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Clear standards
But the key word is treatment
Methods In this 48-week, phase 2 trial, we randomly assigned adults with biopsy-confirmed MASH and fibrosis stage F1 through F3 in a 1:1:1:1 ratio to receive once-weekly subcutaneous injections of survodutide at a dose of 2.4, 4.8, or 6.0 mg or placebo
This discouragement often leads to premature discontinuation, as evidenced by real-world data showing that 75% of patients without meaningful early weight loss will not achieve clinically significant results after six months of behavioral therapy alone
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