Drug intelligence / Profile preview

HRS-7058 + SHR-A2102 + BP102

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
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Overview

HRS-7058 + SHR-A2102 + BP102 is an investigational combination therapy being developed by Shandong Suncadia Medicine (a subsidiary of Jiangsu Hengrui Pharmaceuticals) for the treatment of advanced malignant solid tumors. The regimen includes **HRS-7058**, a selective small molecule inhibitor of extracellular signal-regulated kinases 1 and 2 (**ERK1/2**), which are key components of the MAPK/ERK signaling pathway often dysregulated in cancer. **SHR-A2102** is an antibody-drug conjugate (ADC) consisting of a humanized monoclonal antibody targeting **Nectin-4** conjugated to a potent cytotoxic payload, typically a topoisomerase I inhibitor. **BP102** is a biosimilar of **bevacizumab**, a monoclonal antibody that binds to vascular endothelial growth factor A (**VEGF-A**) to inhibit angiogenesis. This multi-pronged approach aims to achieve synergistic anti-tumor activity by simultaneously targeting intracellular signaling, cell-surface antigens, and the tumor microenvironment. It is currently being evaluated in Phase II clinical trials for patients with advanced solid tumors who have progressed on standard therapies.

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Targets

TOP1 (DNA Topoisomerase I)VEGFA (Vascular endothelial growth factor A)PVRL4 (Nectin cell adhesion molecule 4)KRASG12C (Kirsten rat sarcoma viral oncogene homolog G12C)

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