Drug intelligence / Profile preview

AK119 + AK112 + mFOLFOX6

Development stage
Unknown
Lead developer
Kangfang Sainuo Pharmaceutical
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

This is an experimental **combination therapy** consisting of three components: - **AK119**: an investigational monoclonal antibody targeting CD73 (ecto-5’-nucleotidase), being developed as an immuno-oncology agent to inhibit adenosine-mediated immune suppression in the tumor microenvironment, with the intention to enhance anti-tumor immune response. - **AK112**: an investigational bispecific monoclonal antibody targeting PD-1 and VEGF, designed to provide checkpoint inhibition (PD-1) and anti-angiogenic (VEGF) effects concurrently, aiming to maximize immune-mediated anti-tumor activity and inhibit tumor-driven vascularization. - **mFOLFOX6**: a standard-of-care cytotoxic chemotherapy regimen comprised of oxaliplatin, leucovorin (folinic acid), and fluorouracil (5-FU), widely used for gastrointestinal cancers, particularly colorectal cancer[1][2][5]. mFOLFOX6 works primarily by disrupting DNA synthesis and repair, and is administered intravenously. The combined therapy is being investigated (2023–2025) primarily for **advanced or metastatic colorectal cancer** and other gastrointestinal malignancies as part of clinical trials. The rationale is to simultaneously target multiple pathways of tumor growth: immune suppression (AK119), immune checkpoint and angiogenesis (AK112), and direct cytotoxicity (mFOLFOX6).

02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TS (Thymidylate synthase)NT5E (Cluster of Differentiation 73)VEGFA (Vascular endothelial growth factor A)DNA

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