Pembrolizumab, an anti-PD-1 antibody, inhibits PD-1 and PD-L1 interaction to relieve T and B lymphocyte deprivation for sustainable antitumor
by I Baraibar 2024 Cited by 97Arthralgia and myalgia have been widely reported with anti-PD-1/PD-L1 agents (approximately 10%), especially anti-PD-1 drugs [107]. These are
The anti-PD-1 mAb nivolumab, pembrolizumab has recently been approved by the FDA. These drugs inhibit checkpoint binding of PD-1 and PD-L1 between T cells and
life expectancy of ≥ 12 weeks. Exclusion criteriac. Prior treatment with lenvatinib or any PD-1, anti-PD-L1, or anti-PD-L2 drug. Prior anticancer
Additionally, several new drugs based on the anti-TIGIT and anti-PD-1/PD-L1 combination, such as AZD2936 and MK-7684 A, and novel combination strategies, such as anti-TIGIT plus anti-PD-1/PD-L1 agents plus chemotherapy or chemoradiotherapy, are being evaluated clinically (Table 1). These advances are expected to expand the benefits of the anti
The first anti-PD-1 mAbs, nivolumab and pembrolizumab, were approved by the US Food and Drug Administration (FDA) in 2024 and the first anti-PD-
Drugs Targeting the PD-1/PD-L1 Pathway. A small, first-in-human trial of the anti-PD-1 drug nivolumab reported promising results, and
by C Su 2024 Cited by 52To date, several anti-PD-1/PD-L1 immune checkpoint agents have been approved for the treatment of NSCLC, including two anti-PD-1 drugs pembrolizumab and
Drug class: anti-PD-1 and PD-L1 monoclonal antibodies (immune checkpoint inhibitors) drugs, over-the-counter medicines and natural products.
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