Ladies and gentlemen, welcome to the Euroapi 2025 full year result. The call will be structured in two parts. First, a presentation by the Euroapi Group management team, represented by David Seignolle, CEO, and Olivier Falut, CFO. Afterwards, there will be a Q&A session. During this session, you may ask question in two ways: by submitting a written question in the box below the player, or by joining the conference call and dial pound key five on your telephone keypad to enter the queue. I will now hand over to Sophie Palliez, Head of Financing, Treasury, and Shareholder Engagement. Madame, please go ahead. Thank you. Thank you, Laura, and welcome everybody. Before we start this presentation, we would like to emphasize that some of the information we will share with you today is looking forward and not historical. This information is based on projections and assumptions concerning Euroapi's current and future strategy, future financial results, and the environment in which we operate. These looking forward statements and information do not constitute guarantees of future performances. They may be subject to certain risks and uncertainties which are difficult to predict and generally outside the control of the group. They could cause actual results, performances or achievements to differ materially from those described or suggested. That said, let me give the floor to David Seignolle. Thank you, Sophie, and welcome everybody. Let me begin on Page 5 with the key takeaways from 2025. Our teams fought on all fronts to protect our market position in an increasingly competitive environment. For example, Vitamin B12 as mentioned here. It was also another year of declining API volumes for Sanofi. Fortunately, on the Sanofi side, this was partially offset by a strong commercial CMO activity, particularly in anti-infective and skin care. At the same time, we saw growth in sales of key APIs with other clients, such as opiates, et cetera, et cetera. While the top line was under pressure, we continued to make strong progress on everything that we can control. We sustainably reduced our external expenses and our personal costs. We maintained strict working capital discipline with another year of improved inventory management. We continued to invest selectively in CapEx to prepare the company for future growth. All of this reflects a real strengthening of our cost discipline across every function. Despite the top line headwind, our transformation remains firmly on track. We have executed the initial phase of our plan on schedule in all the areas we control, some even earlier than planned. That includes our product portfolio rationalization, our industrial footprint simplification, and our organization and processes. Taking a quick look at 2025 from a financial perspective on Slide 6. Net sales came in at EUR 848 million with Sanofi sales down 26.4%. Other clients up 9.7% as reported. Our core EBITDA came in at EUR 66.2 million, a 31% increase from 2024, with a core EBITDA margin of 7.8%. Our EBITDA was close to EUR 10 million versus -EUR 44 million in 2024. CapEx stood at EUR 77 million, with 55% of that allocated to growth and performance projects and supporting the company's return to back on track for sustainable long-term trajectory. Turning into Slide 7, the challenges we faced this year did not weaken our commitment to sustainability. First, our near-term carbon emission reduction targets were validated by the SBTi. This is a strong confirmation that our trajectory is aligned with the Paris Agreement. Looking at our 2025 emissions, we are already seeing meaningful progress. We have achieved half of our targeted reduction for Scope 1 and 2, and we have already exceeded our target of Scope 3. This is a major milestone for the company. On diversity, given the current reorganization underway, we have fell short of our 2025 targets on diversity. However, it is important to keep a long-term perspective in mind. In 2023 and 2024, our diversity ratio increased and even exceeded our objectives. The underlying trend remains positive. On safety, which is something a bit painful to me, but despite our continuous effort, the injury rate remained stable in 2025. Most incidents were minor, often related to slip, trips and falls. That said, even one incident is one too many, and the accident prevention plan launched in 2025 will continue to be rolled out in 2026 with a stronger focus on root cause analysis and proactive prevention. With that, I will now hand over to Olivier, who will walk you through our financials in more detail, and I'll come back later to look at the perspective. Thank you, David. We'll start the review of the consolidated items with the evolution of net sales. Net sales reached EUR 848.2 million in 2025 versus EUR 911.9 million in 2024, representing a decrease of 7%. The current impact on net sales was almost nil. The currency impact, sorry, of net sales was almost nil, and the 1.2% perimeter impact is related to the Haverhill divestment. On a comparable basis, sales declined by 5.9%. We take a look at the net sales per activity on Page 10 now. API solutions to Sanofi decreased by 34.2% due to, first, an intolerable comparison base related to the stock clearance of Buserelin, which positively impacted 2024 sales for EUR 21 million. The decline of volume of Sevelamer in H1 2025 and the sales of Haverhill at the end of June 2025. Last, EUR 50 million reallocation of Opella sales to other clients starting in May 2025, following the change in control of Opella. Excluding Opella, sales to Sanofi in 2025 compared to 2024 only would have decreased by 25.7%. CDMO sales to Sanofi decreased by 4.9%. Higher demand of Pristinamycin and PLA commercial sale contracts was more than offset by the decrease in revenue from the phase 3 BTK inhibitor project. API solution to other customers increased by 18.6% since beneficial from, first, an active cross-selling strategy, then 31 additional new clients in 2025 which generated high single-digit net sales in 2025. Last, the EUR 50 million reallocation of Opella sales. Without the change, sales to other clients would have increased by 4.5%. CDMO sales to other clients decreased by 13.6% as a result of the downsizing and discontinuation of three carve-out major commercial contracts and the slowdown of early stage CDMO business. Turning to the core EBITDA evolution on slide 11. Core EBITDA reached EUR 66.2 million in 2025. This represent a 7.8% margin, up from 5.5% in 2024. The evolution in core EBITDA margin was driven by the following elements. The stock clearance of Buserelin in 2024 for EUR 21 million or -4.9 percentage points. Volume impact for -1.0 percentage points, which is mainly due to the discontinuation of CDMO contracts. Price and mix positively contributed by 1.3 points, a positive 0.3 points from the discontinued products. Industrial efficiency led to an additional 1.2 percentage points of core EBITDA margin. Energy and raw material increased the margin by 0.9 points. Strengthened financial discipline and lower personal cost in OpEx allowed to gain 1 point of core EBITDA margin. While Brindisi weighted -1.4 points in 2025, and on the other hand, the divestment of Haverhill allowed to gain 0.6 points. Total non-recurring items on Page 12 now. Total non-recurring items related from core EBITDA, from EBITDA, sorry, stand at EUR 56.3 million in 2025. The vast majority of these exceptional items are directly related to the FOCUS-27 plan. We recorded EUR 36.1 million of idle costs, which mainly concern the rationalization of the Frankfurt site. We also recognized EUR 6.6 million of internal and external costs related to the transformation of the company. Employee-related expenses in part linked to the redundancy plans amounts to EUR 13.7 million, which mainly concern again Frankfurt and the divestment of Haverhill. Looking now at items below EBITDA on slide 14. Please, sorry. Operating income amount to negative EUR 130.6 million in 2025 compared with negative EUR 120.4 million in 2025. Depreciation and amortization remain broadly stable year-on-year. The increase of assets impairment to negative EUR 77.8 million reflect discontinuation of Vitamin B12 productivity project in Elbeuf, following a reassessment of its economic potential, and a revision of growth assumptions to align with the latest market dynamics. As we move below operating income now, net financial expenses improved EUR 7.5 million in 2025 versus EUR 19.1 million in 2024. This decrease reflects lower financial expenses following the implementation of the financing plan. The 22.8.9, sorry, income tax. Sorry, 72.9 income tax expense includes the depreciation of assets, of factor assets following the update of growth assumptions. Taking together these items results in the net loss of EUR 211.2 million compared to EUR 130.6 million lost in 2024. Turning to working capital dynamics on slide 14 now. As part of our commitment to improve working capital, we have maintained the progress achieved on both months on hand and DSO since the implementation of FOCUS-27. Months on hand stood at 7 in 2025 and DSO at 30 days. CapEx now on Sage 15. CapEx reached EUR 77 million in 2025, which represent 9% of total 2025 net sales. 55% of CapEx was dedicated to growth and performance, mainly supporting the capacity increase and efficiency projects on peptide and oligonucleotides, prostaglandins and corticosteroids. 21% of CapEx related to compliance. As a reminder, these investment address safety, quality and environmental topics, and a significant share of them are mandatory. 24% of remaining CapEx correspond to the maintenance of the existing assets base. Moving now to Slide 16, which covers the evolution of the net cash position. We ended 2025 with a net cash position of EUR 68.2 million, compared with EUR 24.6 million at the end of 2024. Cash flow from operating activity generated EUR 128.5 million of the cash in 2025. This was mainly driven by the working capital, which contributed for EUR 120.1 million. This improvement mainly reflects further reduction in inventory totaling EUR 38.9 million. Decrease of trade receivables supported by factoring program launched in March 2025. Out of the EUR 45.4 million reduction of receivables, EUR 26.5 million were factored by year-end, with remaining decrease reflects enhanced cash collection. Other current assets and liabilities includes EUR 36 million paid by Sanofi to reserve minimum availability capacity for five selected products. EUR 21 million upfront grants from the IPCEI program. EUR 6.5 million related to the monetization of research tax credit in France. Including the EUR 77 million of CapEx that was re-reviewed in previous slide. Free cash flow before financing activity stood at EUR 51.5 million in 2025 compared to EUR 15 million at the end of 2024. Finally, cash from financing activities include the cost of debt of EUR 3 million in significant decrease following the debt refinancing in 2024. This concludes the review of the 2025 consolidated results, and I will hand it back to David. Thanks, Olivier. Before moving to full year 2026 guidance, let me walk you through the main operational and business drivers that will underpin sales profitability and cash development for the year. Net sales will be strongly impacted by the rationalization of the API portfolio that we have engaged in two years ago. As we've said, the discontinued API accounted for around EUR 70 million of sales in 2025, including EUR 20 million related to stockpiling. Although the manufacturing of these API has been stopped, we still expect a residual EUR 10 million-EUR 15 million revenue from this product in 2026 as we continue sales through existing inventory. This means between EUR 55 million and EUR 60 million headwinds in 2026 that we decided upon. The other impacts are the continued decrease of the sales to Sanofi and further discontinuation of commercial CMO contracts. Turning to profitability, the industrial efficiencies and additional OpEx savings we anticipate should be offset by unfavorable fixed cost absorption resulting from lower volumes. Our EBITDA will also be impacted by the restructuring costs that are foreseen in 2026. We will maintain a strong focus on working capital discipline and a CapEx to sales ratio is expected to be around 8% of sales. All in all, on Page 19, due to the impacts of our portfolio rationalization and considering the challenging business environment, we expect a decrease of around 10% in net sales in 2026 on a comparable basis. Our own decision to streamline our portfolio accounts for around 90% of that decrease. In this context, we will accelerate our transformation to protect profitability, and we expect to maintain the full year 2026 core EBITDA margin broadly in line with financial year 2025. Moving to the next slide and an update on FOCUS-27. On Page 21, let me recall first what FOCUS-27 was fundamentally about. It was designed around four structural pillars to reshape Euroapi into a more competitive, more profitable, and more resilient company. First, a streamlined API portfolio. We are concentrating on highly differentiated and profitable products, reducing exposure to commoditized segments where structural pressure is intensifying. Second, a focused CDM offer where we are leveraging recognized capabilities and strong technology platforms to position ourselves where complexity, reliability, and regulatory excellence matters most. Third, a rationalized industrial footprint and disciplined CapEx. We are simplifying our manufacturing network and prioritizing high return investment and improving asset utilization. Four, organizational transformation. We are building a leaner, more agile company aligned with our strategic priorities and able to compete in a faster-moving environment. These four pillars remain absolutely valid today. On Page 22, let's have a look at what has been delivered over the last two years. Despite the demanding environment, we have executed the core structural actions of FOCUS-27 and reinforced our fundamentals. On the portfolio, 66% of our sales in 2025 are now coming from differentiated products. This compares with 57% at the end of 2023, and we are on track to achieving our target of 70% by the end of 2027. The planned discontinuation of the low-margin products was almost completed at the end of last year, which will impact our 2026 top line, as already said, accounting for 90% of our top-line reduction. Regarding the CDMO goals, 70% of the projects are late stage, improving visibility and reducing the risk. On the industrial footprint, Haverhill has been divested, productivity has improved across all sites. One workshop in Frankfurt has been mothballed, and 380 positions have been reduced across the company ahead of our original plan. On the organization and cost base, key functions have been reorganized, R&D has been refocused, and close to EUR 20 million of OpEx savings have been delivered over the past two years. Overall, Euroapi today is a leaner and more disciplined organization than it was in 2023. Moving to Page 23. Capital discipline has also been a very strong priority under FOCUS-27. This is clearly reflected in our CapEx trajectory. Investment decreased from EUR 137 million in 2023 to EUR 108 in 2024, EUR 77 million in 2025, and I've even mentioned that we will be close to 8% for 2026. From a CapEx to sales ratio starting at 14%, back in 2023. This reflects a deliberate shift towards stricter prioritization, higher return of projects, and certainly better care and discipline around CapEx expenses. We have continued to invest in strategic platforms such as peptides or oligonucleotides, and in high barrier APIs like prostaglandin and corticosteroids. At the same time, we took disciplined actions to discontinue the Vitamin B12 capacity project following market deterioration and technical constraints. Moving to slide 24, let me briefly step back at where we are on our key KPIs for FOCUS-27. Since 2024, we have incurred EUR 44 million of transformation and restructuring costs ahead of the 25% originally mentioned for those two years. This reflects the fact that the project or the restructuring program is ahead of schedule, but it doesn't change the total expense expected envelope of EUR 110 million-EUR 120 million, although we will do every effort to limit that. On incremental core EBITDA, we had initially targeted EUR 75 million-EUR 80 million, incremental by 2027 compared to 2024. With 2026 and 2027 net sales now expected to be below initial assumptions, additional under activity is anticipated. This incremental core EBITDA target will not be achieved in 2027. On CapEx, EUR 185 million has been invested over 2024 and 2025 against an initial EUR 350 million-EUR 400 million envelope for 2024-2027. Although we maintain this envelope, we will be looking for all opportunities to either limit our CapEx to projects offering the highest return and reinforcing competitiveness or optimizing the CapEx expenses. Let me be clear, this is not about slowing down. It is about allocating capital where the returns are sustainable and defensible. Turning to Slide 25, sorry. As we have just discussed, FOCUS-27 and the transformation of the company are on track. However, over the past year, the business environment has evolved faster than initially anticipated. Competition from low-cost Asian players has intensified, increasing price pressure in natural APIs. At the same time, we're also seeing large pharmaceutical companies outsourcing more late-stage and complex projects. This creates opportunities, but competition is obviously selective and execution must be precise. Sovereignty initiatives are promising. They have not yet translated into tangible economic incentives at this stage. We are working or helping towards this evolving. In addition to this external environment, it is fair to say that we also face internal challenges with early stage CDMO roadmap progressing at a slower pace than anticipated, and the discontinuation of the Vitamin B12 project. This is the context in which we are accelerating and sharpening the execution of FOCUS-27 and launching new initiatives. Moving to slide 26. On the portfolio side, we will further reduce our exposure to commoditized API, structurally pressured small molecules, and concentrate our resources on high-barrier segments such as prostaglandins, corticosteroids, and opiates. On these three segments, we have solid competitive advantage that we will leverage, including further innovation programs that we have mentioned before. This includes technology edge and strong market position in prostaglandin, as well as strong expertise and flexible capacities in corticosteroids and opiates. On operations, we'll continue improving operational performance, standardizing and improving our processes, for example, through leveraging technology. We will also strengthen the commercial CMO business. We can offer reliable and sovereign manufacturing to customers looking for de-risking their API supply chain. This will help securing volumes and improve capacity utilization in our sites. On the organization front, we will further streamline structures, simplify processes, and align skills and capabilities with a more de-demanding environment. We have done a lot since the launch of the plan, we see further opportunities to improve our operating model towards a fit for purpose and linear organization. In parallel, we are launching additional initiatives. First, we will enhance commercial excellence and expand our API customer base in underleveraged territories. Let me give you two examples. North America, which is the largest and fastest-growing API market worldwide, accounted for only 8% of our total sales in 2025. If we go south to Latin America, we only serve 10% of the top drug product players over there. Second, we will refocus the CDMO business on strategic customers and on complex molecules, notably PNO, peptides, and oligonucleotides. This means we'll stop diluting our commercial efforts and concentrate on strategic customers and projects that we can succeed upon, and increase focus on complex molecules projects, for example, high added value peptides or oligonucleotide projects, including RNA therapies. Third, we will optimize our supply chain to structurally reduce our costs while maintaining end-to-end control. This is one very important way to increase competitiveness and adapt to the current environment. Our objective is obviously to adapt the operating model to a structurally tougher market and restore a sustainable path to profitable growth. Moving to our long-term ambition as a conclusion. While we recognize that the recovery is taking longer than initially anticipated, reflecting structural evolution of the market, we are taking the necessary actions to build a more competitive, sustainable, and financially resilient operating model. Looking towards the near future, our positioning is clear. We aim to be the European-based sovereign supplier of complex API, a reliable CMO partner, and a trusted CDMO player for new drug developments. At the same time, this positioning must be supported by a sustainable operating model with a cost-competitive supply chain, a lean and capital-efficient industrial footprint, and obviously an agile organization. Our long-term strategy is anchored in discipline and certainly value creation. This is where our focus is now in the interest of all our stakeholders. Thank you for your attention. We are now ready to answer your questions. If you wish to ask a question, you may do so by submitting a written question in the box below the player or by joining the conference call and dial pound key five on your telephone keypad to enter the queue. If you wish to withdraw your question, please dial pound key six on your telephone keypad. We have a first question from Clément Bassat for Portzamparc. Please go ahead. Hello, good morning. Thank you for taking my questions. Basically, I have four. The first one about the top line. What is your 2025 base top line? I assume it is your published figure, minus EUR 70 million from discontinued API, which leads to EUR 778 million. This would imply a top line 2026 of EUR 700 million following your expected 10% decrease in top line. Just to confirm if I am correct. Second question. Regarding the EUR 78 million impairment on Vitamin B12, does this include a portion of the CapEx invested from the current FOCUS-27 plan? Are you considering further impairment in 2026 following the discontinuation of the other API? Third question, just to confirm, you are maintaining restructuring costsadds EUR 100 million. This is only cash related, spread through 2027. Finally, your CapEx was limited to EUR 77 million in 2025. This decrease is a decision to preserve cash or just to adjust to your expected future top line. Thank you. Thank you, Clément, for all the questions. Let me, I may ask you to repeat some of them at some point, just to be precise. Let me, let me start with answering and maybe Olivier will step in at some of those. The top-line assumptions that you've made, if I followed, I think are not the way we think about those. The, there is no such comparable visits at EUR 778 million, which you mentioned, removing 10% of that, getting to EUR 700 million. What we are looking is around 10% versus comparable basis, which you would only reduce the sales of Haverhill in 2025. So you can make on that, I don't want to make it for you. We have not mentioned any specific numbers, but we are not seeing such a drop as you calculated. I'll come back to the B12 impairment question. Yes, the investment of B12 was part of the EUR 350 million-EUR 400 million total envelope. Most of these investments on B12 were made in 2023 and 2024. Some even earlier... Sorry, 2024 and 2025. Some even earlier to that, to that period. The impairments are all related to that. There is no such plan to further impairment in 2026. There is just the adjustment of these impairments plus the, the impairment we did on, on the terminal value of the company. There is no such thing to do, to do anything else. The I wasn't clear on the restructuring. I'll leave you to come back to it afterwards. Finally, the CapEx of EUR 77 million in 2025. I think it's a bit of both. I think the company has been used to spending far too much money on CapEx in the past, probably referring back to the time that we were a large pharma company where the cash was not a problem. I think over the last couple of years, we have learned to be more disciplined with spending cash, spending CapEx, looking at different ways to fix problems than to invest in new equipment. Maybe in some cases, reutilizing elements or not looking for the gold-plated solutions, but more the practical solution that a CDMO, CMO organization needs and not a large pharma. There is no such thing to say that we want to limit to the further growth. I think we're still committed to investing significantly in the future. For that, we have a couple of projects such as IPCEI or the morphine project, where we are looking at new ways of manufacturing the morphine and all of these products being either funded by or partially funded by France Relance or France 2030 or the IPCEI program. There will be significant investment that will come at the right time. All in all, we need to look that a sub-EUR 800 million revenue company should not be spending EUR 100+ million on a yearly basis. Yes, Clément, can you go back to the question number three on the restructuring, please? Yes. You are maintaining restructuring cost of EUR 100 million, but have in mind that restructuring costs are composed with cash and idle costs. The EUR 100 million for me, I understand this is only cash related, expected in 2026, 2027, and maybe also 2028. Just to confirm, you are talking just about cash related amounts. Yeah. The last part of your sentence is correct. It's talking about cash amounts. It's only covering 2026 and 2027. All right. -looking at different, views on the top line for 2026 and 2027 at this stage, than was originally anticipated. As a result, if we need to adapt the organization to those new levels, we will have to do. There will be a time to engage in those discussions if they need to happen. Mm-hmm. All right. Thank you, Clément. Very clear. All right. Thank you very much, David. Thank you. Now we have a question from Zain Ebrahim from J.P. Morgan. Please go ahead. Hello. Zain Ebrahim, J.P. Morgan. Thanks for taking my questions. My first question is just in terms of the China API increased competition that you're seeing. It sounds like Vitamin B12 is a key segment where you're seeing that competition, maybe anti-infectives as well. Can you talk through which divisions or product categories you're seeing that competition in? How much of the headwind you're expecting in 2026 is due to price reduction on those product categories versus volume lost to some of the extra competition? That's my first question. Maybe I'll pause there. I can ask my follow-up. All right. Thank you. Look, I think unfortunately, this is a strong industry as we see, or China has entered into a stronger industry-wide program. And we see that across various industries, and it's valid in ours, and they are looking at every single product. The reality is we have the small commodity programs and products, sorry, that are very much impacted because in this specific case, not only they are benefiting from large volumes, from very low cost of labor, low energy costs, significant new equipment with, I mean, state-of-the-art, et cetera, plus in some cases, subsidies by the government. In those cases, it's quite difficult to compete. For whomever wants to supply and to get materials from Europe, we will maintain, and we have some of these customers. Now, I believe the trajectory over the next 2 years on those type of products is gonna continue to decrease, and we will have to fight back and to provide answers in the cases we can. For those specific categories, I think it's all over the all over the the ball. The reality, though, is we have quite a strong value proposition on the typical strength category of products that we have in the company. Prostaglandin, we are the global leader in prostaglandin by either the number of products that we look, by the experience and history that we have, and the quality of our products. We aim to maintain that. We are actually reinforcing this offering by looking at different further improvements or innovation projects on site. We have launched, as you know, a strong capacity increase to support the growth in the future and we continue to accelerate down this path. The second element to that would be the opiates, where, you know, not only we benefit from a somehow protected market with all those morphine and derivatives products, we have... We are working towards significant innovation project in the future, as mentioned before, and these are benefiting not only for subsidies, but will be supported from our side, from CapEx investment to increase in the future. We don't necessarily foresee challenge on the price on that specific category either. Finally, the corticosteroids. I think the corticosteroid is maybe a little bit of a different animal. We are, there is a lot of players in the world. We are the only one, except with one other site in the U.S., which is fully integrated from A to Z of manufacturing of corticosteroids outside China. This is a strength, especially when we talk about sovereignty. We have discussed about sovereignty through COVID and challenges. We see sovereignty through shells nowadays. We see some geopolitical issues now which may endanger some logistic routes further in the next couple of weeks and months. We still believe that this is not gonna be simplified in the future and our sovereign solution will be helpful. That being said, for corticosteroids, yes, we are challenged on price. Yes, we will probably do some efforts because we have significant projects to innovate and to improve our value proposition to cut costs significantly through new chemical routes in the future. That is what IPCEI actually want, the work package two of IPCEI is about, and that's a strong avenue for us to reinforce our value proposition in the future. I can't just further comment on the impact of volume or price related to our 2026 earnings. You had a follow-up? That's very helpful. But yeah, my follow-up was on the discontinuation of API, which is helpful in terms of the quantification of the headwind to 2026 sales. Should we expect any further discontinuations in addition to what you'd already planned? There were 13 API before, I believe. Just any further discontinuations given the portfolio prioritization you're undertaking and can we expect a return to sales growth? Like, it sounds like obviously, 2026 you're giving guidance for. 2027 you said is below expectations, when can we expect to see that? Yeah. That's a couple of questions. Let me just get them in order. Are we expecting further discontinuation of products? No. The answer is no. Now, this being said, you never know what's gonna happen. I think, it's healthy for any company to look at their portfolio regularly. At this stage, we have not decided to further prune our portfolio. Actually, we are looking at growing that, and that's part of our additional activities for commercial that we mentioned. We are looking to new geographies. We are looking to seeing if we can have additional offerings, and how we would progress on that specific front. The when are we expecting to grow, was the second part of your question. Well, the earlier the better, obviously. What we are seeing for 2026 is still some reduction as we mentioned. I just want to come back to the fact that 2025 saw a significant reduction in Sanofi's sales. We just mentioned we gained 31 new clients and the sales to other clients than Sanofi was up close to 10%. It's definitely a way forward that while we want to maintain some level of Sanofi, we know that the inherent share of the Sanofi business for the future is to reduce. On that specific front, because maybe the question is gonna come and I can anticipate it, we are, you know, we have an MSA up until 2027 that we are working towards extending. We have already five products that are extended until 2032. One specific with Opella now until 2031. We are working towards concluding the terms of the extension of the other products beyond 2027. Whilst we, our focus is to, you know, manage the reduction of Sanofi over time, we are heavily focused on selling to other clients and cross-selling, acquiring new, et cetera, et cetera. The first elements of the strategic move we did last year with merging the two organization commercial and into one and led by an expert in commercial operations in the CDMO and CMO space in our industry with the arrival of Frédéric Robert in our organization is proving us right. The problem is, as you very well know, it takes time to bring new clients in and register those. I would hope to see continuous momentum into acquiring new clients and new sales, into 2026 and 2027. Very clear. Thanks very much. As a reminder, if you wish to ask a question, you may do so by submitting a written question in the box below the player or by joining the conference call and dial pound key five on your telephone keypad to enter the queue. Maybe we can move to the questions that we have from the website. There's a bunch of them, so I'm gonna try to summarize them and by key subjects. The first subject is about the CDMO business. Our analysis of the reasons of the slowdown of the pace versus what initially expected, and maybe what type of future we see in the CDMO business and how we manage to recover specifically growth in that in that field. CDMO. All right. The CDMO, as I think mentioned earlier, was, is indeed lower than anticipated. Definitely not at the level where the equity story of the IPO was at. I think over the last couple of what we've learned over the last couple of years is, one, we need to be focused. We can't answer 250, 300 RFPs every year, with the organization we have, with the resources we have, the sites and R&D labs that we have, because that prevents providing the right attention to the clients, to the requests, the RFPs, understanding the exact needs, et cetera, et cetera. That's why we decided to be a lot more focused into either, not the very early preclinical stage, and to specific areas in which we know we have a competitive advantage. There is. We have two main R&D labs that support the CDMO, one in Frankfurt, which has very strong expertise on the BNO side, and in Budapest, which can very much work on complex small molecules, such as the prostaglandin and others. In fact, we are still working with providing very complex and strategic projects for the future, such as, for example, developing the backbone of any future development of a large American Big Pharma. That's the first learning. The second learning we had is, you know, it's a lot more complicated than one would think to get into the CDMO world. CDMO world. The clients know that, you get into a lot more questions that you need to answer around what kind of raw material will I be using? What kind of processes will I develop? How can I scale up? What will be the implication and the challenges that I will see? Navigating in all this ambiguity hand in hand with the customer is not something that this organization was used to in the past with working with one internal client only, which was Sanofi at the time. All of this takes time to build the capabilities, and I believe we are doing the right things. We are bringing the right talents, and we are working more hand in hand with the customers across all of this. For the future, what we see? Well, we see continuous, let's say, difficulty to navigate in this space because there are a lot of players. There are a lot of actually even Asian players that are coming in with different, let's say, approach to the business than European have. However, there is still place for all of us to work to provide local manufacturing, local scale-up with the right expertise, and certainly proximity to the customers. The key point is we will also be thinking CDMO and CMO very much differently. The CDMO is everything that I said, working very much in research and development, align, or accompanying the customer, through the journey of their own development. While CMO is a very simple, tech transfer, smooth tech transfer type of approach with a reliable supply chain of existing commercial products. Those CDMO and CMO, as we want to differentiate, require different set of skills. Different set of skills either by our commercial and customer-facing individuals, and also on the side with very lean and effective and efficient certainly operations on the ground. As a result, we will approach those two businesses very differently moving forward to be able to answer our customers. One question is about core EBITDA in 2025, which improved significantly despite revenue declining. How much of the improvement is structural versus temporary cost savings? I guess from this area, the answer is quite simple, right? In term of cost savings and improvement of the organization and the model, pretty much everything is sustainable. We improved the structure in term of industrial footprint. We improved the model in term of organization, in term of SG&A. The R&D have been also redesigned. I would answer clearly that the whole is sustainable, provided that, as I comment before, there is one-offs that are not sustainable obviously like the Buserelin, the Buserelin issue, meaning impact of 2024. For the rest, it's pretty much sustainable. Those EUR 20 million of OpEx that we have mentioned are definitely here to stay and will remain as is. This is part of a new structure, a new baseline of our costs. Everything that is being done at the site, or in procurement and et cetera, will continue to bring efficiency on a yearly basis. Question on Asian imports. How can you compete against Asian imports? Where is your, where do you think you have a sustainable edge to compete against those Asian imports? The, the... How we can compete? I think there is a, there is a where and how, I guess, was the question, right? The, the key point is, we will not be able to compete on everything. As customers just want price, I think it will be difficult, just on that pure front. This being said, difficult doesn't mean impossible. As I mentioned earlier, we have a significant amount of our portfolio that is today still very much competitive and for which we have further innovation programs to reinforce this competitiveness in the future, which will either allow us to increase commercial margin or to provide more competitive offerings to our customers. The second part is, of the question was. What are your competitive edges decisioning? Yeah. That I mentioned. I think the second element is the fact that we are based in Europe. As I mentioned, I think a lot of customers want reliable supply. Our reliable supply, our very China-independent supply chain, even for raw materials, is actually today the only one available in Europe. Let's face it. For whomever customer in Europe or in the U.S. that want a risk-free supply chain, China-independent supply, well, we are here available. This being said, I think on all those customers that want pure pricing, not really caring either about ESG or pricing, that's where I think we need to look at things maybe a bit differently. That's what is mentioned in the cost of our supply chain improvements that we want to do in the future. It could very well be that buying some raw materials or intermediate in a lower cost country could be coming handy for us, not by depleting our sites, but by able to reduce the pricing that we will in turn be able to offer to our customers, increasing those volume, and actually at the end, probably having higher volumes in this specific site that is manufacturing the API than we used to have. I think we need to be able to play on both levels. One is top-notch player of premium quality API. Two, being a European source, sovereign source to China independent supply or sovereign supply. Three, for those customers that want price, let's play here as well. What is the current level of capacity utilization across your main API sites? What level could you consider as normalized for the business? Do you have an objective in the midterm? Objective in the midterm. The look on the capacity utilization, I don't think we comment on that, but we would expect around, let's say, about half of our capacity or a bit more half of our capacity being utilized at this stage. There is no surprise if I say to any of you, if I say that in the chemical industry in Europe, given the cost structure and everything, all our, all my peers, let's say, would agree that 75%-80% utilization is a minimum to have sustainable long-term perspective. In our situation, we know that, at this stage, given the elements of, underutilization that we have, which hurts or will hurt, or which at least offsets all the efficiencies we are bringing from a cost standpoint, any additional volume that will fill up this available capacity will not only generate commercial margin, but also, reduce those underutilization that hit our P&L. We are working on that, and I think that's why we are discussing very heavily now how do we increase our offering in terms of portfolio, how do we augment that, and how do we play more on the CMO, or European-made CMO, type of market, because I think that's, that can be win-win for both customers and ourselves. Thank you. Do we have any question online? I do not have any more question online. Okay. Maybe one last to conclude on from the webcast. If you had to prioritize one key execution risk that could derail the execution of the plan, what would it be? I think the key point today is we need to have everyone on the top line. We have proven over the last two years that whatever we can control, we can simply deliver. The teams have done outstanding job across sites, across organization in the last two years to actually prove that. That's why our, despite the whole headwinds we've seen, our core EBITDA has increased significantly between 2024 - 2025, and that we landed 2025 with actually a positive EBITDA. Those, as we said, are sustainable measures that will keep yielding results in the future, and we expect further actually on that. Now we need the whole organization to be working top line. What I mean the whole organization is, we need to be able to support our commercial folks that go and talk to customer on a daily basis. We need to provide them with high quality materials, with a competitive value proposition. We need to equip them with top-notch products, maybe provide them more products, provide with the right CMO value proposition, CDMO and R&D expertise. Definitely when they need support and when they are able to seize clients, we need to be 100% on time delivering against customer expectations. I think the key point here is, restoring growth will come by having a full organization focused on growth in the future to support the commercial folks, delivering on that ambition. Thank you. I think if there's no more question online, this will end our webcast today. Thank you for attendance. Thank you for the questions. As usual, our the Investor Relations teams and the management remains at your disposal should you have any follow-up question. Thank you, and have a good day.