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Reviewed by Dr Sarah Mitchell, PhD · Editorial Board
Mounjaro vs Wegovy in the UK
Tirzepatide (Mounjaro) and semaglutide (Wegovy) are the two cornerstone licensed GLP-1 weight-management products in the UK. This page sets them side by side: mechanism, trial outcomes, NHS pathways, dose schedules, side-effect profiles, and the practical factors that usually decide the choice.
At a glance
| Mounjaro (tirzepatide) | Wegovy (semaglutide 2.4 mg) | |
|---|---|---|
| Mechanism | Dual GLP-1 + GIP agonist | GLP-1 agonist |
| Manufacturer | Eli Lilly | Novo Nordisk |
| Mean weight loss (trial, 68–72 wk) | ~20–22% at top dose | ~15% at 2.4 mg |
| Injection | Weekly subcutaneous (KwikPen) | Weekly subcutaneous (FixDose pen) |
| Dose range | 2.5–15 mg weekly | 0.25–2.4 mg weekly |
| UK NHS pathway | NICE TA1026 | NICE TA875 |
| Other UK indications | Type 2 diabetes | (Same active ingredient: Ozempic for T2DM, Rybelsus oral) |
Mechanism
Both activate the GLP-1 receptor. Tirzepatide also activates the GIP (glucose-dependent insulinotropic polypeptide) receptor — a second incretin pathway. The dual mechanism is the basis for the larger trial-effect size; in practice both drugs achieve their effect through appetite suppression, slowed gastric emptying, and improved glycaemic control.
Trial outcomes
Reported trial outcomes (SURMOUNT for tirzepatide, STEP for semaglutide):
- Tirzepatide SURMOUNT-1 (adults with obesity, no diabetes, 72 weeks): mean weight loss of around 16% (5 mg), 21.4% (10 mg), and 22.5% (15 mg) vs ~2% placebo.
- Semaglutide STEP 1 (adults with overweight or obesity, no diabetes, 68 weeks): mean weight loss of around 14.9% at 2.4 mg vs ~2.4% placebo.
A direct head-to-head trial (SURMOUNT-5) reported tirzepatide 15 mg producing greater weight loss than semaglutide 2.4 mg in adults with obesity.
Trial averages don’t predict individual response. Some patients lose more on semaglutide than the trial average; some lose less on tirzepatide. The trial numbers are a useful prior, not a guarantee.
NHS access
Both are NICE-recommended for NHS use. In practice, NHS access isn’t typically a patient choice between the two — local formularies, specialist-service capacity, and supply availability determine which product a patient is offered. Both pathways require BMI thresholds and specialist-service involvement.
Side-effect picture
The GI profile is broadly similar between the two. The dose-response curve for tirzepatide is steeper — patients moving from 5 mg to 15 mg often need to slow titration to manage escalating nausea. The 12.5 mg and 15 mg tirzepatide steps are where most discontinuations cluster.
Practical factors that usually decide
- Availability. Whatever the NHS service or private clinic actually has in stock.
- Tolerability. Individual response varies; switching is a normal clinical conversation.
- Comorbidities. Patients with T2DM are often steered toward whichever product their diabetes pathway uses.
- Cost (private). Pricing changes; don't fixate on a single number.
- Trial-effect size. A meaningful prior for ‘which to try first’ but not a guarantee.
Sources & further reading
- NICE TA875 — semaglutide for weight management — nice.org.uk
- NICE TA1026 — tirzepatide for weight management — nice.org.uk
- MHRA — gov.uk
- NHS — obesity treatment — nhs.uk