Drug intelligence / Profile preview

nivolumab

Development stage
Approved
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Nivolumab is a fully human monoclonal antibody targeting the programmed death 1 (PD‑1) receptor, functioning as an immune checkpoint inhibitor. By binding to PD‑1 on T cells, it blocks the interaction with its ligands PD-L1 and PD-L2, thereby releasing the inhibition of T-cell activity and enhancing anti-tumor immune responses. Nivolumab is used in the treatment of various cancers including melanoma, non-small cell lung cancer (NSCLC), renal cell carcinoma, classical Hodgkin lymphoma, head and neck squamous cell carcinoma, urothelial carcinoma (bladder cancer), colorectal cancer with microsatellite instability-high or mismatch repair deficiency, hepatocellular carcinoma (HCC), esophageal cancer, gastric/gastroesophageal junction adenocarcinoma, and malignant pleural mesothelioma. It can be administered alone or in combination with other agents such as ipilimumab. Nivolumab was developed by Medarex and Ono Pharmaceutical; Bristol Myers Squibb acquired Medarex in 2009[2][4][5][7].

Brand names
Opdivo欧狄沃保疾伏
Other names
纳武利尤单抗纳武单抗
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)

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