FDA approves atezolizumab for first | 合法醫療器材資訊網
FDAapprovesatezolizumabforfirst-linetreatmentofmetastaticNSCLCwithhigh...OnMay18,2020,theFoodandDrugAdministrationapprovedatezolizumab ...
On May 18, 2020, the Food and Drug Administration approved atezolizumab (TECENTRIQ®, Genentech Inc.) for the first-line treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors have high PD-L1 expression (PD-L1 stained ≥ 50% of tumor cells [TC ≥ 50%] or PD-L1 stained tumor-infiltrating immune cells [IC] covering ≥ 10% of the tumor area [IC ≥ 10%]), with no EGFR or ALK genomic tumor aberrations.
Today, the FDA also approved the VENTANA PD-L1 (SP142) Assay (Ventana Medical Systems, Inc.) as a companion diagnostic device for selecting patients with NSCLC for treatment with atezolizumab.
Efficacy was evaluated in IMpower110 (NCT02409342), a multicenter, international, randomized, open-label trial in patients with stage IV NSCLC whose tumors express PD-L1 (TC ≥ 1% or IC ≥ 1%), who had received no prior chemotherapy for metastatic disease. Pat...
FDA approves atezolizumab for first | 合法醫療器材資訊網
FDA approves atezolizumab for PD | 合法醫療器材資訊網
FDA approves atezolizumab plus bevacizumab for ... | 合法醫療器材資訊網
Tecentriq (atezolizumab) FDA Approval History | 合法醫療器材資訊網
TECENTRIQ (atezolizumab) | 合法醫療器材資訊網
Label (PDF) | 合法醫療器材資訊網
Atezolizumab | 合法醫療器材資訊網
【羅氏抗PD-L1 (SP142) 兔單株一級抗體檢驗試劑】許可證字號:衛部醫器輸字第033118號
器材品名:羅氏抗PD-L1(SP142)兔單株一級抗體檢驗試劑許可證字號:衛部醫器輸字第033118號註銷狀態:註銷日期:註銷理由:有效日...
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