Amivantamab (JNJ-61186372) is a humanEGFR-METbispecific antibody with immune anticancer activity. Amivantamab inhibits ligand binding, promotes endocytosis and degradation of receptor-antibody complexes, and induces Fc-dependent cytokinesis in macrophages and antibody-dependent cytotoxicity in natural killer cells^[1].

Amivantamab (JNJ-61186372)(0.05-1 mg/mL) 导致 Ba/F3 细胞活力显着且剂量依赖性降低，EGFR 下游信号通路磷酸化 EGFR (pEGFR)、磷酸化 AKT (pAKT)、磷酸化 ERK (pERK) 和磷酸化 S6 (pS6) 也显着降低^[2]。
Amivantamab (JNJ-61186372) 可以通过下调 EGFR 和 MET 信号通路在具有 EGFR Exon20ins 突变的 NSCLC 患者来源的癌细胞中具有有效的抗肿瘤活性^[2]。

Amivantamab (JNJ-61186372) (i.p, 30 mg/kg, twice a week, 15 days) 可以有效减小在雌性无胸腺 BALB-c/nu 小鼠的 EGFR Exon20ins 突变的 NSCLC 异种移植模型中的肿瘤体积，具有体内抗肿瘤作用^[2]。

Liquid

2171511-58-1

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