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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]

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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

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

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