What this page establishes
- In SUSTAIN-7 at week 40, semaglutide 0.5 mg lowered HbA1c by 1.5 percentage points versus 1.1 for dulaglutide 0.75 mg, and semaglutide 1.0 mg by 1.8 versus 1.4 for dulaglutide 1.5 mg.
- Trulicity is licensed to reduce major adverse cardiovascular events in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors. Doses: 0.75, 1.5, 3 and 4.5 mg weekly.
- Ozempic is licensed to reduce major adverse cardiovascular events in adults with type 2 diabetes and established cardiovascular disease, and separately for kidney outcomes in type 2 diabetes with chronic kidney disease.
Quick answers
Which one controls blood sugar better?
In SUSTAIN-7, semaglutide beat dulaglutide at both dose pairs tested. Dulaglutide is now licensed up to 4.5 mg, which that trial did not test, so the result is a comparison at the doses studied rather than at current maximums.
Read the full answer
Which is better if I have not had a heart attack but have risk factors?
That is the one population where the labels clearly differ. Trulicity’s cardiovascular indication covers multiple risk factors without established disease.
Read the full answer
Ozempic’s requires established cardiovascular disease. This is a prescribing decision, but the labels are not equivalent here.Do either help with weight?
Both reduce weight as a secondary effect and neither is licensed for weight management. The weight-licensed brands in this class are Wegovy, Zepbound, Saxenda and Foundayo.
Read the full answer
Trulicity is dulaglutide from Eli Lilly, Ozempic is semaglutide from Novo Nordisk, and both are once-weekly injections for type 2 diabetes. SUSTAIN-7 compared them directly, and the labels differ in a way that matters more than most brand comparisons admit.
The head-to-head
SUSTAIN-7 was an open-label phase 3b trial across 194 sites in 16 countries, comparing semaglutide against dulaglutide added to metformin at two matched dose pairs.
At week 40, semaglutide 0.5 mg lowered HbA1c 1.5 percentage points against 1.1 for dulaglutide 0.75 mg, and semaglutide 1.0 mg lowered it 1.8 points against 1.4 for dulaglutide 1.5 mg. Semaglutide arms also lost more weight and more often reached target HbA1c.
Dulaglutide has since been licensed up to 4.5 mg, above the 1.5 mg tested here.
The licence difference that gets left out
Trulicity is licensed to reduce major adverse cardiovascular events in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors.
Ozempic’s cardiovascular indication requires established cardiovascular disease.
That difference covers a real and large group: people with risk factors who have not yet had an event. On that population Trulicity has a licensed claim and Ozempic does not, which is the opposite direction to the head-to-head result.
What Ozempic has that Trulicity does not
A kidney indication. Ozempic is licensed to reduce the risk of sustained eGFR decline, end-stage kidney disease and cardiovascular death in type 2 diabetes with chronic kidney disease. Trulicity carries no renal outcome indication.
The evidence, one row per claim
| Claim | Tier | Source |
|---|---|---|
| In SUSTAIN-7 at week 40, semaglutide 0.5 mg lowered HbA1c by 1.5 percentage points versus 1.1 for dulaglutide 0.75 mg, and semaglutide 1.0 mg by 1.8 versus 1.4 for dulaglutide 1.5 mg. | established | SUSTAIN-7, Lancet Diabetes & Endocrinology (Pratley et al. 2018) |
| Trulicity is licensed to reduce major adverse cardiovascular events in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors. Doses: 0.75, 1.5, 3 and 4.5 mg weekly. | established | FDA Structured Product Label, BLA125469 (via openFDA) |
| Ozempic is licensed to reduce major adverse cardiovascular events in adults with type 2 diabetes and established cardiovascular disease, and separately for kidney outcomes in type 2 diabetes with chronic kidney disease. | established | FDA Structured Product Label, NDA209637 (via openFDA) |
Sources
- SUSTAIN-7, Lancet Diabetes & Endocrinology (Pratley et al. 2018)
- FDA Structured Product Label, BLA125469 (via openFDA)
- FDA Structured Product Label, NDA209637 (via openFDA)
Keep reading
- Ozempic vs Mounjaro: The Diabetes Head-to-HeadBoth are licensed for diabetes, and unusually for this category there is a randomised trial of one against the
- Victoza vs Ozempic: Daily Liraglutide Against Weekly SemaglutideAn older daily drug against a newer weekly one, with a randomised trial between them.
- Ozempic vs Wegovy: Same Drug, Different Licence and Maximum DoseTwo brands, one molecule. The difference is regulatory and it is only 0.4 mg wide.