Dual-agonist survodutide reduces liver fat and weight in phase 3 MASLD trial

In the SYNCHRONIZE-MASLD phase 3 trial, 216 adults with obesity and metabolic dysfunction-associated steatotic liver disease received weekly survodutide 6.0 mg or placebo for 48 weeks. Survodutide met both co-primary endpoints, with 84.2% achieving ≥30% reduction in liver fat content (MRI-PDFF) versus 24.3% on placebo, and significant weight loss compared with placebo. About six in ten treated participants reached normalization of liver fat. The study used a dose-escalation period to 6.0 mg followed by a maintenance phase and included extensive safety monitoring. Secondary endpoints showed favorable changes in liver enzymes, liver stiffness/volume, insulin resistance, and other noninvasive liver tests. These results support survodutide as a potential therapy for obesity and MASLD, with data sharing and ongoing follow-up planned.
- Survodutide in adults with obesity and metabolic dysfunction-associated steatotic liver disease: SYNCHRONIZE-MASLD, a randomized, double-blind, placebo-controlled phase 3 trial Nature
- Weight loss drug maker sinks 25% after new safety data spooks investors CNBC
- Boehringer-Zealand's obesity drug shows promise in cutting visceral, liver fat Reuters
- Zealand Pharma Shares Slide After Boehringer Study Shows Obesity Shot’s Side Effects WSJ
- ADA: Boehringer execs claim survodutide tolerability 'consistent' with class despite phase 3 update Fierce Biotech
Reading Insights
0
5
46 min
vs 47 min read
99%
9,270 → 118 words
Want the full story? Read the original article
Read on Nature