Mashi 2023: I-Abemaciclib (Verzenio, Eli Lilly and Company) kanye nokwelashwa kwe-endocrine (tamoxifen noma i-aromatase inhibitor) kugunyazwe i-Food and Drug Administration (FDA) ukuze kusetshenziswe i-adjuvant yeziguli ezikhulile ezine-.
March 2023: Study Type : Interventional (Clinical Trial)Estimated Enrollment : 30 participantsAllocation: N/AIntervention Model: Sequential AssignmentIntervention Model Description: a "3+3" design is used to determine Maximum..
SHANGHAI, CHINA, December 12, 2022 An independent and creative biotechnology company called JW Therapeutics (HKEX: 2126) focuses on developing, manufacturing, and selling cell immunotherapy products. At the 64th American Society ..
Feb 2023: I-Dostarlimab-gxly (i-Jemperli, i-GlaxoSmithKline LLC) yanikezwa imvume ye-FDA yokwelapha iziguli ezikhulile ezinomdlavuza ophindaphindayo noma othuthukile we-endometrial oqhubeke noma ngemva kwalokho.
Agasti 2022: Ezigulini ezikhulile ezinomdlavuza webele ongalungiseki noma one-metastatic HER2-low (IHC 1+ noma IHC 2+/ISH) ezithole ukwelashwa ngamakhemikhali kwangaphambilini esimweni se-metastatic noma ezihlangabezane nokuvela kwesifo phakathi noma phakathi nezinyanga eziyisithupha.
Mashi 2022: I-Food and Drug Administration igunyaze i-olaparib (Lynparza, AstraZeneca Pharmaceuticals, LP) yokwelapha i-adjuvant yeziguli ezikhulile ezinegciwane elisusayo noma elisolwa ngokususa i-BRCA-mutated (gBRCAm) h.
Dec 2021: The following drugs are approved as of date for the treatment of liver cancer:. Please check the prescribing information before taking the drug. Atezolizumab Avastin (Bevacizumab) Bevacizumab Cabometyx (Cabozantinib-S-M..
Agasti 20, 2021: Muva nje ngoMeyi, i-2021 Lumakras (sotorasib) yamukelwa yi-US Food and Drug Administration njengokwelashwa kokuqala kweziguli ezindala ezinomdlavuza ongewona omncane wamangqamuzana wamaphaphu asebenze okungenani uhlelo olulodwa lwangaphambilini ..
On February 15, 2019, pembrolizumab (KEYTRUDA, Merck) was approved by the Food and Drug Administration for the adjuvant treatment of patients with melanoma with the involvement of lymph node(s) after full resection. The approval ..
NgoFebhuwari 6, 2019, ngokuhlangana nokushintshaniswa kwe-plasma kanye nokwelashwa kwe-immunosuppressive, i-Food and Drug Administration igunyaze i-caplacizumab-yhdp (CABLIVI, Ablynx NV) yeziguli ezindala ezine-thrombotic cystopeni.