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Home » Topics » Conferences » American Association for the Study of Liver Diseases

American Association for the Study of Liver Diseases
American Association for the Study of Liver Diseases RSS Feed RSS

Liver
Gastrointestinal

Dual-targeted approach for hepatobiliary diseases presented

Nov. 28, 2024
Rectify Pharmaceuticals Inc. has conducted preclinical testing on RTY-694, an oral dual-targeted positive functional modulator for use in the treatment of hepatobiliary disorders.
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Liver illustration
Gastrointestinal

CLM-022, an NLRP3 inflammasome inhibitor, reverses chronic and acute liver inflammation

Nov. 27, 2024
NLRP3 inflammasome activation, pro-inflammatory cytokine production and pyroptosis are key features of inflammation that contribute to liver fibrosis progression, cirrhosis and end-stage liver failure. Pyroptosis, a lytic form of inflammatory-regulated cell death, is regulated by multiprotein complexes expressed in both parenchymal and nonparenchymal hepatic cells. Researchers from Genfit SA presented preclinical efficacy data on CLM-022, a synthetic pentacyclic triterpenoid derivative designed to target the NLRP3 complex.
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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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Gastrointestinal

New preclinical data on CVI-2742 for treating MASH

Nov. 21, 2024
The efficacy and capabilities of CVI Pharmaceuticals Inc.'s CVI-2742, a THR-β agonist, were tested in nonhuman primates.
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Gastrointestinal

RTX-001, an engineered macrophage therapy with hepatic regenerative effects

Nov. 21, 2024
As a consequence of chronic liver disease progression, severe cirrhosis, decompensation and fibrosis culminates in end-stage liver disease (ESLD). There are no treatment options approved for ESLD, but, among others, regenerative therapies with autologous, nonengineered, pro-regenerative macrophages have shown good tolerability and improved transplant-free survival in the clinical setting.
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Photomicrograph of liver biopsy in a patient with cirrhosis, showing bridging septal fibrosis and regenerative nodules.
Gastrointestinal

FAP inhibitor AZD-2389 improves liver fibrosis and MASH

Nov. 20, 2024
Astrazeneca plc has developed a potent oral fibroblast activation protein (FAP) inhibitor, AZD-2389, that avoids the cleavage of FGF21 and α2-AP. AZD-2389 was tested in cynomolgus monkeys with diet-induced MASH.
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Infection

Bifunctional molecule capsid modulator and cGAS agonist achieves complete cure in AAV-HBV mice

Nov. 30, 2023
LW-231, under development by Shanghai Longwood Biopharmaceuticals Co. Ltd., is a novel bifunctional molecule designed to simultaneously modulate hepatitis B virus (HBV) capsid assembly and activate cGAS-STING pathway. Preclinical data were recently presented.
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Illustration of the liver, gallbladder, stomach, and pancreas
Gastrointestinal

Lerna Biopharma presents first-in-class GalNAc-siRNA therapeutic for treatment of liver diseases

Nov. 23, 2023
Researchers from Lerna Biopharma Pte. Ltd. (formerly Cargene Therapeutics Pte. Ltd.) recently presented the discovery and preclinical evaluation of a first-in-class GalNAc-siRNA therapeutic, CG-LR1, being developed for the treatment of liver diseases.
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Transmission electron micrograph of hepatitis B virus particles
Infection

A-7387 inhibits bile acid transporter and blocks hepatitis infection

Nov. 21, 2023
Researchers from Ipsen Ltd. and affiliated organizations presented the discovery and preclinical characterization of a novel NTCP inhibitor, A-7387, being developed for the treatment of HBV and HDV infections.
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Liver disease
Gastrointestinal

HNF4A upregulation confers protection in liver fibrosis

Nov. 21, 2023
Omega Therapeutics Inc. has presented preclinical data on hepatocyte nuclear factor 4-alpha (HNF4A) modulation in fibrotic liver disease models to enhance its key role and suggest it as a potent therapeutic target.
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