Drug intelligence / Profile preview

HRS-7058 + SHR-1826 + SHR-1316

Development stage
Unknown
Lead developer
Hengrui Pharmaceutical
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Oral, Intravenous
01

Overview

HRS-7058 + SHR-1826 + SHR-1316 is an investigational combination therapy under clinical development for the treatment of advanced solid tumors. HRS-7058 is a novel, selective small molecule inhibitor targeting KRAS G12C mutations, designed to inhibit tumor growth in cancers harboring this mutation[2][7]. SHR-1826 is an antibody-drug conjugate (ADC) targeting c-Met, developed for use in combination with other antitumor therapies in advanced solid tumors and non-small cell lung cancer[3][5][7]. SHR-1316 is a monoclonal antibody that targets programmed death ligand 1 (PD-L1), functioning as an immune checkpoint inhibitor to enhance anti-tumor immune responses; it has shown efficacy when combined with chemotherapy in esophageal squamous cell carcinoma[4]. The combination aims to leverage targeted inhibition of oncogenic signaling (KRAS G12C), direct cytotoxicity via ADC against c-Met-expressing cells, and immune checkpoint blockade through PD-L1 inhibition.

02

Targets

MET (Mesenchymal-epithelial transition factor receptor)KRASG12C (Kirsten rat sarcoma viral oncogene homolog G12C)CD274 (Programmed cell death protein 1 ligand 1)

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