Good day ladies and gentlemen and welcome to Repligen Corporation's First Quarter 2021 Earnings Conference Call. My name Illie [Ph] and I will be your coordinator. All participations will be in listen-only mode. [Operator Instructions]. Please note this event is being recorded. Following the company’s formal remarks, there will be a question-and-answer session. In order to accommodate all individuals who wish to ask questions, there will be a limit of two questions at a time. I would now like to turn the call over to your host for today's call, Sondra Newman, Head of Investor Relations for Repligen.

Thank you, Illie. Good morning everyone. We appreciate you joining us this morning in a busy season. We’ll be covering today our financial results and business highlights for the three months period ended March 31, 2021. We’ll also update our financial guidance for the current year 2021. President and CEO, Tony Hunt will cover business updates; and our CFO, Jon Snodgres will cover our financial results and guidance. As a reminder, the forward-looking statements that we make during this call, including those regarding our business goals and expectations for the financial performance of the company are subject to risks and uncertainties that may cause actual events or results to differ. Additional information concerning risks related to our business is included in our annual report on Form 10-K, our quarterly reports on Form 10-Q, the current report on Form 8-K, which we filed today and other filings that we make with the SEC. Today’s comments reflect management's current views, which could change as a result of new information, future events or otherwise. The company does not obligate or commit itself to update forward-looking statements, except as required by law. During this call, we’re providing non-GAAP results and guidance. Reconciliations of GAAP to non-GAAP financial measures are included in the press release that we issued this morning, which is posted to Repligen’s website and also on sec.gov. The non-GAAP figures in today’s report include the following; revenue growth at constant currency, gross profit and gross margin, operating expenses including R&D and SG&A, operating income and operating margin, income tax expense, net income and earnings per share as well as EBITDA and adjusted EBITDA. These adjusted financial measures should not be viewed as an alternative to GAAP measures, but are intended to better enable investors to benchmark Repligen’s current results against historical performance and the performance of peers when evaluating investment opportunities. Now I’ll turn the call to Tony Hunt.

Thank you Sondra and good morning and welcome to our Q1 earnings call. We are delighted with our performance in the first quarter of 2021 where a combination of accelerating demand from COVID accounts and robust demand for a non-COVID business drove our overall performance. For the quarter, revenue was up 88% coming in at a $142 million with organic growth up 69% versus Q1 2020. COVID related programs made up approximately 25% of our revenue and 46 points of our total growth. Revenue from acquisitions we made in 2020 including ARTeSYN accounted for over 14 points of overall growth. Finally we were especially pleased by the performance of our base business which accounted for 27 points of our growth and approximately 68% of our revenue reflecting continued strong demand for our products. As noted in our February call, the strength and orders that we saw in Q4 last year carried over into 2021, with an exceptional quarter in orders, driving not only our revenue beat, but also our increased guidance. Orders for the quarter were up more than 150% versus prior year, with customers now planning out into the second half of this year. Based on these developments, we now expect to finish the year with revenues in the range of $565 million to $590 million. We anticipate COVID vaccine and therapeutic programs will contribute approximately 25% to 27% of overall revenue on our non-COVID based business to grow at or above 20%. Before jumping into our quarterly results, I want to provide a progress update on our strategic initiatives for 2021. Our number one priority, as it has been for the last 12 plus months is building out our capacity to support accelerating demand across all of our businesses. As you know, our industry is seeing unprecedented demand…

Thank you Tony and good morning everyone. Today, we are reporting our financial results for the first quarter 2021 as well as updating our financial guidance for the year. Unless otherwise mentioned, all financial measures discussed reflect adjusted non-GAAP measures. As you've seen in our press release this morning, we delivered record revenue and strong earnings growth for the first quarter of 2021, while continuing to see a significant order load. As Tony mentioned, our performance reflects COVID tailwinds, which accounted for approximately $35 million and about half of our revenue growth in the quarter, strengthened our base business which was up 31% along with nearly $11 million of incremental revenue from our 2020 acquisitions. We are benefiting from an acceleration in demand for our products in general, and the healthy biologics market that continues to move towards more flexible and efficient biologics manufacturing processes. With product innovation and differentiation at our core, we continue to drive technology leadership in the first quarter through three new product launches that Tony discussed, through the integration of our most recent acquisitions that complement and broaden our systems and fluid management offerings and through expanding the applications for our products into a larger set of drug modalities. With increased demand, we continue to focus on expanding our manufacturing capacity with a three plus year time horizon to support increasing adoption of Repligen branded consumables and systems. Now transitioning to our first quarter of 2021 revenue commentary. On our top line, we realize record revenue of $142.8 million in the first quarter of 2021. As mentioned, this represents growth of 88% as reported, and 69% organic growth. Within these figures our reported growth includes a four point tailwind from foreign exchange, and a 14 point tailwind from our 2020 acquisitions. Overall, COVID program revenues…

Thank you. [Operator Instructions]. Our first question today comes from Julia Qin with JPMorgan.

Hi, good morning. Congrats on the strong quarter. So maybe starting with guidance on the COVID revenue expectations, could you help us understand what led to the increased revenue expectations? How much of that is the new spike protein ligand? And how much is maybe just new commercial production scale up? And does guidance include the new capacity that's coming online in 3Q?

Yes, great question, Julia. I, when you look at the increase in our COVID guidance, most of it is coming from the demand uptick that we're seeing for both commercial vaccines that we're in for mid-to-late stage vaccines that are under development. So I think when you look back to where we were in February, we had many of the orders in for Q1and into Q2, we've seen a lot more quarters come in, as we went through Q1, which is now going into the second half of the year and a little bit even into next year. So, in terms of capacity, we're constantly adding capacity. So our guidance reflects where we believe we will be in capacity. But it doesn't reflect yet as we go through the year. But what happens in Q2, Q3 Q4 in terms of the demand curve.

Got it. Thank you. And then in the prepared remarks, you caught out some pretty strong traction for some key new products, including TFDF and the Spike Protein Resin, so just wondering how much contribution from these new products do you see in the first quarter?

Oh, in the first quarter it is still minimal, compared to what we did a few million dollars. That's basically what those products contribute in the first quarter. I really think that the benefit of the new products are, what's going to happen in 2022 and beyond? Right, it's great that we've gotten we've launched these products really happy with how FlowVPX is, is gaining traction in the marketplace. It's already been well seated, with the FlowVPE technology been out there for two to three years. So I think the reaction to that product was really positive. As I said, on the spike resin, we're seeing a lot of evaluations going on. But as we've may have, as you may remember, in prior earnings calls, we've said that, the opportunity for the spike resin is going to be in next generation vaccines and of course it will be for protein based vaccines. And then finally, TFDF I think we've been pretty clear that we believe that that technology and product will double every year for the next few years. And we're right on track this year to double.

Got very helpful. Thank you and congrats again.

Yes, thank you.

Our next question comes from Dan Arias with Stifel.

Good morning, guys. Thanks for the questions here. Tony, a couple on gene therapy if I could maybe starting with sales activity. I know the difficulty there had been access for evaluations last year. Are you feeling like you're approaching or at a level where the ability to get in there and do a proper demo is now relatively unimpeded? Are you still working through that situation? And then as a follow up, if I could…

Yes.

Go ahead. I'll just ask the second one after the answer to first one. I was just going to ask as a just sort of a follow up on your comment about 17 new accounts in that area. I was wondering if you could help us with looking across the next 12 to 18 months in that market? Are you able to parse out how much of what you think you see comes from new project and trial work for new business to you, versus progression of existing trial work to the later stages versus marketed product demand?

Okay. Yes, so maybe I'll start with the progression. I would say most of our growth will come from the accounts that have been seated over the last few years. So it's not that we get into a single process at a gene therapy account. I like every everybody else in bioprocessing, we're looking to get platforms, so you pick up new drugs as they come through the pipeline. So for sure, I think when you look at our top accounts, they continue to grow. They continue to expand, the idea with our commercial team, if you remember a year ago, we put a gene therapy, go to market team in place, that team has done a tremendous job. They work with the sales people, they work with the field applications, folks. And that's what you know, we focus on in terms of bringing new accounts online, we don't expect that those new accounts will add a tremendous amount of revenue in the first year. But it's all around seeding and keeping the funnel filled up. And I think from that perspective, I think we've done a good job. The second part of this is, is really around, building out our gene therapy, applications labs. So we're in the middle of doing that right now. So when we get into kind of late summer timeframe, we'll be up and running fully functional. So that'll give us the balance of being able to work with key accounts with, top leaders in the space, but also be able to do our own gene therapy applications work here in Repligen. The first part of the question, I believe, was around the gene therapy project evaluations. Yes. I would say that, there's still some restrictions, but nothing like what we were dealing with in sort of Q2, Q3 last year, I think the field applications team sales team have really figured out a way to work with all our accounts. While it's not ideal, we're definitely doing evaluations. And we're making progress. And so, our expectation is that we need to keep building the funnel with new opportunities. I think the challenge we have and everybody in our industry has right now is that, when you look at the COVID demand, which is really strong, you have to balance, the delivery of products to, to the COVID vaccine therapeutic accounts, and also working with the non-COVID accounts to get product to them as well. So that's the idea of adding our extra capacity is that we're going to be able to shorten lead times for the non-COVID accounts as well.

Okay, I know that was deuce, technically, two. So apologies for slipping into third here. But if I could I was, I just wanted to ask, I was reading about clinical trial progression and where these candidates in gene therapy are. And it looks like right now, more than half of them are in phase 2, this is selling gene together. So it's not specific to the gene side where you are. But, if we assume that it's close, do you think that that translates to sort of a surge in buying at some point? And are there capacity considerations there? Or is the expectation that things will sort of naturally space themselves out, so to speak, and so therefore, to be more steady over time?

Yes, and this is just my opinion. I believe it'll be steady over time, as opposed to a huge surge. But that's, that's just where we're where I'm at. And what I, when I look at what's going on in our, in the broader industry, there's surely CDMOs are working rapidly to expand capacity, which I think is a really good leading indicator. We're also along with all our peers, everybody is building capacity. The capacity built out is going to be not only for COVID, vaccines, therapeutics, but it's going to also be very helpful as we look at mAb and gene therapy customers that want lead times that are much shorter than what the industry is providing right now.

Yes, okay. Great. Thanks, Tony.

Our next question comes from Jacob Johnson with Stephens Inc.

Hey, guys, this is Mason on for Jacob. How's everyone doing?

Good.

Good. Just a few quick ones from me. On the gene therapy side, there, there seems to be a shift to using suspension for viral vectors versus the inherent processes. What opportunities this present for your product portfolio?

Yes, so definitely, I think we've spoken about this a little over the last year or so there. There is a move towards suspension cells. Obviously, when you look at the products that we have in our portfolio, whether it's the ATF technology, or any for filtration products or systems, it's going to be pretty well suited suspension cells, that's what we do in the mAb world. It's more scalable, and I think it's just a positive development for, for Repligen for really many of the players in bioprocessing. So if we just see it as positive.

Got it And then protein seem to be performing well, any updated commentary on the Cytiva relationship going forward?

Yes, no proteins business. Really, really good quarter. Honestly, the last couple of years have been very positive for that business, which comprises obviously of ligands and growth factors. Yes, we continue to have our, our dialogue and conversations with Cytiva. I think there's a genuine interest in extending the current contract, and we're working through that process. And obviously, we'll update people when, when that gets done.

Got it? Thanks, guys.

Our next question comes from Puneet Souda with SVB Leerink.

Yes, hi, Tony, John thanks for taking the question. So obviously, first of all, congrats on the on the really impressive quarter. And it's really great to see how you're contributing to being an important part of the COVID vaccines and therapeutics solution out there. So maybe on, you know, COVID was covered a little bit too, maybe if I could talk a little bit in terms of based business, what was the contribution in that based business from mAbs, versus gene therapy versus non-COVID vaccines that you could provide? Obviously, there's a really strong growth there too, but just wanted to see if you have any, if anything, if there's anything you can provide there.

Yes, I don't have the split of mAbs and gene therapy. But, 25% of our, of our beat came from our, in the quarter came from our non-COVID based business. So I think that's, that's a real positive, the things we're seeing across the board, it doesn't really matter whether it's mAbs or its or its gene therapy. But on our base business, you'll what we're seeing right now is, our proteins business has done has really over performed in the first quarter. We're seeing opportunities, where we have lead times that are shorter, where we can take some share for our, be able to deliver to accounts that really need product in a shorter period of time, really happy with our analytics business. That's really accelerated again, in Q1, which I think is very encouraging. And then the yields we did last year, ARTeSYN, EMT and NMS are all performing well. And we're building out that commercial team. So I look at it as really the whole portfolio. I don't really look at it as gene therapy versus mAbs. But we're really happy with the over 30% growth for our, for our base business in Q1, I think that's a reflection of the technologies we have. I think that's a reflection of our, the ability for sales and field applications team to do a really good job with our customers.

Got it? Okay, that's helpful. And then Tony on, there's a quite a bit of discussion about the booster shots and how do you think about that opportunity, longer term? Obviously, these number of these products usually get spect in. So, how should we think about the COVID opportunity, the COVID tail? And, what can vaccines be, or what, what portion of revenue do you think vaccines can be as a mix of your revenue longer term given the ramp up we're seeing here?

Yes, that crystal ball answer is going to be really hard to give in terms of what percent long term, but I think it's pretty clear that, the, the whole therapeutic vaccine part of COVID is going to be with us for a number of years, definitely into 2022 and more, more likely beyond that. I read the same reports you do on booster shots. So if booster shots happened later this year, early next year, that's going to add increased demand, annual vaccines, if that's a reality, obviously, you can see how that adds to the overall demand cycle. And then on top of all that, you there's still a large percent of the global population that's not vaccinated, and we don't really know what way the variants are going to go. So a lot of lot of unknowns. I think as we get, into the second half of this year, it'll become a little clearer on 2022. And even on 2023 as well. But we, we expect that that COVID is here for a number of years, it's going to be a driver of growth, and it's driver growth for our whole industry.

Got it. And then last one, if I could squeeze in in terms of the product portfolio. Tony, is there obviously you highlighted ARTeSYN, are there any other products that are doing remarkably well and part of the larger part of the pickup here in COVID? And on ARTeSYN, are you what was it mostly system sales? Or was there a good mix of systems and consumables that was part of the growth hair and the quarter? Thank you.

Yes, I think ARTeSYN was a combination of systems and consumables. When you look at our overall portfolio, I mean, it's, it's been really impressive, like all our products are doing very well in the marketplace. Obviously, the filtration portfolio, when you see what our guidance is, for the year, where we expect filtration to essentially double, I think that tells you a lot about, where we're winning. But that's not to say that, our whole industry is doing incredibly well right now. So the demand is high. It's really around everybody's ability to produce and keep lead times at a reasonable level. That's what everybody in the industry is focused on. And, when we look at where we're going as a company, I believe that, the combination of the new products, the products we've launched over the last four or five years, we've firmly established ourselves as a technology player in the industry. And I think that's paying off for us.

Great, thank you.

Our next question comes from Paul Knight with KeyBanc.

Good morning, Tony, could you go over the CapEx numbers and where is that CapEx targeted at, is it for OPUS?

I’ll ask John to walk you through that?

Yes, I mean, there's the biggest piece of it Paul is really and, I'm not going to give specific numbers, but we're talking about $55 million to $60 million biggest piece is going into the various filtration product lines, for both flat sheet and hollow fiber, along with the flow paths of businesses. So including, including pretty significant investments we’re making in the new acquisitions. And then there's a bit going into OPUS. And there's a bit actually going into proteins as well, for us to continue to maintain capacity there for expected higher amounts in the future. So those are kind of the big capacity related programs. Of course, there's general maintenance as well, that's probably a $10 million number to $15 million number a year. And then there's SAP, which is going to take another 5 million or so this year, so that that program continues as well.

And then Tony, you've gone over a very robust internal set of products. Do you think your growth in the future now is shifting a bit toward internal projects? Or is there still the same level of M&A opportunity out there?

Yes, look, obviously the portfolio over the last seven years has expanded dramatically. The projects that we can work on the programs we can work on from an R&D perspective, continues to grow and expand. So we have lots of ideas about what we want to do with the technologies that we have. But we also believe that, for us to continue to compete in this industry, we still need to bring new technology in, whether it's through M&A or to the R&D efforts. So expect that we're going to continue to work through the -- continue to keep to the strategy we put in place over the last five years on a go-forward basis.

Thanks.

Our next question comes from Matt Hewitt with Craig-Hallum Capital Group.

Good morning, congratulations on the strong quarter. Maybe, yes, maybe a couple. So you've talked a little bit about the visibility into the second half, maybe even a little bit of next year in the lead times? It sounds like you're staying on top of those both from a capacity standpoint, or you're making more investments, as well as on the headcount side. I'm curious, as you look at those lead times, where are their potential pinch points? Is it more on this that your suppliers getting the products that you need? Is that the potential pinch point? And if so, how are you working with your suppliers to make sure that they're in a position to help you kind of meet the demand that you're seeing?

Yes, I think it's both honestly. Clearly, we're working with our suppliers. I guarantee you everybody in bioprocessing is working with their suppliers. But you never know right? As you go from quarter to quarter of what unexpected supply issues crop up you just have to manage through it. I think in general, the supplier side has been well managed. We worked through any issues that need to get worked through. I think the internal capacity and lead times, we've obviously for the last two years been building out. And that's helped us a lot, honestly, second half of last year and first half of this year, but we also realize that we need to add more capacity. And that's why we're spending the $55 million to $60 million this year. And there'll be a, a significant spend next year as we had capacity in the second half of this year, and we add capacity in 2022. And all of that puts us in a position to be able to support, a billion dollar type company by 2025.

Understood, thanks. And then maybe one last one here. I think last quarter, you commented that the vast majority of the COVID related demand that you're seeing was vaccines, Is that still the case? Or, are there opportunities in the treat on the treatment side as well? And in what kind of demand are you seeing from those customers? Thank you.

Yes, on the therapeutic side, I would say it's similar to what we saw last year. We're in obviously a number of processes. But I think the vast as you said, the vast majority of the revenue is coming from the vaccine side. And that hasn't changed.

Understood. Thank you.

Our next question comes from Ram Selvaraju with H.C. Wainwright.

Hi, thanks so much for taking my questions, and congratulations on a very impressive quarter operationally. With respect to the vaccine outlook in the COVID-19 space. Two quick questions there first, can you comment on the degree to which your vaccine solutions are likely to be applicable to vaccine technologies that may arise in the future that are not specifically reliant upon the spike protein. And secondly, I wanted to understand better to what extent you anticipate two factors potentially driving your business with regard to the COVID-19 vaccine related items. And those are in particular, the need for vaccination campaigns to be accelerated dramatically in emerging countries, especially as we've been seeing, surges running out of control in those areas where vaccine rollouts really have not happened to any great extent. And also, in developed countries, and particularly most notably in the United States, to what extent you expect the broadening of vaccine applicability to younger people, including children as young as now it seems 12 to have on the demand for your vaccine related reagents. Thank you.

Yes, so maybe start with the last question. I do think that the especially in the developed countries, the campaign's that are going on to get people to vaccinate is really important. I think it's hard to put a number on what that means for demand. What we do, honestly, is we're really relying on the players that we're working with to give us the forecast of what they need. And that's kind of what we work to. And obviously, we pay attention to what's going on in the news. But really, it just comes down to what do the big vaccine manufacturers forecast out in terms of their needs, whether it's in the quarter in the year or in the following year. In terms of developing countries, I mean, it it is we're a long way as a as a human race in terms of getting vaccines rolled out to all sort of developing countries. And I think that's something that obviously is going to happen more as we hit the second half of this year. And my guess is all the way through 2022. So that's something that everybody will be focused on. And again, we will rely on the companies and partners that we have in terms of forecasting out what the demand is going to be. To your first question, which was on the applicability of our technologies to future vaccines that are non-COVID vaccines, but just vaccines in general. I think our portfolio of products are very well suited to any vaccine development work that's going on. I think our filtration portfolio hollow fiber technologies has been historically used in vaccine manufacturing. So, to the extent that we see more, viral vector based vaccines or mRNA based vaccines. I think we're well positioned with our technologies to be able to operate in both upstream and downstream parts of that vaccine development work.

Great. And then on the gene therapy side, two questions there. Firstly, if we look at the emergence of specialized gene therapy CDMOS, I think, in our research, we cited the case of this privately held entity called forge biologics. Clearly, we see those as being more potential customers for Repligen, then potential competitors. But we were wondering, to what extent you're seeing as these entrants in the CDMOS space and gene therapy start to emerge, that's having any kind of impact on future demand for your gene therapy solutions. And then secondly, if you think that at any point in the future, any of these CDMO gene therapy businesses might be likely to try to compete with Repligen on any of the product offerings that you have, or if you think they're going to stay in their lane, and you're going to stay in yours. And in point of fact, it's more a complimentary relationship that you see developing in the future. Thank you.

Yes, to your second question. I don't know how that plays out. I think, if you look at, historical data, CDMOS have tended to focus on working directly with customers and developing drugs, whether it's gene therapy, or its monoclonal antibodies aren't really that many examples of CDMOS who have become, bioprocess technology players. So, again, I don't know how that plays out. I don't, I can't really predict the future on that. But, I think you can see what's happened in the past. In terms of companies like Forge Biologics, I think when you look at the gene therapy space, where we've been, working Repligen has been working with CDMOS in the gene therapy space for the last three, four years. And I would say that the CDMOS have represented close to about 50% of the revenue that we have in gene therapy. So, if other CDMOS jump in and start to manufacture, then we would see them as another opportunity to position technologies that we have, and I would imagine everybody else in our industry would look at it the same way. But I think the CDMO industry has been probably one of the biggest drivers of gene therapy growth over the last four or five years. So I fully expect that, the addition of new CDMOS is only going to be viewed as positive.

Okay. And then just one last more general question. If you look at strategically speaking, the impetus that COVID-19 has created for your business and how you think Repligen can best capitalize on this, for the long term. Do you view this in terms of effectively broadening the scope of Repligen’s offerings and expanding Repligen’s customer base as this pertains specifically to vaccines, and possibly also to certain segments of the therapeutics landscape that may have applicability and COVID-19, but may also have implications for future therapeutics down the line that are not related specifically to COVID? Or do you think that in point of fact, given that at least some of the COVID-19 related revenue strengths may be transient in nature, you would look at this as possibly an opportunity that may give you the potential to pursue other strategic acquisitions or other strategic directions that don't have anything to do with COVID-19 or perhaps even vaccines in general. You know, kind of, while you're able to make hay while the sun shines. And I understand that, that's kind of a loaded question, but I think any perspective you can give us would be helpful.

Yes, I don't think our strategy changes around how we compete and play in the bioprocessing market. So we've been, doing the combination of M&A and launching new products, whether the new products come from an M&A that we've done a few years ago, or something that we've come up with internally and decided to develop ourselves. So I don't think COVID changes, how we think about the overall strategy of the company with respect to the importance of M&A or the importance of R&D. In terms of how we think about the COVID opportunity and how it can broaden offerings for us down the road. To me, the most important part of being involved, on the COVID. front is, there's a huge sense of purpose and pride within our company in terms of our ability to produce, deliver, and have a real impact with respect to these vaccines, therapeutics. The other piece that I think is longer term, is the relationships that we develop with these manufacturers, whether it's, pharmaceutical companies, biotech companies, CDMOS, because of the way the vaccines have been rolled out, there are many new players that we haven't worked with before, that we got an opportunity to work with, and, and form a really strong relationship. And we expect that those relationships will extend beyond what's going on with COVID today, and that those are the future opportunities for us. So that's kind of how we view it.

Our next question comes from Brandon Couillard with Jefferies.

Hey thanks. Two part question for John. You did 59% gross margins in the first quarter, kind of just maintaining guidance for the balance of the year? Why would we necessarily see more operating leverage on that line? And then any color you can share with us in terms of the phasing of the expected COVID revenues over the next three quarters? Should we just assume it's ratable, or maybe perhaps more front-end loaded than that?

Yes, I'll let Tony cover the second one. But the first one in terms of gross margin. Yes, we had a great quarter 59.3%. And you're correct, that we held guidance at 57% to 58%. You got we have meaningful investments coming into the into the P&L in terms of headcount, in terms of depreciation expenses coming terms of facility expenses, for added footprint that we've added. So that just really reflects the expected timing and when we expect those things to hit, align with that with the revenue coming through the P&L. Essentially, that's, that's what we're seeing. I would say, if you start to look at that, at that range, we're probably edging towards the higher end, the mid to high end of that range, versus the lower end at this point in time. So there is some movement, but we're just kind of moving up within that range right now.

Yes, and I think Brandon on the on the COVID revenue it’s probably going to be evenly spaced. If you, if you just take the midpoint of our guidance and take out 35 million, you'll see we're probably on the high end of 35 million to 40 million in the next few quarters.

That's it for me. Thank you.

This concludes our question-and-answer session. I'd like to turn the call back over to Tony Hunt for any closing remarks.

Great, thank you. Thanks to everybody for joining us today. Look forward to catching up in August when we'll bring you up to speed on the first half of the year performance. So again, thanks. Thanks, everybody for joining.

The conference has now concluded. Thank you for attending today's presentation. You may now disconnect.