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Tirzepatide: Science, studies and safety data

Tirzepatide is the first-in-class dual GIP and GLP‑1 receptor agonist, developed for the treatment of type 2 diabetes and also studied for weight management. The molecule combines the effects of two incretin pathways, resulting in stronger regulation of appetite and glucose metabolism.

Tirzepatide: Science, studies and safety data

Tirzepatide: Science, studies and safety data

Peptology · 2026-06-04

Tirzepatide: Science, studies and safety data

Tirzepatide: a scientific review of weight-loss efficacy and a comparative analysis with Semaglutide

Tirzepatide is the first-in-class dual GIP and GLP‑1 receptor agonist, developed for the treatment of type 2 diabetes and also studied for weight management. The molecule combines the effects of two incretin pathways, resulting in stronger regulation of appetite and glucose metabolism.

Clinical trial results: body weight

Results from SURMOUNT‑1 (72 weeks)

Long-term effect (88 weeks)

Probability of ≥5/10/15 % weight loss


Other trial findings

Glycaemic control

Cardiovascular and cognitive effects

Weight maintenance



Tirzepatide versus Semaglutide: results

Clinical data (SURMOUNT‑5)

Tolerance and side effects



Safety



Conclusion

Tirzepatide is a dual GIP and GLP‑1 receptor agonist. In SURMOUNT‑1 the mean weight reduction reached up to ~21% at 72 weeks, and in the head-to-head SURMOUNT‑5 trial it was greater than with semaglutide (20% versus 14%). These are clinical trial data; the tirzepatide offered by Peptology is a research peptide intended for laboratory use only.



Frequently asked questions

How does tirzepatide differ from semaglutide?

Semaglutide activates only the GLP‑1 receptor, while tirzepatide also activates the GIP receptor (dual agonist).

Which trial compared tirzepatide with semaglutide directly?

SURMOUNT‑5 (72 weeks): mean weight loss of 20% with tirzepatide versus 14% with semaglutide.

Did the trials include people without diabetes?

Yes, the SURMOUNT-1 trial included people with obesity who did not have diabetes.