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BI1361849 + durvalumab + tremelimumab

Development stage
Unknown
Lead developer
Boehringer Ingelheim
Modality
mRNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics, Vaccines & Immunotherapeutics
Administration
Intradermal, Intravenous
01

Overview

This is a combination immunotherapy regimen consisting of: - **BI1361849** (also known as CV9202): an mRNA-based therapeutic cancer vaccine encoding six non-small cell lung cancer-associated antigens (NY-ESO-1, MAGE-C1, MAGE-C2, survivin, 5T4, and MUC-1). It is designed to induce targeted immune responses against these tumor antigens. The mRNA is protamine-formulated and administered intradermally. - **Durvalumab**: a human monoclonal antibody targeting programmed death-ligand 1 (PD-L1), functioning as an immune checkpoint inhibitor to enhance anti-tumor T-cell activity. - **Tremelimumab**: a human monoclonal antibody targeting cytotoxic T lymphocyte-associated antigen 4 (CTLA-4), also acting as an immune checkpoint inhibitor to further stimulate the immune response. The combination aims to synergistically boost anti-tumor immunity by both priming the immune system with tumor-specific antigens via vaccination and releasing inhibitory checkpoints on T cells. This regimen has been investigated primarily in advanced non-small cell lung carcinoma in early-phase clinical trials[8][1].

Other names
RNActive cancer vaccine (BI1361849)CV9202CV-9202CV 9202
02

Targets

BIRC5 (Survivin)TLR7 (Toll-like receptor 7)CD274 (Programmed cell death protein 1 ligand 1)NY-ESO-1 (New york esophageal squamous cell carcinoma 1)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)MAGEC2 (Melanoma-associated antigen C2)TLR8 (Toll-like receptor 8)MUC1 (Mucin-1 Antigen)MAGEC1 (Melanoma antigen family C1)

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