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

  • Lee M. Kaplan,
  • Elena Startseva,
  • Carel W. le Roux,
  • Sean Wharton,
  • Biykem Bozkurt,
  • Daniel F. Mazo,
  • Jessica von Schlippenbach,
  • Sandra González Maldonado,
  • Samina Ajaz Hussain,
  • Guy W. Neff,
  • Yaneicy Gonzalez Rojas,
  • Charles Smith,
  • Ramy Younes,
  • Arun J. Sanyal,
  • Antonio Olveira,
  • Juan M. Pericás,
  • Mark Leibowitz,
  • Douglas Denham,
  • Kevin Korenblat,
  • Michael Herman,
  • Shekhar Challa,
  • Rasha Youssef,
  • Masi Khaja,
  • Apinya Vutikullird,
  • Humberto Aguilar,
  • Naga Chalasani,
  • James Maher,
  • Ronald Surowitz,
  • Cassandra Steimle,
  • Yaneicy G. Rojas,
  • Antonio Sanchez,
  • Ruth E. Kavcioglu,
  • Julio Vijil,
  • Robert Perry,
  • Guy Neff,
  • Martha G. Navarro,
  • Omer Khalid,
  • Rizwana Mohseni,
  • Michael Zimmerman,
  • Julie Vu,
  • Gregg Lucksinger,
  • Satish Iduru,
  • Dmitry Shuster,
  • Bruce Segal,
  • Paul Hellstern

摘要

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 m2 or ≥27 kg m2 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).