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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.
Peptology · 2026-06-04
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.
5 mg: ~‑15% weight loss
10 mg: ~‑19.5%
15 mg: ~‑20.9%
Up to 25.3 % mean weight reduction versus 9.9 % with placebo.
Tirzepatide significantly increases the chance of achieving ≥15% weight loss compared with Semaglutide.
Tirzepatide leads to a greater reduction in HbA1c compared with Semaglutide 1 mg.
GLP‑1 therapies, including Tirzepatide, are associated with reduced risk of stroke and dementia.
89.5 % of patients retain ≥80 % of lost weight on long-term follow-up.
Mean weight loss after 72 weeks: 20 % with Tirzepatide versus 14 % with Semaglutide.
Patients with ≥25 % loss: 32 % with Tirzepatide versus 16 % with Semaglutide.
Similar profile: most commonly nausea, diarrhea, constipation. Lower discontinuation rate with Tirzepatide.
Common GI effects: nausea, vomiting, diarrhea.
Potential risk of C‑cell thyroid tumors (as with Semaglutide).
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.
Semaglutide activates only the GLP‑1 receptor, while tirzepatide also activates the GIP receptor (dual agonist).
SURMOUNT‑5 (72 weeks): mean weight loss of 20% with tirzepatide versus 14% with semaglutide.
Yes, the SURMOUNT-1 trial included people with obesity who did not have diabetes.