
A once-weekly injectable for weight management in adults
Triple agonist activates receptors for GIP, GLP-1 and glucagon
Not available in the UK
Used alongside a reduced-calorie diet and increased physical activity
Retatrutide is an once-weekly triple hormone receptor agonist. Retatrutide is a single molecule that activates the body's receptors for glucose-dependent insulinotropic polypeptide (GIP), glucagon-like peptide-1 (GLP-1) and glucagon.
Retatrutide is currently not yet available for public use.

Retatrutide is a medication currently in clinical trials for the treatment for obesity and type 2 diabetes, with a particular focus on weight loss.
Most weight loss medications available today work on one or two of the body’s hormone signals- Retatrutide is designed to work on three at once.
It mimics three distinct hormones naturally found in the body:
This unique combination is why it is colloquially referred to as "Triple G." By engaging all three receptors simultaneously, the drug aims to regulate appetite, weight and blood sugar more effectively than its predecessors.
Retatrutide isn't available in the UK yet. It hasn't been approved by the regulators, as it's still going through clinical trials. These studies check how safe and effective a medication is before it can be prescribed.
The power of Retatrutide lies in its triple-action mechanism. Each hormone plays a specific role in how your body manages energy and hunger.
By combining these three actions, Retatrutide tackles weight from several directions at once: reducing hunger, improving metabolic function, and actively breaking down fatty acids which can be used for energy. Early clinical trials have shown promising levels of weight loss.
As things stand, Retatrutide is not yet available for prescription in the UK. The medication is yet to be submitted to the MHRA, the regulators for approval.
The approval process involves rigorous review by the MHRA to ensure safety and efficacy. Following that, NICE (National Institute for Health and Care Excellence) will evaluate it for NHS use. Based on current timelines, UK regulatory approval for Retatrutide could occur in 2027.
With TRIUMPH-1's pivotal results now in, Eli Lilly (manufacturers of Retatrutide) has the primary efficacy dataset it needs to file for approval, and further TRIUMPH trials (including in type 2 diabetes and cardiovascular disease populations) are expected to report through the rest of 2026. Until an application is actually filed and a formal review timeline is set by regulators, any specific date for UK availability is an estimate.
Until then, medications like Tirzepatide (Mounjaro) and Semaglutide (Wegovy) and Orflorglipron (Foundayo) remain the gold standard for medical weight loss in the UK.
Since retatrutide is not yet approved in the UK, any version you see for sale online currently is unregulated and potentially unsafe. These black-market products have not been tested for purity or safety.
Using unverified compounds carries severe health risks. It is critical to wait for approval from the MHRA (Medicines and Healthcare products Regulatory Agency) and only obtain prescriptions from registered UK healthcare providers like Phlo Clinic.
Getting a new medicine to UK patients involves two separate steps:
In practice, this usually means a private prescription route becomes available first, with NHS access following later.
The TRIUMPH-1 trial results were first announced in May 2026 and published in full in the New England Journal of Medicine in September 2026. They showed that retatrutide could help patients lose around a quarter of their body weight, and close to a third for some patients who continued treatment for longer.
The study included 2,339 adults with obesity or overweight who did not have type 2 diabetes. They were treated for 80 weeks.
The published paper's main analysis counts everyone who started the trial, including people who stopped treatment early. The table also shows Eli Lilly's figures for people who stayed on treatment as intended, which is the effect you'd expect if you keep taking it.
The trial also measured other health benefits. People with knee osteoarthritis reported less knee pain. People with obstructive sleep apnoea had substantially fewer breathing interruptions per hour while asleep, around 32–34 fewer on the 9 mg and 12 mg doses compared with about 10 fewer on placebo.
The most common side effects were gastrointestinal: nausea, diarrhoea, constipation and vomiting. These were mostly mild to moderate and resolved during treatment. Around 11% of people on the 12 mg dose stopped treatment because of side effects, compared with about 5% on placebo.
Like other weight management medications in its class, Retatrutide is designed as an injectable treatment. It is administered once weekly via a subcutaneous injection. This means it goes just under the skin rather than into a muscle or vein.
If approved, it will likely come in a pre-filled pen device, similar to devices used for Mounjaro and Wegovy. As with other weight loss injections, consistency will be important, so taking it on the same day each week helps maintain steady levels of the drug in your system.
Each clinical trial showed patients starting at different doses. Phase 2 trials started at 1mg where as Phase 3 trials started at 2mg.
There isn't an official confirmation of Retatrutide strengths or dosing schedule yet, as it's still being studied. However, like other weight loss injections, it was given at a low starting dose in trials and increased gradually over several weeks. This step-by-step approach allows the body to adjust to the medication and helps reduce the chance of side effects
To give your body time to adjust, treatment does not start at the maximum dose. You will likely begin on a low starting dose of 4mg.
If you tolerate the medication well, your clinician will gradually increase the dosage every four weeks. This step-by-step approach, known as titration, is crucial for minimising side effects while slowly building up to the therapeutic maintenance dose where maximum weight loss occurs.
Any dose schedule shown here is a general guide. Your own dose, and how quickly it increases, will be set by your prescriber based on your individual response and tolerability.
Because Retatrutide influences digestion and blood glucose, current research shows it shares a similar side effect profile with other GLP-1 medications. They usually occur when you first start treatment or when you increase your dose.
Common side effects include:
To manage these, we recommend eating smaller, more frequent meals and avoiding high-fat or spicy foods. Staying hydrated is essential, especially if you experience diarrhoea. If side effects become severe or persistent, your clinician may pause your dose increase or adjust your treatment plan to ensure you remain comfortable.
Understanding where retatrutide fits in the hierarchy of weight loss drugs helps manage expectations. No trial has tested retatrutide directly against other GLP-1s, so this is a comparison across separate trials rather than head-to-head evidence.


Mounjaro is a dual agonist, targeting both the GLP-1 and GIP receptors. In the SURMOUNT-5 trial it produced 20.2% average weight loss at 72 weeks and is currently the most effective weight-loss drug on the market.
Retatrutide's triple mechanism adds glucagon receptor agonism on top of tirzepatide's GLP-1/GIP combination. TRIUMPH-1's 28.3% at 80 weeks (rising to 30.3% at 104 weeks in patients who continued treatment) is meaningfully higher than tirzepatide's published results, suggesting retatrutide could set a new bar for the class.
While Retatrutide appears more effective, Tirzepatide and Semaglutide are proven, safe, and available now. For many patients, the dual action of Tirzepatide provides ample support for reaching a healthy weight without waiting for future drugs.


Wegovy is a single-hormone agonist that targets the GLP-1 receptor. It is the most established of the three, with years of real-world use, and its own pivotal trials showed average weight loss of around 15% of body weight.
Retatrutide adds two further mechanisms on top of GLP-1: agonism at the GIP and glucagon receptors. On the current evidence, that broader mechanism translates into a substantially larger effect – the Phase 3 TRIUMPH-1 trial reported 28.3% average weight loss at 80 weeks (24.2% in the earlier Phase 2 trial at 48 weeks), roughly double semaglutide's published figures.
As an investigational medicine, formal contraindications will only be finalised at approval. Based on its drug class, people with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2, and people with a history of pancreatitis, are likely to need careful evaluation or to avoid it, consistent with other GLP-1/GIP medications. Pregnant or breastfeeding individuals would not be candidates. This will be confirmed in the official product information once Retatrutide is approved.
Trial data shows Retatrutide lowers blood glucose in people without diabetes, via its GLP-1 and GIP effects, though as with other medications in this class, this should be monitored by a clinician to avoid blood sugar dropping too low.
At present, there is no confirmed price for Retatrutide in the UK. If approved, the cost will be determined by the manufacturer.
As with other GLP-1/GIP medications, a proportion of weight lost on retatrutide is expected to come from lean mass alongside fat, which is why adequate protein intake and resistance exercise are generally recommended alongside treatment to help protect muscle. Retatrutide-specific body composition data from the Phase 3 programme is still being published in full.
In trials, gastrointestinal side effects like nausea have generally been most noticeable in the early weeks of treatment and after dose increases, easing over time as the body adjusts, consistent with the pattern seen with other GLP-1 and GIP medications.
Retatrutide, a Triple Hormone Receptor Agonist, for Treatment of Obesity. New England Journal of Medicine. Published 29 September 2026. DOI: 10.1056/NEJMoa2604169. Available at: https://www.nejm.org/doi/full/10.1056/NEJMoa2604169
Eli Lilly and Company. Lilly's triple agonist, retatrutide, delivered powerful weight loss in pivotal Phase 3 obesity trial. Available at: https://www.prnewswire.com/news-releases/lillys-triple-agonist-retatrutide-delivered-powerful-weight-loss-in-pivotal-phase-3-obesity-trial-302778859.html
Eli Lilly and Company Investor Relations. Lilly's triple-agonist retatrutide delivered weight loss average. Available at: https://investor.lilly.com/news-releases/news-release-details/lillys-triple-agonist-retatrutide-delivered-weight-loss-average
National Center for Biotechnology Information (PMC). Available at: https://pmc.ncbi.nlm.nih.gov/articles/PMC12026077/
Medicines and Healthcare products Regulatory Agency (MHRA). How we regulate. Available at: https://www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency
National Institute for Health and Care Excellence (NICE). How NICE evaluates new medicines. Available at: https://www.nice.org.uk
