Cytosorbents Corporation (NASDAQ:CTSO) Q4 2022 Earnings Call Transcript

Cytosorbents Corporation (NASDAQ:CTSO) Q4 2022 Earnings Call Transcript March 9, 2023

Operator: Good afternoon, and welcome to the Cytosorbents Fourth Quarter and Full Year 2022 Financial and Operating Results Conference Call. At this time, all participants are in a listen-only mode. Following the formal remarks, we will open the call for questions. Please be advised that the call will be recorded at the company’s request. At this time, I’d like to turn the call over to our moderator, Jodi Hoover. Please go ahead Mrs. Hoover.

Jodi Hoover: Thank you, and good afternoon. Welcome to the Cytosorbents fourth quarter and full year 2022 financial and operating results conference call. Joining me today from the company are Dr. Phillip Chan, Chief Executive Officer; Vincent Capponi, President and Chief Operating Officer; Kathleen Bloch, Chief Financial Officer; Dr. Efthymios Deliargyris, Chief Medical Officer; Dr. Christian Steiner, Executive Vice President of Sales and Marketing and Managing Director of CytoSorbents Europe GmbH; Christopher Cramer, Senior Vice President of Business Development and Dr. Irina Kulinets, Senior Vice President of Global Regulatory. Before I turn the call over to Dr. Chan, I’d like to remind listeners that during the call management’s prepared remarks may contain forward-looking statements which are subject to risks and uncertainties.

Management may make additional forward-looking statements in response to your questions today. Therefore, the company claims protection under safe harbor for forward-looking statements contained in the Private Securities Litigation Reform Act of 1995. Actual results may differ from results discussed today and therefore we refer you to a more detailed discussion of these risks and uncertainties in the company’s filings with the SEC. Any projections as to the company’s future performance represented by management include estimates today, as of March 9, 2023 and we assume no obligation to update these projections in the future as market conditions change. During today’s call, we will have an overview presentation covering the operating and financial highlights for the fourth quarter and full year 2022 by management.

Following that presentation, we will open the line up to your questions during the live Q&A session with the rest of the management team. And now it’s my pleasure to turn the call over to Dr. Phillip Chan.

Phillip Chan: Thank you very much, Jodi, and good afternoon everyone. For the first slide, I’d like to just cover some recent operational highlights. First of all, we ended last year with more than 195,000 cumulative CytoSorb treatments delivered as of the end of the year, up 20% from the end of 2021 and marking 10 years of CytoSorb commercialization. Second, our STAR-T pivotal trial passed the halfway point of enrollment with an acceleration of enrollment aided by addition of new Canadian sites following Health Canada approval of this study. We are on target to achieve 80 patients by spring of 2023 and complete enrollment of the study by the summer of 2023. We also added Dr. Richard Whitlock, Professor of Surgery at McMaster University Medical School and Canadian Research Chair in Cardiovascular Surgery for the Population Health Research Institute, PHRI, as our Canadian Principal Investigator of the STAR-T trial, joining Dr. Michael Gibson and Dr. Michael Mack.

He has an outstanding track record of trial execution and brings a superb network of Canadian clinical trial sites specializing in cardiovascular trials to the STAR-T trial. We also strengthen our cash balance with $5 million in non-dilutive debt financing from Bridge Bank and we also increased our product €“ and our product gross margins recovered in the fourth quarter to 75% and are expected to reach 75 to 80 plus percent as we ramp volume manufacturing. Last but not least, our sales momentum from the fourth quarter of last year has extended into the first quarter of this year to-date with expectation of sales growth in 2023. I’ve left most of the clinical update to Makis to cover later on in his slides. I now have the pleasure of welcoming Irina Kulinets to our management team.

Dr. Irina Kulinets joins the senior management team as Senior Vice President of Global Regulatory. Her goals are to drive U.S. and Canada regulatory strategy, an execution for DrugSorb-ATR as well as to oversee European Union MDR compliance. Irina brings 30 years of experience in regulatory affairs and clinical research with a specialty in medical devices having a track record of success leading to regulatory approval or clearance of many medical products via Class 2 510(k) and Class 3 pre-market approval or PMA pathways in the cardiovascular and neurovascular space. Most recently, Irina served as Senior Vice President of Regulatory Affairs for MicroVention, a division of the Terumo Corporation Conglomerate that generated an estimated $0.5 billion in annual sales last year.

She has also worked for major companies such as Johnson & Johnson, Boston Scientific, CynoSure and others. And she also has extensive experience as a regulator and was appointed as a third-party FDA inspector in 510(k) reviewer on behalf of the FDA to review, assess and approve new technology. With that, I’d like to invite Irina to have a few words. Irina?

Irina Kulinets: Thank you, Phil, for kind introduction, and good afternoon, everyone. I’m excited to be a part of Cytosorbents team and with the current success of Cytosorbents product on many markets and encouraging trends of clinical research. I have high expectations for the patients and physician community using this product worldwide and eagerly anticipate the success of Cytosorbents product on U.S. market. I’m looking forward to leading the registration of this lifesaving product in many important regions. This is great opportunity to participate in success of something so important.

Phillip Chan: Thanks so much, Irina. And now I’d like to turn it over to Kathy to discuss our financials. Kathy?

Kathleen Bloch: Thank you so much, Phil and hello to everyone on the call today. I will be discussing fourth quarter and full year 2022 financial results including revenues and gross margins, and then I’m going to also provide an update on our working capital and our cash runway. Next slide, please. Total revenues for the fourth quarter of 2022, which include both product sales and grant revenue was approximately $9.4 million, a 13% decrease as compared to Q4 2021 total revenue of approximately $10.8 million. Q4 2022 product sales were $7.6 million, a 21% decline over $9.7 million in Q4 2021 product sales. We note however that sales in Germany, our largest market were $3.3 million in the fourth quarter of 2022, which is an increase of 33% over the prior Q3 2022 quarter.

COVID-19 sales were negligible during the fourth quarter 2022 as compared to $1.7 million in the fourth quarter of 2021. In addition, we experienced a decrease in the average exchange rate of the euro to the U.S. dollar, which lowered our fourth quarter 2022 product sales by approximately $865,000 such that on a constant currency basis, fourth quarter 2022 core non-COVID product sales were actually $8.5 million, which represents a 6.4% increase from our $8 million in core non-COVID product sales a year ago. Our grant revenue for the fourth quarter was $1.7 million compared to $1.1 million in the prior year, and our gross profit margins on product sales were 75% for the fourth quarter 2022 compared to 78% for the prior year. And the decrease that we experienced was due primarily to inefficiencies related to the relocation of our manufacturing operations to our new facility which occurred during 2022.

Next slide, please. This chart breaks out our core non-COVID-19 product sales and our COVID-19 product sales by quarter. And as you can see, except for the $300,000 in COVID-19 sales in the first quarter of 2022, COVID-19 product sales have declined to virtually zero for the remainder of the year. Fourth quarter COVID-19 product sales were zero. That compares to $1.7 million in COVID-19 product sales in the fourth quarter of the prior year. Note that Q4 2022 product sales are directionally higher than the immediately prior quarter, a quarter-over-quarter increase of 18%. And I know Christian will be discussing later in the call, we are seeing positive trends in the market, particularly in Germany, our largest market. Next slide, please. Total revenue for 2022 including both product sales and grant revenue was $34.7 million compared to $43.2 million in 2021, a decrease of 21%.

Product sales were $29.4 million, representing a decline of 27% over 2021 product sales of $40.1 million. COVID-19 sales were negligible as we said in 2022 that compares with $6.3 million in COVID sales for the prior year. The decrease in the average exchange rate of the euro to U.S. dollar, lowered 2022 product sales by approximately $3.1 million, such that on a constant currency basis, 2022 core non-COVID product sales were $32.2 million, a 5% decrease compared to $33.8 million in core non-COVID-19 product sales one year ago. 2022 grant revenue was $5.3 million compared to 2021 grant revenue of $3.1 million. And product gross margins for the year were 70% in 2022 compared to 80% in 2021. This decrease is primarily due to the relocation as I previously mentioned.

We expect that as we increase production at our new facility during 2023, we will see gradual improvements in our gross margins, which should equal or exceed the 80% blended gross margins that we typically reported prior to 2022. Next slide, please. This chart shows our annual product sales and it’s also broken down into COVID-19 product sales, the light blue part of the bar and core non-COVID product sales. The darker blue part of the bar, and we note that on a constant currency basis, 2022 core product sales were $32.2 million, which is just 5% lower than core non-COVID-19 product sales of $33.8 million last year. We also like to point out on this chart that core non-COVID-19 product sales are 30% higher than they were in 2019, which is the year immediately prior to the start of the pandemic.

Next slide, please. Lastly, I’d just like to say a few words about our working capital and cash runway at December 31, 2022, we had $23.8 million in cash, which includes $1.7 million of restricted cash. This also includes $5 million of loan proceeds, which we received under our debt facility in December. This is an interest-only loan over the next 12 months and we are very comfortable with this level of debt at the moment. We are in discussions with Bridge Bank about extending our term loan commitment, which is scheduled to expire on March 24, 2023. Based on our detailed 2023 operating budget, we believe we have available cash to fund our operations beyond the next 12 months. Conservation of cash is of course an important corporate priority and we are focused on controlling expenses.

We have and will continue to identify potential cost saving opportunities to reduce our cash burn. During 2022, we reduced our overall headcount by 10%. We shifted our R&D employees to solely grant funded programs and in addition, we’ve reduced our inventory levels providing for additional working capital. We have de minimis capital expenditures planned for 2023 compared to $6.1 million in actual capital expenditures in 2022. Our goal is through a combination of driving an increase in sales and gross margin along with cost cutting measures to significantly reduce our cash burn and to further extend our operating runway. While the first quarter of 2023 is not yet complete, we are observing significant reductions in our quarterly cash burn. Our spend is laser-focused on and fully aligned with our strategic priorities, most notably our STAR-T clinical trial designed to support U.S. FDA marketing approval for DrugSorb-ATR.

And now I’ve brought up clinical trials. It seems like the perfect time to turn the call over to our Chief Medical Officer, Dr. Efthymios Deliargyris. Please go ahead, Makis.

Efthymios Deliargyris: Thank you, Kathy and hello to everyone on the call today. For the next few minutes, we’re going to discuss primarily the progress and the STAR-T trial, also provide an update on the remaining company clinical programs and of course, highlight some major data releases that happened already this year. So next slide, please. So the headline for today’s clinical update is that we have made solid progress and now have increased visibility as we’re moving forward. The strategy that we discuss with you on the last earnings call on focusing all our resources, all our clinical resource on the STAR-T trial and expanding to Canada, I’m very happy to report that it’s paying off. STAR-T is enrolling fast and has now crossed the halfway point with more than 50 patients enrolled.

We can now reiterate the timelines previously stated that we will hit the next milestone of 80 patients this spring and of the trial will fully enroll this summer. The STAR-D activities remain on pause and the plan also remains to resume this study upon completion of STAR-T. Also very encouraging of the enrollment rates with STAR-T registry, in fact, we have enough patients enrolled that we will have the initial data readouts before the first half of this year. We’re also accelerating our trials in critical care, specifically our process, randomized clinical study and our COSMOS international registry, which we will focus on this year to accelerate enrollment. And finally, the positive data flow for CytoSorb will continue in 2023 with a constant stream of presentations and publications in large international conference and peer-reviewed journals in all therapeutic areas including critical care, liver and kidney and cardiac surgery.

Next slide, please. Now let’s spend the next couple of slides talking about STAR-T. As I mentioned, we now have good visibility of the way forward. Just as a reminder, at the end of last year in December, we received a green light from the DSMB who finished their first safety review after the first 40 patients were enrolled and recommended that we continue to study as planned without any modification. Since that time, we have experienced accelerating enrollment and now the majority of sites participant in the trial are actively contributed. Canada came on quickly and came on fast, but has already contributed multiple patients in the study and it’s accelerating enrollment also. Now that we are passed the halfway point, we’re working closely with our regulatory colleagues.

And as a side note, I would like to also welcome, be very thankful for Irina joining us, such an experienced regulatory expert that will be critical in driving the filing to the FDA upon completion of the trial. And as we’ve shown you before, on the bottom of the slide, you see the table outlining the three milestones of the trial with the first one that has already been completed that were reviewed already. The second one, which is what we should be looking for next happening in this spring once we hit 80 patients enrolled. And then the final milestone, which represents the full enrollment of the study with 120 patients, the follow analysis of the DSMB closed out review, which we anticipated will take place this summer. Next slide, please.

I want to give you a little bit more insight in the next few months as the trial is coming to completion. So let’s talk a little bit about what to expect in the near future for the STAR-T trial. First of all, we estimate that the trial will be fully enrolled by the time the previously scheduled interim analysis process would be completed. The process that requires a soft database log with full data cleaning and full event adjudication, I’d also like to remind you that performing an interim analysis comes with a statistical price, the so-called spend of alpha. Therefore, now based on the fast enrollment, we have an opportunity to preserve all the alpha for the final analysis by forgoing the interim analysis and we plan to do so. I will emphasize that this positive development is a direct result of the fast enrollment of the trial, which is directly related to the highly motivated investigative sites in U.S. and Canada, and it’s not at all related to any safety or other known concerns.

So what we should be looking for next is the enrollment of 80 patients, which similar as we did in late last year will trigger a press release. And from that point on the following €“ the second DSMB safety review, we anticipate that the interval between enrolling the 80 patients and executing the DSMB review will likely be similar to the one from the press review and approximately eight weeks. Next slide. Now, for the next couple of minutes, I’d like to provide you with a brief update on the progress we’re making on the remaining company clinical programs. First in line, let’s talk about process, a randomized clinical study in patients with refractory shock that we’re executing in multiple sites in Germany. We now have the majority of those sites open and are in the process of executing an important protocol amendment that will allow earlier initiation of therapy and should also contribute to faster enrollment.

This optimization of the trial was informed by observations from other studies, including our own CTC registry with its excellent results, but also from testimonials from real world use that suggest that CytoSorb benefits are maximized with earlier initiation of therapy. This approach is also aligned with our commercialization strategy of offering treatment now to patients before they develop organ failure and require organ support like continued renal replacement therapy with the use of a standalone hemoperfusion pump. We anticipate this amendment to be completed in the first half of the year and to drive faster enrollment process in 2023. Now let’s turn our attention to the STAR registry. I’m happy to report that enrollment in the registry is exceeding our own projections.

We believe that this is in large part driven by the increasing adoption of ATR or anti-thrombotic removal as the standard of care in many European heart centers. We already have more than 200 patients enrolled, and 2023 is an exciting year since we’re going to have the initial data readouts starting with the presentation for the very large international conference of interventional cardiology EuroPCR in Paris this May. We also have submitted an additional analysis to the largest cardiovascular conference in the world, the European Society of Cardiology meeting that will take place in Amsterdam in August. And we also plan to present the European Association of Cardiothoracic Surgery in Vienna next October should our submissions be accepted of course, these meetings.

Finally, let’s talk about COSMOS. This year will be the year of COSMOS. We will focus our attention and increase our resources and prioritize progress in this important registry. We believe that this platform allows enrollment for all the remaining CytoSorb applications with the exception of antithrombotic removal across multiple therapeutic areas. And that the data from this COSMOS registry will generate a wealth of high quality evidence both from the clinical benefits but also the value proposition of CytoSorb for the years to come. We’re happy with the opening of the first few sites €“ the first two countries, Germany and Spain and the first few sites and are happy to see that enrollment has shown a slight uptick in the recent months. Just as a reminder, the CTC registry, we have discussed previously in detail and the final results presented at the international European Society of Intensive Care Medicine meeting last year, and now the main results have been submitted for publication.

So please be on the lookout for the formal paper to be released shortly. Next slide please. During our last earnings call, we discussed about the flurry of new data in cardiac surgery that were presented at the European Association of Cardiothoracic Surgery. The study that really stood out was the multi-center analysis on staph endocarditis patients that was presented. I would like to spend a little more time now and refer you to the reference listed on the bottom for you to actually get the study online €“ find the study online, since it has now been formally published. Staphylococcus aureus endocarditis is the most serious type of endocarditis. It carries the highest risk of morbidity and it carries mortality rates that can approach 40%.

In this multi-center study, a total of 130 patients would confirm staph aureus endocarditis underwent cardiac surgery and valve replacement. 75 of those patients were treated with CytoSorb, while 55 of those patients underwent surgery without CytoSorb. The main results are summarized on the slide. On the left hand side, on the diagram you see on the bottom left the need for vasopressor support. These are drugs that are given intravenously and try to maintain blood pressure in the presence of hemodynamic instability. And patients who were treated with CytoSorb had reduced need for such agents throughout the early post-operative period from right after surgery out to day three after the operation. However, what’s more compelling is that the investigators specifically looked at three different mortality rates.

First of all, patients who expired because of sepsis and that was significantly lower among those treated with CytoSorb 8% versus 22.8%, then they look at 90 day mortality that was 21.3% versus 40% in the control group. This represents a really significant absolute risk reduction of 18.7% in mortality, which in turn would translate to a number needed to treat to save the life of 5.3%. The authors stated that they believed that these compelling benefits were in large part related to the fact of the ability of the CytoSorb device to remove not only cytokines but also staphylococcal specific toxins, but those staphylococcal hemolysin and toxic shock toxin. Next slide. And finally, the highlight recently that you have probably already seen in our recent press release is the fact that we are very happy to report that for the first time our technology has been mentioned in practice guidelines, specifically the 2023 European Society of Anaesthesiology and Intensive Care issued guidelines for the management of severe perioperative bleeding.

And they have included intraoperative hemo absorption in these guidelines with a statement saying that it may be considered as an adjuvant therapy to reduce leading complications in patients on ticagrelor or rivaroxaban undergoing emergent cardiac or aortic surgery on CPB. Next slide please. And you will probably hear a few more words about this major development and how it’s going to inform our commercialization strategy from Christian coming up next. So in conclusion, we now have visibility for STAR-T with more than half of the patients enrolled and we’re confident in the timelines of hitting the second milestone this spring and completing the trial enrollment this summer. We will proceed straight to final analysis with fully preserved alpha.

There is no longer rationale for interim since the full enrollment will complete before the interim could be executed. We anticipate that we will have top line results from STAR-T by year’s end approximately three to four months after the last patient completes the study. STAR-D remains on hold and the plan remains to restart right after we complete our operational responsibilities with STAR-T. STAR registry is ahead of schedule with anti-thrombotic removal now becoming increasingly standard of care in real world practice. And finally, this year we’ll prioritize both process in COSMOS with the intent of speeding up enrollment and generating critical evidence in our critical care applications. I also would like to remind you that we have a fully staffed very capable medical affairs team that the priority in Europe is to support our business in all of our therapeutic areas.

We anticipate increasing adoption of our therapy in 2023 based on the feedback we get from ongoing interactions with KOLs and users who continue to express high enthusiasm about our therapy. Also, we believe that the constant stream of new and positive data presented at international conferences and the continuous flow of new positive publication across all of our therapeutic areas will be major tailwinds for our business and adoption of our therapy. So thank you for your attention. And with this, I would like to turn it to Christian. Christian?

Christian Steiner: Yes. Thank you, Makis. And good afternoon to everyone in the United States and to good evening to Europe. Kathy and Phil have already described to you the overall situation and the status of our business development. The macroeconomic situation has not improved and remains to be challenging in many ways. I want to give you a few more insights about our commercialization outside the United States and share with you what we are seeing in the markets. I do believe that we are already in the middle of the stabilization of our CytoSorb commercialization. Although the environment in the markets characterized by shortage of personnel at the hospitals, inflation, energy costs and so on has not improved. But again, we have improved.

Next slide please. In the first quarter 2022, we could further improve the number of customer visits in our direct markets. However, we are still significantly below the number we have achieved before the pandemic. For example, in Germany it’s still approximately 25% lower. The shortage of personnel on ICUs leaves little time for meetings with industry representatives and for educational events. However, over the last 12 months, we could continuously increase our face-to-face time with customers. This led to the beginning of a turnaround we have experienced in Q4 2022. We could stop the decline of our business and increase the revenues by 16.9% compared to the quarter before. This is 15.3% higher than the comparable last quarter before the pandemic in Q4 2019.

More customers are buying again, they’re buying more frequently and placing average bigger orders. That shows us that the patient population is somehow normalizing and more treatments are conducted. Next slide please. So much has been said already about the impact of the pandemic on the medical device business and about a challenging new situation in the healthcare systems. This chart is showing on an annual basis that although we have suffered from all these circumstances and needed to digest a 27% decline from the pandemic years, we nevertheless could close the first post-pandemic year 31% higher than the last pre-pandemic year. I believe that this is the last only call we need to speak about the pandemic and its impacts. Although markets will not go back to their observation, we from now on can concentrate on quarter-over-quarter and year-over-year growth.

Next slide please. This growth will partly be driven by several phase initiatives we have reported to you in the last few earnings calls. These are ongoing and we will keep you updated regularly. But a very significant growth catalyst for the next product and years will be that we are now ready to start addressing new additional customer groups and entering the mainstream market in certain indications. The chart in the lower part of the slide is showing the early markets in green on the left and the big mainstream market on the right. Our draw so far was mainly coming from those early market customer groups. Some of our geographically market like Germany, Austria, Italy, are now mature enough to start crossing the chasm towards mainstream customers.

The possible application field for CytoSorb are so many-fold that we have to focus on only a few indications which are most advanced. And these are the following. Number one, reversal of vasoplegic shock, which includes also the septic shock, number two, intra and post-operative use of CytoSorb in the infected endocarditis and number three, antithrombotic drug removal in cardiac surgery patients. The first of those three indications is representing the biggest business opportunity, but also it’s the most complex application as many co-founding factors influencing the therapy outcome. The second and the third indication are part of our cardiovascular therapeutic area and represent smaller business opportunities, but also promised a possibility to faster get standard of care status.

I will give you some more insights about our activities in all three therapeutic areas, cardiovascular, critical care, and liver kidney with my next three slides. Next slide please. The biggest means for our therapeutic area cardiovascular is that hemadsorption therapy has made it into the new guidelines of the management of severe perioperative bleeding by this European Society of Anaesthesiology and Intensive Care, which has been published on March 1 this year. Makis has already reported to you about this major treatment, but I just wanted to add two facts which are very important to us from a consolidation point and investor point of view. The authors obviously avoided product named CytoSorb, but only CytoSorb is specifically approved for the removal of ticagrelor and rivaroxaban and this guideline entry is solely based on CytoSorb data and evidence.

Furthermore, in this therapeutic area, several very relevant studies on CytoSorb therapy effects in infective endocarditis patients have recently been published or are submitted for publication. The body of evidence in the field is growing and we can see the increasing excitement and momentum in the community. The attendance at Congress’ symposia and education event is rising and we also can say that the support from renowned KOLs is getting stronger. Next slide please. In the therapeutic area critical care, we also can report a significant step forward in the acceptance of our therapy by key opinion leaders. Although, not yet in guidelines, the therapy has been integrated as a therapy option for certain patients in the consensus paper on sepsis associated acute kidney injury by leading European nephrologist and intensivist published just a few days ago.

Also of great potential impact, several publications on the impact of CytoSorb on the underlying mechanisms of several diseases are either out or will be published within the next few weeks. Please confirm and support the medical rational of CytoSorb therapy. In general, we see a new openness and a lot of excitement about our therapy in the intensive care community and with KOLs. All the progress on the medical scientific side is feeding our marketing stories and argumentation lines and I’m sure we would see an impact of this development within the next few months and quarters. Next slide please. Last but not least, I want to speak about our third and youngest therapeutic area, liver and kidney. We have started two awareness campaigns on an international level and we see a lot of interest arising in these two fields.

One, CytoSorb liver support in patients with liver dysfunction and two, CytoSorb protects the kidneys rhabdomyolysis. There is no real solution for the medical needs in these two fields, and CytoSorb has initially shown remarkable results. Inspired by those findings, there was recently an expert meeting on the topic rhabdomyolysis at the biggest German intensive cares in Braman, Germany. Leading nephrologists and intensivists in this field have started to get to consensus on the use of CytoSorb in this application as well. Next slide please. This slide should just illustrate for you how we are representing our company and the CytoSorb therapy at different medical conferences and trade shows, the two pictures in the lower part of this slide show that our symposia are attracting many, many attendees.

Next slide please. So to summarize, we had a very challenging year 2022 with a declining business due to the in the healthcare markets caused by the pandemic. The macroeconomic circumstances have not yet improved and will remain challenging in 2023. However, 12 months of hard work have resulted in the turnaround we have seen in Q4 2022. And this stabilization has continued so far in Q1 of this year, and I’m very convinced that we just have started a new phase of growth for this company. I hope, I could give you some insights and a little flavor from the markets. And with this, I want to hand over to my colleague Vince Capponi, our President and Chief Operating Officer. Vince?

Vincent Capponi: Thanks, Christian. As we prepare for commercialization in the U.S. and Canada, our core sales and marketing team has established a go-to-market launch plan, identifying key personnel and sales operations to facilitate rapid entry into the market with a total addressable market of $250 million for ticagrelor alone, we believe a blended sales model of direct and distributors will provide broad access to the market in a cost effective manner. Our COVID-19 distributor experience in North America has aided us in identifying distributors in both Canada and the U.S. that we can leverage to supplement our direct sales effort. We believe this blended sales approach will allow broader market access to the market and drive faster revenue growth in the early stages of launch with experienced distributors as part of the sales team.

Regarding the antithrombotic removal application, we continue to receive positive feedback from our EU customers where we see ongoing adoption and growth in the market. A device capable of meeting this unmet medical need to reduce the risk of postoperative bleeding for patients that have undergone CPB has had positive feedback. Even among our U.S. clinical trial sites, we see enthusiasm for the development of a medical device for antithrombotic removal. If STAR-T trial is successful and based on our experience in Europe, we believe there is significant upside ahead of our intraoperative use of DrugSorb-ATR during CPB and add-on applications related to hospital-wide use as a pre-operative treatment and subject for future label expansions. Reimbursement is a key consideration when launching a new medical product.

We believe though €“ we believe DrugSorb-ATR would likely fall under this TCET or Transitional Coverage for Emerging Technologies reimbursement program for breakthrough devices under CMS. A favorable program announcement from CMS probably in late April, which strengthened the value proposition for DrugSorb-ATR, especially in the elderly Medicare population, a major demographic we will address with DrugSorb-ATR. However, given the value proposition, we believe DrugSorb-ATR presents the TCET would be helpful, but not necessary for us to be successful in the market in our opinion. In summary, as we finalize our commercial launch plans, our core commercial team is working closely with our clinical team to gain voice to the customer. In addition, as we look to the commercialization, we are closely €“ we are working closely with our regulatory team, gating our built out of the commercial operations in line with our regulatory filing.

Next slide please. Regarding the new facility, the end of 2022 marked a significant milestone for the company with the successful transfer of polymer manufacturing to the new facility and complete integration of the company under one roof. The polymer plant is fully commissioned and producing polymer today, supplying our device manufacturing lines. An early look at KPIs, suggest we should continue to see improvements in efficiency as a result of consolidating the operation under one roof and a contiguous manufacturing space and scale. We’re currently ramping production replace inventories that we utilize to bridge transfer of the operations and look forward to continued improvements in efficiency as we gain experience running the new plant.

Moving now to cost of goods. The 2022 gross margins dip to 70% driven by the two plant shutdowns associated with the transfer of operations and several other non-recurring items. We expect to see continuing increases in gross margin to historical levels of 80-plus-percent as the year progresses in hand with increased sales as we experience recovery in our core business. Next slide please. R&D and product development teams are focused in two key areas, HemoDefend-BGA and DrugSorb-ATR. The HemoDefend market opportunity is a large covering three market segments encompassing military, civilian and plasma processing industries. Our initial entry into the market will be focused on military applications associated with the universal plasma fresh whole blood and freeze dried plasma applications.

Follow on commercialization efforts will address the larger civilian market encompassing blood transfusions and the plasma processing industry. We continue to receive strong government funding for our research programs. In 2022, we received an additional $6.1 million in grant funding for our HemoDefend-BGA product and Phase 1 grant for CytoSorb-XL to address endotoxin removal. The backlog of grant funding is approximately $11.5 million currently, and it’s important to note that the funding is non-dilutive, providing a cost effective vehicle to advance the CytoSorb polymer platform. Product development continues to drive the DrugSorb technical manufacturing plan for finalizing packaging and validation of DrugSorb-ATR in our new facility. This work in conjunction with our clinical trial data will support our future regulatory submission and the launch of DrugSorb-ATR in the U.S. and Canada.

In conclusion, the R&D team remains focused on advancing these programs to support the development and monetization of these assets. Thank you. This now concludes my remarks. Let me turn it back to Phil.

Phillip Chan: Thank you very much, Vince. So our earnings released today covers much of this in greater detail. But just to give you some expectations for 2023. First of all, as you’ve heard today, we expect completion of the STAR-T pivotal trial in the U.S. and Canada this year with regulatory submission FDA and Health Canada to follow. We have increased visibility on the likelihood now of DrugSorb-ATR contributing to future sales should the STAR-T trial be positive. We expect the rebound in international sales growth this year with economic relief for hospitals expected throughout Europe. And we have many new initiatives to drive sales growth, including new clinical data. We are now conducting full CytoSorb production from our new Princeton manufacturing facility with an expectation of a restoration of product gross margins to the 75% to 80%-plus range.

We have been able to achieve historically. And we also expect more normalized year-over-year comparisons now that we believe that the euro has bottomed in 2022 and the fact that we did not have any COVID-related revenue or nominal COVID-related revenue in 2022. And as Christian mentioned, we will not need to make these core versus non-core comparisons next €“ this year. Last but not least, we have €“ expect to have reduced cash burn with tight control over expenses with no major capital expenditures with our current cash balance expected to be more than sufficient to drive our 2023 operating plan. With that, that concludes our current prepared remarks. Operator, please open the call up for the Q&A session.

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Q&A Session

Operator: Thank you. Our first question comes from Mike Sarcone with Jefferies. Please go ahead.

Mike Sarcone: Hey, good afternoon and thanks for taking my questions.

Phillip Chan: Hey, Mike.

Mike Sarcone: So my first one, just, as it relates to STAR-T, can you maybe talk to us about how you’re thinking about approval, timelines, post submission and top line data presentation?

Phillip Chan: Yes, thank you. Thanks, Mike. Makis and Irina, would you like to comment on that?

Efthymios Deliargyris: Sure, Phil.

Irina Kulinets: Yes. Thank you, Phil. I can comment on that. At the moment, we’re developing our regulatory strategy and would be able to inform the investment community when the regulatory strategy would be finalized. We’re still waiting for results of clinical study and we’ll be acting exactly upon receiving the favorable results.

Mike Sarcone: Okay, thank you. And just my second question you’ve talked about a continued focus on reducing OpEx and you’ve made some progress so far. Can you just elaborate, are there any areas for incremental improvement that you could streamline even further?

Phillip Chan: Kathy, did you want to take that?

Kathleen Bloch: Sure, Phil. I can take that. We’re constantly looking at making sure that we’re focused on our core initiatives and we do this in waves, right? You do one pass and then another pass and then another pass. One of the things that we did as Mike has talked about earlier, was we pause our STAR-D trial. So we can €“ we saved and estimated $4 million in costs in 2023 by just putting that trial on pause. So we’re always looking for opportunities where as we review our budget versus actual, where we have non-essential things, I can tell you that not having capital expenditures this year will save us $6.1 million. But we’re open to other opportunities as we review our operating results and our budget versus actual comparisons. I think you’ll see dramatic reductions in the burn this year. Really dramatic.

Mike Sarcone: Okay, great. Thank you.

Phillip Chan: Thanks, Mike.

Operator: Our next question comes from Josh Jennings with TD Cowen. Please go ahead.

Josh Jennings: Hi, good afternoon. Thanks for taking the questions. Phil, it was great to see you earlier this week, and congratulations again on the guideline announcement. I was hoping to just ask first on the guidelines. I think there’s be some star registry readouts as well throughout this year. And how should be thinking about, I guess, the commercial adoption ramp for drugs or ATR in the €“ maybe the second half of 2023 or maybe throughout 2023. Are these big catalysts, or is the STAR-T trial really going to be the big driver of adoption? Not only approval of adoption in the United States, but also the big driver adoption internationally?

Phillip Chan: Thanks, Josh. Micus, did you want to take that question?