib igunyazwe yi-FDA yokwelashwa komdlavuza wamaphaphu we-metastatic ongewona omncane ngokuguqulwa kwe-BRAF V600E

I-Food and Drug Administration (i-FDA) igunyaze i-Encorafenib (i-Braftovi, i-Array BioPharma Inc., inkampani ephethwe ngokugcwele ye-Pfizer) kanye ne-binimetinib (Mektovi, Array BioPharma Inc.) ngoNovemba 2023 njengemithi engasetshenziswa ukulungisa inkinga.

I-Bosutinib igunyazwe yi-FDA yeziguli zezingane ezine-myelogenous leukemia engapheli
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I-Bosutinib igunyazwe yi-FDA yeziguli zezingane ezine-myelogenous leukemia engapheli

Nov 2023: Ezigulini zezingane ezinonyaka owodwa nangaphezulu ezinesigaba esingapheli (CP) Ph+ chronic myelogenous leukemia (CML), esanda kutholakala (ND) noma engazweli noma engabekezeleli (R/I) ekwelashweni kwangaphambilini, iFood and Drug Admini. .

Talzenna talazoparib
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I-Talazoparib ene- enzalutamide igunyazwe yi-FDA yomdlavuza wendlala yesinye we-HRR oguquliwe we-metastatic castration-resistant prostate

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..

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I-Crizotinib ivunyelwe yi-FDA ye-ALK-positive inflammatory myofibroblastic tumor

 Julayi 2022: I-Crizotinib (Xalkori, Pfizer Inc.) yanikezwa imvume yi-Food and Drug Administration (FDA) yokwelapha abantu abadala kanye neziguli zezingane ezinonyaka ongu-1 ubudala nangaphezulu ezitholwe zinezinkinga ezingalawuleki, eziphindelelayo.

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ILorlatinib ivunyelwe yi-FDA ekwelashweni kwe-NSCLC ye-ALK-positive metastatic.

Agasti 2021: I-Lorlatinib (i-Lorbrena, i-Pfizer Inc.) ithole ukuvunyelwa okujwayelekile kwe-FDA kweziguli ezinomdlavuza we-metastatic non-small cell lung cancer (NSCLC) ezinamathumba azo yi-anaplastic lymphoma kinase (ALK) -positive, njengoba kunqunywe uhlelo lokusebenza lwe-FDA ..

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ILorlatinib ivunyelwe yi-FDA ekwelashweni kwe-NSCLC ye-ALAS-positive metastatic

Agasti 2021: I-Lorlatinib (i-Lorbrena, i-Pfizer Inc.) ithole ukuvunyelwa okujwayelekile kwe-FDA kweziguli ezinomdlavuza we-metastatic non-small cell lung cancer (NSCLC) ezinamathumba azo yi-anaplastic lymphoma kinase (ALK) -positive, njengoba kunqunywe uhlelo lokusebenza lwe-FDA ..

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Umuthi wokugoma we-COVID-19 - Konke obufuna ukukwazi

UDkt. Julie Gralow uphendula imibuzo ngomgomo we-COVID-19. Singaqiniseka kanjani ukuthi imithi yokugoma iphephile uma yenziwa futhi yagunyazwa esikhathini esifushane kangaka? Umphakathi wezokwelapha ubusebenzela ukwenza imigomo ye-COVID-19 itholakale.

Qala ingxoxo
Siku-inthanethi! Xoxa Nathi!
Skena ikhodi
Sawubona,

Siyakwamukela kuCancerFax!

ICancerFax iyinkundla yokuphayona ezinikele ekuxhumaniseni abantu ababhekene nomdlavuza oseqophelweni eliphezulu ngemithi yokwelapha yamangqamuzana efana ne-CAR T-Cell therapy, ukwelashwa kwe-TIL, nezivivinyo zomtholampilo emhlabeni wonke.

Sazise ukuthi yini esingakwenzela yona.

1) Ukwelashwa komdlavuza phesheya?
2) Ukwelashwa kwe-CAR T-Cell
3) Umuthi wokugomela umdlavuza
4) Ukubonisana ngevidiyo eku-inthanethi
5) Ukwelashwa kweProton