Drug intelligence / Profile preview

SHR-8068 + adebrelimab + oxaliplatin + capecitabine + paclitaxel + cisplatin

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a combination regimen consisting of six agents used in clinical trials for the treatment of advanced gastric and esophageal cancers, as well as other solid tumors. The components are: - **SHR-8068**: A monoclonal antibody targeting cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), acting as an immune checkpoint inhibitor to enhance antitumor immune responses[1][2][3][4]. - **Adebrelimab**: A high-affinity, humanized IgG4 monoclonal antibody against programmed death-ligand 1 (PD-L1), also functioning as an immune checkpoint inhibitor to promote T-cell-mediated antitumor activity[3][6]. - **Oxaliplatin**: A platinum-based chemotherapeutic agent that forms DNA crosslinks, inhibiting DNA replication and transcription in cancer cells[7]. - **Capecitabine**: An oral prodrug converted to 5-fluorouracil (5-FU) in the body, which inhibits thymidylate synthase and disrupts DNA synthesis in rapidly dividing cells[7]. - **Paclitaxel**: A microtubule-stabilizing agent that inhibits cell division by preventing microtubule depolymerization. - **Cisplatin**: Another platinum-based chemotherapy drug that causes DNA crosslinking and apoptosis in cancer cells. This combination is being investigated primarily for unresectable or metastatic adenocarcinoma of the stomach or gastroesophageal junction, and esophageal squamous cell carcinoma. The regimen leverages both immunotherapy (immune checkpoint blockade) and cytotoxic chemotherapy for synergistic antitumor effects[5].

02

Targets

TS (Thymidylate synthase)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)CD274 (Programmed cell death protein 1 ligand 1)DNATUBB (Tubulin (alpha and beta subunits))

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