Good day, and thank you for standing by. Welcome to the Valneva Full-Year 2022 Financial Results Conference Call. At this time, all participants are in a listen-only mode. After the speakers' presentation, there will be a question-and-answer session. Please be advised that today's conference is being recorded. I would now like to hand the conference over to your speaker today, Vice President of Global Investor Relations, Joshua Drumm. Please go ahead.

Hello and thank you for joining us to discuss Valneva's full-year 2022 consolidated financial results, which were published today and are available on our website. It's my pleasure to welcome you today. I'm joined by Valneva's CEO, Tomas Lingelbach; and CFO, Peter Buhler, who will provide a brief overview of our business and our financial results for the period, as well as updated financial guidance and a summary of anticipated upcoming milestones. There will be an analyst Q&A session at the conclusion of the prepared remarks. Before we begin, I'd like to remind listeners that, during this presentation, we will be making forward-looking statements which are subject to certain risks and uncertainties that could cause actual results to differ materially from those expressed or implied by these forward-looking statements. You can find additional information about these risks and uncertainties in our periodic filings with the Securities and Exchange Commission and with the French Market Authority, which are also listed on our company website, www.valneva.com. Please note that today's presentation includes information provided as of today, March 23, 2023, and Valneva undertakes no obligation to revise or update forward-looking statements except as required by applicable securities laws. And with that, it is my pleasure to introduce Thomas to begin today's presentation.

Thank you, Josh, and good afternoon, good day to all of you. Well, 2022 was a year marked by our ability to adapt to a changing environment and showed our resilience. We achieved several key milestones that underpin our unique value proposition. We made continued progress across the R&D pipeline with our chikungunya vaccine now under BLA review. On Lyme disease, we started the Phase 3 pivotal efficacy study, VALOR, together with Pfizer. On COVID-19, we were the first company to achieve a full marketing authorization by EMA. However, given the changing environment around COVID and the prospect of that vaccine, we decided to not further invest in development and stop manufacturing the COVID vaccine. We accelerated our preclinical activities with the aim to build a new, exciting R&D pipeline, up and beyond Lyme and chikungunya. We have seen a significant rebound of the commercial business, and we clearly capitalized on the strong recovery in the travel segment. We complemented our commercial portfolio with additional third-party product sales. We have reported strong full-year 2022 revenues and cash position with revenues of about €360 million, and product sales year-on-year increase well above 80%. Our cash position at the end of 2022 was close to €290 million. We also strengthened our shareholder base with a successful upsized follow-on offering which included now also our new major long-term shareholders and Pfizer. With that, let me go straight into our programs and into the business update, and I will start with chikungunya, page six of the presentation. By way of reminder, our chikungunya program is the most advanced chikungunya program in development worldwide. It is a live-attenuated vaccine candidate targeting long-lasting high sero-response after a single shot. Basically, the Phase 3 study met all primary endpoints in terms of sero-response rate, but also in terms of lot-to-lot consistency. We reported positive 12-month antibody persistence data and the long-term persistence trial that will measure the sero-response rate over time, targeting at least five years. The adolescents' trial is fully enrolled by now, and we expect first data mid-2023. We are under priority review for the BLA. A PDUFA action date has currently been assigned for end of August, 2023. And we expect to commence other regulatory processes in the second half of this year, including EMA. The program also received FDA Fast Track and Breakthrough and EMA PRIME designations, as you know. In terms of target population and overall geographic reach, we have explained before that we see, of course, the non-endemic countries, and here primarily travelers, military, but also the possibility of outbreak preparedness and stockpiling. On the other hand, the endemic use where we have a partnership agreement with CEPI and Instituto Butantan. From there, let me turn now over to the key data for chikungunya. Sero-response, 99% after a single vaccination; this immunogenicity profile has been sustained even after 12 months. We have seen a similar sero-response rate in the elderly, which is particularly encouraging. Based on that high sero-response rate, we see also a 100% seroconversion. Regarding safety data, VLA1553 was generally well tolerated. We had, as expected for a vaccine of that class, solicited systemic adverse events, but the majority of solicited adverse events were mild or moderate. Only 2% of study participants reported severe solicited adverse events, most commonly fever. In terms of future commercialization, as we repeatedly communicated, VLA1553 fits perfectly within our existing commercial infrastructure. We have a high-caliber team with significant experience in the vaccine space. We are currently adding a significant amount of talent as we prepare for the commercial launch and market access for this brand new vaccine in a brand new indication. We are all extremely excited about the prospect of being in a position to launch such a product. Let's go to Lyme. It is, again, following our pipeline differentiation around first-only or best-in-class, the only Lyme disease vaccine in advanced clinical development today. It is a multivalent recombinant protein-based vaccine covering the six main serotypes of Lyme borreliosis prevalent in the northern hemisphere. We initiated the Phase 3 study on the back of positive results from three Phase 2 studies, including in a pediatric population. You know that as part of the ongoing Phase 3 study, there were GCP issues observed that led the study sponsor and our partner, Pfizer, to stop a significant part of the study subjects included in the study. Given the seasonality around Lyme development, we currently have a review of the trial design and the associated timeline ongoing. By way of reminder, regarding the data that have always been extremely strong for Lyme, and of course, also the GCP issues that we have been facing now as part of the Phase 3 conduct do not change the picture on the underlying science and value of this program. All three Phase 2 studies showed strong immunogenicity. The product has been in more than a thousand people, including the pediatric population. We have seen as part of the booster studies a very strong anamnestic response which is of utmost importance for a product that is expected to be boosted over time. When we look at our pipeline, you basically see that we are currently reviewing most of our or some of our preclinical and previous clinical candidates regarding the next clinical entry. We have a Zika candidate for which we conducted a Phase 1 study. We did not progress it further because of the work that we commenced on COVID. However, we are currently evaluating a potential clinical re-entry at the end of this year or very, very early next year. Given that we could leverage one of our existing platforms, and given that WHO made a clear recommendation for Zika vaccines to be based on inactivated whole-virus technologies. hMPV, human metapneumovirus, is a program that we developed throughout the preclinical phase. It has reached the end of the preclinical phase, with the initial preclinical proof of concept being completed. But given that the market is shifting in the development arena towards combination vaccines, RSV hMPV, we've decided to evaluate a potential partnership before taking it potentially into a first trial in humans. Our lead program in our preclinical shop today is Epstein-Barr virus. We target the completion of the antigen identification for such a complex development in an area of very high unmet medical need by the end of 2023. The two other programs that we have in early R&D are Campylobacter and parvovirus. We are still evaluating whether we will put them into preclinical R&D and development as of now or not. This is something we will decide over the course of this summer. With that, I would like to hand over to Peter to provide us the financial reports.

Thank you, Thomas, and good morning or good afternoon to all of you. Let's look at the financial review of our fiscal year 2022. Total revenue grew by 3.8%, which is fiscal year 2021, driven by strong product sales growth. Total product sales reached €114.8 million, an increase of 82.3% versus the prior year or 66.7% in constant currency. 2022 product sales include €29.6 million of VLA2001, our COVID-19 vaccine. Product sales excluding our VLA2001 sales reached €85.2 million exceeding our guidance of €70 million to €80 million. Moving on to slide 14 looking at product sales details, IXIARO sales reached €41.3 million, a decrease of 8.4% versus the prior year as a result of fewer shipments for the U.S. military. A decrease in sales to the U.S. military was partially offset by a significant increase in sales in the travel market of 300%. DUKORAL sales reached €17.3 million compared to €2.4 million in 2021, an increase of more than 600% once again driven by the recovery of the travel market. Third-party product sales increased by 72% to reach €26.5 million for the fiscal year 2022; this represents a record level for this product segment as Valneva managed to increase third-party product sales consistently over the last two years. The very positive sales performance in our travel vaccine is related to the travel market recovery faster than expected. Finally, as already mentioned, we shipped the COVID-19 vaccine for an amount of €29.6 million to certain member states of the European Union as well as to the Kingdom of Bahrain. Moving on to slide 15, looking at the P&L. We already covered product sales. Other revenues reached €246.5 million and primarily consist of one-off revenues derived from the advanced purchase agreements with the European Commission and the United Kingdom. The cash related to these revenues was received in 2021 and early 2022. Also included in the other revenue line is the added impact related to the amendment of the VLA15 agreement with Pfizer and updated cost sharing. Further details will be included in our universal registration document in 20-F that we plan to publish next week. Total revenues reached €361.3 million slightly exceeding our guidance of €340 million to €360 million. Looking at expenses, we observed a significant increase in cost of goods, which is mainly a result of one-off items related to the winding down of our COVID-19 program following reduced market demand. Research and development expense decreased from €173 million in 2021 to €104.9 million in the fiscal year 2022 and stayed well within the revised guidance of €95 million to €110 million communicated during our nine-month result release. The decrease compared to the prior year is mainly driven by lower spending on our VLA2001 program but also by decreased spending on clinical trials of our chikungunya vaccine as the program advances to its licenses. Marketing and distribution trends remained stable compared to the prior year at €23.5 million and contained €7.3 million of cost for our chikungunya vaccine candidate, twice the amount spent a year ago as we prepare for potential launches. G&A expense decreased significantly from €47.6 million in 2021 to €34.1 million in 2022. All expense lines benefited from substantial long cash adjustments related to the positive effect of the costs related to the company's share-based compensation due to the share price performance in 2022. Overall, an upside of €25 million resulted in '22 compared to a total of €37 million in 2021. Other income of €12.2 million mainly consists of R&D tax credits and other expenses related to the provision for the ongoing Vivalis/Intercell litigation procedures. Total other income decreased compared to the prior year due to the lower R&D spend and a relative decrease of R&D tax credits. In 2022, Valneva generated an operating loss of €113.4 million compared to €61.4 million in the prior year and an adjusted EBITDA of negative €69.2 million versus minus €47.1 million in the prior year. Next slide, please. Looking at our COVID business segments, we see total revenues of €309.6 million with a total cost of goods and services of €267.1 million. COVID cost of goods includes significant costs related to the write-down of the COVID program. The company recognized major costs related to a write-down of all COVID-related inventories and agreements, particularly the discontinuation of a third-party manufacturing contract. The operating loss for the COVID segments in 2022 reached minus €42.8 million. The business outside COVID generated total revenues of €51.7 million. As already mentioned, the negative other revenues were driven by the revised agreement with Pfizer. Cost of goods and services reached €57.3 million and sales of €9.2 million for technologies and services, €3.3 million for vaccine candidates and €41.8 million for commercialized products. Gross margin of product sales reached 45.5% compared to 36.5% in 2021. Cost of goods for commercialized products also includes impairment charges related to DUKORAL. Total operating loss for the business outside COVID was €70.6 million compared to an operating loss of €65.3 million in 2021. The increased operating loss is driven by the negative revenues related to the Pfizer agreement. Moving on to slide 17 and looking at our balance sheet, total assets decreased from €817 million at the end of 2021 to €621 million at December 31, 2022. The main decrease in assets relates to a sharp decrease in inventories primarily related to the full write-down of all COVID-19-related inventory. Cash and cash equivalents at the end of 2022 were at €289.4 million compared to €346.7 million at the end of the prior year. Next slide, Valneva's equity was strengthened in 2022 through a global offering of €102 million at the end of the third quarter, as well as private investment in Valneva shares for a total value of €90 million. At the same time, total liabilities decreased by €245 million, particularly driven by a decrease in contract and refund liabilities resulting from revenue recognition of deferred revenues related to the COVID-19 agreements. Borrowings and other non-current liabilities remained stable. While total borrowings increased due to an increase in Deerfield & OrbiMed loans, these liabilities decreased due to amortization and the foreign exchange impact. Provisions decreased due to lower costs of share-based compensation, driven by the decrease in Valneva's share price. Overall, Valneva significantly improved the debt-to-equity ratio in 2022. Now moving on to the financial outlook on slide 20, we expect product sales to reach €130 million to €150 million, but this includes marginal remaining VLA2001 sales under the supply agreement. Further €90 million to €100 million of other income are expected in relation to the sale of the PRV expected upon potential approval of chikungunya vaccine candidates. Investments into research and development are anticipated to reach between €70 million and €80 million. This concludes the finance section of this call, and I would like to hand back to Thomas for the news.

Thank you so much, Peter. Yes, so we see for the year 2023 quite a significant number of catalysts and interesting news flow. As mentioned earlier, chikungunya is, of course, the adolescent study results that would come mid-year. Please keep in mind that we expect to extend the label in the United States post-licensure and probably include the data directly for the initial filing in other markets. Of course, then it's all about our launch here, the potential BLA approval, and the launch, and upon successful approval, the PRV and the potential PRV sale that Peter mentioned earlier. We aim to accelerate bringing this novel and unique vaccine to many markets as quickly as we can. Hence, you should expect additional ex-U.S. regulatory submissions in the second half of this year. On Lyme, of course, we all understand that it is important that we get clarity on our Phase 3 clinical study plans. We need to have this as quickly as we can so that we can restart enrolling people in time. As we are running the antibody persistence studies in an ongoing manner, we will also expect additional antibody persistence results in the second half of this year. Then on IXIARO and military, we expect a potential new DoD contract still towards the later part of H1, the progression of the selected preclinical programs towards clinical entry, so we will take a clear decision which one, and by when. As we reported earlier, we are reviewing and evaluating potential augmentations of our clinical pipeline through program acquisitions or partnerships in the R&D environment. When you look at our strategy and how we see the company evolving over time, we prepare slide 23. You see that our value proposition will gradually be extended. The additional potential growth drivers include the continued recovery of the travel market to pre-COVID levels and beyond, new U.S. DoD contracts for IXIARO, further expansion of our third-party distribution segment, and potential in-licensing or acquisition of additional clinical and/or commercial-stage products. With that, we conclude our presentation and hand back to the operator to take your questions.

Thank you. We will now take the first question; it comes from the line of Maury Raycroft from Jefferies. Please go ahead, your line is open.

Hi. Congrats on the progress, and thanks for taking my questions. I was going to ask one about the Lyme disease program. So, for the Phase 3 Lyme proposed protocol modifications that would allow Pfizer and Valneva to remain on track for a 2025 filing, I'm guessing you can't provide too much into exact interactions with FDA. But can you talk about some of the scenarios or moving parts involved with being able to maintain that, the timelines?

So, Maury, hi, good day. It's, of course, an excellent question. You would certainly understand that, as you rightly pointed out, there is very little we can say at this point in time. We don't want to disturb this ongoing process. It is very clear that, as we discussed previously, of course we did lose a significant number of people in the season 2023. Given the seasonality, you only have a certain window where you can recruit people. One scenario is just to add another season, which is the obvious one that you already figured out for yourself, and just restarting again this summer or the next tick season, 2024. There are other, what I would call, more creative scenarios that may potentially allow still a filing, but those are in the making right now or in discussions, and we can't comment on those.

Got it, understood. And for CHIKV, I'm wondering if there's been any new correspondence with the FDA related to potential foreign advisory committee meeting? And, in looking ahead, how are you preparing for the February 2024 ACIP vote and maybe talk about how outcomes from that vote could impact your launch strategy?

An excellent question. First of all, we are making progress in the ongoing review process. At this point in time, there is nothing that has come up unexpectedly. Otherwise, of course, we would have reported it. As far as the work plan is concerned, no decision has been taken yet as to whether a dedicated work plan for this program will be needed or not. It goes without saying that we are preparing at full speed, at full steam for such a work plan. Our teams are well-prepared, and we are putting everything together to enable a very positive work plan, should it be required. Regarding the ACIP, the ACIP process has been very clearly outlined. We had already a number of presentations on the program. We will continue following the path as we are invited to present. Of course, we do hope and do assume a positive vote as part of our launch plans for the United States.

Got it. Okay, thanks so much for taking my questions.

Thank you. We will now take the next question. It comes from the line of Evan Wang from Guggenheim Securities. Please go ahead, your line is open.

Hey, guys, thanks for taking the question. Following up on Lyme, just as you guys are having these discussions, have you seen this kind of situation before? Have FDA or EMA provided any kind of commentary or is there any precedent that gives confidence that a modification could be reached? And then I have a follow-up after.

I would say the situation with Lyme; it's in a way unprecedented because of the seasonality of the disease. Under normal circumstances, if you did not have a seasonality to be considered, you lose, for whatever reason, people in your clinical study, and then you just continue recruiting, and the recruitment takes longer. Here, we have, of course, the situation where you need to recognize the seasonality because otherwise you don't get the necessary case count in a placebo-controlled efficacy setting. As such, there is probably not any precedent to such a specific situation. Now, the discussions with FDA on primary endpoints, secondary endpoints, co-primary endpoints, parallel endpoints; these are discussions that I have been through in my more than 30 years of vaccine development many, many times, and this is certainly nothing unusual. These are things that need to be based on different statistical modeling. This is clearly something that is not new to any regulatory authority. But, by the end of the day, it is always a matter of risk, benefit, and judgment. That's all I can say at this point in time.

Got it. And I have a follow-up on chikungunya. Can you expand a little bit more on your travel commercial infrastructure? And in particular, how it compares to that of Bavarian Nordic?

First of all, we do have our own commercial operating entities and organizations in the U.S., Canada, the U.K., France, the Nordics, and Austria. We are working with Bavarian Nordic under a commercial agreement where, in some of the markets where we have our own infrastructure, we sell Bavarian Nordic products, and in other markets where Bavarian has an infrastructure, they sell our products. As we've said previously, this whole collaboration is going to be under review. But for now, both parties have made a clear commitment to respect their respective contractual obligations going forward.

Great. And I had one last one on hMPV. It seems like maybe there's more emphasis on partnering. Am I interpreting that right, or are there still plans to bring that into clinical-stage development?

So I would say, right now, we have, as I mentioned earlier, reached the point of preclinical proof of concept completion. This means we need to take a clinical entry decision on this asset. But the point is that we are talking here about a pre-fusion candidate that requires an adjuvant. Standalone hMPV does not really make sense from a product development perspective. The first trial in humans is certainly valuable. But whoever would then later combine this asset with an RSV vaccine would need to go largely back to the drawing board because of the specifics around adjuvantation. Therefore, we have given it a slight pause and look to see whether it would be more valuable to bring this asset into a partnership model with one of the RSV candidates, and therefore have a more efficient development route. Should this not be seen as a viable and value-generating option, then we will certainly consider taking it into the clinic in order to increase the asset's value.

Great. Thanks, guys.

Thank you. We will now take the next question. It comes from the line of Max Herrmann from Stifel. Please go ahead, your line is open.

Hi. Thanks very much for taking my questions; three, if I may. Firstly just some financial clarity just on the COVID vaccine inventory write-off in the fourth quarter. Was interested to find out what that was? Secondly, on the Epstein-Barr virus candidate, how do you view the field given the mRNA vaccines ahead of you in the clinical ready? And then just a little bit more clarity on the refund liabilities at €136 million; what do they actually relate to? Is that to do with the Pfizer funding or what's within that? Thank you very much.

Max, let me start with the non-finance question first about EBV. As you know, Valneva's strategy is certainly based, and Valneva's R&D pipeline strategy is basically based on our clear idea to have assets where we can play a differentiating role; first-in-class, best-in-class, only-in-class. If we entered into a space where others are more advanced, we will evaluate our candidate and then take a decision before we enter the clinic, of course.

Okay, understood. Thank you.

Thank you.

Yes. Thanks, Max, for the question. So, first question on the COVID inventory write-off. The approach we took and communicated previously was that we have 8 to 10 million doses of the COVID vaccine in our inventory. The approach we took at the end of 2022 is basically to take a full write-down on semi-finished and finished products but also on specific raw material related to the COVID vaccine. We, of course, continue our efforts to try and sell these products in the market. Given where we are today, we decided that this will be a prudent approach to wholly write-down those inventories.

Regarding your second question, the refund liabilities, which is by and large Pfizer-related. There is a small historic remaining part that relates to an old use case, contract or refund liability that we had last year, but basically, the large majority of the refund liabilities is related to Pfizer.

And just on my inventory write-off, are you able to quantify it? Because it's quite odd not to list, so I'm unclear about what the actual amount was. I mean does that mean that you have written off the product you all your inventory now? The stuff that you plan to ship to Bahrain that you have kept a cost? Just trying to understand the implications.

Yes, your assumption is absolutely correct. We basically rolled off everything except the remaining shipments for Bahrain. That will still be included in our inventory, and that's a relatively small amount. Overall, you can assume a write-off in the financial year 2022 of roughly €130 million. That goes into our cost of goods.

Okay, great. Thank you.

Thank you. We will now take the next question. It comes from the line of Rajan Sharma from Goldman Sachs. Please go ahead, your line is open.

Hi, thanks for taking my questions. Just on the market of travel vaccine. So, if you could just kind of help us understand what proportion of the revenue growth in 2022 was driven by volume versus price? And how we should think about this dynamic into '23 and into the mid-term? Secondly, just again kind of the commercial vaccine business. There are some additional detail in today's release which was helpful on growth margins. I am just wondering how we should think about this into 2023. Is it safe to assume that it's kind of up '22 levels? And what would be the pushes and pulls to this? And then, just one follow-up on Lyme; in a scenario where there are additional trials required, I just wanted to clarify if your potential contribution to those costs is capped at a certain level? Thanks.

Let me start with the Lyme section. It's important to note that the study is ongoing. It means we have to study why it's not stopped. It's only a matter of when do you recruit the necessary additional people into the study because you lost some of them. The second part relates to what kind of readout you keep and when you do the readout. This is always in relation to readout after primary immunization versus readout after priming class; more from the clinical development point of view. On the cost side of things, we have not had any discussion yet regarding any potential incremental costs, and this is something that will be discussed as soon as we have an agreed development plan going forward.

With regard to your volume versus price question, when we look at the IXIARO as you can see on the slide, at constant exchange rates, we look at a downside of about 18.6% versus the prior year. We are looking at the upside rate to price of around 10%, so the differences are, of course, volume-driven. When we look at DUKORAL, we have volume upside versus the prior year of roughly 400%, and then the distance to the total 600% of services per year would be price-related. I think you had a second question, but if you could just repeat that one.

Yes, sure. It's just on the gross margin on the travel vaccines; you have some additional information in the release today. I was wondering whether those '22 levels are a fair assumption for margins going forward.

Yes, so we look at a much stronger gross margin than for IXIARO than for DUKORAL in 2022. As you can see, the gross margin improved significantly versus the prior year. We would expect this improvement also to continue as we continue to increase volumes.

Okay, that's fair, that's very helpful. Thank you.

Thank you. We'll now take the next question. It comes from the line of Samir Devani from Rx Securities. Please go ahead, your line is open.

Hi, everyone. Thank you for taking my questions. I have three that are mostly related to finance. First, regarding the guidance for other income at €90 million to €110 million, I wanted to confirm that this is essentially non-cash revenue recognition. Next, concerning the Pfizer Phase 3, did you make a cash contribution to that in 2022? If so, could you clarify where that appears in the cash flow since you mentioned it doesn't go through the P&L? Lastly, about your distribution of marketing expenses, we noticed a slight increase in Q4; is Q4 a good benchmark as we move into this year? Thank you.

I'll start with the first point on guidance. Other income, as we mentioned, is related to the PRV we expect to receive upon approval of our chikungunya vaccine candidate, and as we expect to sell this PRV, it will be cash-related because we will recognize that other income as we get to cash. To be very clear, we expect this to go not into other revenues with other income, i.e., further down in the P&L. In regard to the Pfizer Phase 3 cash, the way the agreement works is that we basically pay every quarter our share to the trial. Indeed, to your point, that does not go into the P&L but it would go against the balance sheet against the refund liability we talked about previously in Max's question. As for distribution and marketing expenses, what you see in Q4 is an increase compared to prior year's previous quarters driven, of course, as we prepare for the chikungunya candidate launch. It's safe to assume that you could see further increases there as we strengthen the commercial infrastructure in view of the new launch.

Okay, that's great. Thanks very much.

Thank you. We will now take the next question. It comes from the line of Suzanne Van Voorthuizen from VLK. Please go ahead, your line is open.

Hi, thanks. Yes, it's Rohan calling in for Suzanne. I just have one confirmatory question, so since you've mentioned that you've written off all COVID-19 inventory in 2022, if I understand correctly that we will see no financial impact for the current year?

We will continue to have some R&D expense as we continue to finalize certain clinical trials that we have started in the past. We will not initiate new clinical programs, of course, but we do need to ramp up the clinical trials; that cost is included in our R&D expense. We do not expect further inventory write-offs to that point. Of course, we also mentioned the final shipments to Bahrain. That was, of course, driven by revenues. That's basically what we expect for 2023 in terms of COVID hitting there.

Okay, thanks. And then, one final question. So, last year's R&D day, you presented on various preclinical programs, such as Zika, hMPV, and UBC, which we expect in terms of updates on these programs during this year? Thanks.

Our objective is to have a clinical entry by the end of this year or very early next year, but it's one or two programs. It's still something that we're going to decide out of our own pipeline, but we will definitely inform markets about which program we expect to enter into clinics. This would certainly be a new development for this year. We have ongoing discussions about reviewing potential additional external opportunities to inject into our clinical pipeline since we have clinically relevant capacity and capability. That's an ongoing process as reported in the expected news flow and catalyst section.

Thank you. We will now take the next question. It comes from the line of Rajan Sharma from Goldman Sachs. Please go ahead, your line is open.

Hi, thanks for taking my additional questions. I just wanted to follow-up on the BD M&A piece or the external sources of innovation. Would your preference on that be kind of a knowledge platform that you potentially don't have in-house right now, or would you be looking at specific assets? And then, just secondly, to follow-up again on my initial question on kind of volume versus price, so I was just wondering, were you able to kind of take price increases on DUKORAL third-party products on IXIARO in 2022, and do you expect to be able to do that in 2023? Thank you.

Yes, thanks, Rajan. Let me start with your second question. So, yes, we did increase pricing across the board for basically most IXIARO and those are some of our third-party products. We are also looking at continuous price increases in certain countries going forward.

Your first question regarding BD M&A. Valneva is a technology agnostic company, right? We are not a technology company; we go by indication, looking for indications where we can still play a pioneering role. I mentioned earlier that Valneva has historically worked with literally all vaccine technologies out there except mRNA. Of course, we will also be open to work on a specific indication on mRNA, but it’s not our interest to acquire a technology company or a technology platform. We'll focus on specific indications and specific assets.

Okay, that makes sense. Thank you.

Thank you. There are no further questions at this time. I would like to hand back over to Thomas Lingelbach, CEO for final remarks.

This one I hand over to my friend, Josh.

Well, thank you, everybody for your time and participation today. Please note, an archived version of today's webcast will be made available later today. A PDF of the slides presented during today's call is already accessible on the company's website. We look forward to a productive 2023 and to welcoming you back for our next conference call in the not-so-distant future. Thank you and enjoy the rest of your day.

That does conclude our conference for today. Thank you for participating. You may all disconnect.