Agusta 2023: Pralsetinib (Gavreto, Genentech, Inc.) An ba da izini akai-akai ta Cibiyar Abinci da Magunguna don manya marasa lafiya tare da ciwon daji na huhu na huhu (NSCLC), kamar yadda FDA ta ƙaddara.
Yuli 2023: Hukumar Abinci da Magunguna ta ba da izini ga glofitamab-gxbm (Columvi, Genentech, Inc.) don sake dawowa ko ɓarnawar babban lymphoma B-cell, ba in ba haka ba (DLBCL, NOS) ko manyan ƙwayoyin B-cell ly.
Jan 2023: Mosunetuzumab-axgb (Lunsumio, Genentech, Inc.), CD20-directed CD3 T-cell engager don manya marasa lafiya tare da relapsed ko refractory follicular lymphoma (FL) bin biyu ko fiye zagaye na tsarin jiyya, rece.
Dec 2022: Atezolizumab (Tecentriq, Genentech, Inc.) an amince da shi ta Cibiyar Abinci da Magunguna (FDA) don manya da marasa lafiya na yara tare da sarcoma mai laushi mara kyau ko metastatic alveolar.
Maris 2022: Hukumar Abinci da Magunguna ta amince da rituximab (Rituxan, Genentech, Inc.) tare da haɗin gwiwar chemotherapy don CD20-positive diffuse big B-cell lymphoma (DLBCL), Burkitt lymphoma (BL), Burkitt-like lymphoma.
Nov 2021: Hukumar Abinci da Magunguna ta amince da atezolizumab (Tecentriq, Genentech, Inc.) don maganin adjuvant a cikin marasa lafiya tare da mataki na II zuwa IIIA ciwon huhu mara ƙaranci (NSCLC) wanda ciwace-ciwacen su ya ƙunshi PD-L1 magana o..