Thank you for standing by. Welcome to Schrödinger's conference call to review Fourth Quarter and Full Year 2024 Financial Results. My name is Kevin, and I'll be your operator for today's call. All lines have been placed on mute to prevent any background noise. After the speaker's remarks, there will be a question-and-answer session. Please be advised that today's call is being recorded at the company's request. Now, I would like to introduce your host for today's conference, Ms. Jaren Madden, Senior Vice President of Investor Relations and Corporate Affairs. Please go ahead.

Thank you, and good afternoon, everyone. Welcome to today's call during which we will provide an update on the company and review our fourth quarter and full year 2024 financial results. Earlier today, we issued a press release summarizing our financial results and progress across the company, which is available on our website at schrodinger.com. Here with me on our call today are Ramy Farid, Chief Executive Officer; Geoff Porges, Chief Financial Officer; and Karen Akinsanya, President of R&D Therapeutics. Following our prepared remarks, we'll open the call for Q&A. During today's call, management will make statements that are forward-looking and made pursuant to the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995, including, without limitation, statements related to our outlook for the full year 2025, our plans to accelerate the growth of our software business, and advance our collaborative and proprietary drug discovery programs, the timing of initiation of and readouts from our clinical trials, the clinical potential and properties of our compounds, the use of our cash resources as well as our future expenses. These forward-looking statements reflect our current views about our plans, intentions, expectations, strategies and prospects, which are based on the information currently available to us and on assumptions we have made. Actual results may differ materially due to a number of important factors, including considerations described in the Risk Factors section and elsewhere in the filings we make with the SEC, including our Form 10-K for the year ended December 31, 2024. These forward-looking statements represent our views only as of today, and we caution you that except as required by law, we may not update them in the future, whether as a result of new information, future events or otherwise. Also included in today's call are certain non-GAAP financial measures. These non-GAAP financial measures are not prepared in accordance with generally accepted accounting principles and should be considered only in addition to and not a substitute for or superior to GAAP measures. Please refer to the tables at the end of our press release, which is available on our website for reconciliations of these non-GAAP measures to the most directly comparable GAAP measures. With that, I'd like to turn the call over to Ramy.

Thanks, Karen, and thank you, everyone, for joining us today. 2024 was an exciting year for Schrödinger. We exceeded our software revenue expectations, established a new drug discovery collaboration, and expanded our software agreement with Novartis. We continue to advance our collaborative and proprietary pipeline. We advanced the science underlying our platform, including initiating a project to predict toxicity associated with off-target binding and launching a new enterprise informatics platform for biologics. 2024 was also marked by important milestones at companies we co-founded. Ajax and structure progress their clinical programs, and Morphic was acquired by Lilly for $3.2 billion, resulting in approximately $48 million for Schrödinger. As we look to 2025, I'm optimistic that this broad momentum will continue. Total revenue for the year was $208 million. Software revenue was $180 million, representing just over 13% growth, and fourth-quarter software revenue grew 16% to $80 million. The strength of our business is also reflected in our 2024 KPIs. The number of software customers with an annual contract value of greater than $5 million increased from 4 million to 8 million, and the number of customers with ACV of greater than $1 million increased from 27% to 31%. Total ACV increased by 24% to $191 million. Our software customer retention was 100% for customers with ACV of at least $500,000. We believe this strong performance of our KPIs is a direct consequence of the impact our technology is having on our customers' programs. Our priority for 2025 is driving continued increases in the adoption of our computational technology and enterprise informatics platform. It is clear that the computational landscape in the industry is changing rapidly, and that our unique integration of physics and AI/ML methods is producing powerful solutions for drug discovery and materials design. This year, we plan to release several new products and solutions that reflect our continued investment in the platform, including our predictive toxicology technology, where we have already enabled more than 50 off-targets. We are also planning to release enhancements to our biologics discovery technologies and additional applications of AI/ML methods that are accelerating and broadening the impact of our physics-based methods. Our platform is having a big impact on our ability to rapidly progress a broad pipeline of collaborative and proprietary discovery programs. This year, we look forward to sharing initial Phase I clinical data from our three lead programs. Karen will provide a detailed update later in the call. We are well positioned for a transformational 2025, and we look forward to providing updates over the course of the year. I will now turn the call over to Geoff.

Thank you, Ramy, and good afternoon, everyone. We are very pleased with Schrödinger's financial performance in 2024. Our software growth exceeded our expectations and showed the resilience of our business through changing industry cycles and the headwinds of large contract renewals in prior years. The revenue contribution from hosted contracts continues to increase, and we expect this will gradually reduce the Q4 concentration of our revenue. The strong software results for the year is reflected in the excellent progress we have made in our KPIs and in the financial guidance we are providing for 2025. Our drug discovery collaborations and portfolio are expanding, driven by the landmark new agreement with Novartis and new programs added to the existing Otsuka and Lilly collaborations. Finally, our proprietary clinical programs are reaching key data milestones with significant clinical disclosures from three programs coming this year. I'll now summarize our financial results, beginning with Q4. Total revenue in Q4 was $88.3 million, an increase of 19% compared to Q4 2023. The increase was driven by higher software and drug discovery revenue. Software revenue was $79.7 million, an increase of 16% compared to Q4 2023. The increase was mainly due to higher hosted revenue from large customers who have transitioned from on-prem to hosted licenses over the last two years. On-prem software revenue increased by 3% to $55.4 million as new multiyear deals that closed in Q4 2024, including Novartis, matched the contribution of multiyear deals closed in Q4 2023. Hosted revenue increased by 86% to $11 million. Maintenance revenue was $5.9 million and increased by 3.5%. Maintenance revenue was driven by support for on-prem contracts from prior periods and offset reductions in maintenance from customers switching to hosted licenses. Services declined by 23% as the existing services projects were completed or expired. Contribution revenue was $4.9 million, reflecting the new predictive tox project funded by the Bill & Melinda Gates Foundation. Overall, hosted revenue contributed 14% of total software revenue in the quarter, compared to 9% in Q4 2023. We are very encouraged by the software result with strong growth in the top 30 global pharma accounts, offsetting continued churn in our small and mid-cap customer segments. Small biotech companies continue to embrace our software, but equally, each year, we are seeing a number of our biotech software customers being acquired. These outcomes are positive for the industry and add to the validation of our platform, but also contribute to the churn in our SMID-cap Biotech segment. Drug discovery revenue was $8.7 million in Q4, compared to $5.5 million in Q4 2023. The increase was due to milestones received in the quarter and amortization of upfront payments from existing collaborations, very little revenue was recognized for the new Novartis collaboration in the quarter. Turning to margins. The software cost of revenue was $13.3 million in the quarter, compared to $8.7 million in the same period in 2023. The increase was mainly due to the costs associated with the predictive tox project, along with higher royalties. The software gross margin was 83% in Q4, compared to 87.4% in Q4 2023. The decrease in gross margin was due to the lower profitability of the predictive tox project. Drug discovery cost of goods was $10.9 million, compared to $7.9 million in Q4 2023. The increase was due to higher royalties as well as some increases in FTE and technology expenses. Overall, our cost of revenue increased by 46% compared to Q4 2023, and the overall gross margin declined from 77.6% in Q4 2023 to 72.6% in Q4 2024. The decline was due to higher drug discovery expenses and the higher cost of software. Looking ahead, we expect this trend to continue for the balance of this year as more of our R&D expenses associated with internal projects moves into cost of goods for drug discovery and as the predictive tox project continues in 2025. Our largest operating expense remains R&D. R&D declined from $51.5 million in Q4 2023 to $49.4 million in Q4 2024. The decline was due to lower CRO spending and lower FTE allocation for projects that were discontinued during the year. Sales and marketing expenses in Q4 decreased by 2.5% to $9.7 million based on relatively stable headcount and associated expenses, and G&A was essentially flat at $25.8 million, mainly associated with higher professional services being offset by decreases in royalties. Total operating expenses were $84.8 million, compared to $87.2 million in Q4 last year, and the loss from operations was $21 million compared to $29.6 million in Q4 last year. The change in fair value was a loss of $22 million based on the mark-to-market of our equity and structured therapeutics and the small changes in private company valuations. This compares to a loss in value of $8 million in Q4 of 2023. Other income was $3.5 million in Q4 compared to $6.6 million in Q4 2023; the lower income was due to a lower cash balance and the unfavorable effect of currency fluctuations in foreign currency balances. Total other expense was a loss of $18.5 million compared to a loss of $1.9 million in Q4 last year, resulting in a net loss before taxes for the quarter of $39.3 million, a net loss after taxes of $40.2 million or $0.55 per diluted share. This compares to a net loss of $31 million or $0.43 per diluted share in Q4 of last year. The fully diluted share count for Q4 was $72.9 million, and for the year was $72.7 million. The share count increased by 1% compared to the same period in the prior year. I'll now summarize the full year 2024 financial results. Full year revenue was $208 million compared to $217 million in 2023. Software revenue grew by 13.3% from $159 million to $180 million, with two-thirds of the growth coming from hosted software and one-third from contribution revenue. Hosted revenue grew from $20 million to $35 million due to an increasing number of large accounts transitioning to hosted licenses. Hosted contracts contributed 20% of software revenue for 2024 compared to 13% in 2023. On-prem contract revenue was flat at $104 million, as new large multiyear on-prem contracts signed this year more or less offset those signed last year. Contribution revenue increased due to the impact of the predictive tox project funded by the Gates Foundation. Drug discovery revenue was $27 million for the year compared to $58 million in 2023. The reduction was due to the impact of non-recurring milestones received from partners in 2023. Software gross margin for the year was 79.5% compared to 81.5% in 2023. The change in gross margin was due to the higher costs associated with the contribution revenue in 2024 compared to 2023. Overall, gross margin was relatively stable at 64% compared to 65% in 2023. Operating expenses increased by 7.3% compared to 2023, with R&D increasing by 11% to $202 million, sales and marketing increasing by 7% to $40 million, and G&A increasing by 1% to $100 million. Our operating loss for the year was $209 million compared to $177 million in 2023. Other income was $23.6 million this year compared to $220 million in 2023 and a net loss in 2024 was $187 million or $2.57 per diluted share compared to net income of $41 million or $0.54 per diluted share in 2023. The profit in 2023 was driven by the gains associated with the distribution from Nimbus and the gains in the value of our stake in Morphic during 2023. Our net cash used in operating activities was $31 million in Q4 compared to $37 million in Q4 2023. Our net cash used in operating activities for the year was $157 million in 2024 compared to $137 million in 2023. Our cash and marketable securities balance was $367 million at the end of Q4 2024 compared to $469 million at the end of Q4 2023. Our cash position at the end of Q4 2024 did not reflect the effect of the receivable from Novartis, which added $150 million to our cash balance in January. I'll now provide our initial financial guidance for 2025. We expect our software revenue growth to be in the range of 10% to 15% and currently expect drug discovery revenue to be in the range of $45 million to $50 million. We expect a further increase in the proportion of our revenue from hosted contracts, which should slightly reduce our fourth-quarter weighting of software revenue and bolster our revenue in earlier periods. Our current expectation is that software revenue will be in the range of $44 million to $48 million in Q1, and the drug discovery revenue will be weighted towards the later quarters of the year. Our software gross margin is likely to be in the range of 74% to 75% compared to 79.5% in 2024. The reduction is driven by the increase in the contribution revenue from the predictive tox initiative. Our operating expenses are likely to grow by less than 5% in 2024, with certain expenses shifting from R&D to cost of goods associated with the predictive tox initiative and newly announced collaborations. We now expect net cash used in operating activities in 2025 to be lower than in 2024. In 2025, we expect the growth of our software business to continue to be driven by increasing adoption of our technology by large customers. Many of these companies have not scaled up their investment in our technology and are increasingly interested in improving the productivity of their drug discovery efforts. We are already having encouraging discussions with many of the companies who have not yet adopted our technology at scale and anticipate that the enhancements to our platform, including capabilities for biologics and expanded integration of AI and machine learning with our physics-based methods should contribute meaningfully to our growth this year. While we are fielding inquiries from new and emerging biotech companies, we don't expect small companies to contribute meaningfully to our growth this year. Our exposure to China is less than 5% of revenue, and we don't expect significant growth from that market this year either. To conclude, Schrödinger had an excellent year in 2024, with strong results that leave us well positioned operationally, financially, and strategically entering 2025. We have many opportunities to drive continued growth in our software business and our collaborations are poised to contribute significant value in 2025 and beyond. Our balance sheet is strong, and our operating metrics, including KPIs and operating expenses are trending in the right direction. I'll now turn the call over to Karen to comment on our therapeutics R&D.

Thank you, Geoff, and good afternoon, everyone. 2024 was a productive year as we advanced our collaborative and proprietary pipeline. In November, we signed a significant new drug discovery agreement with Novartis, and we recently expanded our collaborations with Otsuka and Lilly. Dose escalation studies for SGR-1505 and SGR-2921 progressed, and we initiated our Phase 1 study for SGR-3515. These achievements laid the groundwork for important milestones this year with the expected presentation of initial Phase 1 data from all three clinical stage programs. Beginning with our collaboration portfolio, we are pleased with the addition of another target to our discovery collaboration with Lilly. Today's announcement of an exciting new program in a high-value therapeutic area builds on the agreement initially signed in 2022 and the advances made by the team on a challenging initial target. Last month, we announced the expansion of our collaboration with Otsuka, adding another program to the existing agreement. The expansion of these two partnerships, as well as our collaboration with Novartis, reflects the excellent track record we have established for delivering differentiated molecules and robust pre-clinical packages for high-value targets. Turning to our clinical programs, our most advanced Phase 1 program is our MALT1 inhibitor SGR-1505. MALT1 is a clinically validated target for leukemias and lymphomas. It is downstream of the BTK pathway and regulates NF-kB signaling, which is elevated in B-cell malignancies and in patients with BTK inhibitor resistance. Our ongoing Phase I dose escalation study is evaluating SGR-1505 in patients with relaxed refractory B-cell malignancies and we expect to report safety, pharmacokinetic, pharmacodynamic data, as well as preliminary PK/PD relationships and efficacy data at a medical meeting in the second quarter. Our goal is to provide an initial understanding of the profile of SGR-1505 to inform further development. Enrollment is also ongoing in our Phase I study of SGR-2921, our CDC7 inhibitor in patients with acute myeloid leukemia or myelodysplastic syndrome. As a reminder, the objectives of this Phase I study are to evaluate the safety and tolerability of SGR-2921 and to determine the recommended Phase II dose and schedule. The study is progressing well with multiple dose escalations completed, and we continue to anticipate reporting initial clinical data in the second half of this year. Third, our Phase I study of SGR-3515, our Wee1/Myt1 co-inhibitor, is also advancing. Our ongoing dose escalation study will evaluate the safety, PK/PD, preliminary antitumor activity, and dosing schedule in patients with advanced solid tumors predicted to be sensitive to Wee1/Myt1 inhibition. This includes ovarian, uterine, and breast cancers, in addition to other solid tumors with elevated replication stress. SGR-3515 inhibits both Wee1 and Myt1, and the concurrent loss of these two proteins converts amplified vulnerability in cancer cells, termed synthetic lethality. Our intermittent dosing schedule is intended to maintain efficacy while allowing recovery from any potential mechanism-based hematological toxicity. We are pleased with our progress in this study and anticipate reporting initial data in the second half of this year. Beyond our clinical programs, we are also progressing early discovery programs for targets involved in inflammation and neurodegenerative diseases. Recently, we selected a development candidate for our EGFR C797S program for osimertinib-resistant non-small cell lung cancer, including brain metastases. Over the past three years, we have advanced several programs into the clinic and partnered some of our early-stage programs. We continue to see additional opportunities for value creation emerging from our portfolio through licensing, new ventures, or collaborations. We are very much looking forward to sharing clinical results from all three clinical programs throughout the year. I'll now turn the call back to Ramy.

Thank you, Karen. As you heard, we had a very successful 2024, and I would like to take this opportunity to thank our dedicated employees for their hard work and accomplishments. I'm very excited about our outlook for 2025, and we look forward to providing further updates across the business throughout the year. At this time, we'd be happy to take your questions.

Thank you. Ladies and gentlemen, we will now begin the question-and-answer session. Your first question comes from the line of Michael Yee of Jefferies. Please go ahead.

Hey, this is Kyle Yang for Michael Yee. Thanks for taking our question and congratulations on the quarter. I have a few quick questions. First, what is your assumption behind your 2025 drug discovery revenue guidance? Can you share what portion of that revenue comes from the Novartis partnership? Second, could you update us on your one program? I know you previously used data from J&J's first-generation molecule as a benchmark. How should we view that benchmark now that J&J has started a second-generation molecule?

Do you want to cover the first?

Let me start off with your question about the 2025 revenue guidance for drug discovery. The increase in the drug discovery revenue that we're forecasting is pretty broad-based. It comes from quite a few different collaborations as you would imagine. Part of it is the amortization of the upfront payment from the Novartis collaboration, which we've indicated will be over multiple years. I wouldn't want you to think that it's most of that revenue, because we're just scaling up all of those activities on those projects. I imagine we're going to be at peak recognition of that upfront payment probably 18 to 24 months from now, but it's a significant portion. But there are a number of other programs. As we announced today, we have a new collaboration with the Lilly agreement. We announced a new program in the Lilly agreement, and a new program in the Otsuka agreement at the beginning of the year. Both of those contribute, and the progress that we're making in some of our other collaborations, such as BMS, also contribute. So it's really pretty broad-based. And that's similar for the guidance that we provided on software, frankly, as well.

Yes. So as you pointed out, there is a lot of excitement about more wide mechanisms. That's reflected, I think, in the number of companies that are seeing this target. We are very pleased with the progress we're making in our Phase I trial. Just to remind you, this diverse escalation study is focused on the PK/PD safety, which we think is super important for this mechanism in terms of combinations, as well as initial signs of clinical activity. Now in terms of the bar, I would say that we're really focused on understanding the performance of our molecule in this trial. As you point out, there are other companies entering this space. But our focus this year is laser-focused on describing the profile of our molecule. And as you have, we will be sharing some of that data in the second half of the year at a medical conference with an update on the profile so far from this dose escalation study.

Hi. This is CJ on for Mani. Congrats on the quarter and thanks for taking our question. Our question is, you previously noted that seasonality becomes more Q4 weighted over time. Is this something that's happening at a pace that we would start to show this year? Or is this something we would see more long-term over the next half-decade?

You mentioned that our seasonality is increasingly weighted, but perhaps you meant it will become less weighted over time. We believe that revenue distribution will gradually become less focused on Q4. It's challenging because we continually find great opportunities in the fourth quarter as we have in recent years. However, we expect to see more distribution this year. That's why we highlight hosted revenue, as it serves as a foundation that persists throughout all four quarters. I believe the Q4 weighting will decrease, but I want to point out that Q2 and Q3 will still tend to be lower quarters compared to the others this year. Additionally, our Q1 guidance reflects the influence of deals we signed in Q4, with revenue recognition for several things we finalized in Q4, especially hosted deals. Therefore, some of that revenue will carry over from Q4 into Q1.

Hey, guys. This is Steve on for Scott. Thanks for taking our question. What do customers take into consideration when potentially moving from on-prem to hosted? And how do you see the percentage of your book transitioning to hosted progressing over the next couple of years? And then as a follow-up, what is the level of demand been like for combination drug discovery and software arrangements from existing and new customers?

So maybe I'll give you a sense of the cadence of the transition from on-prem to hosted. And then Ramy, maybe you can talk a little bit about the basis for making that decision? And then Karen, you talk about the drug discovery question. So in terms of the cadence, I pointed out in my prepared remarks, I think that there was about a five to seven percentage point difference in the amount of our software revenue that came from hosted contracts in 2024, compared to 2023, and also about the same in Q4 compared to Q4. I think that that's a reasonable goal in terms of the continuation of the trend. We previously indicated that we don't envisage a sudden or even rapidly accelerated switch, but that sort of cadence of transition, we think is reasonable as a base assumption going forward.

Yeah. And let me just remind you what we mean by hosted in the large majority of cases. What this means is that we're hosting a license server, not the underlying software. When we do host for the license server, it allows us to deliver the licenses a little bit more seamlessly to the customer. But as far as the customer is concerned and actually as far as we're concerned as far as the burden on us or the impact it has on us, it's extremely small. Remember, it's just hosting a license server, not software to sell.

Yeah. And I think the last question was about combination deals.

Yes, we see strong demand for combination drug discovery and software arrangements. Both our drug discovery and software teams invest considerable time engaging with potential partners and software customers to showcase our programs and our approach to drug discovery. This has resulted in several combined deals over the past few years, and we anticipate that trend will continue. While it's difficult to quantify the extent of this demand, we are enthusiastic about these opportunities. For instance, the Novartis deal not only allows us to see them scale up the platform but also provides us the opportunity to demonstrate how we utilize the platform effectively, ensuring they get the maximum benefits.

Great. Thanks for taking the questions. I wanted to actually maybe just piggyback off of that prior question just a little bit and ask a bit more about kind of customer retention feedback and how you're thinking about new product offerings. Can you maybe just give us a sense of what are some of the stickiest aspects that your software users are responding to that they're kind of telling you about that's really driving some of this retention and driving up ACV over time? And then really just curious how some of that feedback is impacting your capital allocation strategy on where to focus new product offerings and R&D investment moving forward?

The customer retention is exciting because the technology is positively affecting projects. We're consistently hearing from our customers that they are producing fewer molecules to reach a development candidate, and the quality of those molecules, as well as their chance of success, is increasing. They are reaching development candidates faster. This impact makes them highly dependent on the technology, and not using it isn't really an option when the results are so beneficial. Additionally, the high retention rate suggests there are no viable alternatives to our technology. We're continuously enhancing the platform in significant areas, which also contributes to retention. As customers see our ongoing improvements, it fosters a partnership dynamic; they invest in us, knowing that their feedback will lead to software enhancements and new technologies. For instance, our upgrades in the biologics space, especially in enterprise informatics, have been very well received. There is considerable excitement around our developments in predictive toxicology, particularly the off-target panel, addressing a critical need in drug discovery. This also opens up new budgets, enhancing the technology's overall impact across the enterprise, beyond just one area. Another notable area is formulations, especially crystal structure prediction, a new technology we released last year that has garnered positive feedback. Customers recognize our advancements in science and the tangible effects on their projects.

Great. Thanks. I want to ask about some of the KPIs you release in terms of 2024 performance. Just taking a look at the number of customers with ACV over $5 million ACV of top 10 customers, it seems like a really jump in those top 5, top 10 accounts from a software perspective. Maybe just a follow-on to the prior question, but just sort of what are you seeing there? Why does it feel like a little bit of a step function, and how sustainable is that? And is this a little bit of a one-time jump, or are you seeing something that's making you reassess that?

Yes. No, we can address that. It's a great question. We've talked a lot about this: that to see impact from this technology has to be used at scale. You have to explore huge numbers of molecules to solve this incredibly complicated drug discovery and material design problem that we all face, this multi-parameter optimization problem. It requires exploring huge amounts of chemical space. And that can only be done by using the technology at scale. It has become very clear that, in some sense, there's an inflection in the value that gets created when you reach that $5 million-plus spend, which gives you access to enough technology to support enough programs to really see an impact. But as we have said over and over again, that's not — we don't think that's the TAM. We don't think that's the limit. We know internally in our 25 to 30 programs or so that we're working on internally, we're using the technology at a much larger scale in that. So yes, these companies can see impact at the $5 million to $10 million range or so. But it turns out there's still room to experience significantly more impact by actually spending quite a bit more than that. And again, we have evidence of that through our own partnerships and our partner's experience that they get access to that level of technology. Companies like Lilly and now Novartis and so on, and I think they're going to start to see what's required to achieve the kind of outcomes that we've achieved and that Karen mentioned is that reflects — that's reflected in our track record.

Hi. Good afternoon. Thanks for taking our question. So we had two. First on the revenue guidance, I was wondering if you could just talk us through what drives the bookings there? Just wanted to understand some of the sensitivities that flow into each end of the range? And then secondly, on MALT1, also you mentioned that the data update here is going to be a medical meeting in 2Q. I was just wondering, do you think you'll be in a position to evaluate partnerships for that program post that data cut? Or do you think you'd want to see more follow-up or more data points before evaluating potential BD for MALT1?

So on the revenue guidance, we provided revenue guidance for Q1 and then for the full year. As you can imagine, Vikram, the confidence or uncertainty that we have about the outlook for Q1 is much higher than for the full year because we're kind of two-thirds of the way through the first quarter as well. And as I mentioned in an earlier question, we have some deals that closed late in Q4 that are delivering revenue in Q1. So there's a pretty broad foundation behind that Q1 number. For the full year, we're still going to have a pretty big chunk of revenue that we'll have to deliver in the fourth quarter. And the confidence we have in that is based on several things. First, you heard Ramy talk about on the penetration in much of the industry. Yes, we have eight customers over $5 million, but that still leads an awful lot of the industry that is well below that. In fact, it's substantially below that, where we think we have an opportunity to advance discussions. The second is that, of course, we are deploying all the new capabilities into the technology, which results in both new customers coming in and saying, 'Hey, that would be really useful, we will step up.' And then existing customers that have already stepped up taking their utilization to a higher level. The third thing I'll say is that we — because of the hosted contracts that we've put in place, a hosted contract in a strange way puts future revenue in the bank rather than an on-prem contract where you take all the revenue upfront. So compared to prior years, the situation we're in, in terms of the base of revenue that we have a high degree of certainty about, for 2025 is actually higher than it's been in prior years because of that hosted revenue contract. So all of those elements give us a very solid way of confidence about the revenue guide for the year. Now the top and bottom end just depends on what the magnitude, the step-up in those large customers is particularly towards the end of the year. And as those discussions mature, we'll think about where we actually think the year is going to end up. But we've got a very high degree of confidence at this stage.

So on MALT1, I think it's important to just restate that this is an ongoing dose escalation trial. As you know, we spend a lot of time with potential partners, aligning on what kind of profile people are looking for what would be impactful in the hemo space for MALT1, but I will emphasize again that what we will be sharing in 2Q is the data cut-off when we submit the abstract. So it will be ongoing. And I think as we approach a more complete study, we will have a second round, obviously, discussions, further rounds of discussions with companies as the year progresses. So yes, we get an interim update, I think, at the medical meeting.

Hi. This is Malcolm Hoffman on for Evan. Thank you for taking our question. Wanted to ask if you guys can think of any impact that you could foresee from recent proposed US tariffs, in order to exposure to China is only roughly 5% of revenue. Did any of this be meaningfully impacted by those ongoing disputes? Just trying to get your context there. I appreciate it. Thanks.

I appreciate your question, which is quite sensible given the circumstances. Total revenue from China is actually significantly less than 5%, sitting in the low single digits. We expect it to recover in the near future, but we don’t perceive a lot of risk associated with that. To complement your question, our exposure to the NIH is under 1%. Overall, our exposure to US academic institutions across various business segments is in the high to mid single digits, and our total exposure to the US government, including the NIH, remains considerably less than 1%. While there's some turmoil currently, it seems to be a challenging environment for local economic research, but we don’t anticipate it will significantly impact our business.

Good afternoon, and thank you for the update. I have three different lines of questions, so I will ask them all and then allow you to respond before I come back with follow-ups. First, regarding the drug discovery revenues, how should we view the timing for those? While I understand you may not know exactly when milestones will occur, with the Lilly contract signing in January, is there anything specific we should consider? I'm trying to determine how we should allocate those revenues throughout the year.

I mentioned earlier that we expect the revenues to be somewhat weighted towards the latter part of the year. The Novartis contract will make a contribution, which will increase as we initiate the project teams. Similarly, with the new program, the Lilly collaboration, and other partnerships, we are prepared to start but it will take some time to ramp up the project teams, and revenue will be recognized as those teams become operational. Overall, while we don’t anticipate a heavy back-end weighting, revenue should gradually rise throughout the year.

Yes. As I indicated, the feedback has been really excellent. It's clear there's a wide recognition that this solves a real challenge that essentially every single project faces at some point. As far as the quality of the science and the accuracy of the methods, it's impressive, and that's also being recognized widely. As far as when it will be released, we're not in the habit of announcing ahead of time dates for actual releases, but we are committed to releasing it this year. I look forward to sharing with you announcements around that release and more information as we have more and more customers using it. I will say, this is kind of important. Maybe you can hand it over to Karen, we are using it already. So our collaborators have access to it, and it's had a big impact on a number of our projects.

Yes, that's correct. As you know, the internal drug discovery team gets early access to the technology. It is actually something we've been using in ongoing programs, both our own and collaborators, as Ramy said, and being able to dial in and dial out the profiles we want and those we don't want is really a very powerful tool.

I'll hand it over to Geoff to give some thoughts. But let me just first make clear, and this is something we've talked about before, that we have a number of small companies that are using the software potentially, if you think about the number of programs they have at a higher scale than the large majority of our pharma customers. So the good news there is that there are plenty of relatively small companies that are recognizing the value and using it. That's a good sign. But the broader question, maybe Geoff, you can.

Yes. So I may have conveyed the wrong impression. It's not that small pharma or biotech companies are reluctant to use the software or actually even lagging. In that segment as a whole has churn in it, frankly, because some of them are so successful, they just keep being acquired. And that is a lot of validation for our platform, and then the acquirer finds out how they discover their molecules. So that's causing some churn. But the other thing is that we're all seeing the headlines about companies that are restructuring and focusing on advancing just their clinical program or concentrating down just to one core therapeutic area or something. And naturally, that has an effect on their appetite for investing in discovery. So what I would do — my direct answer to your question would be for that segment to again be a growth driver for us, what we want to see is kind of a renewed commitment to providing capital for drug discovery in emerging biotech companies, which is still pretty tepid, the environment for that.

Thank you very much. I have two questions. Regarding the predictive toxicology business, you made several announcements in 2024 about the partnership and the revenue contribution from the Gates Foundation. You mentioned that most of the revenues will be recognized in 2025. Geoff, could you clarify how we should model that revenue recognition and where it appears in the model, as well as any details related to sequencing? My second question, directed at Karen but still relevant to Geoff, involves the three clinical assets you discussed over a year ago during your R&D Day regarding potential candidates for clinical advancement. What is the current factor preventing you from selecting another candidate to move into the clinic? Also, do you have a preferred candidate at this time?

Great. Thanks, Chris. In terms of the predictive tox revenue, you are 100% correct. We indicated that most of the revenue would be recognized in 2025. We recognized $6 million in revenue for that initiative in 2024 between Q3 and Q4. And then the total grant, I believe we've disclosed, is around $19.5 million. So, most of the balance of that will be recognized in 2025. There is a bit of a tail that will continue into 2026, but that's kind of the cadence of that recognition.

Yes. I'd say on the programs, I think the focus in 2025 is really on the three programs that we have in the clinic. As we've said, we're excited about the progress, and we intend to share data on those programs this year. With respect to the pipeline behind those programs, we have, as you know, last year, partnered some of our early programs with Novartis, and we want to stay flexible in terms of the decision when to partner, when to advance programs to the clinic. We've got our hands pretty full right now in the clinical space with our three advanced assets. But we do have other opportunities that will emerge from the pipeline over the coming years. And I think the merits of each of those assets, not just within the target product profile that we've been focused on, but also within the landscape. There are a lot of companies pursuing similar exciting targets, and we'll have to decide when the time is right, whether that's one that we will take into the clinic ourselves or whether we will partner.

This is Ike Lee on for David Lebowitz. Thanks for taking our question. We have one on the Wee1/Myt1 inhibitor, SGR-3515. For the Phase I study results coming out later this year, are there any safety signals that you are going to be very focused on, particularly given past discontinuations in this class? And to what degree do you think you have an advantage there based on the work that you've done with the dual mechanism approach? And then two, I guess, on a related note as well, when you say you're canvassing different solid tumors, is there one of particular interest that stands out to you before we see the data?

Yes. So I mean, I think, first of all, with respect to safety, what we have shared with you in the past is what we've observed pre-clinically that the ability to dose intermittently with a dual inhibitor that essentially allows you to take the break off Wee1, that's the Myt1 contribution. But in our preclinical studies, we observed that this allowed for more efficacy while you were in a dosing holiday. As you know, we're currently exploring that in our Phase I trial. We are not going to be providing an update necessarily on this call about the profile. That's something that we're reserving for later on this year. But you're right to say that it's very clear. Wee1 has efficacy. The focuses are how do we maintain efficacy while ensuring that people can tolerate the drug. And so that's going to be a focus during the course of this trial, to fully understand the safety profile, as well as the efficacy profile, or at least initial clinical activity coming out of the dose escalation trial. I also want to just answer this question on tumor types. I think what we've seen time and time again with Wee1 is that there's activity there in some pretty important tumor types: platinum-resistant ovarian cancer, uterine serous carcinoma. We're seeing repeatedly with different molecules that there's activity there, and that's something that we will be looking to replicate with our proof of mechanism aspect of our trial. But as you know from previous comments, we're also excited about other tumor types that have the potential to respond to Wee1. I think we also know CCNE incur some additional sensitivity. We are interested, of course, in exploring that in other tumor types, but we haven't been sharing a lot about the beyond ovarian and uterine strategy at this time that will emerge later on.

There are no further questions at this time. With that, ladies and gentlemen, that concludes your conference call. We thank you for participating and ask that you please disconnect your lines.