Replay available

Biovica International (Stockholm:BIOVIC B) Q3 2026 Earnings Call

Biovica International (Stockholm:BIOVIC B) Q3 2026 earnings call, held 2026-03-18. Watch the replay and read the transcript on 6ix.

Wed, March 18, 2026 at 9:00 AMendedReplay
Biovica International (Stockholm:BIOVIC B) Q3 2026 Earnings Call
Company
Biovica International AB (OMXSTO:BIOVIC_B)
Period
Q3 2026 earnings call
Date
Wed, Mar 18, 2026, 9:00 AM ET
Replay
Watch the replay on this page · 35 min

On 6ix: 6ix.com/event/biovica-international-ab-publ-biovicb-q3-2026-earnings-call

Replay

Transcript

Automated transcript · Written by software from the replay's audio. It can mishear names and figures; the replay is the record.

0:00 Hello everyone, and welcome to our earnings call for the third quarter of our fiscal year. Today, it will be me and our CFO, Anders Morian, will do the presentation. And the agenda will be first a short introduction about Biovica. We'll go through the highlights, then Anders will go through the financials, and then we'll end with a summary and a Q and A session. The Q and A session will be done this way that we will have Filipe Lindfist, our analyst from Redeye, into the call asking questions, but you can also submit questions that will be answered in writing and appended to the presentation that will be put on our homepage after the call.

0:52 So I'll start with Biovica and our product Divatum. Divatum measures what's the core of cancer, which is self proliferation, and the way we do it is through a blood sample from the patient that is analyzed using our assay in our lab or in an external lab. And by doing so, you will get a precise understanding how the tumours are proliferating, which is an indication of how aggressive the disease is, which is of course is important when making treatment decisions. Also, it has proven to be an excellent tool for monitoring of treatments and to get feedback over time and get quick feedback earlier and then with other methods like imaging.

1:41 This has been proved in several clinical trials. We have more than 30 peer reviewed articles and that has been studies that have been performed with some of the leading oncologists in the business at some of the most well renowned institutions and like John Hopkins, Washington U, Mayo Clinic, etc. And the majority of these trials are within our first application, the breast cancer area, although there are potential also outside to expand into other large area where the DIVITUM can add benefits both to patients being on treatment and as well as treating physicians and payers, because you will also have able to reduce waste for expensive treatments also benefits society and payers.

2:40 These clinical trials create a solid foundation for our commercial activities and our go to market process and also create demands from pharma companies developing new therapies within this area that are using our product in that phase. As I said, the first application is with the in the breast cancer area, more specifically in the metastatic breast cancer, where we have our five ten ks clearance, and that we are active especially so in on The US market that we serve the market from our US CLIA lab situated in San Diego serving all the 50 states here in US. Lately also we have presented clinical data showing that we have a strong application also in early phases of breast cancer when monitoring so called adjuvant treatment, a market which is significantly larger.

3:40 We also developed a second version of the test, the so called LDT, that we can provide from our lab in San Diego within this space as well. There's potential here to expand into other areas and we see several mega trends that is playing to our advantage. One is that people are staying longer and longer on treatment and also on more expensive treatments with severe side effects and you want of course to improve the precision of monitoring. This is especially true for our two main focus area targeted treatment and also immuno oncology treatments.

4:26 And same thing with the precision oncology, want to you have more and more precise treatments that has a more narrow target and also that drives the demand for more precise monitoring. And the third trend would be pharma integration that pharma is using biomarkers and biomarker tests more and more when they develop new therapies and the diagnostic product very closely related to the new drug, then that drives also demand for improved monitoring. You could also add a fourth trend maybe which is dose optimization, something that the FDA is pushing through their product optimist initiative which has the focus to not overdose but to give enough to maintain efficacy and of course you need then good efficacy biomarkers.

5:23 So this all boils down to that we are well positioned to meet these new trends and has as a unique product that measure what's really essential in cancer and also have the ability to impact great values. Currently, according to IQVIA, more than $200,000,000,000 per year are spent on oncology treatments within this area. So there's also potential not only to improve to help patients with a better treatment outcome, but also to be more efficient when spending these large resources on cancer therapies. So if we move into our third quarter and the highlights for that, we start with the financials, Anders will go through these more in details, but if you compare year on year for the third quarter, we had a 40% growth, and it's even more if you compare it in local currency. That local currency would be dollars.

6:26 The majority of our sales, more than 90%, is in dollars. So when the dollar currency is affected, you can see that in our top line as well. And if you look accumulated over the first three quarters, it's also still a strong improvement, even also so in local currency. One important KPI is our operating cash flow. We have been reducing this steadily during the last two years. If you compare versus same quarter last year, it's a significant reduction. If you compare for two years, I think we brought it down from 25, 30 millions per quarter now to 11.5, so that's a trend that we welcome and that's an important KPI for us moving forward as well.

7:22 Our cost position at the end of the quarter is SEK88 million. If you look at the clinical area in US and in Europe, we continue to sign commercial agreements with our target customer category, is the NCI, NCCN designated cancer centers. We announced that in December. We believe more and more we're getting traction on The US market and is focusing our resources, and so that meant that we agreed jointly with our Nordic distributor to terminate the distribution agreement in The Nordics. The activities that we're currently doing in The Nordics we can do ourselves also.

8:12 Pharma services has been has had a great momentum now for for quite some time and so that is continuing which we'll get into on a separate slide and when it comes to the clinical area we are continuing to present new clinical studies especially in these areas that are important to us CDK4c inhibitors, dose reduction and monitoring. Just this morning we had a PR out that we will be presenting a study within immuno oncology or ICI immune checkpoint inhibitors on the upcoming AACR conference.

9:01 We also have initiated a CEO succession and at the last slide I'll give a little bit background and my thoughts around that. So in general, think we're seeing momentum in both our areas. We see strong growth and we expect to continue growing going forward. So, you look at The U. S. Highlights, if you compare it quarter by quarter, you see maybe not such positive trend, and I will still want to claim that we overall see a strong growth. All quarters are not the same in our business, especially quarter three is a little bit of slow quarters with both Thanksgiving and then you have the Christmas and New Year's holiday.

9:50 And if you add that add a storm in US last week in January, where all the samples from the East Coast had to be thrown away. Of course, you can have a short term impact, but I think if you break down the numbers, you can see that we've had a weak October due to what we communicated lastly that we lost we lost already from a clinical trial which takes some time until we turn that around to clinical use. That was the commercial agreement we signed then in December, and we see the pickup. We still have such low it's still a bit volatile our business, so we'll get impacted of events like that.

10:44 But since November, we see a steady trend that we are improving and also beginning of Q4 is better, and I would say that in general we see a strong momentum in our US business as well. It's taken a bit longer to get to this point than expected, but more and more we are seeing an increase in demand and also more spontaneous accounts opening up from both patients and oncologists getting knowledge about Diwitum from already users that recommends and that is growing our business. We've also seen actually patients choosing oncologists that can offer Divitum versus oncologists that are not offering Divitum. So, yeah, we see an increased momentum and we're very pleased with that.

11:39 And on top of that, we also have several initiatives that we are convinced that will further drive the growth. One thing is the large IDN that we have been talking about now for quite some time. We have completed the protocol. We've spent it's been pretty intense period the last couple of months. We worked together with them to ensure that what we know right in the protocol, the way we design the trial, that we optimize for a successful outcome of the trial. So I think it's worth that extra time to make sure that it is a successful outcome. The next step is submission to IRB that will take place now very soon, and then if we can do that, we believe we can initiate the trial this summer.

12:30 This has a great potential both during the actual trial, but also after the trial to unlock this large organization for a system wide adoption and also becoming a very strong reference case for others. The early breast cancer, also see that this is starting to happen more and more. We see, for instance, we have a center in Florida that has made a decision to expand usage into the early breast cancer area for adjuvant monitoring, and they will over certain time here, will increase patients from today's twenty to around one hundred.

13:16 So that illustrates the impact that having earlier breast cancer expanding to that that one can have. That also is done like an observational trial, so we will get some important data because that's an area where we don't have as much data, and it's essential to strengthen the clinical data in that area to further strengthen our value proposition. And completed their market research, which is preparation for our go to market work, and as communicated earlier, we expect to launch this together with them in the fall of twenty six. They have both a significant sales organization and also a very efficient process to target with sophisticated IT systems, so this is a great opportunity to us to leverage on a totally different scale sales organization to target the big community oncologists segment.

14:25 This morning we did a PR about the upcoming AACR. We have two abstracts that will be presented as posters. One is personalized dosing in the CDK space, both the existing foursix but also next generation. This is an important area for us because this is an area that the FDA is pushing through their project optimus and I think we have a unique offering here, so it's very very good that we also can prove that with data in more than trials than we have achieved so far, so very positive. Another area that's interesting for the future is the immuno oncology area.

15:10 Here's a collaboration with a few Italian institutions and also here, Davidson performs very well and it's an area interesting for the future where we have ongoing patents and also now ongoing collaboration with both academia and pharma companies. Moving over to pharma, that's also one important area of our business. We're currently active in the left hand phase of the process here, service and kit sales. We are working with the majority of companies developing next generation CDK inhibitors, and so we have a portfolio of around, yeah, I would say 20 plus now projects, and we see here that the volumes are increasing month by month, so it's very very positive, and that we can add value here.

16:15 Companies are coming back for the next project and the next project, and the business is growing over time as they're moving also forward from we're involved already in preclinical phases until phase one, phase two and going forward also phase three hopefully. So strong momentum in this business. The CDK area is an exciting area. It is currently an area with a $12,000,000,000 of yearly sales from three leading drugs Pfizer, Novartis and Eli Lilly have their respective drugs in this area. The future market is expected to be even even bigger with about five times the volume, and it's driven both by new drugs coming to the market and the expansion into the earlier phases of breast cancer for adjuvant treatment.

17:20 And so we're well positioned here. We're working with the majority of the companies developing these new drugs, and we're participating both in preclinical and clinical trials, and we're used for, yeah, as a treatment efficacy marker. And there's a lot of events here during this quarter that just passed. I'm here in The US, so I can see every day in the lab we're receiving samples and we've been able to bring in extra personnel at the end of the period, and so we'll do so also during this fourth quarter. So we're seeing that the momentum is growing, and it has been a trend that has now been ongoing for several quarters.

18:12 Here's also an area where we think we can drive the revenues even further by extending our commercial organization, and we're looking to increase our commercial organization with a US based rep, specifically for the pharma business. That was my highlights. And Anders, if you can if I can leave it to you to go through the financial updates, then I'll be back and do a little summary and Q and A. Perfect. Thank you very much, Anders. Quick look at the financials. Q3 sales about SEK3.3 million in total. If you look in local currency as Anders said that's mainly or 90 plus percent being U. S. Dollars, it's more than 60% growth.

19:12 IVD tests grew about 21 on a yearly basis, even though the challenges that Anders mentioned with converting that clinical trial into IBD or clinical use and also on top of that the snowstorm that hit Mid And Eastern U. S. That actually made us lose about one and a half week of samples not receiving our CLIA lab in California due to the snowstorm late January. Pharma services grew about 57% in Swedish kronor. It's about 70% plus in local currency. The major growth driver there is the pharma test services.

20:02 We see that trend, that's a trend that we have seen now for quite some time. Most of the really large tier one pharma companies are preferring to send the samples to our CLIA lab mainly in US, but also to our lab here in Uppsala where I'm sitting right now. We are still supplying kits to some smaller pharma customers, but we expect that kit supply to actually increase a little bit going forward because we see quite a lot of interest from Chinese CROs that are planning to start initiating trials for really large pharma companies in China and in China there is a prohibition of exporting human samples out of Mainland China, so that's why they need to buy the kits from us to be able to perform the sample or testing on the Chinese trials.

21:06 So go to the next slide Anders. This is an overview of the year to date sales, about SEK8.6 million, that's a growth of 36% in Swedish and a little bit more than 50% in local currency. Here you see that the IVD tests in The U. S. Grew about 46% year to date. It's about 60% in local currency and our pharma service grew 40% and as you can see here it's the same pattern here that the former test service is growing significantly whereas the former kit supply is slightly declining.

21:53 Go to the next slide Anders. Last slide on financials, as Anders mentioned improved cash flow. Of course that's very important for us to try to minimize cash burn. So our operating cash flow before change in working capital improved with about SEK 4,400,000 versus the same period last year and that's of course then driven by increased sales and lower operating expenses and net operating cash flow improved by million versus same period last year. We closed the quarter with SEK88 million in our bank at the end of the reporting period.

22:39 So that's it in terms of financials. I'll hand it back to you Anders to do a summary and then a Q and A session. All right. Thank you very much Anders. So to summarize, U. S. Clinical business. So we have reestablished a strong trend and we expect to see this in sequential quarterly growth, especially that we have multiple initiatives also that we expect is going to be positively impact the sales development during the coming months and quarters.

23:26 We're now laying a foundation to be able to scale this on The US market, and especially after with the Tempus partnership and also with the big IDN on top of the foundation that we already have. Pharma services, we have now had momentum for several months, and we've built up this portfolio of agreements that we're now seeing also that we are executing, and we see the revenues and samples coming in every day. I think the position here in CDK inhibitor development, especially the next generation, is very, very interesting.

24:12 It's an area with a lot of attention. It's a large part of the oncology therapy spend. And so there's a lot of potential here and also looking further ahead on the checkpoint inhibitor area, it's even greater potential. So I would say that we're well positioned, and I think we can grow with more resources, and we're looking to close that. So good momentum across both segments, and also events going forward that would further accelerate growth. I also want to reflect a little bit and also give a background to the succession that I've been now here in The US non stop for two and a half months now, and it's given me access to people and companies in the business and a better understanding of The US market.

25:15 I think it's been very, very inspiring. I've seen we brought in people that has challenged us and see what we can do to improve. That has been part of very successful companies in the business. There are several companies here on West Coast that has been gone from 0 to billion dollar companies in oncology diagnostics, and of course you want to learn, see what they have done, what we can learn from them. And you can say that to a great extent we're following their path and also both with the combination of setting up your CLIA lab, having control over the reimbursement, making sure that you have a solid science foundation, targeting the right type of oncologists in the beginning, and also complementing your business with pharma services.

26:10 So we have all those pieces in place. You can also see that the initial sales on the clinical market has been slow in the beginning, and then after a few years, you see that you start getting the momentum. So we're following that path. So we can say that on this beginning, we have a lot of building blocks that is in place, which is the foundation I was talking about on the previous slide. We have constraints also. Our main constraints are resources. I strongly believe in the strategy, so we're doing a lot of stuff with little resources.

26:58 But I think we have a strategy that is also addressing this. When we see that we have a model that is scaling, like now on pharma, where every rep can bear their own cost and some margin, extending the organization and we're also improving efficiency on our US clinical sales. I think we have doubled the sales over, if you look back a few years, and we have reduced the cost to one third. So the efficiency wise, we're taking big, big steps, And now when we're going getting momentum and traction, and together with partnerships, I see that we can build on this. So it's very inspiring to do that, to see that. But also I realized that US is where we have the momentum, where people have built this kind of companies, their experience and their reference cases, so I'm even more convinced that the next CEO should do something that I have difficult to do, but to spend more time in The US market, and preferably also have the relationship that I've been developing now over some time to have a strong network from the start, being coming from the business having this network.

28:25 So I think this is a great foundation for the next CEO to continue to build on this journey and be able to create an impact company that can both create significant value for patients, for healthcare providers and society, as well as the shareholders. That is a little bit of a background and some reflection and lessons learned. With that, I'd like to open up for the Q and A session with Filip. Are you there? Yes, I'm here. And thank you for taking my questions. So let's start with one of the bright spots in quarter, which was Pharma Services. So you said in the Q2 earnings call that you expected Pharma sales to pick up in Q3 and Q4, which was true now for Q3.

29:18 Do you expect this to continue even beyond Q4 and onwards? Yes. First of all, we hope to do a strong Q4. We're not giving away, as you know, financial target at this point. But we know your target and we're aiming to be in that, yeah, in the vicinity of that. And with the Q4 that we have ahead of us, we think there's a good chance that we will be able to do that. And the good thing with the pharma services business is that we have the agreements and we have plans, we know we will receive the samples, so we're able to forecast that pretty good.

30:05 Although sometimes there are delays outside of our control, so it's not 100%, but we know for sure that we will get a lot of that volume, we know that will happen, and of course, if it's a delay in a couple of weeks, can spill over to the next quarter. But yeah, so the answer to that question is yes, since we have those agreements, we have it planned with our customers, we're pretty sure that those revenues will come, yes. All right. And I see that time is running out, but maybe a couple more from my end. Sure. What are your expectations on costs in your Q4 and also for your next year? Anders, maybe you could elaborate a little bit on that?

30:51 See if we can switch this. Sure. Are not giving away any guidance on that as we have earlier communicated. But I would say that my guess is that we will be in the same range that we are right now. It might vary a little bit, 1,000,000 up and down from that perspective, but we should be fairly stable. Of course, the most difficult part there is the dollar exchange rate. A couple of weeks ago it was down to SEK8.70 on Swedish kronor, now it's somewhere around SEK $9.40, which is a significant change and we still have a lot of expenses in dollars from our U. S. Subsidiaries.

31:43 So it's very, very hard to say exact numbers in terms of that because there's a lot of things that has an impact on our spend level. That's I can't tell you any more than that. I'm sorry for that. No, but if I can build on that, if you get the picture back. So I agree with Anders, if you take a step back, we're not looking to significantly change our organization other than in areas where we will get a payback with more, that we can increase revenues by investing. So the good example is the pharma services. Otherwise, we're looking to maintain the organisation and the spending until we have a more secure and forecastable cash flow and a more solid financial position.

32:35 So no big change. And then on top of that, it's a very uncertain world with both a dollar currency rate that is flipping up and down and also tariffs on top of that. But it's not game changing. It's on the margin. Yeah, sure. And the last question for me, a broad one, and you can give a high level answer, but can you elaborate on your high level plan to achieve reimbursement in The US? I mean, you're taking steps towards it, but what's the high level plan? So this is something that also when we did these workshops with people from the who have built this bigger companies. So we got so mean the clinical data is the foundation for all commercial activities in this business, you say, but we're looking also into do clinical trials with payers that generate that kind of data. So, because we already have reimbursements for Medicare, we have client bill agreements, so then it would be the private payer segment to generate targeted data towards that. So we have ongoing initiatives looking to that, and we have ongoing clinical trials already that I think will improve that as well. So I think that is not something that will take place immediately, but over a few years, I think we will be able to show a very strong health economic

34:07 business case for payers, so I think it will be a strong side of ours. Currently, private payers is not a very big volume of ours, so Medicare client bill is the majority, It's not that we're leaving so much on the table right now, but over time this becomes an important factor to put in place and we're working on, we have a plan on that. Yeah, super. Yeah, that's all for me. So thank you once again. Thank you very much. Thank you everyone for listening to our call and over now from San Diego and Uppsala.

Follow Biovica International AB into a list and get an email when it puts out news.

Latest news releases

Companies on this call

Speakers

Not disclosed

CEO

Philip Lindqvist

Analyst, RedEye

Anders Morén

CFO

More from Biovica International AB