Menopause and the drugs in this class overlap for an obvious reason: weight distribution changes around the transition, and the drugs act on weight. That overlap has produced a great deal of writing and very little evidence, and the gap between the two is unusually easy to measure.
We measured it two ways — by searching the approved labels, and by counting the registered research. Both came back smaller than expected.
Labels read 13 September 2026 from DailyMed, the National Library of Medicine's index of current FDA labelling; the trial count was taken from ClinicalTrials.gov the same day. Nothing here is medical advice, and nothing here is a dose or a schedule; our editorial standards explain why.
The word is not in any label
We searched the full current labelling of all four leading products — Ozempic, Wegovy, Mounjaro and Zepbound — for "menopause" and every variant of it.
Zero occurrences, in all four documents.
Not in the indications. Not in the warnings and precautions. Not in section 8, which is where labels address use in specific populations including pregnancy, lactation, paediatric and geriatric use. Not in the clinical studies sections describing who was enrolled.
The absence is worth pausing on, because labels are not silent about populations in general. All four have a good deal to say about pregnancy and lactation, and about patients with kidney impairment, and about paediatric and older patients. A population defined by a hormonal transition affecting roughly half of all adults at a predictable stage of life is simply not a category these documents use.
That has a practical consequence. When a reader asks what the label says about menopause, the accurate answer is not "it says to be cautious" or "it says there is no concern". It is that the question is not addressed, and an absence is not a reassurance.
The registered research, counted
A ClinicalTrials.gov query for studies combining menopause or postmenopausal status with semaglutide, tirzepatide, liraglutide or GLP-1 interventions returned 15 registered studies with a combined planned enrolment of 963 participants.
For scale: that is every registered study in this intersection, added together, against the 1,961 participants of STEP 1 or the 2,539 of SURMOUNT-1 — single trials in the same drug class.
And the 15 shrinks on inspection.
Two are not studies of these drugs at all. Both test a topical cosmetic serum in postmenopausal patients and were captured by the search because of the population rather than the intervention. A third dates from 2008 and tested an inhaled GLP-1 formulation that never reached the market, in 20 people.
Ten of the 15 have non-industry lead sponsors — universities and academic medical centres. Five are industry-led.
Where the industry money actually goes
Four of the five industry studies are Novo Nordisk's. None of them asks whether these drugs do anything for menopause.
| Study | Participants | What it actually measures |
|---|---|---|
| NCT01508858 | 21 | Whether liraglutide changes the blood levels of an oral contraceptive drug |
| NCT02845219 | 25 | Whether oral semaglutide changes the pharmacokinetics of ethinylestradiol |
| NCT05153564 | 27 | Blood levels of a bone marker with semaglutide and a co-administered compound |
| NCT07010432 | 144 | An amylin analogue and bone metabolism |
Postmenopausal women appear in the first two because their hormone levels are stable, which removes a confounder from a pharmacokinetic measurement. They appear in the latter two because postmenopausal bone loss is the reason to study bone in that group. In all four, the population is an instrument.
This is the finding, and it is not a criticism of the studies. Each is a legitimate piece of work. But anyone reading "there are industry-sponsored trials in postmenopausal women taking these drugs" as evidence that the manufacturers are investigating menopause has drawn a conclusion the registrations do not support. The industry interest in this population is real and it is aimed at contraceptive interactions and bone chemistry.
It is also worth noting which question the manufacturers have not asked. The two interaction studies examine oral contraceptives. The interaction most relevant to women at this stage of life is with menopausal hormone therapy — and that is being examined in a 96-participant academic study, NCT06715514, looking at hormone therapy alongside GLP-1 agonists and their effects on glucose and energy regulation.
The single study on the actual question
One registered study anywhere tests one of these drugs against menopausal symptoms as its subject:
NCT07218445 — "The Effect of Tirzepatide on Menopausal Vasomotor Symptoms and Biological Aging in Post-menopausal" women. Sponsor: the Mayo Clinic. Planned enrolment: 40. Status on 13 September 2026: recruiting.
Vasomotor symptoms are hot flushes and night sweats. Until that study reports, statements about whether these drugs help with them — in either direction — are not resting on trial evidence, because there is no trial evidence yet to rest on.
Two larger academic studies sit adjacent to the question rather than on it: a 200-participant University of Colorado study on the menopausal transition and mid-life women's health, and a 200-participant Ohio State study combining food, fitness and medication. Neither is designed to isolate what these drugs do to menopause.
What an absence of evidence is, and is not
The 09-11 analysis on this site of GLP-1 drugs and PCOS found 31 registered trials and 3,631 participants, with every lead sponsor classified as non-industry. That absence had a clear shape: an active academic field with no commercial interest behind it.
Menopause has the opposite shape at the same low level of total evidence: fewer studies, a third of the participants, and industry sponsors who are present but asking their own questions. Both are absences; they are not the same absence, and the difference tells you something about why each gap exists.
What neither is, is evidence of harm or of futility. A question that has not been studied has not been answered either way. The honest position is that the mechanism makes the question reasonable, one 40-person trial is running, and everything else currently offered on the subject is extrapolation from trials that did not record menopausal status.
What this page does not answer
It does not say whether anyone should take one of these drugs during or after the menopausal transition, and it contains no dose and no schedule. It also cannot say how the drugs perform in this population relative to others, because the published labelling does not report results split by menopausal status — the subgroup analyses in the labels are by sex, age, race, ethnicity and region, and menopausal status is not among them.
Related reading: the population question with a fuller evidence base is PCOS; the bone and body-composition question sits alongside muscle loss; and what happens when treatment stops is on stopping a GLP-1.
Sources
- DailyMed, OZEMPIC (semaglutide) injection (SPL version 20), WEGOVY (semaglutide) injection / tablet (version 19), MOUNJARO (tirzepatide) injection (version 40) and ZEPBOUND (tirzepatide) injection (version 40) — full label text searched on 13 September 2026 for every variant of "menopause"; zero matches in each.
- ClinicalTrials.gov, searched 13 September 2026 via the public API for registered studies whose condition includes menopause or postmenopausal status and whose intervention includes semaglutide, tirzepatide, liraglutide or GLP-1 agents. Result: 15 studies, 963 combined planned enrolment, 10 non-industry and 5 industry lead sponsors.
- Individual registrations read the same day: NCT07218445 (Mayo Clinic, tirzepatide and vasomotor symptoms), NCT06715514 (menopausal hormone therapy with GLP-1 agonists), NCT01508858 and NCT02845219 (contraceptive pharmacokinetics), NCT05153564 and NCT07010432 (bone).
- The PCOS comparison figures are carried from our own GLP-1 and PCOS page, where the same registry search method was applied on 11 September 2026.
A registry count is a measure of what has been registered, not of everything being studied, and studies are added continually. The count above is dated and the query is described so that it can be repeated.
