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Its relatively short treatment duration, high curative potential, and cost-effectiveness render it a feasible and impactful intervention, even in resource-limited settings [11]

Going forward, increased vaccine studies in the Syrian hamster model may provide critical preclinical data, as the Syrian hamster appears to replicate human COVID-19 immunopathology more closely than rhesus macaque models 75

Conclusion: The results suggest that EA3571 has well-tolerated favorable safety profile and improves MASH by enhanced GLP-1 level due to inhibiting enteropeptidase/trypsin on the luminal side in patients with MASH