An Exelixis Product for the Clinical Management of HCC
Supported by: An Exelixis Product for the Clinical Management of HCC
Presenter:
Julio A. Gutierrez, MD, MS
Supported by: An Exelixis Product for the Clinical Management of HCC
Presenter:
Julio A. Gutierrez, MD, MS
Supported by: Mallinckrodt Pharmaceuticals
Presenter:
Kris V. Kowdley, MD, AGAF, FAASLD, FACP, FACG
Supported by: Labcorp
NIS4® is a blood-based test designed to effectively identify patients with at-risk metabolic dysfunction-associated steatohepatitis (MASH, formerly NASH). The more recently developed NIS2+™ is an optimized version of NIS4® that was
Supported by: Intercept Pharmaceuticals, Inc.
Join us for an informative presentation that discusses taking treatment for Primary Biliary Cholangitis (PBC) a step further. Learn about an approved therapy for patients with PBC.
Presenters:
Kris Kowdley,
Supported by: Alnylam Pharmaceuticals
AHP is a rare, genetic disease characterized by debilitating, potentially life-threatening attacks of which the cardinal symptom is severe, diffuse abdominal pain. This presentation will provide a disease overview an
Supported by: Ipsen
In primary biliary cholangitis, it is important to look beyond the liver to make meaningful improvements for patients, so how can we optimize regular disease monitoring alongside the impact of symptoms on patients’ lives? Join us to
Supported by: Novo Nordisk
Join us as we review the pathophysiology of metabolic dysfunction-associated steatohepatitis (MASH, formerly known as NASH, non-alcoholic steatohepatitis), including the impact of underlying metabolic comorbidities. We will als
Supported by: Perspectum
In this session we will introduce cT1, a well-established biomarker in liver disease derived from MRI technology. cT1 has played a pivotal role in numerous clinical trials focused on Steatotic Liver Disease, proving its effectiv
Supported by: Genentech, A Member of the Roche Group
This program will provide an overview of HCC disease and staging, IMbrave150 including the clinical trial design, patient characteristics, pivotal efficacy and safety data, and exploratory subgroup ana