Thoughts on the Market
Cheaper obesity medicines could unlock broader demand, while supply-chain bottlenecks and premium-drug innovation may also shape how the market evolves.
The introduction of lower-cost semaglutide generics in India, Canada, and Brazil is driving significant volume expansion, with India seeing a six-fold increase in volume within months. While API and device supply remain robust, fill-and-finish capacity may face bottlenecks. Meanwhile, differentiated brands like tirzepatide and new oral formulations continue to capture premium market segments.
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Key takeaways
In India, semaglutide generics captured 80% of volume by April 2026, driving a six-fold increase in volume compared to February. The Indian GLP-1 market is projected to grow from $125 million in 2025 to over $1 billion by 2030.
212223Semaglutide patents expired in India in March 2026. In Europe, expiration is expected in 2031, and in the U.S. from 2032. Canada and Brazil are currently introducing generics, providing a blueprint for future U.S. and European market dynamics.
111319While API and device supplies are expected to remain robust due to Chinese manufacturing capacity, fill-and-finish capacity requires highly controlled clean rooms and up to three years to build, posing a potential bottleneck for generic manufacturers.
25262830Tirzepatide, which targets both GLP-1 and GIP pathways, offers better efficacy and tolerability, allowing it to command a premium price. In the U.S., tirzepatide holds about 60% of the market share, indicating sustained branded growth alongside generic entry.
333436New oral GLP-1 options, particularly non-peptide-based ones that are easier to scale, are attracting new users who were not previously on injectable versions, further expanding the overall market size.
37404244Ask GenPod next
“How might the expiration of semaglutide patents in Europe and the U.S. impact branded drug pricing strategies?”
“What are the regulatory hurdles for generic GLP-1 approvals in the U.S. compared to India and Canada?”
“How do non-peptide-based oral GLP-1s differ in manufacturing complexity compared to peptide-based options?”
Background reading
Market Context
Approximately one billion people worldwide live with obesity, including over 100 million in the U.S. The introduction of lower-cost generics is expected to improve affordability and drive demand in under-penetrated markets like India, Canada, and Brazil.
91114Questions
Generics are being introduced in India, Canada, and Brazil. India was the first market, with 13 companies launching 26 generics. Canada has launched two generics with four more awaiting approval. Brazil approved one generic last month with 17 others in regulatory review.
111213151718The main potential bottleneck is in the fill-and-finish stage, which requires highly controlled clean room space and up to three years to build capacity. API and device supplies are expected to remain robust due to investments by large Chinese companies and existing device manufacturers.
252627283031Tirzepatide targets both GLP-1 and GIP pathways, offering better efficacy and tolerability than semaglutide. This differentiation allows it to command a premium price, with tirzepatide holding about 60% of the U.S. market share.
333436Oral GLP-1 medicines, including both peptide-based and non-peptide-based options, are expanding the market by attracting new users who were not previously on injectable versions. Non-peptide-based orals are noted as being easier to scale for a larger global market.
37404244Experts
Sources and disclosure
This listening guide is based on a podcast episode from 'Thoughts on the Market' published on July 13, 2026. The insights are derived from the provided transcript and notes.
Cheaper obesity medicines could unlock broader demand, while supply-chain bottlenecks and premium-drug innovation may also shape how the market evolves. Our analysts Terence Flynn and Thibault Boutherin break down the investor implications.
Read more insights from Morgan Stanley.
----- Transcript -----
Terence Flynn: Welcome to Thoughts on the Market. I'm Terence Flynn, Morgan Stanley's U.S. Pharma and Biotech Analyst.
Thibault Boutherin: And I'm Thibault Boutherin, Morgan Stanley's Europe Pharmaceuticals Analyst.
Terence Flynn: Today, how cheaper GLP-1 obesity medicines could reshape access, pricing, and supply chains; and what the first generic markets may signal for Europe and the U.S.
It's Monday, July 13th at 10am in New York.
Thibault Boutherin: And it's 3 pm in London.
Terence Flynn: Around one billion people live with obesity worldwide, including over a 100 million in the U.S. Right now, the introduction of the first lower cost generics of semaglutide, a GLP-1 medicine, in some international markets, could have consequences on affordability and demand.
Thibault, what are the first countries seeing the introduction of sema generics? What are the current dynamics, and why should global investors pay attention?
So, so far generics are being introduced this year in three countries: in India, Canada and Brazil.
And if we look at India, this is the first market where the generics are being introduced.
The patent for semaglutide expired in March 2026, and 13 companies have launched 26 generics across different formulations: autoinjectors, vials, and pills, which price is lower than the branded drug.
And because the India market was quite under-penetrated for GLP-1, we are seeing affordability driving volume expansion.
In Canada, two generics have been launched so far.
Four other generics are waiting for approval, and more are being filed.
And finally, in Brazil, one generic was approved last month, and we are expecting these generics to be launched in Brazil in July.
And 17 other generics are in different stage of regulatory review in Brazil, and we would expect more to enter the market by the end of this year.
And the reason why we focus on these markets is because we believe they could provide a blueprint for what could happen later in the U.S. and in Europe; in particular for Canada, which shares some characteristics with Europe and the U.S. And the patent for semaglutide will expire in Europe in 2031 and in the U.S. from 2032.
Terence Flynn: Great. Maybe on the India front, I know that's at the leading edge. What happened with patient demand when price came down?
So, what we saw in India is a surge in volume when generics were launched, and the volume in April 2026 were already six times higher than the volume in February.
And that expansion has been driven mostly by these generics launch, which captured 80 percent of semaglutide volume in April.
And our India team expect that the GLP-1 market in India will actually expand in value from $125 million in [20]25 to more than $1 billion by 2030, despite lower prices as we see better, you know, greater volume and greater adoption of GLP-1s in India.
Terence Flynn: The other thing, you know, you and I have discussed is the supply chain, and one of the questions is the ability of some of the generic manufacturers to scale semaglutide. So, maybe talk to us about the current capabilities. And could we see bottlenecks in the supply chain formation here?
Thibault Boutherin: Yeah, sure. So, there are three key elements to watch on the supply chain. The first is the active pharmaceutical ingredient or API, and that's the semaglutide molecule itself. The second element is the device and the device components, and the third element is the fill and finish, which is basically putting all of these things together.
On the API side, so semaglutide molecule, we believe there will be no bottleneck in supplying for generics as we see a handful of large Chinese companies, out of China, building multi-ton capacity for semaglutide. So, we believe there will be no shortage of API to supply the generic supply chain for injectables.
On the device, these are the same device companies that are supplying the branded version of semaglutide, and other GLP-1s for the device that are also supplying the generic makers. And we are seeing meaningful investments being made, so we don't believe there will be a bottleneck here.
Where we could see a bottleneck emerging is on the fill and finish side.
Fill and finish requires highly controlled clean room space to minimize contamination.
It requires regulatory approval, and it takes up to three years to build fill and finish capacity.
And so, that's where if there is not more investment being made over the next few years, there could potentially [be] a bottleneck emerging for the generic companies.
Terence, while semaglutide generics will definitely represent a challenge for the existing branded version of this GLP-1, there are some insights in these emerging dynamics that suggest that tirzepatide, the other GLP-1, could be less at risk. Can you touch a bit on some of these dynamics?
Terence Flynn: Absolutely. So, just to remind listeners that semaglutide targets a pathway called GLP-1. Tirzepatide actually targets two pathways. The first is GLP-1, and the second is GIP. And there are some data comparing these molecules, both in Type 2 diabetes and obesity. And tirzepatide gives not only better efficacy but also improved tolerability.
And so, what you're seeing in some of the ex-U.S. markets is segmentation, where there are some consumers that are willing to pay a premium price for tirzepatide. Our team in Brazil has done a lot of work on this front looking at this dynamic and, you know, we expect that to play out in many geographies.
So, despite the entry of lower-cost generic versions, we think you will still see segmentation of the market between differentiated brand and the lower-cost generics. And that as a result, you will continue to see branded growth.
In the U.S. right now, market share is about 60 percent in favor of tirzepatide. And so again, you're seeing a differentiation between these two molecules.
Thibault Boutherin: And beyond the introduction of generics GLP-1s, there are other dynamics in the industry that are driving this market. And the introduction of oral drugs this year has been a big topic. Terence, what are your views on the role that orals could play on the market?
Terence Flynn: Yes, as a lot of people are probably aware, the many of the existing GLP-1 medicines are injectable.
And so those are delivered once a week with a needle.
But there are now additional oral options of these GLP-1 medicines.
They started off first for Type 2 diabetes, but they have now broadened into obesity as well, following some recent FDA approvals.
And what we're seeing is that the introduction in the U.S. so far is expanding the market. So, the majority of people that are taking the oral versions of these medicines are new users to GLP-1s. So again, you're getting market expansion.
When you think about the orals as well, one of the other questions is capacity. I know, Thibault, you were talking about the supply chain. There are similar questions for these oral medicines because not all of the oral medicines are the same. Some are easier to manufacture than others, and as a result, that's another variable to consider.
So, some of these are what's called peptide-based orals, and some of these are non-peptide-based orals. And the non-peptide-based orals are much easier to scale, for a larger global market. And so that's definitely another variable that we're monitoring and that I think investors need to consider.
Thibault Boutherin: And beyond the pill versions of these GLP-1s, we are seeing more innovation in the drug pipeline of the industry, which could be a key driver of differentiation against the c
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