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Survodutide

All articles tagged with #survodutide

Dual-agonist survodutide reduces liver fat and weight in phase 3 MASLD trial
health1 month ago

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.

Zealand Pharma slides on safety concerns around survodutide
business1 month ago

Zealand Pharma slides on safety concerns around survodutide

Zealand Pharma’s shares fell about 25-26% after late-stage survodutide data showed notable GI adverse events, with a 19% discontinuation rate and more than 40% of patients reporting vomiting, raising questions about safety/tolerability despite up to 16.6% average weight loss versus placebo. Analysts warned the safety profile could limit commercial potential amid strong competition from Novo Nordisk and Eli Lilly, contributing to a steep year-to-date decline as Zealand works with Boehringer Ingelheim and Roche.

"Weight-Loss Drug Shows Promise in Treating Liver Disease in MASH Patients"
health2 years ago

"Weight-Loss Drug Shows Promise in Treating Liver Disease in MASH Patients"

Boehringer Ingelheim and Zealand Pharma's drug, survodutide, has shown success in a Phase 2 study for the treatment of the liver condition MASH, with 83% of patients experiencing significant improvements compared to those who received a placebo. The study met its primary endpoint of improvements in MASH without the worsening of fibrosis, and secondary endpoints, including an improvement in fibrosis, were also achieved. This development comes amid increasing competition in the obesity medicine field.