Drug intelligence / Profile preview

polyinosinic-polycytidylic acid + atezolizumab

Development stage
Unknown
Lead developer
Genentech
Modality
MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intratumoral, Intramuscular, Intravenous
01

Overview

This drug is a **combination of polyinosinic-polycytidylic acid (poly I:C) and atezolizumab**. Polyinosinic-polycytidylic acid is a synthetic double-stranded RNA that acts as an agonist for toll-like receptor 3 (TLR3) and retinoic acid-inducible gene I-like receptors (RIG-I, MDA5), stimulating the innate immune response, enhancing adaptive immune functions, acting as a vaccine adjuvant, and promoting antitumor activity through type I interferon induction and direct apoptosis in some cancer cells[2][4]. Atezolizumab is a monoclonal antibody immune checkpoint inhibitor that targets programmed death-ligand 1 (PD-L1), thereby blocking its interaction with PD-1 and B7.1 receptors on T cells and antigen-presenting cells, facilitating immune-mediated tumor cell killing[1]. The combination is under investigation as a novel immunotherapy for solid tumors, aiming to potently augment immune response by leveraging the immune-priming effects of poly I:C with the checkpoint blockade provided by atezolizumab[3].

02

Targets

DDX58 (Retinoic acid-inducible gene I protein)CD274 (Programmed cell death protein 1 ligand 1)IFIH1 (MDA5)TLR3 (Toll-like receptor 3)

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