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Survodutide diabetes phase 2 · GLP Finds editorial

Survodutide versus semaglutide: an early comparison in diabetes

A short trial compared selected survodutide and semaglutide regimens in type 2 diabetes.

The takeaway

Survodutide showed promising weight results in a short diabetes trial, alongside more treatment-stopping side effects. The doses and study design matter when interpreting the comparison.

Who was studied?

Researchers randomized 413 adults with type 2 diabetes taking metformin; 411 received treatment. Eight groups tested six survodutide regimens, placebo, or semaglutide for 16 weeks. Blood sugar was the primary outcome; weight was secondary.

Estimated weight loss at week 16 in selected groups; 413 randomized across eight groups
Percent of starting weight; secondary outcome
Survodutide 1.8 mg twice weekly8.7%Semaglutide 1.0 mg once weekly5.3%

Original visual based on the study.

Estimated weight loss at week 16 in selected groups; 413 randomized across eight groups
Group or measureResult
Survodutide 1.8 mg twice weekly8.7%
Semaglutide 1.0 mg once weekly5.3%

What changed?

Estimated average weight loss reached 8.7% with survodutide 1.8 mg twice weekly, versus 5.3% with semaglutide 1.0 mg weekly. These are selected groups, not results for every survodutide dose.

Across all survodutide groups, 15.9% stopped treatment because of adverse events, compared with 4.0% on semaglutide and 5.1% on placebo. Digestive symptoms were common.

What limits the comparison?

Participants knew when they received semaglutide. Survodutide doses increased rapidly, and the study was short. This was not a comparison against weekly semaglutide 2.4 mg for obesity, nor evidence of a universal winner.

Boehringer Ingelheim funded the trial.

Sources

Blüher and colleagues, Diabetologia, 2024; correction.