Good day, and thank you for standing by. Welcome to the Biodesix Fourth Quarter 2023 Earnings Conference Call. At this time, all participants are in a listen-only mode. After the speaker's presentation, there will be a question-and-answer session. To ask a question during the session, you will need to press star one one on your telephone. You will then hear an automated message advising your hand is raised. To withdraw your question, please press star one one again. Please be advised that today's conference is being recorded. I would now like to hand the conference over to Chris Brinzey, Investor Relations. Please go ahead. Thank you, operator, and good morning, everyone. Thank you for joining us today for a discussion of Biodesix's fourth quarter and year-ended 2023 business highlights and financial results. Leading the call today will be Scott Hutton, Chief Executive Officer. He will be joined by Robin Harper Cowie, Chief Financial Officer. After the prepared remarks, we will open the call for Q&A. An audio recording and webcast replay for today's conference call will also be available online, as detailed in the press release announcement for this call. Today, we issued a press release announcing our business highlights and financial results for the fourth quarter and year-ended 2023. A copy of the release can be found on the investor relations page of the company's website. Actual events or results may differ materially from those projected as a result of changing market trends, reduced demand, and the competitive nature of the diagnostics industry. Such forward-looking statements and their implications involve known and unknown risks, uncertainties, and other factors that may cause actual results or performance to differ materially from those projected. The forward-looking statements discussed on this call are subject to other risks and uncertainties, including those discussed in the Risk Factors section and elsewhere in the company's annual report on Form 10-K for the year ended December 31, 2023, which was filed today with the Securities and Exchange Commission. Additional information concerning factors that could cause results to differ materially from our forward-looking statements are described in greater detail in the company's press release issued today and in the company's filings with the SEC. This call will also include a discussion of non-GAAP financial measures, which are adjusted to exclude certain specified items. A reconciliation to the most directly comparable GAAP financial measure is available in the press release we issued today. I would now like to turn the call over to Scott Hutton, Chief Executive Officer. Scott? Thank you, Chris. Happy to share that 2023 was a great year of execution at Biodesix. We've been focused on three goals: driving increased revenue through the adoption of our lung diagnostic test and our biopharma and diagnostic services, implementing operational efficiencies to improve gross margins, and maintaining a strict cost discipline. In 2023, we delivered approximately 38,700 lung diagnostic tests, which represents 65% growth over 2022. We increased our gross margins over the course of the year to 77%, and we improved our fourth quarter Adjusted EBITDA by 55% over the comparable period. Our team and culture have never been stronger, and you see that strength reflected in our results. I want to express my sincere gratitude to our team for their hard work and dedication to improving the lives of patients and the healthcare professionals that serve them. Our top priority remains the ongoing adoption of our five blood-based tests for patients with potentially cancerous lung nodules and those with lung cancer. This past quarter, we delivered approximately 10,900 test results, reflecting growth of 54% as compared to the approximately 7,100 test results delivered in the fourth quarter of 2022. This is the sixth straight quarter of at least 50% year-over-year growth, primarily driven by our Nodify CDT and XL2 lung testing volumes. Lung nodule management is by far the largest market we serve and will continue to be the largest driver of lung diagnostic test volume growth. Our industry-leading commercial team was responsible for driving this outstanding growth in 2023. We continued to invest and expand our organization throughout the year, finishing with approximately 50 fully trained representatives, with an additional 10 that came on board late in quarter four. On average, our sales representatives begin paying for themselves within 2-3 months. Therefore, we expect these new teammates to begin contributing in the first quarter of 2024. We also validated the benefit of adding associate sales consultants into existing territories, working alongside established team members to improve account retention and penetration while building a bench for future expansion. As a result, 2024 will see an ongoing expansion that includes splitting existing territories into more manageable geographies as the business grows, with an increase in the number of territories holding both a sales consultant and an associate sales consultant that will accelerate adoption within those territories. In the second half of 2023, the publication of the primary endpoint for the ORACLE prospective registry study was published. The data showed that use of the Nodify XL2 test resulted in a 74% reduction in costly and unnecessary biopsies and/or surgeries on patients with benign lung nodules. In addition to this data, an independent group of academic medical centers published a 73% reduction in unnecessary procedures... clearly demonstrating the clinical utility of Nodify in the real-world clinical setting. Peer-reviewed publications such as these are critical to help expand physician adoption of our test, as well as expanding payer coverage. In addition to the growth in volumes driven by our sales team, broadening reimbursement coverage remains an important part of our growth strategy. In July, the Nodify CDT test was awarded Advanced Diagnostic Laboratory Test, or ADLT status, by the Centers for Medicare and Medicaid Services. Receiving ADLT status is a major milestone for the Biodesix team, as this is reserved for innovative tests with Medicare coverage that provide clinical value and new diagnostic information that cannot be obtained from any other test or combination of tests. The ADLT status is a public recognition of unique clinical utility. Nodify CDT joins Nodify XL2 and VeriStrat in having received that important classification. In late fourth quarter, Geisinger Health Plan issued a positive coverage decision for Nodify Lung testing, including both the Nodify CDT and Nodify XL2 blood-based proteomic test. Geisinger Health Plan was the first commercial plan to cover Nodify CDT. The combined coverage of both Nodify CDT and Nodify XL2 testing recognizes the importance of these tests in assisting healthcare professionals in lung nodule management to help improve patient outcomes. Moving on to our biopharmaceutical services business, we generated exceptional momentum in the second half of the year, with more than 35% year-over-year growth in each of the last two quarters. We are encouraged with the strong growth this quarter and are pleased to see an increasing number of samples received from several different biopharma companies running multiple clinical studies and an increasing number of incoming RFPs and opportunities. In addition, our team continues to deliver on test process automation and workflow optimization projects that have driven a steady increase in gross margins over the course of 2023, ending the fourth quarter with 77% gross margin, an increase of 11 points over fourth quarter of 2022. We've been exceptionally effective in providing our tests with industry-leading turnaround times and have made great strides in becoming even more efficient in the delivery of those tests. Finally, our commitment to a cost-disciplined approach while growing and expanding the business continues to deliver tangible results. Adjusted EBITDA in the fourth quarter improved 55% over the same period in 2022. We've built a commercial and operational platform that will help facilitate long-term, consistent, sustainable growth, and I believe everyone is beginning to appreciate the leverage that exists within the business model and our efforts to demonstrate the team's significant progress and outstanding execution on our path to profitability. Before I turn the call over to Robin, I'd like to reiterate our commitment to transform the standard of care in lung cancer and improve patient outcomes with personalized diagnostics. Lung cancer is still the deadliest of all cancers, as it claims more lives annually in the United States than the combined total of the next three deadliest cancers: breast, prostate, and colon cancer. Time is of the essence when it comes to diagnosing and treating these patients. By discovering, developing, and commercializing tests with demonstrated clinical utility and best-in-class turnaround times, we believe that our diagnostic tests play a critical role in these efforts to treat the right patients quickly and effectively. With that, let me turn it over to Robin to review the fourth quarter and year-end 2023 financial performance. Thanks, Scott. Fourth quarter total revenue was $14.7 million, a 53% increase over the prior year. Full year revenue in 2023 was $49.1 million, a 49% increase over prior year, excluding 2022 COVID revenue of $5.2 million, and a 28% increase over full year revenue in 2022, including COVID revenue. As Scott mentioned, we delivered approximately 10,900 lung diagnostic test results in the fourth quarter, up versus approximately 7,100 test results for fourth quarter 2022, and approximately 38,700 lung diagnostic test results for full year 2023 versus 23,500 test results for the full year 2022, a 54% increase and 65% increase, respectively. Test volume in the quarter was our 6th straight quarter of at least 50% year-over-year growth. Lung diagnostic revenue in the fourth quarter was $12.8 million, compared to $8.2 million for the fourth quarter of 2022, an increase of 55% over prior year. Lung diagnostic revenue for the full year 2023 was $45.1 million, a 54% increase over the full year 2022. As we've discussed in prior earnings calls, we continue to experience delays in some Medicare Advantage payments for our Medicare-covered tests from certain payers. While we continue to work with the plans to resolve the administrative hurdles, the backlog continues to grow and ended the year at approximately $3 million-$3.5 million, up from $2.5 million-$3 million reported in our third quarter earnings call. We will continue to provide updates in our calls as we work towards a satisfactory resolution. Biopharmaceutical services revenue was $1.9 million in the quarter, compared to $1.35 million in the fourth quarter of 2022, and $3.9 million for the full year 2023, compared to $3.7 million for the full year 2022, an increase of 38% and 6% over the respective prior year comparable periods. As a reminder, this business can fluctuate due to several factors, including contract timing and project execution. While we had a strong quarter, we did experience a delay in the receipt of samples for a large project, resulting in approximately $600,000 in revenue, pushing from the fourth quarter into the first half of 2024. Overall, we ended the year with $7.9 million contracted, but not yet recognized as revenue. The decrease in contracted revenue from the third quarter is something we typically see as we complete contracts and record higher revenue totals like we did in the second half of the year. However, it's important to note that the number of incoming requests have continued to be strong in the first 8 weeks of 2024, and we have a robust pipeline. Since the beginning of the year, we have signed new contracts and increased our total dollars under contract, but not yet recognized, to $9.1 million as of today. Gross margin percentage in the fourth quarter, 2023, increased to 77% versus 66% in the prior year quarter, and 76% in the third quarter of 2023. Current gross margin trends reflect the growth in our lung diagnostic testing and successful completion of projects to decrease costs and optimize testing workflows. The steady improvement across 2023 resulted in full-year gross margins of 73% versus 63% for the full year 2022. We anticipate the ability to maintain margins in the mid-70s going forward. Overall operating expense, excluding direct costs and expenses, was $18.2 million in the fourth quarter 2023, compared to $20.2 million for the same period of 2022, and $17.4 million in the third quarter of 2023. The decrease in operating expense versus the prior year quarter is primarily the result of a decrease in R&D expense and G&A, partially offset by increased sales and marketing costs to support lung diagnostic sales growth to enhance product awareness and drive adoption. Total operating expenses, excluding direct costs and expenses for the full year 2023, were $77.4 million versus $74.6 million in 2022. For the full year 2023, the slight increase as compared to the prior year period is related to increased sales and marketing expense, partially offset by the realization of savings from our prioritization of projects that are expected to result in near-term revenue and the delay of longer-term projects. Operating expense for the fourth quarter 2023 includes $1.1 million in non-cash stock compensation expense, as compared to $2.1 million during the fourth quarter 2022. For the full year 2023, non-cash stock comp expense was $5.4 million, compared to $6.0 million for the full year 2022. Net loss for the fourth quarter 2023 was $9.1 million, compared to a $20.3 million net loss for the same period of 2022, and $10.9 million for third quarter 2023. Net loss for the full year ended 2023 was $52.1 million, compared to a $65.4 million net loss for the full year 2022. The decrease in net loss for both the quarter and the full year was driven primarily by the increase in revenue, improvements in gross margin, and reduction in certain operating expenses, including R&D expense, as well as a reduction in non-cash stock-based compensation. Fourth quarter and fiscal year 2023 included a gain of $0.1 million and loss of $1.3 million, respectively, from the change in fair value of warrant liabilities associated with our term loan facility with Perceptive Advisors. While fourth quarter and fiscal year 2022 included a one-time loss of approximately $4.0 million and $7.0 million, respectively, for the extinguishment of debt. To provide better clarity of progress on our path to profitability, during the third quarter, we started reporting Adjusted EBITDA, which excludes certain non-cash items and COVID-19 testing revenue and direct costs and expenses. Adjusted EBITDA for the fourth quarter, 2023, was a loss of $4.9 million, compared to a loss of $10.8 million for the fourth quarter, 2022, a 55% improvement and 11% improvement over the third quarter of 2023. Adjusted EBITDA for the full year, 2023, was a loss of $32.7 million, compared to a loss of $43.2 million for full year, 2022, and a 24% improvement. The improvement in Adjusted EBITDA in both the fourth quarter and for the full year demonstrates our focus on actively managing our operating expenses, our success in improving gross margins, and driving growth in top-line revenue, resulting in a decrease to our cash burn. We ended the year with $26.3 million in unrestricted cash and cash equivalents, as compared to $19.8 million at the end of the third quarter, an increase of $6.5 million, which included the addition of the remaining $12.2 million from the $27.5 million private placement announced in August, and $10 million that was drawn from the second tranche of our $50 million term loan facility with Perceptive Advisors. This was offset by our Integrated Diagnostics milestone payment of $3.5 million, an additional $3 million for one-time CapEx used to complete work on our new facility, which is now fully operational, and cash used to fund operations and working capital. I do want to remind you of a required shift in the display of the milestone payments to Integrated Diagnostics on our statement of cash flows. As I mentioned last quarter, payments made through the third quarter of 2023 have been classified as cash outflows from financing activities in our statement of cash flows. However, beginning with a portion of the milestone payment made in the fourth quarter, as well as all milestone payments to be made in 2024... These payments are now classified as cash outflows from operating activities due to the applicable U.S. GAAP requirements. For clarity, the dollar amounts are not changing, just where they are required to be captured on the statement of cash flows. Finally, turning to 2024 guidance. We plan to deliver $65 million-$68 million in total revenue, driven primarily by growth in lung diagnostics, with modest increases from our biopharma services offerings. This guidance does not include any expected revenues from the Medicare Advantage backlog. Now let me turn it back to Scott. Scott? Thanks, Robin. We've again achieved impressive and high double-digit growth in the past quarter, attributed to the exceptional performance of our consultative lung-focused commercial team, who've been instrumental in fueling our success. We've improved our already strong gross margins and made substantial progress on our path to profitability. 2024 is a year of execution on our three goals: driving increased revenue by accelerating the adoption of our lung diagnostic tests and biopharma services, implementing operational efficiencies to improve gross margins, and maintaining a strict cost discipline. By aligning these three strategic efforts, we're confident in our ability to sustain our aggressive growth trajectory, make progress on our path to profitability, and deliver value to the healthcare professionals, their patients, and all shareholders. We are transforming the standard of care and are excited to be making such a significant impact. Finally, we've completed the move into our new 80,000 sq ft, state-of-the-art corporate office and clinical laboratory in Louisville, Colorado. We believe this new facility provides another competitive advantage as it enables us to grow and expand in an efficient and effective manner. With that, I'll turn the call over to the operator for questions. As a reminder, to ask a question, you'll need to press star one one on your telephone and wait for your name to be announced. To withdraw your question, please press star one one again. Please stand by while we compile the Q&A roster. Our first question will come from the line of Andrew Brackmann with William Blair. Hi, Scott. Hi, Robin. Good morning. Thanks for taking the questions. I have a few. Maybe just start here on revenue guidance for the year. Nice to see that solid growth outlook that you, that you talked about, but can you maybe help parse out some of the build there? I guess I'm just looking for things related to sort of rep adds, utilization increases, new accounts, revenue per test. Any color there might be appreciated. Thanks. Yeah. Good morning, Andrew. Thanks for the question. Yeah, you know, we talked a lot about sales force expansion and growth, and as you've just heard, we exited the year right at about 50 sales reps contributing. We're going to continue to grow and expand that sales force. What we do know from a past performance and obviously a modeling perspective, we've seen our sales professionals come on and start to pay for themselves in about 3 months. The one thing we're mindful of is as we continue to expand into territories where we haven't had representation prior, that ramp may be a little bit slower. And then as we look at promoting associate sales consultants into open territories, which we've done, we had five that we promoted towards the end of the year, which really demonstrates that our plan and approach is working. We still know that those are going to be junior, young sales professionals. So, we've really looked at this, trying to improve forecast accuracy, ensure that we put them in a position to succeed. What we've seen from a sales rep productivity number really is we can get them into that $750,000-$1 million per rep in a pretty reasonable timeframe. One of the things we've disclosed in the past is, we have seen some sales professionals get north of $1.5 million per rep, but we cut their territories, so we were never really striving to see, you know, could we get them to $2 million? We wanted to make certain that we could cut territories and then demonstrate that they could grow again. We just wrapped up our national sales meeting, Andrew, and share this with you. We have a back-to-back top sales rep of the year. What makes that most remarkable is two years ago, she won with an associate sales consultant. At the end of the year, we split her territory, promoted the associate sales consultant into one half of that territory. They both finished in the top five. So what we've really proven out is we can go deep. I use the word consultative. I think the more we put our sales professionals in healthcare professional offices, they're going to find that we are consultative, we bring tremendous value, and the value of our test, the clinical value of our test, isn't really questioned. So again, we haven't seen where we can cap out on that sales rep productivity number just yet. So we factored all of the past performance into modeling, really what we think in that guide range is achievable for us this year. Is that helpful? Very helpful. Thanks for, thanks for all that color. I guess related to sort of the outlook here, you're making really nice progress on the margin front and sort of reducing operational burn. Can you maybe just sort of talk about how we should think about further reductions in that burn metric this year and the sort of leverage that you expect in the model throughout 2024? Yeah. You know, Andrew, you've actually been out here, and you've seen the facility. The new facility really should empower us to continue to make some improvements. We've focused over the last 3-4 years on workflow and operational efficiencies. And obviously, we've made those and achieved those. One of the things most may not appreciate is that the old facility was really constructed for one product in the laboratory. And so we ran out of space. We were limited in what we were able to do. Moving into the new facility gives us the ability to, you know, to move forward with growth and expansion in mind. So we think that we're set up to continue to improve that. We're also mindful that we believe we've got industry-leading gross margins. We're aware of one, maybe two other diagnostic companies that are in the ballpark, maybe slightly better. So we also want to be realistic. We're still forecasting for modest improvements there to take us into that mid and keep us in that mid-seventies range. Yeah, from an operating expense standpoint, it remains one of our top goals and focus for 2024. Maintaining that strict cost discipline, being very efficient and effective with our cash, to keep driving down our overall burn and make continued progress on our path to profitability. That's great. And then maybe if I could just a bigger picture question here. You know, it's been a couple of years since USPSTF updated their screening guideline. We should hopefully get some sort of update on the development of quality measures there for screening later this year. So I think it's sort of safe to say there's going to be a lot of tailwinds and nodule identification over the next couple of years. For Biodesix in particular, you know, aside from continuing to invest in that commercial team, I guess, can you talk about some of the things that are in your control to really ensure that you're going to be that go-to solution for nodule management as all these tailwinds sort of play out here over the next few years? Thanks. Yeah, it's a really insightful question, Andrew. Thank you. Yeah, I think you're right. We're all eager to see what USPSTF change in screening guidelines does and what that impact is. You know, obviously, everybody's got their fingers crossed that it improved those numbers and that we see more early detection and diagnosis. Because we're dealing with the deadliest of all cancers, we know right now that the first thing that will improve outcomes is that early detection and diagnosis. So we'll eagerly sit back and wait for that. We also know, and we've seen what the HEDIS measures did in breast cancer, and so right now, we're anticipating HEDIS measures for lung cancer to go into effect in the third and fourth quarter of this year. That'll also continue to drive not only increased awareness, but hopefully it helps drive broader adoption of nodule management clinics, screening programs. So for us, as you, as you referenced, the expansion of our sales force is not just about hiring new sales professionals, it's empowering them to partner with those healthcare professionals and clinicians to work on nodule management programs. And so we spend a lot of time in peer-to-peer education, where some physicians will share their experiences on nodule management programs, their experiences with patients that have been identified through a screening program. So, we're collaborating across this entire care continuum, and we think that's one of the ways that not only will we become a trusted partner, but that this becomes sustainable, right? It's not just about driving test volume adoption. It's about building relationships and partnering to make the biggest impact we can in the deadliest of all cancers. All right. Thank you. I'll leave it there. Thanks, Scott. Thanks, Robin. Thanks, Andrew. Our next question will come from the line of Kyle Mikson with Canaccord Genuity. Hey, thanks. Congrats on the year. Robin, two questions for you to start on financials. On working capital, I think, like, current assets, such as accounts receivable, stepped out materially in Q4. Just wondering why that was and anything to read into in terms of how net working capital and cash conversion cycle could kind of progress in the near term. And then secondly, could you, you probably did this, but could you quantify the MA backlog in terms of revenue? Like, you know, either revenue or volume, I guess that'd be, that'd be helpful just to kind of understand how to, you know, the apples-to-apples comparison in this guidance year. Thanks. Yeah, absolutely. And good morning, Kyle, and thanks for the questions. Working capital did see a step up towards the end of the year. We do typically see that in fourth quarter, just from timing and holidays. We see insurance companies slow down a little bit towards the end of the year. But also with the increase in test volumes, we do expect an increase in AR. There are no delays or anything of concern to be aware of. About the Medicare Advantage backlog, it's really just a couple of Medicare Advantage companies. The rest are paying quite well and on time. It is now about $3million-$3.5 million worth of backlog. That's up about $500,000 from the fourth quarter, or sorry, from the end of the third quarter, so that increased in the fourth quarter. We removed all of that from our guidance for 2024, so we do not have any anticipated collections on the backlog included in our guidance. We also remove any anticipated collections from current claims from those impacted health plans, from the guidance as well, to try and minimize any sort of variability that you see in our revenue. Now, obviously, that means if we're able to get to rapid resolution there, that we should see some upside, and we are working diligently with those plans to get these administrative hurdles resolved. So once we have anything more to share on that, we will be very happy to share it. Yeah, that was great. Thanks so much, Robin. And then, Scott, one for you on, I guess kind of, some of the legislation kind of guideline stuff out there. So the first is on the biomarker legislation. You know, obviously, expanding private payer, commercial payer coverage has been kind of an ongoing effort for you. You have these biomarker laws that could really, like, kind of deepen your penetration, possibly in that, in that segment, produce the heavy lifting for you. So is, is that fair to say? I mean, I think Colorado is going to be evaluating that legislation this year, I believe. So is that a tailwind, or, or not, I guess? And then just secondly, I think NCCN has this new concurrence, tissue and, blood-based testing, you know, guidelines for-- recommended guidelines for lung cancer. I mean, does that affect you at all? I'm just wondering if these things are maybe like drivers of performance, like in this year, that wouldn't be affected or included, I mean, in this guidance range. Yeah. Good morning, Kyle. Great questions. You know, I'll start with the last. Definitely there is an opportunity for us there in the tailwind, especially on our IQLung portfolio of the franchise, where we offer two genomic blood-based tests and then our proprietary VeriStrat test, where we measure a patient's immune system status or ability for the immune system to respond to that tumor. You know, for us, it does create an increased awareness. We have the most rapid turnaround times for those tests. And I think some aren't quite aware, we actually do offer tissue testing to our biopharma partners, so that fits squarely kind of in our wheelhouse. I think on the individual state biomarker bills, I think Robin may be the best to provide an update on that, and I'll turn it over to her. Yeah, it's a great question. There have been a lot of biomarker bills passed over the last couple of years, with Louisiana, Arizona, Illinois leading the way. You're right, Colorado is considering it in this legislative session. We really look at this as maybe a door opener. They are focused on the payers and trying to help get more rapid payer coverage for tests that have been proven and have, you know, Medicare coverage or other reviews that prove that the tests have clinical utility. Our team are actively working with health plans in the states that the bills have already gone live, and we'll see how that turns out. The big question is, most of the states have not yet implemented the regulations that will dictate how they will require the coverage and how it will be enforced. So it's really a work in progress, but it's something we're tracking very, very closely. Okay. Actually, on that note, would... You know, since, you know, NCCN guidelines was so important for the private payer, commercial payer segment, would this kind of, you know, reduce the need to get into guidelines or kind of even negate that, kind of push by you? Yeah, it's a really good question. You know, I think we're approaching it as if it won't negate it. I think for us, getting into the guidelines, whether that's NCCN, ACCP, Fleischner, that really would be a great tailwind for us. As we've stated before, ACCP, which is the CHEST guidelines, would be the most appropriate for us. You know, this is where developing and presenting the best data possible, and as you get that out there, enabling and empowering physicians to make the right decisions. You know, we've highlighted historically that CHEST or ACCP has been delayed. They're behind. So they've made very few actual updates for lung nodule management and lung cancer detection and diagnosis in the last couple of years. So, if we can agree that they're behind, it's really a matter of when do they catch up and then how broadly do they go in updating those guidelines. NCCN, right, is gonna be slightly more on the treatment guidance front, which could benefit us on our IQLung. So we're gonna continue to fuel that by funding studies, producing and publishing the best and highest quality data possible, and working with those private payers to make certain that if they have questions, we're answering those questions with data. Okay. That was great, Scott. And there's one more before I hop off about the, the portfolio, the product portfolio. So I think the, the pipeline tests were not mentioned possibly at all in the prepared remarks. Maybe just like, you know, either update us on these tests, like at the MRD tests or, or, or PIR or anything like that, and then maybe, like, we should expect any, any news or updates this year or next year, possibly from, from those assets. Yeah. Thanks, Kyle. Yeah, just as a reminder for everybody, we have three products in our pipeline. We have a Primary Immune Response test, where we're able to identify those patients that will respond favorably to an immunotherapy regimen. We also have Risk of Recurrence, which is a pre-surgical resection blood-based test, where we can identify those patients with the highest likelihood of recurrence. And then MRD would be our post-surgical resection blood-based test, where we can identify those patients with minimal residual disease who are also likely to recur. We believe we'll be the first company to have both a pre-surgical and post-surgical blood draw that can help identify those patients with the highest likelihood of recurrence. that those two tests would cover both, kind of a multi-omic approach, both proteomic and genomic. Given our prioritization of kind of progressing towards profitability, Kyle, we've slowed commercialization of those, so we're not planning on launching any of those three tests here in 2024. I think everybody understands when you first launch a test and you have to build kind of that experience and that data, oftentimes those are no-pay tests. So for us, ensuring that we've got a path to reimbursement for those will help guide us in our timelining, timeline of commercialization. We'll continue to provide updates as we progress. I wouldn't anticipate hearing much on the risk of recurrence or primary immune response front. We've already, you know, discovered, developed, and validated those. Those are still being offered for biopharmaceutical partners in a research use only basis. The MRD project, though, I fully expect we'll be providing updates here in the coming weeks and months as we continue to progress and collaborate with Memorial Sloan Kettering. They've been a tremendous partner, and I think what you'll find is working together collaboratively, we believe that this is an engine that will enable us to fuel future growth and potentially add additional products in addition to the MRD product. Okay. Have these pipeline tests been driving some of the biopharma revenue recently, or could that be upside going forward? It definitely is upside. Yeah, we offer them, Kyle. It really is dependent upon the different biopharmaceutical companies, their studies, you know, the critical questions they're trying to answer that they think we can help them answer. It was not, or those two were not the big drivers in the fourth quarter. We saw a tremendous amount of continued interest in our really our treatment guidance portfolio. So everything within IQLung, you know, the GeneStrat ddPCR, the GeneStrat NGS, and the VeriStrat test. Those were the big drivers of biopharma interest. And I think fair to say that early in 2024, it continues to be that way. A lot of interest. We're making a lot of progress on numerous fronts with a handful of major biopharmaceutical companies. Mm-hmm. Yeah, thanks, Scott. Thanks for having me. Appreciate it. Yeah, thank you, Kyle. Our next question will come from the line of Tejas Savant with Morgan Stanley. Hi, team. Good morning. Thanks for taking the questions, Madison on for Tejas. I was just wondering, to start off, with lung diagnostics volume growing at about 65% in 2023, driven primarily by Nodify Lung testing. Just wondering how sustainable you think that growth is as we start to see tougher comps, year-over-year in 2024? Yeah. Hi, Madison. Good morning. Great, great question. You know, for us, it's really a factor of the number of sales professionals we have, the opportunity within the territories we place them, and in some cases, whether that territory and sales consultant has an associate with them. You know, with 6 straight quarters of greater than 50% growth, that's really the bar that we've established and the goal that we've challenged the team to, to kind of, you know, hit and exceed that growth performance. We stated that we hired 10 additional sales professionals at the end of 2023. The nice thing is, is based upon our track record, we know that within about 3 months, they're gonna be paying for themselves and contributing, and so, we did that with that goal in mind. We really wanted them to be, you know, hired, trained, onboarded, out in the territory and fully capable of contributing as soon as possible in 2024. So we'll continue to invest in the sales and commercial channel expansion. Historically, we've hired approximately six sales reps per quarter. Obviously, we shared that we hired 10 in the fourth quarter, so we've demonstrated we can increase that number. We just wanna be very mindful of that expense and cash burn, and making certain that we set them up for an immediate or a near-term return. So we believe that we can continue to achieve those strong numbers. You're spot on. As we've continued to grow, the year-over-year comps become more and more challenging. It would be really challenging if we were static and not continuing to expand the sales force. We still know that there's a number of pulmonologists that we haven't reached, because of our limited coverage. And we also know that we're less than 1% penetrated into this market opportunity, and it's a massive opportunity. So we feel confidently we can continue to grow, expand, invest in that commercial channel, and that we'll see a return on that investment. Got it. Okay, that makes sense. I think you previously talked about an interim analysis for the ALTITUDE study. I was just wondering if we should be expecting to see some data from this sometime this year? Yeah. So as a reminder, ALTITUDE is our prospective randomized trial for Nodify, that's being conducted at a number of major academic institutions in North America. We implemented a DSMB, a Data Safety Monitoring Board, in 2023. So the nice thing about that, Madison, is it - an interim analysis is really out of our control. The Data Safety Monitoring Board will help guide that and direct that, and they're meeting on a quarterly basis. So that select group of individuals will come together again in March, and then I believe June is the following meeting. So I think we'll learn more as we progress through those meetings. At this point in time, we're not anticipating an interim analysis, but what I am able to share at this point in time is, we have seen enrollment improvement and increase over the last 18 months, kind of exiting the pandemic. And we've actually brought on a few additional academic institutions. So we feel confident that this is gonna continue to be a meaningful data relief. It's still just a question of when the Data Safety Monitoring Board and the primary investigators deem that to be necessary. If we were to do something this year, it would be at CHEST in that October-November timeframe. So we'll learn more, and you can expect greater insight into that in the following earnings calls. Got it. That makes sense. Thanks so much for the time, guys. I'll hand it on over. Great. Thanks, Madison. That concludes today's question and answer session. I'd like to turn the call back to Scott Hutton for closing remarks. Thank you, operator. We've worked long and hard to build the best pulmonology-focused sales team in diagnostics, and believe that this is just the beginning of our growth, as we just scratched the surface with less than 1% penetration of this addressable market. With first mover status in lung nodule management and an ever-increasing body of robust clinical data, we're building the momentum we've already created as we increase our clinical and payer adoption in this extremely large and underserved population. Ultimately, it's all about healthcare professionals and the patients they treat, and we believe in our ability to make a more significant impact in the future. This year, we delivered 65% lung diagnostic test volume growth, saw a return to growth in our biopharma services business, expanded our sector-leading gross margins to the mid-seventies, and improved Adjusted EBITDA by 24%. At Biodesix, we have a culture of teamwork, quality, and execution, and constantly work to deliver on our goals to increase our reach and adoption and improve our operational effectiveness and efficiencies on our path to profitability. 2024 is a pivotal year of execution, and we look forward to updating you on our continued progress and success on the next earnings call. Thank you. This concludes today's conference call. Thank you for participating. You may now disconnect.