Last clinically reviewed: 20 August 2026 Published 19 August 2026

Switching from Mounjaro or Wegovy to Foundayo weight loss tablets safely

Switching from long-term injectable tirzepatide or semaglutide to Foundayo (orforglipron) has been studied for weight-loss maintenance, but the evidence does not create a self-directed switching schedule. ATTAIN-MAINTAIN tested a specific trial protocol in people who had completed 72 weeks of injectable treatment, while current UK patient information gives a different general Foundayo starting schedule. Whether, when and how to change treatment therefore remains a prescribing decision. [1][2][3]

Paul John
Written by Paul John MPharm, IP
James Reynolds
Reviewed by James Reynolds MPharm, DipClinPh, PgCert Derm, SCOPE, IP

Key takeaways

  • ATTAIN-MAINTAIN directly studied people moving from long-term injectable tirzepatide or injectable semaglutide to once-daily orforglipron for a further 52 weeks. [3]
  • Among participants whose weight had plateaued, orforglipron preserved more of the previous weight reduction than placebo in both prior-treatment groups. [3]
  • The trial did not compare switching with continuing Mounjaro or Wegovy, so it cannot show that Foundayo is equivalent to staying on an injectable treatment. [3]
  • ATTAIN-MAINTAIN did not study people moving from oral Wegovy to Foundayo, and people with diabetes were excluded. [3][4]
  • There is no Mounjaro, Zepbound or Wegovy-to-Foundayo dose conversion in the current UK Foundayo Patient Information Leaflet. [2]

Can you switch from Mounjaro or Wegovy to Foundayo?

There is now direct clinical evidence for a particular type of transition: people who had completed long-term injectable tirzepatide or injectable semaglutide treatment and then moved to orforglipron for weight-loss maintenance. That evidence comes from the phase 3b ATTAIN-MAINTAIN trial. [3]

It does not mean everyone taking Mounjaro or Wegovy can follow the same transition. The people in the trial had completed 72 weeks of injectable treatment, had lost at least 5% of their body weight, and did not have diabetes. The trial therefore most closely reflects a maintenance situation after sustained treatment, rather than an early switch during dose escalation or a change made for every possible clinical reason. [3]

Foundayo is the UK brand name for orforglipron. The MHRA authorised it on 10 August 2026 for weight loss and weight maintenance in eligible adults, as well as for treatment of type 2 diabetes. It is a prescription-only medicine. [1]

Foundayo, not ‘Foundation’

If you searched for ‘switching from Mounjaro to Foundation’, ‘Foundation pill’ or ‘Foundation dosage’, the medicine referred to in this context is Foundayo. Foundayo is the licensed brand name for orforglipron in the UK. [1][2]

‘Foundation’ is not the medicine name, so we use Foundayo throughout the rest of this guide.

Mounjaro, Zepbound and tirzepatide: what is the difference?

Mounjaro contains tirzepatide and is a UK brand used for weight management and type 2 diabetes. Zepbound is a US tirzepatide brand. [5][6]

That matters for search wording. Someone looking for ‘switching from Zepbound to Foundayo’ is asking about the same active ingredient studied in the tirzepatide cohort of ATTAIN-MAINTAIN. For a UK reader, however, Mounjaro and tirzepatide are the clearer terms to use when discussing current UK treatment. [3][5][6]

What did ATTAIN-MAINTAIN actually study?

ATTAIN-MAINTAIN was a randomised, double-blind, placebo-controlled phase 3b trial at 29 sites in the United States. It included 376 adults who had completed SURMOUNT-5 and achieved at least 5% body-weight reduction after 72 weeks of injectable treatment. [3]

 

Prior tirzepatide group

Prior injectable semaglutide group

Participants randomised

205

171

Previous treatment

Tirzepatide 10mg or 15mg maximum tolerated dose once weekly

Semaglutide 1.7mg or 2.4mg maximum tolerated dose once weekly

Previous treatment duration

72 weeks

72 weeks

Required previous response

At least 5% body-weight reduction

At least 5% body-weight reduction

Diabetes

Excluded

Excluded

Randomised treatment

Once-daily orforglipron or placebo

Once-daily orforglipron or placebo

Follow-up

52 weeks plus safety follow-up

52 weeks plus safety follow-up

The study population is important. It did not test a person taking a low starter dose for a few weeks, someone changing because of every possible side effect or clinical problem, a person with type 2 diabetes, or someone taking oral Wegovy. [3]

What happened after switching from tirzepatide?

For the primary analysis, the researchers looked at participants whose body weight had plateaued by the end of SURMOUNT-5. At week 52, those assigned to orforglipron maintained an estimated 74.7% of the weight reduction they had achieved during SURMOUNT-5, compared with 49.2% among those assigned to placebo. [3]

A key secondary result looked at how many participants retained at least 80% of their previous weight reduction. In the tirzepatide cohort, this was 43.7% with orforglipron and 16.4% with placebo. [3]

These are group-level trial estimates, not predictions for an individual person. They also do not mean that everyone maintained exactly three-quarters of their previous loss.

What happened after switching from injectable Wegovy?

The semaglutide cohort showed the same broad direction of effect. Among participants whose weight had plateaued, those assigned to orforglipron maintained an estimated 79.3% of their previous weight reduction at week 52, compared with 37.6% with placebo. [3]

In the secondary threshold analysis, 55.0% of the orforglipron group maintained at least 80% of their previous weight reduction, compared with 6.9% of the placebo group. [3]

Again, these figures describe a specific trial population after long-term injectable semaglutide treatment. They should not be read as a promise of how much weight an individual will maintain after changing treatment.

Does this mean Foundayo is equivalent to staying on Mounjaro or Wegovy?

No. This is the most important limitation when interpreting the trial. ATTAIN-MAINTAIN compared orforglipron with placebo after participants stopped their previous injectable study treatment. There was no group that continued tirzepatide or semaglutide.

The trial therefore answers ‘what happened when people moved to orforglipron rather than placebo?’ much more directly than it answers ‘is changing to Foundayo as effective as staying on Mounjaro or Wegovy?’ The authors identify the missing continued-injectable comparator and the one-year study duration as limitations. [3]

There is another qualification. From week 24, participants assigned to placebo who regained at least 50% of the weight they had previously lost could receive rescue orforglipron. By week 52, only 31.3% of the tirzepatide-placebo group and 18.2% of the semaglutide-placebo group had completed treatment without receiving active therapy.

This was intended to limit the harm associated with substantial weight regain, but it means later comparisons are not a pure active-treatment-versus-untreated-placebo contrast. [3]

The strongest conclusion from ATTAIN-MAINTAIN is that orforglipron preserved more previous weight reduction than placebo after long-term injectable treatment. It does not establish equivalence to continuing the injectable medicine, nor does it identify the best maintenance strategy for every patient.

Alex Gibbins
Alex Gibbins MPharm, IP, FRPharmS

What about switching from oral Wegovy to Foundayo?

ATTAIN-MAINTAIN does not provide direct evidence for this transition. Oral Wegovy is now authorised in the UK for weight management and contains semaglutide, but its pharmacokinetics and dosing are not interchangeable with the weekly injection.

Current UK product information specifically notes that the effect of switching between semaglutide tablets and injections cannot easily be predicted because oral semaglutide has greater variability in absorption. [4]

The semaglutide participants in ATTAIN-MAINTAIN had used injectable semaglutide 1.7mg or 2.4mg once weekly. The trial did not include people taking oral Wegovy before moving to orforglipron. A specific oral-Wegovy-to-Foundayo regimen should therefore not be inferred from the injectable evidence. [3][4]

What Foundayo dose is used when switching from Mounjaro, Zepbound or Wegovy?

There is no simple dose-equivalence table in current UK patient information. More importantly, the ATTAIN-MAINTAIN study protocol and the general UK Foundayo starting schedule are different. [2][3]

Question

ATTAIN-MAINTAIN research protocol

Current UK Foundayo patient information

Starting treatment

12mg investigational orforglipron capsule, equivalent to the 9mg tablet strength used in the marketed formulation

General starting dose is 0.8mg once daily for 30 days

Dose increases

Every four weeks in the trial until 36mg or maximum tolerated dose

At least 30 days at each dose stage before a clinician may increase the dose

Timing after previous injection

First study dose was ideally given within 14 days of the last SURMOUNT-5 injection

No general Mounjaro/Wegovy-to-Foundayo switching interval is stated in the current PIL

The researchers deliberately tested a higher transition dose in people with extensive prior injectable exposure to explore whether the usual escalation period could be shortened. The paper itself says this raises a question for further investigation; it does not turn that higher dose into a general rule for routine practice. [3]

The current UK PIL, by contrast, gives 0.8mg once daily as the general Foundayo starting dose, followed by clinician-directed increases no sooner than every 30 days, and tells patients not to change their dose unless instructed by their doctor. [2]

Clinical caution

Neither column is a personal switching instruction. A trial protocol cannot be converted into ‘Mounjaro 10mg equals Foundayo 9mg’, and the general 0.8mg starting schedule does not by itself answer what is appropriate after every type or duration of previous GLP-1 treatment.

How soon after the last Mounjaro or Wegovy injection was Foundayo started in the trial?

ATTAIN-MAINTAIN aimed to give the first study dose within 14 days of the final SURMOUNT-5 injection. [3]

That timing describes how the study was run. The current UK Foundayo PIL does not state a general switching interval after tirzepatide or semaglutide. It should therefore not be turned into a rule such as ‘start Foundayo 14 days after your final injection’. [2][3]

Clinical caution

Do not create your own washout, overlap or timing plan from the trial. The appropriate interval depends on clinical assessment and should be set by the prescriber managing the change.

What do we know about side effects during the studied transition?

During the first four weeks of ATTAIN-MAINTAIN, nausea, vomiting or diarrhoea were reported in 10.5% of the tirzepatide cohort and 9.5% of the semaglutide cohort. Most gastrointestinal adverse events were mild to moderate, and no dose de-escalations were required during those first four weeks.

Across both cohorts, discontinuation because of adverse events ranged from 4.8% to 7.3% among participants receiving the maximum tolerated orforglipron dose. [3]

This is useful tolerability evidence for the people who were actually studied. It is not evidence that switching will be easy for everyone, and it does not justify using the trial's higher starting dose without an individual prescribing decision.

Safety information that matters when changing treatment

Starting a different prescription medicine is not only a question of dose. The Foundayo PIL tells people to speak to a doctor, nurse or pharmacist before taking it if they have a history of pancreatitis, severe problems with stomach emptying, gallbladder problems, eye or vision problems, severe heart failure, or upcoming surgery under anaesthesia.

It also highlights dehydration risk with vomiting or diarrhoea and low blood sugar risk when Foundayo is used with insulin or a sulfonylurea. [2]

Tell your prescriber about all medicines and supplements you take. Foundayo has listed interactions with several medicines and with St John's wort, and the PIL gives specific advice for people using insulin, sulfonylureas and medicines for high blood pressure. [2]

Clinical caution

Foundayo should not be used during pregnancy or breastfeeding. The PIL also states that orforglipron may reduce the effectiveness of oral hormonal contraceptives and advises considering a barrier method or non-oral contraception for 30 days after starting Foundayo and for 30 days after each dose increase. If you are planning a pregnancy, the PIL advises discussing a treatment change with your doctor and stopping Foundayo at least three weeks in advance.

The following symptoms need clear action rather than waiting to see whether they settle:

What you notice

What to do

Severe pain in the stomach and back that does not go away

See a doctor immediately. The PIL lists this as a possible sign of acute pancreatitis. [2]

Breathing problems, swelling of the face or throat, wheezing, fast heartbeat, pale or cold skin, dizziness or weakness

Get immediate medical help. These can be signs of a serious allergic reaction. [2]

Severe tummy pain with a swollen tummy, vomiting, or being unable to pass wind or open your bowels

Seek urgent medical advice. The PIL lists bowel obstruction as a serious side effect. [2]

Sudden changes in vision or other unusual visual symptoms

Tell a doctor promptly. [2]

Persistent vomiting or diarrhoea, particularly if you cannot keep fluids down or have kidney problems

Contact a clinician because dehydration can contribute to kidney problems. [2]

Urgent patient warning

Severe, persistent stomach-and-back pain or symptoms of a serious allergic reaction need immediate medical attention. Do not wait for a routine medication review.

ATTAIN-MAINTAIN gives direct evidence that, in a selected group of adults who had completed 72 weeks of injectable tirzepatide or injectable semaglutide, moving to orforglipron maintained more of their previous weight reduction over the following year than moving to placebo. [3]

That is useful evidence for maintenance after long-term injectable treatment. It is not a universal switching protocol. The study did not include oral Wegovy switchers or people with diabetes, did not compare Foundayo with continuing Mounjaro or Wegovy, and used a transition regimen that differs from the general starting schedule in current UK Foundayo patient information. [2][3][4]

For those reasons, the evidence can inform a conversation with a prescriber, but it cannot tell an individual reader which dose to start, how long to wait after a final injection, whether treatments should overlap, or whether changing medicine is the right option for them.

Common questions

How we wrote this article

This article was created in line with our editorial standards. Medical information is checked against UK-relevant guidance and reliable sources, which may include the NHS, NICE, the MHRA, medicine safety information, recognised clinical guidance and peer-reviewed research.

Medical content is reviewed regularly and updated sooner if clinical, safety or regulation guidance changes. This article is general information, and not a substitute for personal advice from your own prescriber.

Something wrong or outdated? Email: support@lotusweightloss.co.uk

References

  1. Medicines and Healthcare products Regulatory Agency. UK first in Europe to authorise orforglipron for weight management and type 2 diabetes. GOV.UK, 10 August 2026. gov.uk
  2. Eli Lilly and Company Limited. Foundayo 0.8mg film-coated tablets — Patient Information Leaflet. Electronic Medicines Compendium. Last updated 12 August 2026. medicines.org.uk
  3. Aronne LJ, et al. Orforglipron for maintenance of body weight reduction: the double-blind, randomized phase 3b ATTAIN-MAINTAIN trial. Nature Medicine. 2026;32:2679–2687 nature.com
  4. Novo Nordisk Limited. Wegovy 25mg tablets — Summary of Product Characteristics. Electronic Medicines Compendium. medicines.org.uk
  5. Eli Lilly and Company Limited. Mounjaro KwikPen — Summary of Product Characteristics. Electronic Medicines Compendium medicines.org.uk
  6. US Food and Drug Administration. Zepbound (tirzepatide) prescribing information. 2026 accessdata.fda.gov
PERSONAL ASSESSMENT

Is your next step
a suitability check?

Every consultation is reviewed by a qualified
prescriber to check whether weight loss treatment is right for you.

Start an assessment
Paul John
Paul John MPharm, IP

Paul John MPharm, IP is a Clinical Pharmacist Prescriber at Lotus Weight Loss with over 15 years of experience across community and NHS care. He has held national leadership roles in blood-borne virus services in Wales and has contributed to work recognised by the BMJ for clinical leadership.

View Paul John's profile