Drug intelligence / Profile preview

anti-miR-21-SNA

Development stage
Preclinical
Lead developer
Nagoya University
Modality
Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, MicroRNA (miRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Antisense Oligonucleotides (ASOs) → Long RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Single-strand DNA → Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Modified DNA Oligonucleotides → Antisense DNA → DNA Therapeutics → Nucleic Acid Therapeutics
Administration
Subcutaneous
01

Overview

anti-miR-21-SNA is an antisense oligonucleotide (ASO) synthesized from serinol nucleic acid (SNA) that targets microRNA-21 (miR-21). Developed by researchers at Nagoya University, this acyclic artificial nucleic acid therapeutic is designed to inhibit miR-21, which is aberrantly upregulated in cystic kidney diseases such as autosomal dominant polycystic kidney disease (ADPKD) and nephronophthisis. The SNA backbone provides high nuclease resistance and stable hybridization with target RNA without the need for toxic phosphorothioate modifications. In preclinical models, systemically administered anti-miR-21-SNA accumulates preferentially in the kidneys, where it suppresses renal cyst growth, improves renal function, and modulates pathways associated with mitochondrial metabolism, apoptosis, and tissue fibrosis.

Other names
anti-miR-21 oligonucleotideanti-miR21 oligonucleotideanti-miR 21 oligonucleotideanti-miR-21-serinol nucleic acidanti-miR21-serinol nucleic acidanti-miR 21-serinol nucleic acidanti-microRNA-21 oligonucleotide synthesized from serinol nucleic acidanti-microRNA21 oligonucleotide synthesized from serinol nucleic acidanti-microRNA 21 oligonucleotide synthesized from serinol nucleic acidanti-microRNA-21-serinol nucleic acidanti-microRNA21-serinol nucleic acidanti-microRNA 21-serinol nucleic acid
02

Targets

miR-21 (MicroRNA-21)

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