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Alright, everyone, and welcome, everyone. And thank you for joining us to discuss Insight Molecular Diagnostics third quarter 2025 results. If you have not seen today's shareholder letter, please visit Insight Molecular Diagnostics Investor Relations page at investors.imdxinc.com. Today's prepared remarks build upon the information already shared in this robust letter. Joining us today are Insight Molecular Diagnostics President and CEO, Josh Riggs, Chief Science Officer, Ekke Schutz, and CFO, Andrea James. We also have our analysts with us as panelists. After our prepared remarks, our analysts may ask questions. Before turning the call over to Josh Riggs, I'd like to go over our safe harbor. The company will make projections and forward statements regarding future events. Any statements that are not historical facts are forward-looking statements. These statements are made pursuant to within the meaning of the safe harbor provision of the Private Securities Litigation Reform Act of 1995. We encourage you to review the company's SEC filings, including the company's most recent Form 10-Ks and subsequent Forms 10-Q, which identify risks and uncertainties that may cause future actual results or events to differ materially. Please note that the forward-looking statements made during today's call speak only to the date they are made, and Insight Molecular Diagnostics undertakes no obligation to update them. And with that, I would like to now turn the call over to Josh Riggs.

Thanks, Gabby, and welcome, everybody. If you've had a chance to look at our shareholder letter, you'll have seen that our momentum is building. I'd like to talk a little bit about how we got here before shifting to how we are positioning ourselves for success in 2026. A couple of years ago, we set out to change how transplant patients are managed. The idea was and is simple. Transplant centers should have the tools on-site to monitor their patients. Intuitively, that makes a lot of sense. Each year, hundreds of thousands of tests, hundreds of millions in payments go out for post-transplant monitoring. As of today, not one of those tests is performed at a transplant center, and not $1 of reimbursement accrues to these centers' benefit. In 2026, with the expected FDA authorization of GraftAssure DX, this is going to change. Last summer, we started a pilot program that put a research version of the assay, the same design we were taking to the FDA, in the hands of researchers around the world. We wanted to do three things. One, get feedback on the workflow so that we could get ideas on what needed to be improved. Two, get technical data on the performance of the assay so we could have a sense of how robust our design was in the field. And three, engage with clinician researchers so we could get a look into what clinical demand might be for a regulated product. Feedback from transplant centers' labs helped us optimize our test workflow from two steps down to one step. That improves our turnaround time and ease of use, which means faster results with less labor for our customers. As you probably recall, our PCR-based technology is already much simpler and faster than sequencing-based technology used by major centralized labs. With our one-step workflow, we have further increased these advantages. Just last month, we published a white paper that showed that our performance across multiple centers from Singapore to Switzerland had exceeded expectations. You can find this white paper on our website. This gives us high confidence that the assay will perform well in the very rigorous FDA process. Across the board, in the U.S. and Europe, we are feeling pent-up demand for in-house testing. Because we are a kit-first company, we are seen as a partner in patient management, and institutions are eager to support our mission of broadening access. I should point out that just getting through the FDA is not enough to give us the market. The expectation is that clinicians will want to familiarize themselves with GraftAssure and compare it to legacy technology before making a switch. This could look like head-to-head comparison or interacting through the registry program we recently announced. Case in point, earlier this year, we saw data come out of Heidelberg, a research transplant center in Germany, where they compared the performance of our test to another commercially available RUO assay that is on the market in Europe. This data showed statistical equivalence on the relative measure of ddCF DNA between the two tests. It's great because the market today is largely dominated by the relative measurement method. Showing that we get to the same answer with an easier-to-use technology reduces the barriers to adoption. Recently, we've also seen preliminary results from a 100-plus patient study at a major center here in the U.S. that is a direct head-to-head against a leading U.S. centralized lab test. We and the researchers are very happy with those results. Showing that you can get equivalent to better results with on-site technology is critical to our success. There are more of these types of studies ongoing, and we expect that data will start coming out in the new year that shows clearly that GraftAssure is reliable and that it compares well to legacy technology. The feedback we get from transplant centers, primarily in the U.S., is that they are optimistic about being able to bring testing in-house, but fully expect that some level of head-to-head work will be needed to fully support conversion and internal adoption within their center. We welcome this activity. The more data that gets out there showing positive comparison to cumbersome legacy providers, the faster we'll see broad adoption. Alongside the generation of head-to-head data, we announced the launch of a registry program. The goal of this program is to capture how the industry uses our alternative measurements of ddCF DNA, namely absolute quantification and our proprietary combination model score algorithm, while they use our currently available relative measurement for patient management. The benefits of this approach in our registry are twofold. Firstly, it familiarizes clinicians with our report and test, probably making them more likely to use the technology once it's available in-house. And secondly, it generates real-world data on the utilization and performance of our alternative measures. Early data and publications suggest that these alternative methods may be superior ways of quantifying and analyzing the ddCF DNA data. If we are successful, we should see improved biopsy yield at transplant centers that are using the combination model score because of its expected higher positive predictive value. When the Centimeters score data first came out at the World Transplant Congress this summer, we saw an immediate spike in interest from our clinical partners. So we've been moving as quickly as possible to get the novel score into production. I expect that we will see the first reports going out with the new Centimeters score in 2026. Early access is likely to be limited to participants in the registry. Once the peer-reviewed publication is out, we will start to make it more broadly available and begin a conversation with MolDx on any potential positive billing impact. I'm amazed by the progress we made in such a short time. That is attributable to our team of researchers and development scientists, clinicians, and centers around the world that have embraced our partner-first approach and the strong support from Bio-Rad, who have been with us every step of the way in our planning engagement with the FDA. And now, after almost three years of absolutely grinding on product development with a modest staff, we are in November 2025, very close to our planned FDA submission. While the shareholder letter details our recent accomplishments and our FDA submission timeline, I'd like to add some color on our clinical trial. You can really feel the energy at the sites right now. They're excited. They're engaged. We love to partner with them. Tampa General was the first to bring in samples, and Vanderbilt and Cleveland Clinic were up and running shortly thereafter. These are leading transplant centers in the U.S., and they are genuinely committed to this effort, and that makes all the difference for us. Some of you may have recognized this sentiment in the comments from Dr. Anthony Langone of Vanderbilt University on our August 15 KOL call. He pointed out the issues with the current paradigm of send-out transplant monitoring, many of which can be resolved with in-house testing. Now I'm gonna take a few moments to talk about what's going on at the FDA. After our planned submission in December, we start the clock on their review process, which is listed as 150 days on their website. That being said, the FDA is not accepting new submissions while the government is shut down. We have been told that our FDA reviewer team is still working through the shutdown, which is good for clearing their docket and review backlog. At the same time, the FDA has paused answering questions from companies like ours that are preparing a new submission. It's common for companies like ours to ask the FDA questions on their preferences and what they would like to see. We do have some outstanding questions that we asked in September. Since the government shutdown on October 1, we have not received those answers. We are staying focused on what we can control, which is completing our clinical trial and being ready to submit to the FDA by the end of the year. I want to make clear that the government shutdown does not affect our ability to drive engagement with customers. We can process tests at our Nashville CLIA lab and pursue our registry study even while the government is closed. Looking forward to 2026, we expect to move forward with validation of both heart and lung assays in our lab. That work sets us up to submit for reimbursement for heart in 2026 and lung in 2027. The nice part is that for heart and lung, we can leverage all of the analytical work already done for kidney when we go to the FDA, which really streamlines the regulatory submission process. We are excited about Heartnext. You'll see a chart in our shareholder letter that showcases our assay versus legacy technology regarding the threshold for rejection detection in heart transplant patients. We are in the rare event detection business, and so lower on the bar chart is better. Being able to quantify at low volumes matters when you need to establish a trend line prior to reaching the clinical threshold. We've also made real progress on our registry study, which we announced in September. The study design is complete, the protocol is written, and we already have 10 centers, including three of the top 10 programs in the country, lined up and working their way through legal. We expect that you'll see the registry study show up on clinicaltrials.gov early next year. As we approach FDA submission, I believe the excitement around our company is building. This excitement extends to other companies with whom our products and services are symbiotic. We continue to be thrilled with our relationship with Bio-Rad, which has been mutually supportive and productive. And we continue to pursue strategic relationships that can support our increasing reach and need to scale as we go into 2026. We've been a development-only stage company for the past two to three years, and that period of time is coming to an end. Now we are focused on shifting into a commercial organization. We believe we are building a product that is going to be the de facto standard of care assay. We also have opportunities to grow the pie. There are developments changing the structure of the market itself. We see tailwinds when we look at the potential for reference lab adoption, anti-CD38 approval, and ddCF DNA guideline adoption. We believe we are bringing to market the most precise testing for transplant rejection while broadening access to the test for patients. The margins available to us in GraftAssure, along with a highly concentrated market, represent a rare opportunity to create an exceptionally profitable business line with an operating margin that should be industry-leading. Now let me turn it over to Andrea, then we can take questions.

Thank you, Josh. Hi, everyone. Thank you for joining us. And I also just want to do a quick shout-out to Gabby Woody, who's emceeing this call and whose

If go ahead.

And wonderful Gabby appears to be frozen. So I will just start. Mark Massaro, you popped up on my screen first. Mark Massaro at BTIG. Go ahead. We'll take your question.

Hey. Thanks, Andrea. Yeah, congrats on the progress. Wanted to start with maybe a macro question. Just about the LCD that we're waiting for with Palmetto GBA. I think if I heard you correctly, you know, you're talking about the four-two-two kidney protocol. Is it safe to say that even if the interval is finalized as is, you know, you expect to have that billion-dollar opportunity in front of you? And then maybe, Josh, if I could just get, like, your latest temperature on how you think the final LCD might come in. You know, do you see there's any opportunity for improvement from the interval? And, also, do you think there's a possibility that the limits could potentially be removed?

Oh, man. Some great questions there, Mark. I think you know, I'll start by saying, you know, I think we're hopeful along with the rest of the industry that the brakes get taken off. Here. It feels unnatural to, you know, limit access to a technology that a clinician feels they need to manage their patient. I think we heard some of that commentary from Dr. Langone when he was, you know, speaking in the KOL call. We're behind him 100%. You know, he expects that if he had this technology in-house, that he'd be doing four tests a year. And so, you know, right now, he wouldn't get paid for that under the current draft of the LCD, which is unfortunate. I mean, I think we'll support him in that process as far as negotiating with MolDx on expanding. We haven't heard anything around how that conversation is going, so I don't have any special knowledge there. But, you know, we agree with the industry that this needs to be a clinical decision.

Okay. And then, I think you mentioned this, but, certainly, the increasing organ transplant access model or IOTA—I wanted to just maybe pick your brain on that. You know, to what extent do you think that could be helpful to the utilization of transplant testing? And I'm just curious if you have any thoughts on that as a potential driver.

You know, it's another great reason why you don't take the clinical out of the hand of clinicians. Right? As you're changing how transplant centers are being incentivized to use more at-risk organs and then tell them, well, they can't monitor them on the scale and schedule that they need, it feels counterintuitive to me. You know, we have seen some positive feedback, some negative feedback on the program itself. But in general, I think it drives demand for testing. I think it's natural as you use more at-risk organs that you're going to want to follow those patients more closely. You should expect to see higher rates of AMR in that population. And so then you need to know if you can bring in these next-generation drugs, like the fezartumab or daratumumab. So we're optimistic that it increases demand for technology and, you know, more kidneys going into patients.

Okay. And I'll just ask one more if I can, and then leave some FDA questions for others. But I wanted to ask about GraftAssure core LDT. You know, recognizing you've got the lab up and running in Nashville, maybe just walk me through how you're thinking about that as a potential source of upside. Obviously, I think that could be potentially, you know, a source of, if you will, cash preservation. So can you just give me a sense for what the strategy is on, you know, the LDT?

Thank you. And it's very closely tied to the registry for us. I mean, we've looked at the market initially. I think one of the big reasons we went kit is that we didn't feel like we could compete, at least initially, toe to toe with the big guys that are out there. You know, when the opportunity to do the registry came up, it's like a natural fit for us and a reason to kind of spool up sort of our capabilities with the CLIA lab. And we think the process is gonna be, you know, call it somewhere between four and six months with each site as we kind of negotiate through the various contracts. And I think we've engaged with about 10 right now. That puts us kind of '1, '2 before we start to see patients coming in off of that registry. The expectation is that we'll be able to bill, you know, for the relative measurement of ddCF DNA, which is what our current claim is with MolDx, you know, while we capture the information around those other measures that we have. I'd say, in general, I mean, this has been very normal for the industry. I think, you know, we've seen, you know, very successful registries out there for our competitors. I think we're kind of following in that vein, although with a slightly different clinical question that we're asking. So yes, it should improve the revenue profile for next year. But we're not predicting that that starts in a meaningful way in Q1 or Q2. That's kind of like just when it starts to pick up. Andrea, anything that you would add to that? I know you've been a little bit closer to the numbers on that than I have.

No. I love it. The only thing I would add is you might be wondering, like, what changed? Why are we doing this? And it really is we press released that late-breaking data at the World Transplant Congress. We do have the opportunity to look to see if there is extra clinical utility in our And so that's really what changed and what's driving the strategy. It's we've had new data come out in our favor.

Got it. Thanks, guys. I'll hop back in the queue.

Thanks, Mark.

I'll just keep calling on people. Harrison Parsons at Stevens. Please go ahead.

Hey. Yeah. This is Harrison on for Mason. Thanks for taking the questions this afternoon. So as institutions validate GraftAssure DX head-to-head against current readout assays, what conversion curve are you expecting over the next twelve to eighteen months post-clearance? And what are the gating factors to go from early adopter physicians to center-wide adoption?

Yeah. I'd say Andrea put out a curve in our shareholder letter back in, I think, August. So coming out of Q2 of last year, which gives at least a look at it. I think what we're trying to do is influence that curve right now. I think when we get a little bit more confidence in how clinicians are feeling about the technology and what kind of engagement we're getting, I think we'll update that curve. But right now, that should be considered our best thinking, and then we can share that with you afterwards if you don't have access to it. But I think in general, it's, you know, the market's gonna be very much show me. You know, which is, you know, they've been very comfortable using technology that has helped them, you know, manage their patients for five, six, seven years now. And I think they're gonna want to see that they're getting similar to better results before they jump. I think once there's enough data out there, there's kind of a saturation point where the question comes off of the table. But, you know, certainly in the early days, it's incumbent upon us to help generate that data and get it out there for the industry.

Yeah. And Harrison, if you look in the shareholder letter, we actually put a launch framework graphic where we talk about driving engagement and utilization with potential future customers. We can't start talking about GraftAssure DX as a kitted test until we have FDA marketing authorization. So there's a wall there, and you can't But we can start to drive utilization of our Nashville labs, start talking about a registry study. And so when we talk about influencing the slope of that curve, these are activities that we can do now. Today, and we are doing them actively today.

Got it. Yeah. That I think that all makes sense. And then, I guess, next, so you previously highlighted the favorable PPV data and how, you know, this could be a differentiator for your kitted product. Could you share any broader feedback you've received from clinicians on this point?

Yeah. I think I'm happy to. And, Ekke, if you have any comments, I think you've been out there on the front end with some of our research partners. Love to hear how you think about it. But I'd say it's broadly been very positive. I think there is a general sense that we are, you know, applying biopsy too frequently. And, you know, that a higher positive predictive value perhaps is better suited to the screening application that the world is looking at right now. But let me hand it over to Dr. Schutz, who's been out there. You know, he's obviously the one that created the score. I've been working with our research partners on it, and sort of why they're looking at it and what they're looking for.

Thank you, Josh. Yeah. Harrison, I think what the entire field in transplant was always missing is gets to the fact that if cell-free DNA is normal, is a way of using cell-free DNA as a rule-in test, well. Right now, it's a rule-out testing, so which also you might forfeit a biopsy. But if it's not, then you do a biopsy. But under those where you are doing a biopsy, way more than fifty percent are not turning out to have a rejection. So and that's actually the, I would say, conundrum clinicians are in. And what we are able to provide is a way of testing that if you see, okay, this patient doesn't look normal, which means I would not forgo a biopsy, then your chance of having really a rejection is way over fifty percent. So it's actually really good for the patients. So you are not biopsying patients when you only have a thirty percent chance of that the patients even had something. And that is clearly something that clinicians understand. They don't want to do a biopsy if it's not really necessary. And we have only had really a lot of positive feedback. It's really up to people are saying, oh, that's a change in paradigm for cell-free DNA. And so, yeah, that's why we put it in the center of our registries and, okay, let's convince the field that this is really a huge step forward for your clinical interpretation of cell-free DNA. And I think it's going to more or less get into a world of its own once we can show that there's going to be a lot of clinical debates around are you using do you want to use a test that really has no positive predictive value or do you want to use a test where you can also make the positive decision for a biopsy with way better chance of doing it in the right situation.

Okay. Thank you, Ekke. And then I'd just had one more last question, and then I'll let others go. I guess so at this point, after the government shutdown, is mid-2026 still the right timeline to think about potential regulatory approval or commercial launch, or has that timeline been pushed out at all, if any? Thanks.

You know, it's tough. Government ever opens again. Yeah. I think we're hopeful that the government, you know, gets funded and stays funded. Obviously, the current conversation that's going on in Washington only funds the government through January. I can't predict, you know, what happens if the government shuts back down. I can't predict, you know, what's going to happen to, you know, to our reviewers. I would say, you know, it helps that these reviewers are funded by industry, you know, by and large, you know, through the doofah. But, you know, I can't guess. I mean, I assume as long as everything's normal, and we get through the FDA fine, then, yes, we're still on pace. But outside of that, there's the piece that we don't control.

If I could just add, Harrison, I think the takeaway is that we are still preparing for a mid-2026 launch, and we're not changing anything. And there's things that we can do regardless of the government shutdown, which is focus on the engagement and utilization of our assay, which we are very much gonna focus on. We can drive revenue out of our Nashville lab. We don't need the government to be open to do those things. And then the other thing, and we pointed this out in the shareholder letter, but we got word that our reviewer was working, you know, that's nice to hear that they were working even though they were not accepting new submissions. So just focused on that. And the final thing I would say is when we've talked about the FDA review timeline, we did bake in some time for them to ask questions and for them to respond. The FDA would say that the review timeline is actually shorter than the number of months we gave you. Because we did bake in a bit of cushion for them to ask questions. They stopped the clock. We respond. And so we're still planning on the same thing we've been planning on all along, but, of course, we have as much insight as you do into what's gonna happen with the government.

Great. Thank you.

Of course. Thanks, Harrison. Okay. Mike Matson, I'm gonna take your question. Thank you for coming on video. Oh, I need him. Here.

No problem. Thanks. So, you know, just in terms of the trial, it sounds like it's still on track, you know, for the end of the year. But I was wondering, can you give us any sort of metrics around enrollment or samples that have been collected to date?

Yeah. I would say the, you know, gosh. I guess everybody would say that sample enrollment is going slower than they would like. Yeah. But, you know, we are enrolling samples. You know, there are, I think, we can't actually update our clinical trials that go up listing right now because, you know, the government is shut down. But I think we actually have five sites that are actively enrolling patients at this point. And so I think we're medium to high confidence that we're gonna have all of the samples that we need to complete the submission by year-end.

Okay. And then you mentioned that, you know, in terms of, you know, once the test is commercialized, the centers and the doctors are likely to try to, you know, do head-to-head testing or maybe potentially use the registry. Can you maybe just explain I guess I'm a little confused in terms of how the registry would help them figure out. You know, I understand head-to-head. You run both tests and kinda compare them. But the registry, how does that kinda pull, you know, serve that same purpose, I guess?

Oh, it's a wonderful question. And I think it's really on the engagement and utilization front. And so it's an opportunity for a clinician who's never used our technology before to have, you know, our report in their hands, you know, see how it comes out, see the data, and then use it in their patient and see how it performs in kind of a real-world setting. And so that's that familiarization piece that we're trying to get to. Also, show them the new ways of measuring donor-derived cell-free DNA. So to engage that kind of intellectual curiosity that they have around it. So that, I think, is that's not head-to-head. That's more getting in their head, if you will, and getting them comfortable using our technology.

Alright. And then, you know, in terms of if the doctors, the centers are doing head-to-head testing, how would that work from a reimbursement standpoint? I imagine they can't bill for both, and then I would be sort of helping them out with that. I mean, I don't even know if that's you're allowed to do that, but giving them a price break or test or something like that.

Oh, so, no, it's a great question. And we've done this before in some of our oncology assays, and what we call is a clinical evaluation program. And so it's a specific program. It's where we sign an agreement with them for a certain quantity of samples. And it's, I think the number is 20 samples where they send 20 out to our competitors. They send 20 to us. We don't bill for those samples. We just generate a report because under CMS rules, only one center is allowed to bill per patient. So we basically just eat the cost on that to generate the data for them.

Okay. Got it. And then finally, just stepping back, you know, the mid-2026 launch, what do you think are the biggest risks to that timeline? Is it mainly the FDA, as you mentioned, in terms of them, you know, back and forth there kind of stopping the clock? Or is there something else you would point to, I guess?

Yeah. I guess there's always unknown unknowns. I'd say we feel like we've checked a lot of boxes, kind of your retiring risk over the past, you know, two and a half years. Obviously, government being in flux right now is a big one for us. That can immediately impact the timeline. Outside of that, I think, I mean, that's probably the biggest risk. I don't know, Andrea, if you've got some I know we get this question a lot, and I think you generally have better answers because I'm so optimistic on all of this stuff. It's hard for me to say, you know, where it's all gonna blow up. But Andrea is much more level-headed than I am.

Go ahead, Ekke. Yeah. I think, Mike, we are pretty confident with production and everything. So I think we don't have really a big risk in-house. We are right now producing our third lot for the FDA trial, and it's working out pretty well. Just looked at the results today. So I would really think our biggest risk is the FDA. If they drag it out, then there's not much we can do about it. My philosophy or strategy right now is that whatever we can think of that the FDA might ask us, we shall be prepared to have the answer already before they ask. So which means it's not really stopping the clock. They're always if they're sending out a question, they stop the clock until they have the answer. And my wish is that when they send us a question in the morning, the answer goes out in the afternoon. So that's more or less what I'm trying to do.

Yeah. Okay. That makes sense. Kinda like prepping for an earnings call. You wanna try to predict what the analysts are gonna ask you guys. Right?

Yes. Yes.

Alright. Thank you.

I love that. And, Mike, the other thing is we've communicated with you guys. We had all those pre-submission meetings with the FDA. So that's great because the team has been getting feedback from the FDA. And so it's not like the first time the FDA sees our submission. They're like, what is this? There have been, you know, meetings I have.

Alright. Thank you.

Thomas Flaten at Lake Street. Hey, guys. Thanks for taking the question. So not to get too granular, Josh, but so there's fifty-one days or so until the end of the year and a bunch of holidays. And with five of 10 sites recruiting, you know, are the others gonna meaningfully contribute to the number of samples? And then how many days do you guys need to take that data, analyze it, compile it, get it into a format that is acceptable to FDA, and squeeze it into an application then send it off. Can you just walk us through I know we're getting way in the weeds here, but Sure. Sure. Sure.

Yeah. I'll take the first half of the question, and I'll hand the second half to Dr. Schutz, who's a lot more closer to it than I am. I'd say there are sites that won't contribute to the first phase of the submission. You know, we are looking at this in two waves with the FDA. So the first is to get basically just over the bar, which is, you know, that 85% negative predictive value. And then there's the combo score, which is kind of the second wave of this. And that's where, you know, the other sites come in. We're gonna continue to enroll past the new year. Andrea talked about this in the shareholder letter. I think we have a few more points to prove with, you know, with this study that will create kind of like follow-on submissions. But, you know, Ekke, maybe you can talk us through. I know a lot of focus on the number of events as much as the number of samples that are going into the study.

Yeah. So, Thomas, if we are recruiting as we think we are, we know from each and every one of our co-sites how many biopsies they are doing per month. And from there, we can more or less calculate are we on track? We are on track. And we are right now full steam writing the submission already. So we are not waiting until we have this data. This clinical data are, believe it or not, the smallest part of the entire submission. It's, if you wish, a very simple evaluation. What is the sensitivity? What is specificity, and I can do the calculations in an hour. So what we are doing, we are really preparing the entire submission right now. And at the very last day, if you wish, we just plug in these two numbers from our clinical study and push the submit button.

Got it. Super. Yeah. Got it. Yeah. Okay. Super helpful. Andrea, I know you said your expenses were ticking up a little bit because of the study and FDA expenses, etcetera. How should we think about the first half of next year? I know we haven't gotten there yet, but do you expect the cash burn to moderate a little bit? Or do you expect it to go up as you prepare for launch?

It's a great question. Right now, I would say we're preparing to keep it flat. If we were to go faster and we want to go faster for some reason, we would communicate that to you. I would keep your expenses flat for now. Now I would say flat to, you know? I mean, I think they're gonna grow up a go up a little bit. We are looking at areas where we could invest to go faster. We scrutinize every dollar, and so we haven't greenlit anything yet. But I think we'll come back at you in March, and we'll update you on how we think 2026 is gonna look.

Got it. Appreciate it, guys. Thank you.

Thank you.

Thank you, Thomas.

Alright. Any other questions? Alright. Well, guys, thank you so much for making time for us today. You know, it is fun to get to share sort of the results of all the hard work that the team has put in. I think we're encouraged. We're excited. You know, we've been waiting to celebrate submission for about two and a half years, and you know, it feels like we're finally about to give birth. So, we're excited and looking forward to sharing this positive news when it happens. So thank you, everybody, and we'll talk soon.

Thank you all.

Mike, can you hang up?

You still have 40 participants. Yeah. Everyone can see, I think.