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DOI 10.1038/s41591-026-04479-3

Медицинская библиотека · Nature medicine · 2026

Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial.

Kaplan Lee M, Startseva Elena, le Roux Carel W, Wharton Sean, Bozkurt Biykem, Mazo Daniel F, von Schlippenbach Jessica, González Maldonado Sandra, Ajaz Hussain Samina, Neff Guy W, Gonzalez Rojas Yaneicy, Smith Charles, Younes Ramy, Sanyal Arun J, SYNCHRONIZE-MASLD Investigators

СтатьяРандомизированное исследованиеКлиническое исследование III фазыПеревод пока не подготовлен

Аннотация

Survodutide is a glucagon receptor/glucagon-like peptide-1 receptor dual agonist under investigation for treating obesity and related diseases. The SYNCHRONIZE-MASLD phase 3, randomized, double-blind, placebo-controlled trial included 216 adults (131 female and 85 male) with obesity (defined as a body mass index ≥30 kg m-2 or ≥27 kg m-2 with at least one obesity complication) and at-risk metabolic dysfunction-associated steatotic liver disease (MASLD), defined by MASLD with evidence of liver inflammation and/or fibrosis by noninvasive tests (NITs) or biopsy-confirmed metabolic dysfunction-associated steatohepatitis (MASH). Participants were randomized (2:1) and treated with once-weekly subcutaneous injections of survodutide 6.0 mg (n = 146) or placebo (n = 70). The co-primary endpoints, ≥30% reduction in magnetic resonance imaging-proton density fat fraction (MRI-PDFF)-assessed liver fat content (LFC) and percentage change in body weight (both baseline to week 48), were met. In total, 84.2% of survodutide-treated patients versus 24.3% of placebo-treated patients had ≥30% reduction in LFC using the efficacy estimand (P < 0.0001; treatment regimen estimand: 68.5% versus 28.6%, respectively; P < 0.0001). Mean percentage change in body weight was -12.2% with survodutide and -1.0% with placebo using the efficacy estimand (P < 0.0001; treatment regimen estimand: -8.7% versus -1.4%, respectively; P < 0.0001). The most frequently reported adverse events with survodutide were gastrointestinal, commonly occurring during dose escalation, and were generally of mild-to-moderate severity. In adults with obesity and at-risk MASLD, survodutide treatment was statistically and clinically superior to placebo for reductions in MRI-PDFF-assessed LFC and body weight. Limitations included short trial duration (48 weeks) and limited global reach (participants recruited in the United States and Spain).

Для цитирования: Kaplan Lee M, Startseva Elena, le Roux Carel W, Wharton Sean, Bozkurt Biykem, Mazo Daniel F, von Schlippenbach Jessica, González Maldonado Sandra, Ajaz Hussain Samina, Neff Guy W, Gonzalez Rojas Yaneicy, Smith Charles, Younes Ramy, Sanyal Arun J, SYNCHRONIZE-MASLD Investigators. Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial.. Nature medicine. 2026. DOI: 10.1038/s41591-026-04479-3.

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