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Profil bibliographique

John M. Vierling

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

5Publications signalées
34Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Liver Disease and TransplantationGallbladder and Bile Duct DisordersLiver Diseases and ImmunityProtein Kinase Regulation and GTPase SignalingLiver Disease Diagnosis and Treatment

Les publications récentes

Accès ouvert 2025 article OpenAlex

EFFICACY AND SAFETY OF SELADELPAR IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS AND COMPENSATED CIRRHOSIS IN THE PHASE 3 PLACEBO-CONTROLLED RESPONSE TRIAL

Alejandra Villamil, Ziad H Younes, Christopher L. Bowlus, John M. Vierling et autres

In the Phase 3 RESPONSE trial (NCT04620733), seladelpar, a first-in-class delpar (selective peroxisome proliferator–activated receptor delta agonist), significantly improved biomarkers of cholestasis in patients with primary biliary cholangitis (PBC) over 12 months vs placebo. More patients with cirrhosis met the primary endpoint …

ar, us, cz, it, nl (code pays fourni par la source)

0 citations Annals of Hepatology
Accès ouvert 2024 article OpenAlex

A virtual scalable model of the Hepatic Lobule for acetaminophen hepatotoxicity prediction

Stelian Camara Dit Pinto, Jalal Cherkaoui, Debarshi Ghosh, Valentine Cazaubon et autres

Addressing drug-induced liver injury is crucial in drug development, often causing Phase III trial failures and market withdrawals. Traditional animal models fail to predict human liver toxicity accurately. Virtual twins of human organs present a promising solution. We introduce the Virtual Hepatic …

us, fr (code pays fourni par la source)

5 citations npj Digital Medicine
Accès ouvert 2024 article OpenAlex

Fazirsiran for Adults With Alpha-1 Antitrypsin Deficiency Liver Disease: A Phase 2 Placebo Controlled Trial (SEQUOIA)

Virginia Clark, Charlie Strange, Pavel Strnad, Antonio J. Sanchez et autres

BACKGROUND & AIMS: Homozygous ZZ alpha-1 antitrypsin (AAT) deficiency produces mutant AAT (Z-AAT) proteins in hepatocytes, leading to progressive liver fibrosis. We evaluated the safety and efficacy of an investigational RNA interference therapeutic, fazirsiran, that degrades Z-AAT messenger RNA, reducing deleterious protein …

us, de, pt, nl, it, es (code pays fourni par la source)

29 citations Gastroenterology

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