Drug intelligence / Profile preview

ATI-2173 + tenofovir disoproxil fumarate + AB-729

Development stage
Discontinued
Lead developer
Antios Therapeutics
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Small Molecules
Administration
Oral, Subcutaneous
01

Overview

This combination consists of **ATI-2173**, a liver-targeted prodrug of clevudine and active site polymerase inhibitor nucleotide (ASPIN), **tenofovir disoproxil fumarate**, a nucleoside reverse transcriptase inhibitor (NRTI) and chain-terminating nucleotide analogue, and **AB-729**, a small interfering RNA (siRNA) targeting hepatitis B surface antigen (HBsAg) mRNA. This regimen is being investigated for the treatment of chronic hepatitis B virus (HBV) infection, aiming for functional cure by combining inhibition of viral replication (ATI-2173, tenofovir disoproxil fumarate) and reduction of HBsAg production (AB-729). ATI-2173 is designed for strong liver targeting and reduced systemic clevudine exposure, providing potent and durable suppression of HBV DNA and cccDNA markers[1][2][3][4][5][7]. Tenofovir disoproxil fumarate is approved and widely used in HBV therapy. AB-729 is an siRNA conjugate in development that reduces circulating HBsAg. The combination harnesses complementary antiviral mechanisms to more profoundly suppress HBV replication and antigenemia than possible with monotherapy.

02

Targets

HBV Pol (Hepatitis B virus polymerase)HBV (Hepatitis B virus)

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