Placebo-corrected reductions in systolic and diastolic BP at 4.8 mg
Survodutide
INVESTIGATIONALGlucagon and GLP-1 receptor dual agonist
Survodutide is investigational in the scoped programme below. Study records do not establish approval, safety or personal suitability. Results describe observations and do not provide treatment advice.
INVESTIGATIONAL Global programme; Obesity and metabolic dysfunction-associated steatohepatitis; Subcutaneous injection; as of 2026-07-13. Zealand Pharma
The grade rates how strong the evidence is, not how good or safe the drug is. A low or very-low grade means the evidence is thin, not that an effect is harmful or ruled out.
Survodutide reduced blood pressure (with waist circumference and triglycerides) in phase 2 obesity cardiometabolic analysis.
Reductions in total cholesterol, LDL-C, triglycerides; increase in HDL-C
Survodutide reduced TG, total and LDL cholesterol and VLDL in phase 2 obesity; HDL relatively unchanged.
GI AEs (nausea, diarrhoea, vomiting) markedly more frequent than placebo; dose-dependent, titration-managed; high AE-related discontinuation, mainly GI.
GI events dominant; higher than placebo
Survodutide (BI 456906; Boehringer/Zealand) is a GLP-1/glucagon dual agonist in phase 3 for obesity and MASH. In a 48-week phase 2 MASH trial, MASH improvement without...
In a 48-week phase 2 trial (biopsy MASH, fibrosis F1-F3), the GLP-1/glucagon dual survodutide was superior to placebo for histologic MASH improvement without fibrosis...
In the phase 2 obesity dose-finding trial (NCT04667377), survodutide raised heart rate by a mean ~2.7 bpm (all doses pooled) versus ~0.1 bpm on placebo, with a...
SYNCHRONIZE (phase 3) prespecified MRI substudy: survodutide reduced visceral adipose tissue ~34%, subcutaneous adipose tissue ~28% and lean body volume ~9.8%; fat...
Weight loss driven by increased energy expenditure plus reduced food intake (preclinical)
Acylated (C18) GCGR/GLP-1R dual agonist, once-weekly; engages both receptors in vivo
Serious adverse events comparable to placebo; no safety signal attributed to glucagon receptor agonism
Dose-dependent weight loss vs placebo over 46 weeks in obesity without diabetes