Cerus Corp

NASDAQ:CERS

Earnings Call Analysis

Cerus Reports Growth and Positive EBITDA

Cerus Corporation had a landmark fourth quarter in 2023, marking over 16 million cumulative kits sold and positive non-GAAP adjusted EBITDA for the first time. They expect product revenue guidance for 2024 to be between $172 million to $175 million, fueled by expansion in North America, Europe, and uptake of IFC in the U.S., estimating IFC revenue of $8 million to $10 million. Year-over-year product revenues reached $46.8 million, up 6%, and Q4 saw a 24% decrease in operating expenses. The promising trajectory is built on reducing losses and focusing on sustained profitability with an operational breakeven point below $200 million in product revenues.

Cerus Surpasses Milestone with INTERCEPT Blood System

Cerus Corporation discussed its significant growth and commercial achievements in 2023, particularly highlighting the milestone of surpassing 16 million cumulative kits sold for transfusable INTERCEPT platelet and plasma doses. This reflects the increasing relevance and adoption of their pathogen inactivation technology in transfusion medicine globally. Positive outlooks were expressed for continued growth of the INTERCEPT business, particularly through international expansion and an increasing growth trajectory in the United States.

Financial Stability and Positive EBITDA Achieved

The company proudly announced reaching a financial milestone by posting double-digit sequential growth for Q4 2023, narrowing its GAAP net loss, and delivering positive non-GAAP adjusted EBITDA for the first time in its history. With product revenue guidance suggesting year-over-year double-digit growth and an aim to sustain or improve the bottom line in 2024, investors can anticipate ongoing fiscal health. Fourth quarter product revenues in the U.S. and EMEA showed improvements compared to the previous year, with a notable 22% sequential increase in U.S. revenues from Q3 2023.

Looking Ahead: Revenue and Market Expansion

For 2024, the company set product revenue guidance ranging from $172 million to $175 million, indicating expected double-digit growth from 2023, spurred by the expansion of the INTERCEPT platelet business and the uptake of INTERCEPT Frozen Complex in the U.S. For the first time, Cerus is also providing specific revenue guidance for IFC, expecting it to be between $8 million to $10 million. This guidance is supported by commercial commitments and growing utilization of IFC products in U.S. hospitals.

Optimism for U.S. INTERCEPT Platelet and IFC Franchises

Cerus executives underscored the company's strong sequential and yearly growth in the fourth quarter, with an emphasis on their platelet franchise and progress in the U.S. INTERCEPT Frozen Complex. The stability in inventory levels and consistent ordering patterns are cited as growth drivers, and they remain hopeful for U.S. platelet franchise growth in 2024. The company also addressed further implementation stages and growth opportunities internationally, particularly in Canada and the Middle East.

Streamlined Operations and Gross Margin Improvements

Q4 2023 saw a 24% decline in operating expenses year-over-year due to the prior restructuring and other cost-saving measures, contributing to improved financial performance. Although the company experienced a significant net loss improvement and nearly $5 million positive non-GAAP adjusted EBITDA in Q4, company management remains focused on sustaining or bettering these results.

Strategic Moves for Revenue and Cost Management

Cerus is proactively managing its capital and working capital to support growth and improve operating cash flows, with a particular focus on inventory and payable levels. The company's commitment is evident in their financial maneuvers, ensuring a poised approach for revenue ramp-up and cash flow enhancements in the face of inventory and payment challenges.

INFECT Business Set to Boost Revenue Growth

With an expectation of a 30% to 50% growth rate for IFC compared to the previous year, the company anticipates a substantial increase in hospital activations and collaboration with large blood centers. The potential total addressable market for IFC is estimated between $200 million to $300 million, with sales strategies focusing on both direct hospital sales and partnerships.

Clinical Development and Regulatory Updates

The company is looking forward to the unblinding of ReCePI study data, a BARDA-funded U.S. Phase III trial for INTERCEPT red blood cells. Additionally, they continue to navigate regulatory submissions, with interactions continuing in China as they await further indications from the NNPA.

Pricing Strategies and Disciplined Execution

Cerus is witnessing stable to increasing prices for its product offerings. The company credits its disciplined global sales approach and the perceived clinical benefits of its products, which enable discussions centered around clinical utility rather than price competitions.

Upcoming Conferences and Engagement

Investors can expect to hear more from Cerus during upcoming healthcare conferences, where they will share insights and updates on the company's progress throughout 2024.

Earnings Call Transcript 2023-Q4

[Operator]

Good day, ladies and gentlemen. Thank you for standing by, and welcome to the Cerus Corporation Fourth Quarter and Full Year 2023 Earnings Conference Call. [Operator Instructions] Please be advised that today's conference is being recorded.

I would now like to hand the conference over to Jessica Hanover, Cerus Vice President of Corporate Affairs. Dr. Hanover, you may begin.

[Jessica Hanover, executive]

Thank you, and good afternoon. I'd like to thank everyone for joining us today. As part of today's webcast, we are simultaneously displaying slides that you can follow. You can access the slides from the Investor Relations website at ir.cerus.com.

With me on the call are Obi Greenman, Cerus' President and Chief Executive Officer; Vivek Jayaraman, Cerus' Chief Operating Officer; Kevin Green, Cerus' Chief Financial Officer; and Carol Moore, Cerus' Senior Vice President of Regulatory Affairs and Quality.

Cerus issued a press release today announcing our financial results for the fourth quarter and year ended December 31, 2023, and describing the company's recent business highlights. You can access a copy of this announcement on the company website at www.cerus.com.

I'd like to remind you that some of the statements we will make on this call related to future events and performance rather than historical facts and are forward-looking statements. Examples of forward-looking statements include those related to our future financial and operating results, including our 2024 product revenue guidance, our expectations for bottom line and non-GAAP adjusted EBITDA performance and our expected expense levels, expected future growth and our growth trajectory, the availability and related timing of data from clinical trials and other statements that are not historical fact.

These forward-looking statements involve risks and uncertainties that could cause actual events, performance and results to differ materially. They are identified and described in today's press release in our slide presentation and under Risk Factors in our Form 10-K for the year ended December 31, 2023, which we will file shortly. We undertake no duty or obligation to update our forward-looking statements.

On today's call, we will also be discussing non-GAAP financial measures, including non-GAAP adjusted EBITDA. These non-GAAP measures should be considered a supplement to and not a replacement for measures presented in accordance with GAAP. For a reconciliation of non-GAAP financial measures to the most comparable GAAP financial measures, please refer to today's press release and the slide presentation available on our website.

We'll begin today with opening remarks from Obi, followed by Vivek to discuss recent business highlights, then Kevin to review our financial results and expectations for the rest of 2024. And lastly, closing remarks from Obi.

And now it's my pleasure to introduce Obi Greenman, Cerus' President and Chief Executive Officer.

[William Greenman, executive]

Thank you, Jessica, and good afternoon, everyone. I'd like to open the call by spending a few minutes reflecting on 2023 as well as our expectations for 2024.

During the fourth quarter of 2023, we surpassed the [ 16 million ] mark for cumulative kits sold for transfusable INTERCEPT platelet and plasma doses. It's a significant figure, particularly with respect to the absolute number of patients who receive INTERCEPT-treated blood components on a daily basis across the globe. And it also represents the ever growing and significant role played by our pathogen and activation technology in the evolving health care landscape.

The importance and relevance of pathogen inactivation were also visible during a special webinar in January of this year, hosted by Yale University, the American Red Cross and the Association for the Advancement of Blood in Biotherapies, or AABB. The event was focused on addressing platelet and security with speakers from blood centers such as the American Red Cross and Canadian Blood Services as well as from hospitals, the military and government organizations.

In addition to the recognition of the growing demand for platelets in the face of blood supply vulnerabilities, it is also clear that pathogen inactivation has become a foundational aspect of today's transfusion medicine landscape. It is this dynamic that drives our excitement about the continued potential for the INTERCEPT business, both in the U.S. and across the globe. We anticipate the near future to be driven by both international expansion of INTERCEPT platelets as well as an increasing growth trajectory for INTERCEPT [indiscernible] complex or IFC in the U.S. Vivek will provide additional commentary on our commercial expectations following my introductory comments.

We ended 2023 on several high notes, posting double-digit sequential growth for the fourth quarter, narrowing GAAP net loss attributable to Cerus and importantly, delivering positive non-GAAP adjusted EBITDA for the first time. Per our 2024 product revenue guidance announcement earlier this year, we expect to post year-over-year double-digit growth along with sustaining if not improving bottom line results. Kevin will provide more details in his comments following Vivek.

I would now like to turn the call over to Vivek to discuss our commercial results and progress for the fourth quarter and full year 2023 and along with color on the outlook for 2024.

[Vivek Jayaraman, executive]

Thank you, Obi, and good afternoon, everyone. As Obi indicated, we delivered strong sequential and year-over-year growth in the fourth quarter of 2023. This growth was driven by our platelet franchise globally as well as encouraging progress within our U.S. IFC business. With inventory levels at most of our blood center partners stabilize, we witnessed the return to more typical ordering, manufacturing and reordering patterns. Furthermore, we saw growth in both existing accounts as well as a meaningful step-up in new account activation, notably in our IFC business.

Our platelet franchise delivered strong growth across the globe. In the U.S., we believe that most of our customers have properly adjusted their INTERCEPT inventory in light of product dating issues and are now ordering at more consistent rates. As we make progress on our real-time aging studies, we remain confident in our ability to extend platelet kit shelf life. While we are not currently assuming a material uplift in revenue associated with increased stating, we do believe this will likely lead to more comfort at the blood center to hold inventory.

We continue to see positive traction at our blood center customers and believe INTERCEPT remains the leading technology for platelet safety in the U.S. Our early experience in 2024 suggests that our U.S. platelet franchise is poised for solid growth this calendar year.

Internationally, Canadian Blood Services or CBS is closing in on completing its [indiscernible] of INTERCEPT [indiscernible] across its entire production operation. In the fourth quarter, CBS completed its implementation of INTERCEPT for whole blood-derived platelets which included its largest site in [ Brampton ] in the Greater Toronto area. With this activity now more than 85% of CBS platelet units issued to hospitals are INTERCEPT treated. In other words, the majority of platelet doses issued to hospitals in Canada are now INTERCEPT-treated. CBS remains on track to complete the transition to 100% [indiscernible] platelets in the first half of this year. As it implements INTERCEPT [indiscernible] platelets to 3 sites, 2 of which are already producing whole blood INTERCEPT platelets.

Meanwhile, [indiscernible], which produces approximately 25% of Canada platelet supply continues to advance its validation of INTERCEPT platelets.

Q4 2023 was a strong quarter for our U.S. IC business. We gained commitment from blood centers to distribute ISC, while starting commercial use at a number of influential hospitals. Our field sales organization meaningfully increased our [ inostral ] engagement, and we were able to host effective peer-to-peer educational forums at both key congresses and in one-off settings for hospitals. Real-world use of IFC continues to grow, and it has been encouraging to see the clinical enthusiasm for the offering. This momentum has continued through the first 2 months of 2024, and we feel confident in our ability to deliver compelling growth with our IFC business.

On a going forward basis, we will provide you with more detail on the progress we are making with IFC, and I'm confident you will gain a greater appreciation for why we are excited about this business.

I will now turn it over to Kevin to discuss our results and outlook in more detail.

[Kevin Green, executive]

Thank you, Vivek, and hello to everyone listening. On today's call, I will be discussing our financial results for the fourth quarter and full year of 2023 as well as our product revenue guidance for 2024.

Beyond the line item components of our P&L, I'll be providing a breakdown on our important fourth quarter achievement of narrowed GAAP net loss attributable to Cerus, coupled with reaching our target of non-GAAP adjusted EBITDA breakeven. This achievement marks the first time in the company's history of delivering positive adjusted EBITDA, and we are committed to sustaining if not improving on this measure for the full year 2024 as well.

As preannounced in January, we posted product revenue of $46.8 million for the fourth quarter of 2023, representing year-over-year growth of 6% and up 18% sequentially from Q3. Full year 2023 product revenues of $156.4 million were, as expected, down 4% year-over-year and in line with our guidance.

In the U.S. fourth quarter 2023 product revenues exceeded prior year levels. Importantly, fourth quarter U.S. product revenues were up sequentially by 22% from Q3. In EMEA, fourth quarter product revenues were up 3% year-over-year at around 2% compared to the third quarter of 2023. Year-over-year, FX rates provided a benefit for the EMEA business of around 430 basis points.

On a consolidated basis, FX provided a benefit of around 1.3% and when comparing Q4 2023 to that of the prior year period and little to no impact on the full year comparative results. In addition to our product revenue and not included in our guidance, Government contract revenue totaled $6.6 million in Q4 compared to $7.3 million for the prior year period. The conclusion of enrollment in our ReCePI study is the primary driver for the slight decline. Included in our government contract revenue are the revenues recognized as reimbursement under our contract with BARDA, our agreement with the FDA to further hold blood pathogen reduction and our milestone-based agreement with the U.S. Department of Defense for [ lyophilized ] IFC.

Let's turn now to our product gross profit and gross margins. Our fourth quarter product gross profit was $26 million compared to $24.5 million during the prior year period, an increase of 6% year-over-year. Product gross margins for the quarter were 55.5%, relatively stable when compared to the prior year and up slightly from Q3. These results are consistent with our expectations and our previous remarks during prior quarter calls. Q4 2023 margins improved over 2022 levels primarily due to increased volumes and lower inventory costs compared to the prior year, offset by net foreign exchange rate impact on our reported margins.

Moving on. Our fourth quarter operating expenses, which totaled $31.6 million were over $10 million lower than the prior year period of $41.8 million, a 24% decline. Q4 2023 operating expenses included $4.9 million in noncash stock-based compensation. By specific expense type, fourth quarter R&D expense totaled $14.3 million compared to $18.6 million during the prior year period. The impact of our June 2023 restructuring continue to result in lower ongoing costs combined with lower costs associated with the ReCePI trial enrollment completion.

Ongoing R&D expenses included, but were not limited to, work under our government contracts, CE Mark pursuit for our red blood cell program, development work on our next-generation illuminator, ongoing change control work and interactions with regulatory agencies.

Beyond R&D, fourth quarter SG&A expenses were $17.3 million compared to $23.2 million during the prior year period. Similar to the R&D drivers, SG&A costs were lower year-over-year in part due to the impact of our June 2023 restructuring as well as lower nonrestructuring-related compensation costs. We continue to expect that the financial benefit from our restructuring will provide at least $10 million in annualized savings relative to expense levels at the time of the restructuring.

Let's focus on the bottom line and non-GAAP adjusted EBITDA results, which are perhaps the strongest financial results that we have to talk about on today's call. On the bottom line, reported net loss attributable to Cerus for the 3 months ended December 31, 2023, improved significantly when compared to the same period in the prior year. Net loss attributable to Cerus for Q4 totaled $1.3 million or [ $0.01 ] per diluted share compared to $13.6 million or $0.08 per diluted share for the prior year period. These results are also directly reflected in our non-GAAP adjusted EBITDA measure.

As you can see from the results and which I'm happy to announce, we surpassed our goal of breakeven and in fact, generated almost $5 million of positive non-GAAP adjusted EBITDA. When compared to negative $3.7 million for the fourth quarter of 2022, and negative $1 million during the third quarter of 2023, this result is an improvement of over $8 million and $5 million, respectively. This is a significant milestone in our history. And while we are clearly pleased with the results, we are committed to sustaining, if not improving upon it for 2024.

As we had predicted, the combination of strong growth in our top line coupled with stable margins and closely managed operating expenses allowed us to surpass non-GAAP adjusted EBITDA breakeven in the fourth quarter. While we may have some fluctuations from quarter-to-quarter this year, we expect that with our product revenue guidance, coupled with stable and perhaps slightly improving gross margins, continued leverage from the business and close management of operating expenses will support potential improvement on this measure for 2024.

On the balance sheet and associated cash flows, we ended the fourth quarter with a cash position of $65.9 million of cash, cash equivalents and short-term investments on the balance sheet. In terms of cash utilization, our cash used from operations was $15.2 million for the fourth quarter compared to $1.8 million during the prior year period.

As we've spoken about in the past, we saw significant increases in working capital use, specifically with increased inventory levels. During Q4, we also made a conscious decision to pay down our payables due. As we now look to 2024, we expect that with the anticipated increase in revenues, we will work down our inventory balances, maintain payable levels near December 2023 levels and manage other working capital line items. We expect that these initiatives and results will translate into improvements in operating cash flows for 2024 and could potentially result in positive operating cash flows for the year.

Turning to our guidance. As we preannounced in January, we expect full year 2024 product revenue guidance to be in the range of $172 million to $175 million, reflecting double-digit growth from 2023. We anticipate this growth to be fueled by continued expansion of the INTERCEPT platelet business, both in North America and Europe as well as continued uptake of IFC in the U.S. As Vivek mentioned, we firmly believe in the prospects for IFC, evidenced by our commercial sales agreements with large national blood providers as well as the growing utilization and recognition of the products benefit and an increased number of U.S. hospitals.

For the first time, we are now providing annual revenue guidance for IFC, which for 2024, we expect to be in the range of $8 million to $10 million. Going forward, on a quarterly basis, we plan to break out IFC revenue on a comparative basis to provide visibility into our progress towards our guidance.

I'd now like to turn the call back over to Obi for some closing remarks.

[William Greenman, executive]

Thank you, Kevin. For the first 2 months of 2024 in the rearview year, we remain positive about the rest of the year ahead of us. With respect to the ReCePI trial, the first of 2 BARDA-funded U.S. Phase III trials for INTERCEPT red blood cells, we continue to anticipate providing the top line readout after the data [indiscernible] [ unblinded ] in the near future. Between continued momentum in our commercial business and increased visibility into our pipeline, we look forward to providing you with updates throughout the year. Thank you for your continued interest in Cerus.

I will now turn the call over to the operator for questions.

[Operator]

[Operator Instructions] Our first question will come from the line of Jacob Johnson with Stephens.

[Jacob Johnson, analyst]

Congrats on the quarter. Maybe starting off on IFC, good to see the $8 million to $10 million expectation in 2024. Maybe just for reference, could you kind of give us what that was in 2023? And then as this continues to hit its stride, can you just remind us the potential TAM for this offering and how we should think about the 3- to 5-year outlook for the IFC ramp?

[William Greenman, executive]

Thanks, Jacob. Vivek, I'll let him take this.

[Vivek Jayaraman, executive]

Thanks, Jacob, for the questions. We -- the guidance range for 2024 assumes a 30% to 50% growth rate versus prior year. I think in the past, we've talked about the TAM for the business being on the order of $200 million to $300 million. Part of it is going to be a function, obviously, as the blood center channel picks up the product and we sell through blood centers. It's going to be a combination of direct sales to hospitals and then also sales through [indiscernible] and our partners. But what I think is most encouraging for us is we announced the collaboration with large blood centers at the end of last year. We saw those first orders come through. And through the first 2 months of 2024, we're seeing continued pickup in new hospital activation. So I think we're all encouraged about the growth prospects for this franchise.

[Jacob Johnson, analyst]

Got it. And then maybe, Kevin, for you. Good to see the positive EBITDA in the quarter. You mentioned kind of sustaining, if not improving that, I guess, kind of as we're thinking about 2024 is a reasonable assumption, positive EBITDA for the entire year, kind of like 4Q? Or could we see even kind of EBITDA be positive on a quarterly basis? If you could help us on that side of things.

[Kevin Green, executive]

Yes. So our -- our top line guidance doesn't necessarily suggest linearity. So there is some chop to it. But for the balance of the year, we do expect and are targeting at least neutrality, if not, improvement from the Q4 level. So I think we've got a lot of reasons to believe that, that is very doable and while we may see some chop quarter-to-quarter, I think for the balance of the year, we're moving in the right direction there.

[Operator]

Our next question will come from the line of Emily Christy with Stifel.

[Emily Christy, analyst]

Just a couple for me. I appreciate the transparency on the IFC business. That's great. Just on international, it sounds like Canada is on track with expectations. Can you talk to any other geographies that might be notable in 2024, like if we should expect meaningful contribution from Germany? And then maybe if there's an update from China from the regulatory situation there.

[William Greenman, executive]

Great. Thanks, Emily. I'll let Vivek take the first part of that question, and then I'll answer the China one.

[Vivek Jayaraman, executive]

Sure. Thanks for the question, Emily. We are -- a lot of the growth that we're expecting this year is a combination of continued depth with existing customers, their growth opportunities and geographies where we've already started. So you referenced Canada, we certainly are anticipating got continued progress in Germany. We also believe that the Middle East was recently at the [ MedLab ] Congress in Dubai. There are great growth opportunities there and they tend to draft off of what the U.S. FDA does in terms of the blood banking community in that region. So we feel like there are meaningful pools of growth across the globe in terms of our platelet business.

And then as referenced earlier in the call, the U.S. IFC business will start to be a meaningful growth driver as well. So it's really a combination of factors. But fundamentally, what we're seeing is we're going deeper with customers and there's still significant headroom for growth. Obi, I'll kick it back to you regarding China.

[William Greenman, executive]

Yes. Thanks a lot, Vivek. Yes. So regarding China, we've submitted to the NNPA last year, as you recall, and are in the process of receiving questions and feedback from the FDA. I was a little delayed at the start of this year just because of [indiscernible] New Year, but is underway. To date, we don't have any indication of the clinical trial being necessary, but we're not complete with the [indiscernible] review yet.

[Emily Christy, analyst]

Okay. Great. And if I can just sneak one more in. We don't talk a lot about pricing, but I'm wondering how we should be thinking about pricing power in both new markets and in those where you have high penetration rates already?

[William Greenman, executive]

Yes. Thanks, Emily. Again, I'll turn that back over to Vivek.

[Vivek Jayaraman, executive]

Sure. Yes. We've seen stable to slightly increasing pricing in light of inflation and other things. I feel really good about the pricing discipline that we've been able to execute on a global basis. So I think given the benefits of [indiscernible] reduction and certainly the clinical benefits of IFC, we've been able to have more discussion around clinical utility and value than going in and competing against price. I mean, hospitals and blood banks certainly have budgetary constraints are under pressure, but I think the global sales team has been disciplined in terms of ensuring that we're realizing value for the offering we're bringing.

[Operator]

Our next question will come from the line of Mark Massaro with BTIG. Mark, your line is now open.

[Unknown Analyst]

This is [indiscernible] on for Mark. So just on the 2024 guide, it looks like it calls for a bounce back in platelets in the U.S. business. So I just want to confirm what's excluded from the guide and where you're seeing sources of potential upside? And then maybe if you could also touch on any seasonality we should be modeling for in that.

[William Greenman, executive]

Yes. Thanks a lot, [indiscernible]. So [indiscernible] I'm sorry to turn it back over to you, but your best place to answer that question.

[Vivek Jayaraman, executive]

Yes, no problem. I'm sorry. The first part of that question cut out on my end. Could you repeat that? Or maybe Obi if you could paraphrase that?

[William Greenman, executive]

[indiscernible], do you want to...

[Unknown Analyst]

Yes, just the puts and takes in the '24 guidance seasonality as well.

[Vivek Jayaraman, executive]

Okay. Fair enough. I think as we mentioned earlier, we're seeing sort of stabilization and strengthening across our business. But we have not modeled in, in terms of embedded in our guidance as an example, a restocking of inventory levels at blood centers as we see improved shelf life in the U.S. nor have we modeled in any accelerated assumptions around the recovery of platelet donors in Europe and the U.S., which leads to overall growth in the platelet market.

So what we are really focusing on as we work kind of hand in glove with the blood center operations folks and our deployment teams, we're seeing continued ramp-up in INTERCEPT platelet production and then continued pass through the hospitals.

And then on the IFC side, we're seeing a fairly methodical and strong ramp-up in new hospitals. And when we get into hospitals in a particular clinical discipline, say high risk ove as an example. Once you get a couple of clinicians with experience with the product, we see that product being adopted in other clinical centers in the hospital and see us [indiscernible] depth there. So those are the sort of some modeling assumptions that underpin our current growth assumptions and the guidance for the full year. But we've tried to really I think the silver to the challenges we had historically but recognize we've got a few tailwinds right now at our back, which is a good place to be.

[Unknown Analyst]

Okay. That's perfect. And then just a follow-up. As far as the ReCePI study, which I think should be reading out shortly here, could you just remind us what your expectations are there and just how that's tracking?

[William Greenman, executive]

Yes. Thanks a lot, [indiscernible]. So the database is locked for the ReCePI study, so we should be unblinding that data in the near term. As far as the study design, it's just to remind you all that it's a non-inferiority study design in cardiovascular surgery patients, many of whom were on bypass with an acute kidney injury endpoint, and that was modeled after bunch of publications in cardiovascular surgery recipients who had AKI rates typically who are getting transfused, who typically had an AKI rate in the range of 28% to 30%. And the margin of non-inferiority for the study between test and control is 50%.

[Operator]

That concludes today's question-and-answer session. I'd like to turn the call back to Obi Greenman for closing remarks.

[William Greenman, executive]

Well, thank you again for joining us today and for your interest in Cerus. We will be presenting tomorrow at the TD Cowen's 44th Annual Healthcare Conference, and we look forward to sharing our progress with you throughout 2024.

[Operator]

This concludes today's conference call. Thank you for participating. You may now disconnect.