GSK plc (GSK) Earnings Call Transcript & Summary

September 17, 2020

London Stock Exchange GB Health Care Pharmaceuticals conference_presentation 41 min

Earnings Call Speaker Segments

Unknown Attendee

attendee
#1

This presentation is for Bank of America clients only. If you are a member of the media or the press, please disconnect now.

Graham Parry

analyst
#2

Okay. Good morning, everybody, and welcome to day 2 of the Bank of America Global Healthcare Conference. For those of you who don't know me, I'm Graham Parry, one of the European pharma analysts here at Bank of America. And I'm very pleased today to be able to introduce our first company and, in particular, Emma Walmsley, the CEO of GlaxoSmithKline. As with the session yesterday, if you have any questions, then please enter them directly into the Veracast website and I'll ask them. Alternatively, if you're having any technical difficulties with that, then you can also e-mail them through to me at graham.parry@bofa.com. So Emma, welcome to the conference. Shame we couldn't see you in person, but I think this is the closest that we can get. And perhaps I'll just kick off the -- our fireside chat with a very broad question.

Graham Parry

analyst
#3

At the beginning of the year, you've laid out a 2-year plan to separate GlaxoSmithKline into 2 companies, a pharma and vaccines company and a separate consumer company. Could you just give us an update on progress so far, and perhaps the extent to which COVID has had any interruption in the process?

Emma Walmsley

executive
#4

Sure. Well, first of all, good morning, Graham, and likewise, I'm sorry, we can't do this in person. And a very good morning also to everyone who's joined the call. Well, yes, certainly, when we announced the separation preparation program in February, none of us were expecting the year to play out quite as it did. But I'm really pleased to say that there are no changes overall in terms of our intentions around the separation into 2 exciting new companies that frankly, have never felt more relevant than they do now. And most fundamentally, because what underpins that change program is an enormous amount of work to set both those companies up for success. And all of that is very much on track. There were sort of 3, I suppose major work streams that came with it. The first one was making sure we continue to complete the integration successfully of 2 very large consumer companies, and make sure we are able to stand that up for independents as frankly, the world's only dedicated consumer goods company to consumer health with an incredible portfolio of brands and a very competitive geographic footprint. The second part was to continue on our program to be investing in terms of R&D and in terms of new launches for our biopharma new GSK so that we continue to strengthen, both growth prospects and returns for that business. And then the third part, which is really a lot of kind of operational crunching in a big global complex company is to make sure that we are readying the cost base of the company to support both that investment and make sure that we're competitive operationally and seeing an acceleration in margins for the future as we come out of that. So all of that is very much on track, whether it be reshaping parts of the organization, refocusing our resources behind long term drivers, making good progress on the pipeline, which I'm sure we'll come to in more of your detailed questions. And, frankly, being on track also following this period of investment to get to some meaningful margin accretion. It is frankly, a unique opportunity that had been long debated, long before I was in this job, around the future of the group. And we think that this is a catalyst that is then being added to, frankly, by COVID. We have made good progress, obviously, in an environment globally, economically that's challenging, but great progress with our employees and union representatives around the work that we have to do there. The necessary processes and systems and technologies are put in place for the underpinning for new consumer. And we've all adapted well to -- we're doing this work remotely. I think that's going to be continuing for some time. So there's no change in our expected time lines for delivery, in some ways, opening up further opportunities to simplify ways of working, accelerate culture change, and most of all, emphasize the relevance of our industry and both new companies.

Graham Parry

analyst
#5

Very clear. You touched a little bit there on changed ways of working and perhaps at even accelerating things. Have you found that there are new opportunities for cost saving brought about by COVID through the new ways of working? And perhaps, it's fingers cross, there is a vaccine next year and things begin to return to a lot more normality, how much of that do you think can stick?

Emma Walmsley

executive
#6

Well first of all, we're doing more than crossing our fingers on vaccines, as you know. And I think when you see the way the industry is mobilized there and we're heavily involved, both on vaccines and other solutions. Whilst it's going to take time, and we will -- the world certainly needs more than one, I think we can be optimistic that across the industry, we'll bring some solutions forward. In terms of ways of working, I think there are that's sort of screaming the obvious, which everybody in this call, I think we all know will change for good about the way that we look at simple things of travel and how we operate. And the fact that as a leader, you can be in 3 continents in a day. It might be quite a long day, but you can do that. I think all of that is definitely going to shift permanently. There are obviously big debates, and that obviously has cost savings. But there are also, I think, less direct, as well all the stuff about office working and locations, that takes a bit of time to flow through, but we're all going to be moving to more of a hybrid model. But let's not forget that in our kind of company, the majority of the population is still operating in the field and in factories and a degree of presence is still required, although what we're seeing in terms of telehealth has an impact and how the health care systems start to adopt technology will definitely bring more efficiency and productivity from a reach point of view there as well. But I really think the hybrid model is what is going to play through. I think the other things, though, that are exciting is how this situation is unleashing the spirit of paced innovation and a lot of partnership with regulators. We're seeing, in part through COVID or it's something we were involved in long before that in our vaccines business, new technologies coming through. We think we're extremely competitively paced -- placed around some of the new technologies in vaccines, not least with some recent deals we did, but also some of our in-house platforms, be it in adjuvants or in now mRNA partnerships as well. And thinking of -- our vaccines business is undoubtedly one of the great competitive advantages of GSK, including when you look at our pipeline coming forward. So I think we see COVID, obviously, with the enormous cost and impact that that's bringing. But fundamentally, it creates some efficiency opportunities through technology and the primacy, frankly, at the front line, being far more important in a variety of ways than those of us that work for them in the offices, but it also brings innovation and growth opportunities and an underpinning and recognition of frankly, the enormous both health and economic benefits of preventative care and earlier intervention and preparedness as well. So I think all of that is -- from a very big picture point of view and not worrying about one quarter's impact, really just quite fundamental for our industry and GSK specifically.

Graham Parry

analyst
#7

Understood. So -- and obviously, COVID had an impact in the field on net sales and in particularly on vaccines and vaccination rates. And you called out vaccination or return to normal vaccination rates as a specific risk to guidance, with the Q2 results there highlighting a 3 months delay in return to normality would have a 5% EPS impact. But perhaps help us understand what recovery means in that sense. So what do you need to see to maintain the guidance? What's assumed there? And what would be something which would mean that you would have to then change the outlook for this year?

Emma Walmsley

executive
#8

Well I mean, I think the first one to point out, the most fundamental point, which is there's never been a time where every single household government payer in the world has been more focused on the contribution that vaccines bring than now. And so -- and that includes on the older adult cohorts, too. So I am very confident in the underlying demand around vaccination. And that this is really a question of when, not if, across the portfolio, perhaps with a -- just a bit of a question around travel vaccines in the -- not just the very short term. But I definitely -- and that's a small part of the business. But I think our fundamental confidence in this business and its growth and profit contributions, and the fact that we have a great pipeline here coming through and obviously, the lack of patent cliffs that you have through vaccines, means that this is a short-term challenge. As you said, we updated our guidance at Q2 to highlight exactly what the risk profile would be. And the key element in that is around Shingrix, where you can see the publicly available data, how the recovery is coming through. But we do need to make sure that we can deliver beyond a recovery and into a bounce back and the recovery of some of the lost sales to make sure that we deliver the outlook that we set out at the beginning of the year to deliver our overall guidance. Now what we've seen to date is where lockdown has lifted, you're definitely seeing vaccination rates starting to recover with pediatric vaccines coming back first, as you would expect. Adult and adolescent vaccines are a bit more discretionary. And obviously, with all of our meningitis portfolio, that's a bit dependent. But again, it's just a question of timing on when back-to-school and university, particularly in the U.S., happens. It's less the case in Europe, where it's very much a pediatric vaccine. Shingrix, TRx are already back at pre-pandemic levels, but we've, as I've said, got to see further catch up beyond that from the period of March, and the flu season is really critical for this. And I think, here, we're doing everything that we can, and with our retail partners, to make sure that we have all the plans in place to advise that people can get these vaccinations at the same time as flu vaccines. We've got tremendous support from government bodies, including the CDC, putting in place guidelines about underscoring vaccination. And we have a lot of consumer work going on as well as the supply, of course, to be in place when rebound does come. So I've mentioned travel vaccines is one area where you definitely won't see a recovery. That's hit. But we're watching this carefully, and we'll keep you updated as things progress. But the most important thing here, Graham, is that the underlying demand for this business specifically and vaccines, generally, I think, fundamentally, is only going to continue to increase over time.

Graham Parry

analyst
#9

So actually on Shingrix, I think you just touched on that, that it's just about now to back to growth year-on-year in the last weekly TRx data, which I think captures about 70% of Shingrix' scripts in the U.S. I have to think before we went into COVID, it was probably going around in the 20s to 30s. So is the expectation that you would make back up lost sales for Shingrix as we head into Q4, in particular. Obviously, flu seasons kicked off, we can see flu vaccination rates are picking up quite quickly. So Shingrix being brought along with that? And is this all going to be Q4-loaded rather than Q3-loaded, looking at the prescriptions at the moment?

Emma Walmsley

executive
#10

Yes. Well I'm not going to -- yes, I wouldn't expect -- I'm not going to guide you specifically on Q3 because it continues to fluctuate, as I've said, and it's incredibly local because of lockdowns and it's always a moving picture. But you're right. I mean, you can see publicly what the numbers are currently. It is about a -- the flu season and this tremendous push that you're going to see from governments around that and particularly with the folks in the U.S. And yes, that is what we need to see, partnering with flu to get those injections in arms. And we've done an enormous amount of work to continue to support that towards the year-end. So it's just the timing issue.

Graham Parry

analyst
#11

Great. And then on flu itself, obviously, a lot of governments are now very keen to expand flu vaccinations. Could you just remind us what you've said about capacity plans for this year. I know you were just a little limited in what you could scale up. But then as you think about next year's flu season, are you already in planning to be able to increase capacity further? And maybe you can help us with some numbers on that.

Emma Walmsley

executive
#12

Yes. So you're right. We have mobilized. And I think we've said -- I'm not going to guide for capacity next year but we've said, I think, 50 million doses around flu for this year. So it is -- we started shipping in July. That is a bit of a -- in fact, it's a record for us in terms of volumes that we would go into the U.S. And that will be through Q3 and Q4. Still a bit early days to construe where the season is going to be, but I think we can all imagine that we should be ambitious for that.

Graham Parry

analyst
#13

Great. Perhaps we'll move on to the consumer spend. So just help us understand operationally, what steps need to be taken now -- between now and 2022 to achieve the spend within the 2022 time frame that you've targeted?

Emma Walmsley

executive
#14

Well I think I alluded to that in some of my opening comments. The first thing is that we need to make sure that the integration is completed effectively. I mean, the separation is a big technical piece, but integrating 2 large companies and portfolios, it's not a small undertaking. We've done it all through our Novartis work, that's very much on track, but we need to make sure that, that is completed. Huge amounts of heavy lifting being done through this year, including remotely, but that will continue through and be largely complete next year. Then we have to make sure that we stand up independently, all of the sort of technical systems, which is always the biggest and most complex part of this but also appropriate corporate structures. And then there is obviously also quite a lot of technical work to be done, both with the GSK Board and with our partners with Pfizer to make sure that we plan both for the kind of model of separation in a way that's most appropriate for shareholder interest, and that's another steps that we will go through before bringing a lot more visibility for both new companies to the market in due course.

Graham Parry

analyst
#15

Okay. And then, at the time of the announcement of the Pfizer joint venture and potential spin, you highlighted some metrics around the spinco. So the consumer business, I think you said 3.5x to 4x net debt-to-EBITDA on gearing and then a 30% to 50% dividend payout ratio. What does that mean for the remainco? So what do you expect the gearing of the remainco company to look like. Is it going to be substantially less so that you can do more bolt-on M&A, for example, to continue to build your innovation and pipeline? And what will be -- or when will you communicate something on dividend policy for the remaining business?

Emma Walmsley

executive
#16

Yes. Well both obviously important questions. One of the reasons that, and certainly not the only reason, but one of the key benefits of declaring the separation is, of course, the opportunity to reset the balance sheet for the biopharma company because we are expecting to gear what by then will be a highly profitable and with great prospects to be more so a consumer company, which we will gear up to 4x, and that's all public knowledge, which allows us to bring the gearing of the biopharma business closer in line to what would be the close to where the rest of the sector is. Now I think it would be -- obviously, we continue in terms of prioritization to say our #1 priority in terms of capital allocation is the strengthening of the pipeline, and we are really pleased with the progress that we've been able to make around that. That includes business development. And we've had many examples over the last couple of years in that space that we've continued to drive. So we're not waiting for the separation to be able to move forward on that. In fact, even just in the last few months, we also proceeded further with Advair deal with what we think would be very exciting COVID antibody potentially. And then the deal with CureVac on new technologies in vaccines as well. So we expect those to continue. We're not waiting around on that. But obviously, it will increase our capacity at split. Now in terms of bringing more visibility, we do have disclosure on our dividend intentions for the consumer business precisely because that's always something that's worth agreeing upfront. I'm not about to announce today what the biopharma dividend policy might be, but that will be something that will become clearer well ahead of the separation. And it will be, as you'd expect, about an output of the business' results with the necessary investment in growth and, of course, recognizing the dividend matters, and we expect to deliver strong shareholder returns. So more on that nearer the time.

Graham Parry

analyst
#17

So when you say well ahead of, so if it's 2020 spin, is that something we should think of with your full year '21 results and earnings guidance for the year?

Emma Walmsley

executive
#18

Nearer the time, Graham.

Graham Parry

analyst
#19

Okay. And then in terms of the -- how you think about the dividend for the Remainco business, obviously, dividend has been an important part of the GSK payout. But as you rightly point out, the need to BDL and build the pipeline is also there, so perhaps just help us just talk through the pushes and pulls on capital allocation, post-spin and what will go into your thinking of where the dividend policy would be set?

Emma Walmsley

executive
#20

Well I think it's exactly as I've said, which is our #1 priority, when you think about the purpose of the company and why we exist, we are here to protect human life and fight diseases. And never more than now we all have been aware of the contribution that we can make. And we have to do all of that profitably. But it's always a -- and continues through COVID, attention and a pressure for our sector around how the pricing dynamic comes into play in that. But our #1 job, therefore, is to solve health care problems at scale in a profitable and responsible way. And that means the pipeline is the first priority for capital allocation. And because of the model that we're in, we have a very exciting portfolio for new biopharma. There's tremendous strength in vaccines, which helps in terms of the patent cliff model, and that's going to be a growth market with a good pipeline in there. We have leading positions in infectious diseases and a shifting and growing portfolio in specialty, which is really where we've been investing recently over the last few years, and that has brought good prospects, both in terms of growth contribution because the advances in science, but also in terms of returns because of mix. And that's all this work we've been doing over the last few years to reset the portfolio, prioritize investments in R&D and in innovation and prioritize our executional capability to do that brilliantly, is absolutely our #1 priority. And that includes business development. So that's where capital goes first. But there should be no mistake, we recognize, whilst we're in a multi-stakeholder world more and more, the incredible performance of share -- importance of shareholder returns, and that the dividend plays a big part in that. So one of the changes we made when I came in was to bring transparency to our dividend policy to make sure it was understood as a function of free cash flow, and we will be doing that again, but obviously, with a reset company. We hope that's going to be a reset company with great growth prospects, an acceleration in returns prospects and obviously, we're looking for, at the moment of separation when that comes, that we're going to have 2 companies, which will be exciting from a shareholder return point of view.

Graham Parry

analyst
#21

Great. That's very clear. Perhaps we switch gears to something that you did bring in through BDL, which is Zejula. Obviously, you have the approval for the first-line indicate -- maintenance indication, but very difficult environment to try and forge an oncology drug into. Perhaps just give us an update on how that's gone? I think the number missed the consensus slightly at the Q2, but obviously, very difficult to know exactly what the real underlying demand is. So perhaps help us understand where you see the demand, the initial physician feedback and where you feel you've got perhaps an edge over competitors, they're also recently approved in that indication.

Emma Walmsley

executive
#22

Sure. Well, we are absolutely delighted with the TESARO acquisition and particularly with the data that came through for Zejula and then, most of all, obviously, when it comes to labels and the guidelines that came through. We got the label approved at the end of April, and we had the guidelines that just came through from Astra actually just in August. So all of those have been very good and supportive. And obviously, from a timing point of view, from a new launch in oncology, we have been hit because you've seen -- well, you saw across a degree of stocking in Q1 and then unwind in Q2, and there's definitely an impact on number of new patients diagnosed, and that we're seeing tragically across many areas in cancer. We're seeing an impact on those undergoing debulking surgery and chemo, and that's obviously going on to impact part maintenance in the second half of the year. But again, I think in our industry, more than most, we need to sort of look through this short term. And what we look at, obviously, is how our share is doing -- market share is doing, within first line maintenance. So there are 2 things I'm watching, and we look at. And then on market share, really definitely good progress, which is we expect to keep accelerating as patients start coming through. In May, I think we had a 50% increase in new patient starts on part for us. We went from 14% to -- in the first line to 21%, then we went up to 28%, I think. And because we are in a position where regardless of your HRD status, this is a medicine that is relevant for all comers. And that's incredibly important when it's one drug doesn't mean any testing, there's no combos, so just from a simplicity point of view, before you can get into the economic challenges around that, that's something that we're feeling good, not -- obviously, in the current environment, particularly challenging, but certainly in terms of our prospects. But the thing that's arguably even more important is to make sure that the class grows and we bought TESARO because fundamentally, we believe that the PARP class was undervalued. And secondly, we think that the Zejula is potentially a differentiated kind of PARP with -- and we are the only one out there at the moment with this all-comers label. So -- but we think that the whole PARP class needs to grow. And really, in maintenance, it's only the minority of patients who are actually getting any kind of maintenance therapy. I think it's still in the teens in terms of the numbers of women who are being prescribed a PARP. And that is even lower when you look at BRCA world type patients. And that's got to change because when you know there is an effective treatment available for all those patients, then we need to be able to move that number up. And that's what we think that everybody in the class should be driving for. So pricing prospects. And as you know, we're also moving into a non-small cell lung cancer trial as well before the year-end.

Graham Parry

analyst
#23

And I was going to say, so is non-small cell lung cancer you think the next most important indication? And do you see Zejula having utility across a broad range of indications than just ovarian and lung over time? I think the prostate indication is already licensed out that's -- is that a potential future revenue stream for GSK that perhaps is under-recognized by the market?

Emma Walmsley

executive
#24

Well we definitely think that Zejula is going to be a big growth contributor for us. And part of that is going to be expansion not in prostate, as you say, and that's about identifying the broadest populations that can benefit. We're looking a lot at unique pipeline combinations within our portfolio, and partnering with others. It's really about thinking through where we could have, I suppose, a meaningful benefit because of the differentiation of the strengths of Zejula, where we do think that there is this -- with this high tissue probability that -- and we saw extending to in preclinical work to crossing the blood-brain barrier, could bring some benefits. So there is still enormous unmet need in lung cancer. That study is starting, I think, in first line in combo with pembro. And we believe that we potentially have a better agent. So we'll see how that plays through. And other things are under consideration. We definitely see this as one of our key growth drivers in oncology.

Graham Parry

analyst
#25

Great. And staying with oncology, so move to benra. Obviously, approved now in late lines of therapy, having failed 4 prior regimens in multiple myeloma. Ocular toxicity is the key side effect. And the FDA seems to express rather a lot of concern about that in its briefing documents, which I'd say maybe the physicians were slightly more sanguine about given the late-line of therapy. As you move this into earlier lines, on the 2Q call, you're talking about looking at different dosing regimens. So can you just talk us through how and where we'll see those different dosing regimens? Are they going to be built into the existing Phase III studies that have actually already begun? Or do we need to wait for additional data from proof-of-concept trials before we can actually start to see what lower doses or more extended doses look like?

Emma Walmsley

executive
#26

Yes. So first of all, we're absolutely delighted to have a first-in-class that got full support, both in the U.S. and in Europe for approval. And I think -- now, it's an update on what we're doing around dosing. But the other thing to remember that's really important here is that physicians have a good experience in the later line as well to keep building confidence. So we put a huge amount of effort into our REMS program. And I've been talking because we can do that as often as you like now just on our calls with the front line field force and the teams in the U.S. and definitely -- as well as in Europe. And definitely, you can see very positive engagement for this new solution for patients who are swiftly running out of options. That said, we obviously take the ocular challenges extremely seriously, and dosing is, as I updated on Q2, is something that we're looking at much more closely in our earlier lines of studies as well as novel combinations. We've got both pembro and GSI as well in the DREAMM-5 study going through. So for the DREAMM-7 and 8, these were designed based on incoming data that was coming from the dose-finding Phase I/II studies, which were 6 and 1 other as well. And those if the benefit risk profile that comes through on those is better than the 2.5 mg per kg, then that means we could amend the second line protocols as well. So that's all going on, at the same time is working really hard on making sure the REMS process is as smooth as possible for both patients and physicians, and that's going well so far.

Graham Parry

analyst
#27

Okay. So if I can just clarify this, the DREAMM-7 and 8 could have lower and extended dosing in them but you're waiting for some data from DREAMM-5 in order to be able to start those different dosing regimens, otherwise, you're basing it on the side effects...

Emma Walmsley

executive
#28

So I think it's DREAMM-6, nice, but we can just confirm that precisely with you afterwards, just so I don't get that slightly wrong.

Graham Parry

analyst
#29

It'd be good. [indiscernible]. Great. So...

Emma Walmsley

executive
#30

[indiscernible], Graham, so I don't remember exactly which one as you know.

Graham Parry

analyst
#31

Yes, cool. But the key thing is you're looking at extended dosing. And then the gamma secretase combination with the type 1. And so when should we expect to have some sort of conclusive information on gamma secretase combination whether that's on the...

Emma Walmsley

executive
#32

I'll give a specific answer on that when they're ready.

Graham Parry

analyst
#33

Got it. Okay. And then perhaps, and we touched on it before, but we sort of straight vagued into COVID vaccines earlier, but perhaps to dig into that in a little bit more detailed analysis. So obviously, GSK is one of the largest vaccine companies in the world. Intrigued to understand why GSK hasn't worked on a full vaccine program that chose to use the adjuvants and work with Sanofi on a vaccine. Just talk us through sort of the rationale behind that.

Emma Walmsley

executive
#34

Well first of all, it was an extremely deliberate choice that was made in January. It was in early February, and it's one that we really think continues to be the right one based on the criteria of how do you add the most value at an effective pace. And well, you all know that the protein vaccines are not the first out of the gate because structurally, it's just a different approach than mRNA and some other new technologies. But they are technologies that are proven in a pandemic situation. And the incredible proven advantage of an adjuvant is that it can impact efficacy, and it is -- it remains dose-sparing, and with a particularly good track record in older patients who are obviously the most vulnerable here. So -- and obviously, the most visible partner we have is Sanofi, but it's certainly not the only one. So in the spirit of maximizing chances of success and frankly, underpinned, as you would expect, and you've seen from the industry with the right kind of commitments to quality and safety, doing multiple partnerships with a proven adjuvant where we could turn on capacity very strongly and continue to work on that, should it be necessary, whilst continuing to supply the world with all of the vaccines that are most definitely required because we were talking earlier about core on Shingrix. You fundamentally -- we all have to recognize the impact of COVID on the overall health care systems, including vaccination globally, and it's definitely having an impact. And we have a tremendous health care responsibility as well as a business to keep supplying there. So we have a number of different collaborations that are going on. The world, if it's going to be multidose, is definitely going to need more than one vaccine to be successful. You are definitely going to see in the current environment that we all understand and recognize that -- and with a very hot media attention on this topic, we're going to see all sorts of news, but we're going to see different results on different technologies and different cohorts. And we're just really pleased with the approach that we've made, the commitments we've made for -- we're in trials now. And looking forward, hopefully, to be able to contribute to solutions in a meaningful way through next year. Now that's not to say, by the way, although I think, across the industry, you've seen this mobilization in vaccination. Our conviction is we're still going to need treatments for COVID, both ahead of global vaccination, but also potentially on an ongoing basis, simply because a very few vaccines are 100% on there in terms of efficacy. The best in the world are hitting 90s. So I think there's still sadly, both a responsibility and an opportunity to continue to contribute here.

Graham Parry

analyst
#35

A question we get a lot, and I've got a question from the audience on this specifically now as well is, obviously, you've talked about this being not-for-profit during the pandemic phase. But if this becomes an annual vaccination, is this a potential future revenue stream? And well how do the economics work with Sanofi? And perhaps, if I can add slight subpart of that question, which is of the money that comes in to help you build adjuvant capacity, does that actually increase GSK's ability for pandemic preparedness and the sort of ancillary benefits to the vaccines business from that work that's going on?

Emma Walmsley

executive
#36

Well it's a great and a good long question, but the answer is going to be short, which is I think we'll, first of all, work out whether we've got a vaccine, and then we'll decide about what the economic returns may be once the pandemic phase has settled down.

Graham Parry

analyst
#37

Great. And then I think just the last question in the last minute we've got, you talked on the second quarter call with, I guess, a lot more optimism certainly about your RSV vaccines, so both maternal and also in older adults. And I think there's competition in the pediatric stroke maternal space. Do you think the older adults is possibly, actually, the under recognized opportunity for the market, that the market is perhaps not giving you the credit for at this point?

Emma Walmsley

executive
#38

Definitely. And I've got a number of points to make on this one actually, Graham. I mean, first of all, you talked about -- I remember this question of maternal vaccine because there's a lot of activity in this space because it's an enormous unmet need. The world is looking again, at respiratory vaccines. The scale of it is very significant, and there is obviously work ongoing in maternal vaccines, in pediatric vaccines, and very importantly, where we think we're leading the way in older adults as well. And the point -- one of the points that's been raised is if you've got an antibody for babies, why would you be bothering with a maternal vaccine? And on this one, I would like to point out as a mother that, if you have the option of protecting your precious new baby through a safe and effective maternal vaccine, that's going -- that is definitely going to appeal more than giving your newborn baby -- very newborn baby an antibody injection. And it's important to know that RSV, 50% of the hospitalizations actually occur in the first 3 months of life. So a maternal vaccine is pretty sensible. And we expect that we would get protection for the first 6 months, which is obviously the most fragile time. Then we are developing a pediatric vaccine for older babies, and we expect the data on that to come through in the first half, I think, of 2021. And there are other reasons as well that we think it could be highly competitive because that maternal vaccine would be polyclonal immunity against the whole wider variety of RSV strains. And that could help against the emergence of mutating viruses as well. But the most important thing on this program, and it is relevant as a vaccine both have a program around RSV is this older adult market. When you think that in the U.S., you've got 70 million people over the age of 60 in the U.S. alone versus 4 million baby cohorts. So we have a prefusion antigen in older adults, which is designed to be stable and generate a good solid immune response. And very critically, that older adult asset has ASL1, which is the adjuvant that is Shingrix, which has been -- and this is really one of the challenges that I think is underestimated has shown ability to amplify immune response in older adults. And there are lots of different approaches going on, but we think we've got a very comprehensive and both individually and competitively competitive one, and there'll be -- we'll share more on that later there again.

Graham Parry

analyst
#39

Fantastic. And unfortunately, time is upon us, but that was very interesting and useful. Thanks, again, for joining us Emma. Hopefully, next time, we'll be able to do this in person, but enjoy the rest of the day, and thanks for your time today.

Emma Walmsley

executive
#40

Thanks, Graham. Take it easy. Thanks, everyone. Bye.

Read the full transcript via the API

You're viewing the first half of this call. Get the complete GSK plc transcript — plus 251,000+ transcripts from 12,000+ companies, speaker segments, AI summaries and full-text search — through the EarningsCalls.dev API.

Get the API View API docs →

For developers and AI pipelines

Programmatic access to GSK plc earnings transcripts and 251,000+ others is available through the EarningsCalls.dev REST API. Plans from $24.99/month — full transcripts, speaker segments, full-text search, and the recently-added /api/v1/transcripts/recent polling endpoint for ETL pipelines.