Greetings, and welcome to the INmune Bio's 2025 Fourth Quarter and Year-End Earnings Call. As a reminder, this conference is being recorded. A transcript will follow within 24 hours of this conference call. At this time, it is now my pleasure to introduce Mr. Daniel Carlson, Head of Investor Relations of INmune Bio. Daniel?

Thank you, Cloey, and good afternoon, everyone. We thank you for joining us on the call for INmune Bio's 2025 Fourth Quarter and Year-end Financial Results. Presenting on today's call are David Moss, CEO and Co-Founder of INmune Bio; Dr. Mark Lowdell, Chief Scientific Officer and Co-Founder of INmune Bio; Dr. CJ Barnum, Head of Neuroscience; and Cory Ellspermann, INmune Bio's CFO. Before we begin, I remind everyone that except for statements of historical facts, the statements made by management and responses to questions on this conference call are forward-looking statements under the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. These statements involve risks and uncertainties that can cause actual results to differ materially from those such as forward-looking statements. Please see the forward-looking statements disclaimer on the company's earnings press release as well as risk factors in the company's SEC filings, including our most recent And quarterly filings with the SEC. There is no assurance of any specific outcome. Undue reliance should not be placed on forward-looking statements, which speak only as of the date they are made as the facts and circumstances underlying these forward-looking statements may change. Except as required by law, INmune Bio disclaims any obligation to update these forward-looking statements to reflect future information, events or circumstances. Now my pleasure to turn the call over to INmune Bio's CEO, David Moss.

Thank you, Dan, and good afternoon, everyone. Thank you for joining us for INmune Bio's Fourth Quarter and Full Year 2025 Earnings Call. Today, I'll begin with an overview of our progress and strategic priorities across the business. Mark will then provide an update on our CORDStrom platform with a focus on our RDEB program. CJ will follow with an update on XPro and our Alzheimer's disease development efforts. Cory will then review our financial results. After that, I'll return to highlight our key upcoming milestones before we open the call to questions. 2025 was a pivotal year for INmune Bio. We completed our MINDFuL Alzheimer's trial, advanced CORDStrom towards registration, and continue to position each of our platform programs for the next stage of development. As we move into '26, our focus is very clear. Execute against the most important regulatory clinical and strategic milestones across the portfolio. Starting with CORDStrom, this remains our most advanced program and a major value driver for the company. We recently presented additional patient data that further reinforces the therapeutic profile of CORDStrom in Recessive Dystrophic Epidermolysis Bullosa, or RDEB. These data showed clinical meaningful wound healing, reductions in itch and improvements in quality of life, all with a favorable safety profile. Based on this progress, we're in the final stages of preparing our regulatory submissions in both the U.K. and the United States, and we remain on track to file the MAA in the U.K. by the end of summer of '26. As Mark will tell you shortly, CORDStrom has a clear batch-to-batch manufacturing consistency, which makes the product reproducible ensuring commercial grade uniformity. Further, the clinical mechanism of action of CORDStrom for RDEB has been worked out along with the potency assays, which is an important step for regulators. The repeatable…

Thank you, David, and thank you to everyone who's joined the call today. Welcome. So as David said, CORDStrom showed great promise in the randomized placebo-controlled trial in RDEB, but it potentially extends way beyond RDEB to other forms of Epidermolysis Bullosa, and indeed to other conditions and indications. CORDStrom remains truly revolutionary in the MSC field. And last year, we reported on the fact that since it's created from mesenchymal stromal cell banks from 4 or more pooled donors, it really has unrivaled stability and reproducibility to compare to all of the other mesenchymal stromal or stem-cell products that are being developed or are on the market. Moreover, what we found is that the pooling allows us to select the individual mesenchymal stromal cell donor seedstocks, and we can choose those that have the appropriate potency characteristic for each disease indication, which allows us to tailor the final product to target different disease indications and thus have different drugs. As you know, RDEB is our first disease indication, and over the past 6 months, we've been able to dissect the precise mechanism of action of CORDStrom in RDEB. That's pretty unique for mesenchymal stromal cell product, while the diversity of the product means that working out quite how it delivers its effect is actually very challenging, but we now know that CORDStrom works by secreting an array of chemical messengers called cytokines, which are used by the body to control inflammation. We know that RDEB is predominantly a disease of inflammation, and it's driven by cells in the skin, which are called Type 1 macrophages or M1 cells. These M1 cells secrete inflammatory cytokines, which drive the itch and lead to the scratching, which causes the skin wounds so prevalent in RDEB patients, in which you'll be familiar with.…

Thank you, Mark. I'll give you an update on XPro and where we're headed. MINDFuL was our Phase II trial in Alzheimer's disease. We designed it around a simple question. If we pick patients who have both Alzheimer's pathology, and signs of inflammation in their body, and we treat the inflammation, do they do better? What we saw was very encouraging. The results consistently favored XPro across clinical, behavioral patient-reported and blood and imaging biomarkers. The Phase I identified what works, who it works for and resolved the open questions so that Phase III can be successful. These results directly inform how we designed the Phase III program. We identified the patient population, those with both Alzheimer's pathology and biomarkers of inflammation. Decades of Alzheimer's research show that cognitive changes come first and functional changes follow with time. That's why the Phase III trial runs 18 months, long enough for the cognitive effects we saw at 6 months to show up on the functional measures the FDA requires for approval. The program is built as an adaptive trial with 2 stages. Phase IIb gives us a decision point at 9 months. a clear go or no go before we commit to the full Phase III investment. If the data hold, the trial continues seamlessly into the registrational stage with the CDR sum of boxes, the same primary endpoint used to approve lecanemab, and donanemab at 18 months. We presented this program to the FDA at the end of Phase II meeting earlier this year. The agency reviewed our data, our enrichment strategy, and our trial design and aligned with our approach. We are now moving forward on several fronts. On the development side, we continue to analyze the MINDFul data set to fully understand the impact of XPro treatment. At the same time, we are preparing the Phase III program for initiation, which includes finalizing the protocol based on the FDA's feedback and pursuing the partnerships and funding needed to execute it. There's a lot of work ahead, but the foundation is solid. I'll hand it back to David. I look forward to your questions. David?

Thanks, CJ. Before I hand the call to Cory to go through our financial results, I want to emphasize from a capital perspective, we remain committed to capital efficiency. Our strategy is built on hitting clear data-driven milestones that allow us to maximize shareholder value while minimizing unnecessary burn. We're focused on maintaining the lean execution-oriented culture that has brought us to this stage. With that, let me pass the call to Cory to go through our financial results. Cory?

Thank you, David. Net loss attributable to common stockholders for the year ended December 31, 2025, was approximately $45.9 million compared to approximately $42.1 million for 2024. Research and development expenses totaled approximately $20.7 million for the year ended December 31, 2025, compared with approximately $33.2 million for 2024, with the decrease due to incurring lower expenses in connection with the Alzheimer's trial in 2025. G&A expenses was approximately $10.3 million for the year ended December 31, 2025, compared with approximately $9.5 million for 2024. We also recorded a full impairment of our intangible asset of $16.5 million in 2025 following the release of the Phase II results of the Alzheimer's trial, in which the trial did not meet the clinical endpoint. During 2025, the company sold 3 million shares of common stock for net proceeds of approximately $17.4 million in a registered direct offering. In addition, the company sold approximately 1.3 million shares of common stock for net proceeds of approximately $10.1 million under at-the-market offerings. At December 31, 2025, the company had cash and cash equivalents of approximately $24.8 million. And as of March 30, 2026, the company had approximately 26.6 million shares of common stock outstanding. Based on the current operating plan, we believe our cash is sufficient to fund our operations through Q1 2027. And now, I'll hand the call back to David.

Thanks, Cory. Now I'd like to present upcoming milestones for the company, and then we can start with the Q&A. For CORDStrom program, we have several significant milestones ahead, which will really set our track for 2027. As Mark mentioned, we're on track to file the MAA in the U.K. by mid-summer 2026. A few months after the MAA filing, we expect to submit the MAA to the EMA and then the BLA to the FDA towards the end of the year. We should have feedback from all 3 geographies in '27, if not, approvals by then. I mind investors that it's our belief that a successful BLA application would likely result in the company obtaining a priority review voucher from the FDA, given that the program already has orphan drug designation and rare pediatric disease designation. For XPro, we continue to make strong progress. We've now received the minutes from our end of Phase II meeting with the FDA, as CJ had mentioned, and we obtained positive initial feedback on the accelerated approval pathways or we're active preparing for next steps. We're advancing partnership and funding discussions to support late-stage development of XPro. Stepping back, we entered 2026 with a focused set of objectives and multiple meaningful opportunities to create value, while MINDFuL trial did not achieve its top line primary endpoint due to powering the patient population properly, the totality of XPro data set continues to support our conviction in the program's potential in Alzheimer's disease and other neuroinflammatory disorders. At the same time, we believe CORDStrom is advancing towards a potentially transformative regulatory and commercial inflection point with the broader platform still not fully reflected in the market. We appreciate the continued support of our shareholders and the commitment of our team as we work towards these goals. At this point, Cloey, I'd like you to tell people how they can ask questions and poll for questions.

[Operator Instructions] And we'll take a question from Elmer Piros with Lucid Capital Markets.

David, what I'd like to ask, and maybe Mark can help us out here. If there is any anticipated differences between an MAA and an FDA submission. Have you had interactions with the FDA, what might be their requirements different from the European or from the U.K. agency?

Yes, I'll -- that's a very good question. Yes. So we -- the last time we spoke to the FDA specifically was a little bit about 13 months ago? And what they came back with was some -- one of the things that's been at the top of my mindset is, -- all of the work we've done so far in RDEB, the products being made from umbilical cord donors from the U.K. and there is a sensitivity about using U.K. donor materials in the U.S. And so we asked the FDA specifically whether we would be allowed to use U.K. donor cords for the U.S. submission. And they came back and said, absolutely, yes, but we would have to screen the U.K. donors for the standard globally agreed infectious disease markers, but they'd have to be tested in U.S. labs in clear accredited labs. And so what we're doing at the moment is creating new master seedstock and from donors that we can ethically test in the U.S. So that's the biggest difference. We have to create a new master seedstock, which is ongoing at the moment. But because we -- as I said earlier on, we've worked out the mechanism of action. We now have potency assays. We've been able to demonstrate that we've made 4 different master seedstocks experimentally from U.K. donors, and they've all been consistent. So the next point is that we make for the FDA filing, which you're going through at the moment, will be those that we take through for commercialization globally. So that was the principal question that we had, and it was the principal answer that they came back with The rest of the questions they came back with were identical to those from the MHRA. So yes, we will present exactly the same data set.

Elmer, let me -- if you don't -- Elmer, if you don't mind, let me just add to that. So the plan is what's -- if you -- a few months -- a few weeks ago, we submitted essentially a pre-MAA package to the MHRA, which will -- which really effectively is like a Type B meeting and it kind of -- it kind of smooths the process of the full MAA application speeds the process up that we intend to file midsummer. Once we get the feedback from the MHRA, and as Mark will tell you, they've already set a face-to-face meeting with us. Once we get that, we'll put that together with the answers to whatever questions they have or whatever feedback they give us, and then we'll submit that as a Type B meeting to the FDA in preparation really like a pre-BLA in preparation of the BLA with the FDA. And so that will be the steps that will take place. I think that might have been a little bit of what you're asking, if I'm correct?

Yes, yes, yes. And just maybe one more detail around this. So would you have to have the samples tested in U.S. labs before you submit or you can have that during the submission or during the evaluation and submit it when you have the results?

So what they will ask is for a confirmation that we will only supply drug into the U.S. from U.S. tested donors. But in point of fact, we're making the master cell batch now. So we will have products that have been made from U.S. tested donors before we submit the BLA.

Yes. And maybe one question about the course -- the XPro program. David, have you had interest, any interactions with potential former partners at ABPD? upon feedback, you get .

No, good question, Elmer. We have ongoing discussions with some groups. And one of the things that now you have to realize, we've just got the end of Phase II minutes a few weeks ago, 3, 4 weeks ago now. And -- so everything is being factored out. But 1 of the things we intend on doing this is finding a group to help us on the BD perspective because there's just a lot of not just large pharma but midsized companies, that we think the program is very appropriate for because if you think about it, it's a relatively small investment to see the Phase IIb portion for obviously a very large market, potentially one of the largest markets. The Phase IIb portion reads out as we expect with the right patient population from what we've learned from the MINDFuL trial, then it's a very clear path to the registration program as CJ had talked about linking the cognitive aspects of EMAC to the cognitive aspects of CDR and then getting the functional scale of CDR, which comes after cognitive changes over time. So the link is very logical. The correlation between EMAC and CDR is very logical. And so we think that this package had explained appropriately to the midsized EBITDA biotech companies that have an interest in neurology, all the way up to the large pharma. I think it's going to be a very attractive program.

And it does appear that there are no further questions at this time. I would like to hand it back to David Moss for any additional or closing remarks.

Thank you, Cloey. 2025 was a year of significant progress for INmune Bio. We completed and analyzed the MINDFuL Alzheimer's trial, advanced CORDStrom towards registration in RDEB and positioning commute for its next stage of development in prostate cancer. As we move toward through 2026, our priorities are very clear: advance CORDStrom's towards marketing approval in the U.K., EU and the U.S., secure regulatory clarity on the path forward for XPro and build the partnerships and financial support necessary to bring these programs to patients. On behalf of the entire INmune Bio team, thank you for your continued support and confidence in our mission. We look forward to updating you on our progress in the months ahead. Have a great evening, everybody.

Thank you. This brings us to the end of today's meeting. We appreciate your time and participation. You may now disconnect.