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Home » hepatitis B

Articles Tagged with ''hepatitis B''

Infection

Japanese scientists divulge new isoindoline compounds for viral infections

May 29, 2025
The Institute of Physical and Chemical Research and Kyoto University have synthesized isoindoline compounds reported to be useful for the treatment of viral infections.
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Illustration of liver infection
Infection

ABI-4334 outperforms vebicorvir in HBV suppression

May 13, 2025
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Current therapies for chronic hepatitis B virus (HBV) infection can effectively suppress viral replication but do not achieve a functional or complete cure. Capsid assembly modulators inhibit the assembly of viral capsids, prevent the encapsidation of pregenomic RNA, and interfere with both the formation and amplification of covalently closed circular DNA, which is essential for viral persistence.
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3d rendering of bispecific antibodies
Infection

Cell-penetrating bispecific HBcAg/pre-S1 antibody suppresses HBV replication and secretion

April 1, 2025
Hepatitis B virus (HBV) infection is associated with liver diseases, including chronic hepatitis, which notably increases the risk of cirrhosis and hepatocellular carcinoma (HCC) development. Although some of the current treatment strategies promote virological suppression, they are insufficient to halt HCC development.
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Immuno-oncology

Aligos Therapeutics patents new inhibitors of PD-1, PD-L1 or PD-1/PD-L1 interaction

Feb. 4, 2025
Aligos Therapeutics Inc. has disclosed programmed cell death 1 (PDCD1; PD-1; CD279) and/or PD-1 ligand 1 (PD-L1; CD274) and/or PD-1/PD-L1 interaction inhibitors reported to be useful for the treatment of hepatocellular carcinoma and hepatitis B.
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Hepatitis B virus
Infection

SA-1211, a dual-target siRNA with promising antiviral activity in AAV-HBV mice

Dec. 4, 2024
Researchers from Suzhou Siran Biotech Co. Ltd. presented the discovery and preclinical characterization of SA-1211, an N-acetylgalactosamine (GalNAc)-conjugated siRNA dimer targeting both hepatitis B virus (HBV) and PD-L1 gene expression, being developed as a potential new therapeutic candidate for the treatment of chronic hepatitis B (CHB).
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Infection

Preclinical characterization of Tune-401, a first-in-class LNP-encapsulated epigenetic silencer therapy for hepatitis B

Dec. 4, 2024
Tune Therapeutics Inc. is evaluating Tune-401.
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Transmission electron micrograph of hepatitis B virus particles
Infection

Therapeutic hepatitis B vaccine generates robust HBc-specific T-cell responses in preclinical tests

Dec. 2, 2024
Researchers from presented preclinical data for AVX-70371, a novel therapeutic vaccine being developed for the treatment of chronic hepatitis B virus (HBV) infection.
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Infection

EDP-514 demonstrates favorable preclinical PK profile, excellent target tissue penetration

Nov. 22, 2024
Enanta Pharmaceuticals Inc. has released preclinical pharmacokinetics (PK) data for EDP-514, a potent and selective class II core assembly modulator in phase I development for the oral treatment of hepatitis B.
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Hepatitis B virus rendering
Infection

Epigenic Therapeutics’ epigenetic inactivator cleared to enter clinic for chronic hepatitis B

Nov. 20, 2024
Epigenic Therapeutics Inc. has received clinical trial application (CTA) approval from the New Zealand Medicines and Medical Devices Safety Authority (Medsafe) and the Health and Disability Ethics Committees (HDEC) to initiate a clinical trial for EPI-003, an investigational, liver-targeting antiviral therapy for chronic hepatitis B virus (HBV) infection.
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Illustration of liver infection

The Liver Meeting: A cure for hepatitis B’s low-hanging fruit

Nov. 18, 2024
By Brian Orelli
Patients infected with hepatitis C have had the ability to rid their livers of the virus for some time, while patients with chronic hepatitis B virus infection have been required to take medications for the rest of their lives in the hopes of just dampening damage to the liver caused by the virus. But, at The Liver Meeting 2024, Arbutus presented data from the phase IIa Im-prove study suggesting a cure might be on its way with its DNAi drug, which binds to the viral mRNA promoting its cutting, leading to loss of translation of the viral proteins.
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