Welcome to Cantargia Q3 Report 2025 presentation. During the Q&A session, Welcome to Cantargia Q3 Report 2025 presentation. During the Q&A session, participants are able to ask questions by dialing #Key5 on their telephone keypad. Now, I will hand the conference over to the speakers: CEO Hilde Steineger and CFO Patrik Renblad. Please go ahead. Thank you. Can you see the slides? I cannot see them. All right. Good afternoon, everyone, and thank you for joining the presentation of our financial report for the third quarter and an update from the company. My name is Hilde Steineger, and as you probably are aware, I'm newly appointed as CEO of Cantargia. Next slide. Patrik, may I ask you to change the slides? All right. Slide 2: Safe Harbor. Slide 3? Patrik? Okay. Let me just finish. With me today, we have our newly appointed Medical Officer, Dr. Wolfram Dembke, and our CFO, Patrik Renblad. Slide 4: We reported this morning our interim report for the third quarter and the first nine months of the year. It has indeed been a transformative period for the company, with the Otsuka transaction as the main event. About the same time, about the same period, we communicated the primary endpoint from our TRI4 phase 2 study on the objective response rate, ORR, and the results showed no difference in ORR between the control group treated with chemotherapy and the patients treated with nadunolimab in combination with chemo. We are awaiting the mature overall survival data, which is expected around year-end 2025. I joined Cantargia as CEO on September 1, and I have extensive experience from leadership roles in the pharmaceutical R&D and business development, as well as background in the financial sector as an analyst and venture capitalist. I'm also very happy to introduce Dr. Dembke, who's joined Cantargia as Chief Medical Officer, and I would like to hand it over to Dr. Dembke for a brief introduction of himself. Thank you, Hilde, and thank you very much for inviting me here. It's a pleasure for me attending this meeting. My name is Wolfram Dembke. Just a brief overview about my career: I'm born and raised in Germany, holding a German passport. I studied medicine in Germany, in Essen, and I'm a fully qualified and board-certified hematologist and oncologist. I'm also holding an MBA in international financing. I worked in the industry for quite a while, and I'm still seeing patients at Munich University and, from time to time, at Cambridge University, as I'm a full professor at Munich University, Hematology-Oncology, and in Cambridge, I'm a senior lecturer. I'm also holding a passport in the U.K. I worked at several pharmaceutical companies, and I have extensive experience in clinical drug development. Just to give you a few examples, I was responsible for bringing dasatinib/Sprycel to the market while working at Bristol-Myers Squibb for the CML indication. I was the mastermind behind ipilimumab for malignant melanoma. I was responsible for the relaunch of gefitinib/Iressa in 2014 while working for AstraZeneca and at least in part, let's say 50%, for the launch of Tagrisso, which is osimertinib. I was the European representative for mogamulizumab while working at Kyowa Kirin. I was responsible for the launch of cabozantinib from Novartis. At that time, I was working at Insight, and Novartis had hired me to get cabozantinib, which is a MET inhibitor, to the market. Lastly, I am in a way responsible at the moment as I'm a board member at Moleculin Biotech. I'm responsible; I was responsible for bringing Moleculin Biotech from phase 0, if you like, to the currently active phase 3. My last role was at Otsuka, especially at TAIO, and therefore I was responsible for the development of selpercatinib, which is a RET mutant TKI, and the drug is currently in phase 3, and the filing will be at some stage next year. My research focus is, as you can see, mainly on GI tumors, especially on pancreatic carcinomas. I did my PhD on RAS in England quite some time ago, and for the last two decades, I worked on lung cancers and acute leukemias. From my clinical perspective, I'm seeing pancreatic carcinoma patients on a regular basis. I'm actually treating them. I do know how these patients are suffering from their disease, as pancreatic carcinomas are a very tough disease. I'm now overlooking 35 years in medical oncology and hematology, and during that time, I've seen everything: every trend on the market, including CAR T-cells. I'm treating patients with CAR T-cells, autologous, and allogenic transplantations. It is a matter of my heart to point out that nadunolimab is definitely the best drug I've ever seen for patients with pancreatic carcinomas, and therefore I was really keen joining Cantargia and to bring that drug to the market as soon as possible. That is my driver, and that is something that thrives me, and it is very important for the sake of the critically ill patients. Thank you. Thank you, Wolfram. Let me then go into detail a bit into the Otsuka transaction that we now announced in July and closed in September. As I said, it was in many ways transformational for Cantargia because it provided us with the financial flexibility that has enabled us to reinvest into the next generation of anti-IL-1RAP antibodies. Equally important, the company sees the deal as a validation of both the target and the technological and commercial value of Cantargia's antibody platform. When the deal closed, Cantargia received $33 million, and we are eligible for receiving up to $613 million in upfront and milestones, in addition to up to double-digit royalties. Now, let me review our pipeline and our strategic priorities. Bringing nadunolimab forward in pancreatic ductal adenocarcinoma, or PDAC, remains our key strategic focus based on our very compelling phase 2 data, which I will elaborate a little bit later on in this presentation. We have observed promising results in non-small cell lung cancer, particularly in a subgroup of patients receiving second-line treatment following immunotherapy, more specifically in those with non-squamous tumor types. While these findings are encouraging, they are derived from a limited sample size of only 11 patients. At present, there are no plans to pursue further development based on these preliminary data. Regarding triple-negative breast cancer, as mentioned, we have previously shared the results from our primary endpoint ORR this summer. We are now anticipating more mature overall survival data and expect to provide an initial readout before the end of the year. As mentioned, the Otsuka deal provided the means to invest in our very promising pipeline. With CAN14, we intend to develop an anti-IL-1RAP bispecific antibody for inflammatory and/or autoimmune disease. We are in parallel exploring the options related to anti-IL-1RAP antibody drug conjugates, or ADCs, also as a next step in oncology under our CANXX umbrella and platform project. Last but not least, CAN10 remains a very important asset in our portfolio. Even though it's in very capable hands of Otsuka Pharmaceutical, we will continue to follow and report on the asset as it progresses through development and hopefully later on for approval and commercialization. If successful in all of these steps, the product will provide important non-diluting funding for Cantargia in the future. Let's dive into nadunolimab in PDAC. Once again, I want to emphasize that nadunolimab in PDAC remains our primary strategic focus. A crucial link between our target IL-1RAP and patient is analyzed both with us and several other groups. Several studies have shown that high tumor expression levels of IL-1RAP serve as a marker of poor prognosis, as demonstrated here in the three graphs. On the left, the data from Cancer Genome Atlas mRNA database shows a connection between high IL-1RAP levels and poor survival. In addition, the middle figure from PANCAT shows the same. Our own study, together with Harlev University on biopsies, we could also show the results from protein expression that showed the same pattern. Interestingly also, we were approached by an AI company who has access to a large RNA database. They had identified IL-1RAP as an interesting marker of disease and saw that two genes in two subnetworks enriched for IL-1 high RAP correlated with worse overall survival. To us, these studies confirm that elevated levels of our target molecule, IL-1RAP, in PDAC form the basis for our convictions and are strongly linked to poor patient survival outcomes. PDAC is a devastating disease, often diagnosed at an advanced stage when treatment options beyond chemotherapy are extremely limited. The prognosis remained poor, with median survival between 9 and 12 months. Current chemotherapy regimens have been standard of care for decades, and unfortunately, there has been little progress in improving these outcomes. That said, the field is seeing promising new agents in development, and there have been significant recent investments driving innovation in PDAC. These emerging therapies provide hope for meaningful advances and improved survival for patients in the coming years. In our phase 1b/2a CAN04 study, we enrolled 73 patients with first-line metastatic PDAC who received a combination of nadunolimab and gemcitabine-nab-paclitaxel, or GM. We observed deep and durable tumor responses, as shown in the figure to the right, which translated into a median overall survival of 13.2 months. Although this was a single-arm study, comparison with historical controls marked here in gray line indicates that expected median overall survival with chemotherapy alone is approximately 8-9 months. These findings suggest a meaningful improvement in outcomes with the addition of nadunolimab. Our scientific team analyzed tumor biopsies from 49 patients to assess the expression levels of IL-1RAP. These analyses revealed two distinct groups: 29 patients with high IL-1RAP expression, while 20 were deemed as low expressors. When we then correlated these expression levels with overall survival, the findings were remarkable. Patients in the high IL-1RAP group demonstrated statistically significant median overall survival of 14.2 months compared to 10.6 in the low expression group. As shown in the previous slide, the high IL-1RAP expression in PDAC tumor is clearly associated with poor patient survival, reinforcing the significance of targeting this molecule and the overall survival in patient population. In this study, the data suggests that IL-1RAP expression is associated with better clinical outcomes, underscoring the therapeutic promise of targeting IL-1RAP with nadunolimab. By selecting patients with elevated IL-1RAP levels who are most likely to benefit from nadunolimab treatment, we hypothesize that we will be able to maximize the potential with clinical impact. In conclusion, nadunolimab has now been investigated in over 300 patients, and the accumulated data continue to demonstrate promising safety and efficacy profiles. Clinical results strongly point to a potential unique first-in-class opportunity for nadunolimab in PDAC and also in non-small cell lung cancer. Notably, PDAC patients with high IL-1RAP expression who traditionally have a poor prognosis respond best to nadunolimab in combination with Gem. Over the last year and a half, our team has developed a robust assay to test IL-1RAP in tumor biopsies, which we intend to use in the next pivotal study to test and select patients that are expected to respond the best. Importantly, we shared our results and discussed our next steps with the FDA this summer, which led to the fast track designation for nadunolimab in PDAC patients with high IL-1RAP. Building on these foundations, we plan to advance nadunolimab into a pivotal trial, which, pending funding and regulatory approval, is anticipated to commence mid-2026. Now, let me spend a few moments outlining our existing early pipeline, which we are further investing in. As previously discussed, our CANXX platform continues to offer robust opportunities for antibody innovation. CAN14 is the next initiative emerging from this platform, and we intend to build on the preclinical and clinical experience gained through our CAN10 program. We are advancing an anti-IL-1RAP bispecific antibody for CAN14. For intellectual property and competitive reasons, the second target remains undisclosed, but we anticipate it will address inflammation or autoimmune disease mechanisms. We expect to select a formal drug candidate of CAN14 around year-end 2026. Earlier this year, our scientists shared also promising preclinical data on antibody drug conjugate, or ADCs, and this approach combines cytotoxic payload with targeted IL-1RAP binding, which may offer higher efficacy with reduced side effects. We continue to evaluate this ADC concept within our CANXX project, and we will assess to move forward with this dedicated progress after evaluating the preclinical results. With this overview, I'm pleased then to hand over to our financial update to Patrik. Thank you, Hilde. Our quarter three was indeed transformational. For the first time ever, Cantargia reported revenues and profits. When the Otsuka payment had been duly recognized and converted into Swedish kronor, our revenues amounted to SEK 308.6 million. With operating expenses of SEK 41.7 million in the quarter, our operating profit amounted to SEK 267 million. From that, we deducted SEK 1.5 million in net financial items to reach a profit for the quarter of SEK 265.5 million. It is worth noting that despite reporting a profit, no tax will be triggered due to our accrued tax losses. Our reported earnings per share were SEK 1.07 per share. For the full reporting period or year to date, our revenues were obviously the same, with operating expenses amounting to SEK 126.2 million. We reported operating profit of SEK 182.5 million. Net financial items at SEK 3.2 million, leading to a net profit of SEK 179.3 million, corresponding to earnings per share of SEK 0.72. Looking at our operating expenses, both quarter and year to date, overall costs were similar to the respective comparison periods, with the comment that our R&D costs were significantly lower, both in the quarter and in year to date, due to a ramp down both for nadunolimab and CAN10. This was then obviously offset by increased spend in general and administration, driven by our transformation, both in regards to transaction-related costs, but also the leadership transformation that we have reported earlier in the year. Our end-of-September available funds amounted to SEK 339 million, and we estimate a cash runway into 2028 with our current and ongoing commitments on nadunolimab and the investments that Hilde mentioned for CAN14 and CANXX, but excluding a pivotal program for nadunolimab and also excluding any potential milestone payments payable to Cantargia from Otsuka in that timeframe. With that, I hand the word back to Hilde for closing remarks. Thank you, Patrik. As a closing remark, we have a significant potential to become both first-in-class with an IL-1RAP antibody in treatment of metastatic PDAC. The development is bolstered by a clear biomarker strategy that guides patient selection. We anticipate being ready to initiate a pivotal study by mid-2026, contingent upon secure and necessary funding and regulatory approvals. In addition, strategic partnership with Otsuka has provided crucial external validation as well as financial flexibility, enabling us to reinvest the development of the promising next generation of anti-IL-1RAP antibodies. With these initiatives, we expect to achieve and report several key milestones in the near future. Thank you for your attention, and I now welcome any questions that you might have. If you wish to ask a question, please dial #5 on your telephone keypad to enter the queue. If you wish to withdraw your question, please dial #6 on your telephone keypad. The next question comes from Richard Romanes from Redeye. Please go ahead. Hello and good afternoon. I'll start with a question about nadunolimab. How long would the proposed pivotal study take? Could you tell us something about what funding options you foresee? We have yet to land on the exact design of the study and also the number of patients, so it's a bit difficult to commit to any timelines. This has also to be cleared with the FDA and EMA, of course, the design. If you look at our competitors, they spend around three years, from two and a half to three years in their pivotal trial. With regards to funding, we will, of course, continuously explore all opportunities to support and accelerate our programs. While partnerships can play an important role in this funding strategy, we do not have any specific commitments for the moment. We remain flexible on financial resources. Okay. I noticed this. There's an increased. To me, it seems you are focusing even more on the autoimmune space with CAN14. Maybe if someone could confirm that there, from what I've seen, there are no approved bispecific antibodies in that space. Is that correct? Would you say that this is a more attractive area for investment compared with oncology right now? Maybe Wolfram, do you want to comment on the oncology part, and I can take the bispecific afterwards? I'm not sure whether I got the question right. Was it the rule of bispecifics in this indication? I mean, I haven't seen any approved bispecifics for autoimmune diseases. Is that? This is right. There are some early trials ongoing, but you're right. Currently, no bispecifics are approved for autoimmune diseases. You are right. That is new, and that is, in a way, a land of opportunity for the company. Great. That's just my focus in an open space where there's not so much competition as in oncology. Yeah. My last question was about the significant increase in administrative costs compared with previous quarters. Could you expand on why that is? Patrik, do you want to? Yeah, it's cost-related to the transaction itself, so it's one-off costs to advisors and consultants and lawyers. Okay. Very well. Thanks for taking my questions. The next question comes from Sarah Nick from H.C. Wainwright. Please go ahead. Hello, team, and thank you for taking the question. I just had one regarding the TRI4 study in the triple-negative breast cancer. I know, as you stated, it didn't show a difference in the OR versus chemo alone. As we're awaiting more mature survival data, I was wondering if you could walk us through maybe how you interpret that data in context of pursuing your strategy in pancreatic and non-small cell lung cancer, and maybe specifically if there are any key biological or clinical learnings and how those are shaping your development strategy going forward. Thank you. Thank you, Sarah. I'll leave that question to Wolfram. Yes. First of all, there is no one fit at all. You can't lump all the tumors together. You can't say, "This is the drug, and this drug is the panacea for everything." We have a very good signal in non-small cell lung cancers, and we do have an excellent signal in pancreatic carcinomas. The biology of breast cancer is totally different. Breast cancer is normally a multicentric disease, as we call it, a systemic disease of the breast. There's a totally different biology. We cannot expect that the drug is equally effective in all of these cancers tested. In addition, breast cancer is, in a way, an endocrine-dependent cancer, and that might alter the effect of interleukin-1RAP inhibitors as well. We do see a signal, certainly not strong enough to move on, but this is not our target cancer. Therefore, we are focusing on the other two. We do not expect that we see a negative result in all the other cancers and vice versa. Does that explain? Yeah. Just to clarify, although the primary endpoint was ORR, we are still awaiting the mature overall survival data. The biology of this that we can learn from this study will, of course, help us to make a final decision. Okay. Thank you. That is very helpful. I think there are other logistic aspects here as well. This was a study in a single country, in a single or more or less single institution or few institutions, oligocentric. That will explain some discrepancies in the result as well. It is not a standard phase three trial with well-defined criteria. Okay. Thank you for the extra color as well. Appreciate it. Next question. The next question comes from Mert Bynvort from Van Lanschot Kempen. Please go ahead. Thank you for taking my question. Could you provide any color or an estimate on how much the phase three trial in PDAC is expected to cost? Thank you. Yes. Hi. Again, I think we, as I alluded to with Richard's question, we have not formally decided on the design, and we're not ready to share our design right now. We need to run this through our regulatory interactions, both with the FDA and EMA. Stay tuned. Thank you. As a reminder, if you wish to ask a question, please dial #5 on your telephone keypad. There are no more phone questions at this time, so I hand the conference back to the speakers for any written questions and closing comments. The first question from the web is related to the triple-negative breast cancer study. Do you expect any negative results from that trial on OS? Why do you think that CAN04 will work in PDAC if it doesn't work in triple-negative breast cancer? Yeah, I think we touched on that. I think we can reiterate that even though ORR is the primary endpoint and showed no difference between the two treatment arms, we still would like to see the mature overall survival data before we conclude. I think also Wolfram did sort of run through with the previous question why we expect a difference or why we expect an effect when we enter into development of PDAC. Sorry, let me chime in here. Obviously, this is something that is in the mind of all participants. Let me make it perfectly clear. There is no panacea for all cancers. All cancers are different, and therefore, we need to treat them in a different way. This is the first thing we have to learn. The second thing is, the mammary and carcinoma breast cancer is a very difficult thing and a very heterogeneous tumor. I'll give you a striking example. Pembrolizumab plus nab-paclitaxel resulted in a triple-negative breast cancer and a huge overall survival benefit. Pembrolizumab plus paclitaxel did not show anything. We don't know why that is. It is the same indication. It is obviously the same drug, and it is the same tumor. There are different results. That is something that we know for breast cancer, which is very tricky. This does not apply to non-small cell lung cancers. I'm overseeing 25 years' research in non-small cell lung cancers and even pancreatic carcinomas. This is a totally different type of cancer with a well-defined and a very distinct molecular biology behind. Therefore, this is, in a way, not very unexpected for us. I hope this clarifies. Yeah. Thank you, Wolfram. I think I just want to add that we do have overall survival data connected to high IL-1RAP in PDAC while we are still awaiting that analysis in triple-negative. Thank you. This second question is related to the CAN10 project, as there are other companies advancing their own programs within that area. Could you comment on your patent position and your competitive standing relative to the other programs being active in that area? We first need to know which indication Otsuka will want to target. It is a bit difficult to be precise on the competitive landscape. I also would like to say that the product is in excellent hands with Otsuka Pharmaceutical, and we are not, for the time being, able to disclose any specific details or where they want to go. We will keep you posted as soon as we know more. Yeah. Another question related to the CAN10 program. Is the handover to Otsuka fully finalized, and are all responsibilities on their hand now going forward? Yes. All the responsibility of the product is in Otsuka's hand. They acquired the product, so they have full freedom to operate in their future clinical development. However, of course, the program is important for Cantargia, so we will monitor the progress tightly. Yeah. Going over to the PDAC study, how confident are you that you will manage to require the funds needed to start this study mid-next year? We will look at all different combinations of financing this study. As I'm sure everyone is aware, a pivotal study in PDAC requires quite a substantially large amount. We will come back to our strategy with regard to financing when we have a bit more insight in where we want to go. Thank you. Also related to that study, will that study be a combination with other drugs like Gemcitabine-nab-paclitaxel, or what's the thinking on the combination strategy for that study? We will have a study in combination with standard of care. Now, how standard of care will look like at the time when we conduct the study, we don't really know yet because Revolution Medicines is approaching the market when we are in our study. However, it will be a randomized two-arm study on top of standard of care. Thank you. To financially— Let me chime in here. I know what you're driving at and where you're alluding to. Revolution Medicines is conducting or has conducted a second-line trial, which will have a readout and has already the database lock, and that will come to be filed in due course. This is second-line. We are talking about first-line. The RefMed study, which might have the potential to change the control arm, is not even enrolling one patient. That is 303, and that will take quite a few times. At the end of the day, both first-line studies will run in parallel. This will actually minimize the risk of changing the control arm during the trial. Thank you. Two questions related to the financial aspects. What are you expecting enrolling cost per quarter in the coming next 18 months, excluding the new studies? Could you elaborate a bit on the upcoming milestone payments that you see in the future? Patrik, do you want to take both of them? Yeah. We have approximately SEK 340 million by the end of September. We have said in our cash runway estimate that it will suffice a bit into 2028. We can assume that that's 10 quarters. You don't need a calculator to calculate what the quarterly burn rate will be then, I think. That is sort of a linear, and things in this business seldom happen linear. That is the best answer I can give right now. Thank you. If possible, could you elaborate around the potential correlation between high cross-expression and high IL-1RAP expression, where high IL-1RAP expression indicates high responses to CAN04? Further elaborate around your thinking and strategy around the targeting hard-to-treat cross-driven cancers through the IL-1RAP pathway. I'm not 100% sure I understood the question, but is it sort of how many other which indications we can target? Jonas, do you think that was the question? No, it's more about the correlation between high cross-expression and high IL-1RAP expression and how that sort of affects your strategy. Okay. We are targeting indications that we see a good correlation of where high IL-1RAP is a prognostic marker for poor prognosis. There are at least four or five indications where this is the case. For now, our focus is on PDAC. I think you can understand that as a small company we need to focus. Right now, PDAC is our sole focus. Thank you. The final question is related to whether you will be organizing any presentation together with Otsuka in the near future around the CAN10 project. We don't know, but we don't expect to do that. If we do, we'll, of course, keep you updated. Thank you. There are no more questions coming in from the web. Okay. Thank you, everyone. Thank you for listening and all of your good questions.