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Adults with biopsy-proven MASH and fibrosis stage F1F2F3, with or without type 2 diabetes, and with MRI-PDFF 8% at screening are randomised 1:1:1:1 to efocipegtrutide 2, 4, and 6 mg once-weekly subcutaneously or placebo for 52 weeks (estimated enrolment: N = 240)

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