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The FDA has approved the first AI tool, AIM-NASH, to standardize liver biopsy analysis in MASH clinical trials, boosting efficiency and consistency.
The FDA has qualified the first AI tool, AIM-NASH, to assist in clinical trials for metabolic dysfunction–associated steatohepatitis (MASH), a severe form of fatty liver disease.
The cloud-based system analyzes liver biopsy images to provide standardized assessments of fat, inflammation, and scarring, improving consistency and efficiency in trial data collection.
While final diagnoses remain with human pathologists, the tool aims to reduce variability and accelerate drug development, potentially cutting trial timelines and costs.
It is now available for use in any drug development program under the qualified context of use.
La FDA ha aprobado la primera herramienta de IA, AIM-NASH, para estandarizar el análisis de la biopsia del hígado en los ensayos clínicos MASH, aumentando la eficiencia y la consistencia.