AASLD 2025 The Liver Meeting®

AASLD 2025 The Liver Meeting®
November 07-11, 2025
Washington D.C.

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

Explore more information for Gilead Liver Diseases therapies
Results (22)

INTEGRATED VIROLOGY ANALYSIS OF BULEVIRTIDE (BLV) MONOTHERAPY IN CHRONIC HEPATITIS DELTA: POOLED DATA FROM MYR301 AND MYR204

A Higher Proportion of Unglycosylated HBsAg is Predictive of Faster HBsAg Decline Kinetics In Patients with Chronic Hepatitis B

REAL-WORLD PERSISTENCY OF BULEVIRTIDE THERAPY IN CHRONIC HEPATITIS D PATIENTS IN GERMANY: A RETROSPECTIVE OBSERVATIONAL ANALYSIS

36 MONTHS OF TREATMENT WITH SELADELPAR IS ASSOCIATED WITH STABLE OR IMPROVED LIVER STIFFNESS IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS

PATIENT-REPORTED BURDEN AND HEALTH-RELATED QUALITY OF LIFE AMONG PATIENTS WITH HEPATITIS DELTA: RESULTS FROM A REAL-WORLD STUDY IN EUROPE

IMPROVEMENTS IN PATIENT-REPORTED GENERAL HEALTH AND WELL-BEING IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS TREATED WITH SELADELPAR IN THE RESPONSE TRIAL

EFFICACY AND SAFETY OF SELADELPAR VS. ELAFIBRANOR IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS: A MATCHING-ADJUSTED INDIRECT COMPARISON

PHARMACOKINETICS, PHARMACODYNAMICS, AND SAFETY OF BULEVIRTIDE 10 MG ONCE DAILY FOR 6 DAYS IN PARTICIPANTS WITH SEVERE HEPATIC IMPAIRMENT AND IN MATCHED CONTROL PARTICIPANTS WITH NORMAL HEPATIC FUNCTION

REAL-WORLD EXPERIENCE OF SELADELPAR AMONG PATIENTS WITH PRIMARY BILIARY CHOLANGITIS INCLUDING PATIENTS SWITCHED FROM OBETICHOLIC ACID

REDUCTION IN ITCH-ASSOCIATED DISABILITY AND PRURITUS DISTRIBUTION IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS TREATED WITH SELADELPAR IN THE RESPONSE TRIAL

EFFICACY AND SAFETY OF SELADELPAR IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS AND ELEVATED BILIRUBIN AT BASELINE IN THE PHASE 3 PLACEBO-CONTROLLED RESPONSE TRIAL

SELADELPAR LEADS TO SUSTAINED, CLINICALLY MEANINGFUL IMPROVEMENT IN PRURITUS: RESULTS FROM THE ASSURE STUDY UP TO 30 MONTHS

PERSISTENT LOW VIREMIC RELAPSE VS HIGH VIREMIC RELAPSE AFTER THE END OF TREATMENT WITH BULEVIRTIDE WITH OR WITHOUT PEGYLATED INTERFERON IN PATIENTS WITH CHRONIC HEPATITIS DELTA VIRUS

SELADELPAR LEADS TO SUSTAINED REDUCTION IN CHOLESTATIC MARKERS WITH CONSISTENT SAFETY PROFILE IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS TREATED UP TO 48 MONTHS

ELEVATIONS IN TOTAL SERUM BILE ACIDS DURING BULEVIRTIDE TREATMENT ARE ASYMPTOMATIC AND NOT ASSOCIATED WITH ADVERSE EVENTS OF INTEREST IN PATIENTS WITH CHRONIC HEPATITIS DELTA

REAL-WORLD IMPLICATIONS OF THE NEW AASLD/IDSA HCV "TEST AND TREAT" ALGORITHM: FOCUS ON CARDIOVASCULAR COMEDICATIONS IN HEPATITIS C VIRUS (HCV) PATIENTS RECEIVING DIRECT-ACTING ANTIVIRALS (DAAS)

SUSTAINED EFFICACY AND SAFETY OF SELADELPAR FOR UP TO 36 MONTHS IN PATIENTS WITH PRIMARY BILIARY CHOLANGITIS FROM THE PLACEBO-CONTROLLED RESPONSE STUDY TO THE OPEN-LABEL ASSURE STUDY

A RANDOMIZED, PLACEBOCONTROLLED, PHASE 2 STUDY OF THE SAFETY AND EFFICACY OF COMBINATION TREATMENT WITH SEMAGLUTIDE, CILOFEXOR AND FIRSOCOSTAT IN PATIENTS WITH COMPENSATED CIRRHOSIS DUE TO METABOLIC DYSFUNCTION-ASSOCIATED STEATOHEPATITIS (WAYFIND)

SAFETY, TOLERABILITY, IMMUNOGENICITY, AND ANTIVIRAL EFFICACY OF GS-2829 AND GS-6779, A NOVEL, ARENAVIRAL-VECTORED, THERAPEUTIC HEPATITIS B VACCINE: RESULTS FROM A PHASE 1B STUDY IN VIRALLY SUPPRESSED PATIENTS WITH CHRONIC HEPATITIS B

EXPOSURE TO TENOFOVIR ALAFENAMIDE AND TENOFOVIR DISOPROXIL FUMARATE AND THE RISK OF HEPATOCELLULAR CARCINOMA

CUMULATIVE REVIEW OF SOFOSBUVIR/VELPATASVIR EXPOSURE IN PREGNANT WOMEN WITH HEPATITIS C FROM A PHARMACOVIGILANCE SAFETY DATABASE

IS SVR4 TESTING AN ACCEPTABLE ALTERNATIVE MEASURE OF HCV CURE IN RE-TREATED PATIENTS FOLLOWING DAA FAILURE? A SVR 4/12 CONCORDANCE EVALUATION FROM THE POLARIS CLINICAL TRIALS