PharmaNest, a leader in high-resolution, single-fiber quantitative Digital Pathology and Artificial Intelligence, showcases the performance of its FibroNest Ph-FCS digital biomarker for quantifying fibrosis severity and its clinical utility in Phase 2 and Phase 3 studies for patients with Metabolic Associated Steatohepatitis (MASH).
PRINCETON, NJ / ACCESSWIRE / June 3, 2024 / PharmaNest Inc., a leader in high-resolution quantitative Digital Pathology and Artificial Intelligence, announces today that it will present, alongside its collaborators, seven abstracts at this year's International Liver Congress - EASL in Milan, Italy, June 5-8, 2024. The abstracts highlight the utility and performance of its FibroNest Ph-FCS digital pathology biomarker for quantifying fibrosis severity and its clinical utility in Phase 2 and Phase 3 studies for patients with Metabolic Associated Steatohepatitis (MASH).
FibroNest is the first multivendor, high-resolution, single-fiber digital pathology quantitative image analysis platform for assessing the severity and progression of fibrosis and inflammation in MASH. Presentations include results from the analytical validation of the fibrosis biomarker, focusing on accuracy, reproducibility, repeatability, and intra-liver variability. Additionally, the presentations will demonstrate the biomarker's sensitivity to detect changes and regression of fibrosis in patients with MASH following bariatric surgery, a well-known and efficacious intervention.
Additional oral and poster presentations will describe the utility of the FibroNest method in screening for anti-fibrotic compounds and evaluating complex phenotypes of fibrosis in the extracellular matrix, along with their relationship to intrahepatic cholangiocarcinoma.
"The automated high-resolution quantification of the phenotype of fibrosis severity from the same slides reviewed by pathologists offers a robust and scalable method to generate continuous digital biomarkers that resolve faint changes in fibrosis severity, account for the efficacy of an intervention, and predict liver-related clinical events," said Mathieu Petitjean, Ph.D., CEO and founder of PharmaNest. "Because the approach is fully quantitative and not based on existing staging or grading paradigms, it can be used throughout the drug discovery and development process and across etiologies of fibrosis."
Communications will take place on the following schedule:
These abstracts will be available on the PharmaNest website at the end of the week at fibronest.com/science.
Contact Information:
Mathieu Petitjean
CEO
info@pharmanest.com
(609) 375 2003
SOURCE: PharmaNest, Inc.
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