American Association for the Study of Liver Diseases, The Liver Meeting®

American Association for the Study of Liver Diseases, The Liver Meeting®
November 15-19, 2024
San Diego, California, USA

AASLD-2024.

Explore more information for Gilead Liver Diseases therapies
Results (23)

Kinetics of Hepatitis B Surface Antigen Loss Following 8 Years of Tenofovir-based Treatment in Hepatitis B e Antigen-negative and Hepatitis B e Antigen-positive Patients With Chronic Hepatitis B

Associations Between Biomarkers and Magnetic Resonance Imaging-Derived ANALI Score in Patients with Primary Sclerosing Cholangitis: Analysis from the Phase 3 PRIMIS Study

Similar Rates of Biochemical Response Are Observed Across Virologic Response Categories Over 96 Weeks of Bulevirtide Monotherapy in Patients With Chronic Hepatitis Delta

Long-term safety of seladelpar with up to 5 years of treatment in patients with primary biliary cholangitis

Long-Term Efficacy and Safety of Open-Label Seladelpar Treatment in Patients With Primary Biliary Cholangitis: Pooled Interim Results for 24 Months From the ASSURE Study

Pharmacokinetics, Pharmacodynamics, and Safety of Bulevirtide 2 mg Once-Daily for 6 Days in Participants with Moderate and Severe Hepatic Impairment and in Matched Control Participants with Normal Hepatic Function

Hepatitis B surface antigen (HBsAg) response in patients with chronic hepatitis delta receiving bulevirtide with or without pegylated interferon alfa-2a in MYR204

Assessing the Health-related Quality of Life, Impairment and Productivity among Individuals with PBC and Pruritus: Results from the ITCH-E Study

SELADELPAR AND REDUCTIONS IN LIPIDS IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS WITH AND WITHOUT STATIN USE IN THE PHASE 3 PLACEBO-CONTROLLED RESPONSE STUDY

ATTENUATION, NEAR RESOLUTION, AND PREVENTION OF PRURITUS IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS TREATED WITH SELADELPAR: A SECONDARY ANALYSIS OF PATTERNS OF PRURITUS CHANGE IN THE RESPONSE TRIAL

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

Results From a Phase 2a, Open-Label Study to Evaluate the Safety and Efficacy of Novel Combination Therapies Containing VIR-2218, Selgantolimod, and Nivolumab for the Treatment of Chronic Hepatitis B

Barodelta study: Real world data (RWD) of patient's characteristics, adherence, persistence, and empowerment in patients with chronic hepatitis Delta and treated by bulevirtide (BLV) 2 mg. Analysis from the French National Health Data System (SNDS).

Pharmacokinetics, Pharmacodynamics, and Safety of Bulevirtide 2 mg Once-Daily for 6 Days in Participants Normal and Severely Impaired Renal Function 

Biomarkers Associate with Fibrosis Progression in Patients with Primary Sclerosing Cholangitis: An Ad-hoc Analysis from the PRIMIS Study

Efficacy and safety of BLV monotherapy for chronic hepatitis delta: post treatment results through 48 weeks after the end of treatment from an interim analysis of a randomized Phase 3 study MYR301

The SVR10K study: A Real-World Data with Pangenotypic Direct-Acting Antivirals Across Multiple Diverse Regions

Immunologic Biomarker Dynamics in Chronic Hepatitis B: Insights From a Phase 2a Open-Label Study on Combination Therapies With siRNA, Selgantolimod, and Nivolumab

Immune-Related Adverse Events With Low-Dose Nivolumab in Patients With Chronic Hepatitis B: Experience From 3 Clinical Studies

A Phase 1b, Open-Label Study to Evaluate the Safety and Efficacy of Novel Hepatitis B Virus Combination Therapies in Patients Living with Chronic Hepatitis B (CHB)

Treatment persistence and discontinuation among chronic hepatitis B patients initiating antiviral treatment

Characterization of Changes in Noninvasive Fibrosis Markers Over 8 years of Tenofovir-based Treatment in Chronic Hepatitis B Patients Enrolled in Two Phase 3 Trials

The REAL Study: Real-world Evaluation of ALP Normalization in PBC Patients Receiving Treatment