Good day. And thank you for standing by. Welcome to the Seer First Quarter 2023 Earnings Conference Call. Please be advised today's conference is being recorded. I would like to hand the conference over to your speaker today, Carrie Mendivil, Investor Relations. Please go ahead.

Thank you. Earlier today, Seer released financial results for the quarter ended March 31, 2023. If you have not received this news release or if you'd like to be added to the company's distribution list, please send an e-mail to [email protected]. Joining me today from Seer is Omid Farokhzad, Chief Executive Officer, President and Chair; and David Horn, Chief Financial Officer. Before we begin, I'd like to remind you that management will make statements during this call that are forward-looking statements within the meaning of federal securities laws. These statements involve material risks and uncertainties that could cause actual results or events to materially differ from those anticipated. Additional information regarding these risks and uncertainties appears in the section entitled Forward-Looking Statements in the press release issued today. For a more complete list and description, please see the Risk Factors section of the company's quarterly report on Form 10-Q for the quarter ended March 31, 2023, and in the other filings with the Securities and Exchange Commission. Except as required by law, Seer disclaims any intention or obligation to update or revise any financial projections or forward-looking statements, whether because of new information, future events or otherwise. This conference call contains time-sensitive information and is accurate only as of the live broadcast, May 9, 2023. With that, I'd like to turn the call over to Omid.

Thanks, Carrie, and thank you, everyone, for joining us this afternoon. I will begin our call today with a review of our first quarter results as well as the progress we're making across our core focus areas to drive growth. Thanks to the tremendous effort of the entire team at Seer, we had a solid start to the year and ended the first quarter with $4.1 million in revenue and continued growth in our installed base. Even more importantly, we're increasingly seeing more and more data being shared by our customers, the initiation of larger studies with a growing interest in population-scale studies, and the first customer publications making their way through the peer review process. We have consistently said that the increased publication of customers' and third-party data will be critical to developing the market, and this is exactly what we're seeing. We now have more than 150 public presentations on Seer's Technology to date with additional data expected at the American Society of Mass Spectrometry, or ASMS, annual conference in early June. With this solid start, we're reiterating our 2023 guidance and continue to expect revenue in the range of $23 million to $25 million for 2023, representing significant year-over-year growth of 48% to 61%. While we continue to drive top-line growth, we're taking a very disciplined approach with our operating expenses in order to protect a robust balance sheet. With over $410 million cash, we're well positioned to execute on our multiyear strategic plan and are building a resilient organization that can make a meaningful impact on the advancement of science and medicine. We're committed to leveraging our resources to drive innovation, creating value for our customers and investors, and contributing to the positive trajectory of the proteomics field and human health overall. As mentioned, on the last earnings call this year, we're focused on executing across our four core areas. First, enabling breakthrough discoveries with the Proteograph Product Suite; second, demonstrating the power of our technology; third, catalyzing new applications and markets; and finally, fourth, expanding our industry-leading team. Starting with our first objective, the Proteograph Product Suite is highly extensible and is providing reproducible unbiased access to the proteome with flexibility and scale, allowing us to address many unmet needs in our customers' hands. We're encouraged by the growing enthusiasm for what the Proteograph workflow can enable. As I mentioned in my opening remarks, more customer data is being shared publicly. Dr. Karsten Suhre, a leading multiomic researcher and a Professor of Physiology and Biophysics at Weill Cornell Medicine, has a manuscript under peer review that is now available as a preprint in BioRxiv. This is the first study using the Proteograph Product Suite to perform protein quantitative trait loci or pQTL analysis. I view this study as an important milestone in which the biological value of connecting genomic variant data to deep unbiased proteomic data at the peptide level has been robustly exemplified. In a cohort study of 325 diabetic subjects and controls, Dr. Suhre identified approximately 3,000 proteins and over 18,000 peptides and associated these with genetic variants across the study, allowing them to identify variation in plasma protein concentration among subjects. Importantly, this publication highlights the shortcomings of affinity-based approaches in which the measured abundance of a target protein may be impacted by protein-altering variants that changed their binding epitope of the affinity reagent. Dr. Suhre's work highlights the importance of peptide level resolution to more deeply understand the proteome, which the Proteograph Product Suite is uniquely able to deliver at scale. Another interesting emerging application of the Proteograph is targeted mass spectrometry workflows for quantifying specific high-value human plasma and serum proteins, for example, in obesity and diabetes research. Most assays today in obesity and diabetes research rely exclusively on antibodies, while certain publications have shown this approach has limitations, including failure to detect the intended target for the post-translationally modified biologically active forms. The combination of mass spec-based targeted proteomics combined with the Proteograph workflow provides a solution to this problem with a robust, highly reproducible method for detecting and quantifying the desired protein barriers across a wide range of concentrations at the peptide level. Dr. Jenny Van Eyk, who's a Professor of Cardiology and Director of the Advanced Clinical Biosystem Research Institute and founder of the Precision Biomarker labs at Cedars-Sinai, is leading this work. Dr. Van Eyk is an international leader in clinical proteomics and current President of the Human Proteome Organization, or HUPO. Her team has leveraged the Proteograph Product Suite to identify and quantify clinically relevant biomarkers that are inaccessible to immunoassays. The targeted methods they performed using the Proteograph ensure accurate quantitation of lower abundance proteins that are not easily accessible by standard proteomics workflow, while also allowing the monitoring of several hundred other plasma proteins of interest, which may contain additional biomarker needs. Importantly, this method allows for rapid completion of large-scale studies and the potential for quick diagnostic turnaround in an assay that can be offered as a service to stratify obese and diabetic patients into optimal treatment groups. Her team presented the Proteograph evaluation data at the targeted mass spectrometry assay in diabetes and obesity research meeting that was funded by the National Institute of Diabetes and Digestive and Kidney Diseases late last year and is currently in the process of scaling up this study toward publication later this year. Dr. Van Eyk's research is a great illustration of the unmet needs that the Proteograph workflow can address in the hands of customers and speaks directly to its potential to deliver new clinical applications that have not been possible with existing methods. In January, one of our multiomic liquid biopsy customers, PrognomIQ, announced early results for what they believe to be the largest deep multiomic study to date. This study was run across 1,031 subjects with non-small cell lung cancer or NSCLC and non-cancer controls and demonstrated the power of diverse molecular biomarker to improve sensitivity and specificity in early detection of NSCLC. Last month, they presented new data in two posters at the American Association for Cancer Research Annual Meeting that demonstrated novel biomarker discovery and the potential feasibility of their approach for early cancer detection. Their first poster leveraged deep multiomic profiling of proteins, metabolites, transcripts, and cell-free DNA in blood from NSCLC patients for biomarker discovery. Data showed multiple biomarkers for NSCLC, tested across all holding types with many overlapping biomarkers of interest, and demonstrated a broad ability to distinguish between individuals with and without cancer. The Proteograph played a significant role in biomarker identification, demonstrating the importance of peptide level resolution to drive novel discovery. The second poster demonstrated that a multiomic classifier achieved high sensitivity and specificity for detection of pancreatic ductal adenocarcinoma or PDAC. In the case-control study of 146 subjects in this proof-of-concept study, PrognomIQ leverages multiomic data to identify novel combinations of analytes with both known and unknown relations to PDAC into a high-performance biomarker panel for detection and discrimination of PDAC from non-cancer controls. The high performance of analytes collected from blood draws makes these panels amenable to rapid development and utilization. Results support the feasibility of this approach as a potentially clinically useful test for early detection of PDAC. These results from PrognomIQ illustrate how the Proteograph can drive the identification of novel biomarkers, which can then be utilized in clinical applications. This is just the beginning of what we believe the Proteograph will enable in the hands of customers. In late March, at the US Human Proteome Organization Conference, there was one podium presentation and nine posters highlighting Seer technology, including customer data on COVID-19 vaccine response and an optimized method for the Proteograph with the Thermo Fisher Orbitrap Exploris for AV using FAIMS Pro. The oral presentation covers the first look at the Alzheimer's disease cohort of approximately 1,800 plasma samples using our next product, which is in the hands of several early access customers. We also hosted a well-attended industry workshop with three featured presentations highlighting Proteograph performance, flexibility to address multiple sample types, and ability to drive large-scale studies. In June, at the upcoming American Society for Mass Spectrometry or ASMS annual conference, we are looking forward to more exciting data with 15 Seer and 12 customer abstracts in the program. Customer posters and presentations include using aging in mouse models, translational pharmacoproteomics in Nonalcoholic Steatohepatitis or NASH, improved sensitivity with precision for quantitation in targeted applications, and host cell proteins for biologic manufacturing among others. And we're continuing to drive standardization and partnership with our commercial partners, Thermo Fisher, Bruker, and SCIEX with multiple posters and costs demonstrating the exceptional performance of the Proteograph across these leading mass spec platforms. One customer study of note at ASMS is from Dr. Steve Carr's lab at the Broad Institute. Dr. Carr will have an oral presentation demonstrating the performance of the Proteograph in plasma from multiple myeloma patients using the Bruker timsTOF HT and dia-PASEF. These results are particularly exciting as they show how larger skilled studies that are enabled by the Proteograph with optimized mass spec protocol can enable deeper exploration of the proteome than previously possible. In 2017, Dr. Carr published a seminal paper that achieved a depth of 4,500 proteins in plasma, which has remained the benchmark for deep unbiased proteomics and plasma until now. Importantly, the 2017 study, given the complexity of the workflow, was accomplished on only 16 samples. Dr. Carr's current study identified over 5,900 proteins and is being applied to 300 samples. This is yet another example of the step-function increase in depth and throughput of proteomics that has been enabled by the Proteograph Product Suite. It is exciting to see customer-driven data beginning to make its way into publications of significance. One such notable example of a customer manuscript on their peer review includes the use of the Proteograph to follow the civilian crew of SpaceX Inspiration4, combined with additional multiomic data to further understand the body's response to space flight. This project is providing new opportunities to understand the molecular and cellular changes that occur in humans during space travel. We look forward to sharing more details following the publication of this study. We have visibility to multiple additional manuscripts being submitted by customers in the coming months as more third-party data is generated. We will see more proof of the unique value of Proteograph in driving novel biological insights that will accelerate the next generation of multiomic studies. We feel very confident about our market opportunities and are thrilled by the emerging validation of the Proteograph among our customers. We expect a progressive increase in the velocity of adoption in the coming several quarters. Turning our attention to the second objective, demonstrating the power of the Proteograph Product Suite, we continue to innovate, extend the capabilities of our technology and drive our own abstract and publication. In March, we announced that our paper on bone morphogenetic protein 1 or BMP1 was published in PLOS ONE. This peer-reviewed publication highlighted the importance of the Proteograph in identifying peptide-level insights that discovered links between protein variants and lung cancer progression at the protein isoform level. In upcoming months, we expect to have multiple papers released from Seer in addition to what we are expecting from our customers. These papers will continue to advance the field of nano bio-interactions, proteomic workflows, and large-scale data science, showcasing the disruptiveness of our technology and its unique ability to push boundaries in proteomics. We remain committed to delivering cutting-edge solutions that drive more access to proteomic data. We know that enabling streamlined data processing, analysis, and interpretation is key. Throughout 2023, we will continue to expand our software capabilities and lay the roadmap for large-scale studies with our Proteograph Analysis Suite. We believe that this will be an important component of our workflow and will serve to enable more customers to onboard deep unbiased proteomics at scale. From the very beginning, we believe there would be broad interest to incorporate unbiased deep plasma proteomics into studies at scale, well beyond the existing installed base of mass spec users engaged in proteomic research. That is exactly what we're seeing play out in our discussions. Consistent with our original vision, the market opportunity is large, spanning the mass spec installed base as well as the genomic market with increased appetite for adding multiomic data to genomic data sets. Our next product is meant to capitalize on this need to serve a broader audience. It is already in early access with multiple sites, and we're getting great feedback on its performance. Our first product delivered a step-function change in unbiased proteomics, and this next product does the same. We are really excited about what it will enable in the market, and we look forward to sharing more with you in the upcoming months. Turning to our third objective, catalyzing new applications and markets. Our technology is inherently extensible, PC-agnostic, and is compatible with a diverse range of sample types. The Proteograph Product Suite is being used in a range of applications across our growing customer base in academic research, translational, commercial, pharma, CROs, and even applied markets. One example of a new application that has emerged from our customer base is the use of the Proteograph to detect host-cell protein or HCP. HCPs are proteins produced or encoded by the host organism used to produce recombinant therapeutic protein such as those used in biomanufacturing of vaccines. Removal of HCP is one of the biggest challenges for the production of biopharmaceuticals; an ideal HCP screening assay is high throughput, reproducible, quantitative, and sensitive with high dynamic range. The Proteograph fits this bill. In a study in partnership with a major pharmaceutical company, we demonstrated that the Proteograph Product Suite detects two to six times more HCPs than traditional methods, identifying 98% of the HCPs and overall improving measurements across purification steps. A poster on this work will be presented at the upcoming ASMS biopharma partner. Customers continue to find value in Proteograph proof-of-principle studies as they build the case for capital equipment funding within the organization, including the grant submission process for academic customers. These small studies of 40 to 100 samples are a key enabler for customers to onboard our technology and often result in posters or abstracts of their own, as preliminary insights and potential biomarkers can be uncovered even from small studies of this size. We had the shipment of a Proteograph to a non-human health company in the first quarter, for example, following a small proof-of-principle study conducted for this organization. With our proof-of-principle study program, we have demonstrated the use of the Proteograph in chicken, dog, cat, baboon, and plant tissue across studies looking at COVID exposure, diet, aging, cognitive impairment, multiple cancers, and transplant. We will continue to drive market development efforts such as these studies, collaborations, and key opinion leader work to accelerate and enable broad market adoption. Through these efforts, we're building relationships with key opinion leaders and expanding our scientific advisory board with the recent addition of Dr. Josh Kuhn, Dr. Chris Mason, and Dr. Jenny Van Eyk. Dr. Kuhn is a Professor of Chemistry and Biomolecular Chemistry at the University of Wisconsin-Madison. Dr. Mason is a Professor of Genomics, Physiology, and Biophysics at Weill Cornell Medicine and the Director of the WorldQuant initiative for qualitative prediction, as well as an affiliate of Memorial Sloan Kettering Cancer Center, Rockefeller University, Harvard Medical School, and Yale Law School. As mentioned earlier, Dr. Van Eyk is a Professor of Cardiology at Cedars-Sinai as well as the Director of the Advanced Clinical Biosystems Research Institute, the Founder of the Precision Biomarker Lab, and the current President of the HUPO. These relationships are reinforcing the power of the Proteograph in the hands of these luminaries in their fields. They're partnering with us to imagine a new future in multiomics, and I'm excited to continue our engagement to push the boundaries of what's possible together. Before I turn the call over to David, I want to share an update on our leadership team. Scott Thomas, our Chief Commercial Officer, will be transitioning from here in July. I want to thank Scott for his contribution in leading and developing our commercial organization. Our two senior regional Vice Presidents will lead commercial in the Americas and EMEA, APAC, respectively. We have an excellent team in place, and we're confident we will continue to deliver on the promise of our transformational technology. With that, I will now turn the call over to David.

Thanks, Omid. Total revenue for the first quarter of 2023 was $4.1 million, representing an increase of 22% compared to the $3.3 million in the first quarter of 2022. The increase in first quarter revenue was primarily due to increased consumable kit sales related to the Proteograph Product Suite. Revenue recognized primarily consisted of sales of Proteograph SP100 instruments and consumable kits. Additional sources of revenue include platform evaluation, service, grant, and lease revenue. Product-related revenue for the first quarter of 2023 was $3.6 million, including related party revenue of $1.3 million and consisted of sales of SP100 instruments, consumable kits, and platform evaluations. Service revenue was $69,000 in the first quarter of 2023 and was primarily derived from the completion of a customer service project. As we have mentioned previously, we will continue to be strategic in undertaking certain service projects for customers that we ultimately believe will lead to purchases of the Proteograph. Grant and other revenue was $335,000 in the first quarter of 2023. As discussed last quarter, contributions from grant and research-related collaborations will resume beginning in the fourth quarter of 2022 related to our SBIR grant from the NIH. The grant period will run through May of this year. In addition, we placed some instruments with key accounts that also require these customers to purchase consumables. We recognized a portion of this revenue as lease revenue. Total gross profit was $2.1 million for the first quarter of 2023, representing a gross margin of 51%. Gross margins were aided by the mix of consumable versus instrument revenue and additional grant revenue in the first quarter. This was offset by overhead expenses and other costs of revenue. We expect to see variability in our overall gross margin on a quarter-by-quarter basis as the proportion of instrument and consumable sales will fluctuate in any given quarter. Total operating expenses for the first quarter of 2023 were $29.5 million, including $8.7 million of stock-based compensation, an increase of 18% compared to $25 million, including $8.1 million of stock-based compensation in the first quarter of 2022. Research and development expenses for the first quarter of 2023 were $14.5 million, an increase of 35% compared to $10.7 million in the first quarter of 2022. The increase in R&D expenses was primarily due to an increase in product development efforts related to the Proteograph Product Suite, including employee compensation costs and other related expenses due to growth in R&D personnel and expenses associated with the build-out of our facility. Selling, general, and administrative expenses for the first quarter of 2023 were $15 million, an increase of 5% compared to $14.3 million in the first quarter of 2022. The increase in SG&A expenses was primarily driven by greater employee compensation expenses due primarily to growth in personnel for our global commercial organization. Net loss for the first quarter of 2023 was $24 million compared to $23.6 million in the first quarter of 2022. We ended the quarter with $410.5 million in cash, cash equivalents, and investments. As Omid mentioned, while we continue to drive growth on the top line, we're taking a very disciplined approach to spend in order to protect our robust balance sheet. We'll continue to be very mindful of our level of spend as the year progresses in light of the volatile macroeconomic environment and its potential impact on demand. With disciplined deployment of capital, we believe we are well funded to execute on our strategic plan for many years to come. Turning to our outlook for the year, we continue to expect revenue to be in the range of $23 million to $25 million for 2023, representing significant year-over-year growth of 48% to 61%, similar to 2022. We expect revenue to be more weighted to the second half of the year. At this point, I would like to turn the call back to Omid for closing comments.

Thanks, David. We started the year off with good momentum as more and more customers generated data using the Proteograph, further solidifying the need for large field unbiased deep proteomic studies. It is exciting to see the Proteograph enabling breakthrough science as shown through its power, extensibility, and ability to catalyze new applications and markets. I have never been more excited about the opportunities ahead. With that, we will now open it up to questions.

Our first question comes from TJ Savant from Morgan Stanley.

This is Gabby on for Tejas. So, maybe just to start with what you're seeing right now with your customer base. What impact are you seeing currently from elongated sales cycles in academic versus biopharma customers? And are you seeing any constrained spending from Chinese CDMO customers?

Yes. Thanks, Gabby, it's David. In terms of the customer base, we are continuing to see a somewhat elongated sales cycle. Again, I think the environment continues to be cautious, but at the same time, we are seeing capital being deployed. It's just, I think, as we've said historically, that for a new disruptive technology, it is just a little bit of a longer sales cycle for us in terms of the data coming out and the proof points. A lot of customers choose to run a proof-of-principle study with us, and so that's really what's creating some of the elongated sales cycle. But I'll note that we have had some publications that we met during his remarks, one from Dr. Suhre and another one coming out. So we're excited about those presentations. We're also excited about what's coming up at the ASMS conference in June to continue to have those customer proof points, but again, we are continuing to see that it just takes some time for people to get comfortable with the technology and ultimately decide to bring it in-house.

Great. And then just on your plans to further build your commercial org, could you share maybe progress on that and how many reps you're planning to add before year-end?

Gabby, this is Omid. So we've said that we're not going to be disclosing the specifics of the size of our commercial organization. That said, in terms of the number of sales, that's the organization right now that includes sales support marketing is around 50 people. We think that's the right size. We're going to continue to scale commensurate to demand and revenue coming in, trying to stay about one to two quarters ahead of it. I think we're well in that place right now.

Okay. Great. And then you had mentioned at a conference recently that you believe other omic integration will be in Seer's future. So what is your next focus for enhancing the Proteograph Suite and moving towards achieving that? And I guess just what is the latest feedback you received from your customers? And how are you thinking about improvements to the platform based on that customer feedback?

Sure. Yes, we released the Proteograph Analysis Suite 2.0, PAS 2.0. That was last August. That software allows a user customer to integrate genomic information and proteomic information as part of the analysis. It was the first step to help the customer achieve proteogenomics for a particular subject that they're looking at. We're going to continue to innovate in that space. That looks at genomic information, but we can bring it into transcriptomic information as well on top of that. And so those innovations in terms of analysis are forthcoming. With regards to feedback from customers, look, feedback in terms of the product has been fantastic. We made some claims in terms of how you would see the ecosystem develop the product to be used, and it's playing out exactly as we have predicted. If you look at the paper that Professor Karsten Suhre has under review and he was kind enough to put it on BioRxiv, which is now available that you want to look at it. That paper has generated incoming interest from genomic scientists. I personally view that paper to be a watershed moment, a moment where it becomes clear that we can tie genomic information at the nucleotide level to proteomic information at amino acid and peptide level. When you do that, you begin to look at changes that happen in terms of protein up and down regulation in response to genetic barriers at the population, at the protein variant level, fundamentally disruptive. I think that's the way these carriers study should be. So we're beginning to see customers publish papers that validate that we need to look at the proteome at the level of the protein variant because the complexity of the proteome exists because it's biologically relevant. And Seer uniquely enables that to be done accurately, precisely, and at scale. We have launched product one, which has significantly improved our ability to operate at scale and increase throughput. Customer feedback indicated a desire for deeper exploration, faster results, and reduced sample volume since biological samples are valuable. Consequently, product two is currently with our early access customers, and the feedback has been outstanding. I believe this product represents another significant advancement in the capabilities of our tool. It's an ambitious offering, and we have incorporated customer feedback from product one. I am very excited to share more details in the upcoming weeks and months as we make this product widely available to customers.

Our next question comes from Dan Brennan from TD Cowen.

This is Kyle on for Dan. So how meaningful will third-party publications be to your customer conversations? It is a notable pickup in customer interest/instrument purchases post these publications implied in the '23 guide. And then maybe just going off of that after the first quarter, what's your confidence and visibility into the back half ramp here?

Kyle, let me, I'll take a part of that, and I'll have maybe David answer a part of it as well. So we have visibility to at least a handful of customer papers that are on various stages of publication, including one that you saw is now publicly available on BioRxiv, but others that are in late-stage reviews that should be coming and then others that are being submitted. I had predicted late last year that we would see probably about five customer papers and kind of tilted toward the second half of the year. It may actually be more than that. And then interestingly and importantly, and related to this is also the number of presentations from customers. So we're now seeing customer presentations at conferences, where we weren't even aware of those studies being done or those studies being presented. That's exactly what you want to see; that you put up the abstract book and you see one of your customers have something going on that they're sharing and talking about it. And I think we're also seeing that. So I'm super optimistic, Kyle, that the velocity of customer data presentation is going to be increasing at a progressively sharper slope as we head into the second half of 2023 and then kind of the balance of the year hitting into 2024. So with that, let me turn it to David, and he can give you additional color in terms of revenue. And before I do, I would say that I reiterated the guidance, so I'm confident about the year being in that $23 million to $25 million that we have guided. So with that, let me pass it to David.

Yes, Kyle, just in terms of the 2023 guide, as Omid said, we did reiterate guidance. And so we feel comfortable with that. And as Omid also mentioned, we did have some visibility into some of these papers coming when we did provide our initial guidance. So we certainly had some of those papers baked in. There are other papers that come out or presentations. Again, we feel like that could potentially be a benefit. But I think that will be a benefit in terms of just helping kind of shorten that sales cycle a little bit for us in terms of getting other folks interested in evaluating the technology. So I think we feel pretty good where we are, and we did have the fact that some of these papers would be out as part of our original guidance.

Got it. And then so how is customer interest in the lease program? Is that something you're actively offering to all potential customers, or is it just a select number of potentially more meaningful customers?

Yes, it's a great question. So we've rolled out what we call our strategic instrument placement program. And really, what we're looking to do is identify key parties, whether they be KOLs or large customers with large sample sets, who can again help drive awareness of the technology and really just trying to lower barriers to accessing the technology in the short term. And so we did place some of the instruments we placed in the first quarter were part of that. And so essentially, what that program is, it does require a consumable purchase. So there's a consumable purchase that goes along with that. And then they have, essentially, we replaced the instrument for a period of time. The customer has the option to purchase it at the end of that. And again, it just helps facilitate getting up and using the technology and ultimately helps drive a consumable revenue stream for us. I will say the amount of lease revenue that we recognize as part of that is pretty de minimis. And it's really about continuing to drive consumables and consumable revenue around that. But again, I think the overall objective is to find ways to improve access and help drive, again, presentations and paper publications with accounts that are going to be leaders, either thought leaders and others or large accounts that have large sample sets to help drive consumable volume over the long term. So it's been great. It's been well received by customers. And so we, again, we'll see how it plays out over the balance of the year. But we're certainly feeling it's a good program that is helping us.

Thank you for participating in today's conference. This concludes the program. You may now disconnect.