Good morning, ladies and gentlemen, and welcome to the Diametica Therapeutics second quarter 2026 earnings conference call. An audio recording of this webcast will be available shortly after the call today on Diametica's website at www.diametica.com in the investor relations section. Before the company proceeds with its remarks, Please note that the company will be making forward-looking statements on today's call. These statements are subject to risks and uncertainties that could cause actual results to differ materially from those projected in these statements. More information, including factors that could cause actual results to differ from projected results, appear in the section entitled Cautionary Statements Note regarding forward-looking statements in the company's press release issued yesterday and under the heading Risk Factors in Diametica's most recent annual report on Form 10-K and most recent quarterly report on Form 10-Q. Diametica's SEC filings are available at www.sec.gov and on its website. Diomedica's President and Chief Executive Officer, Mr. Pauls. You may begin.

Thank you, Morgan, and thank you all for joining us today. With me this morning are Dr. Julie Krop, our Chief Medical Officer, and Scott Kellen, our Chief Financial Officer. Q2 was an important quarter for Diomedica, with progress across DL-19 in early-onset fetal growth restriction, preeclampsia, and acute ischemic stroke. We advanced our pregnancy-related clinical strategy, continued preparations for our Phase II early-onset preeclampsia study in Canada and the UK, and made further progress towards reaching the planned Phase 2-3 Remedy 2 Interim Analysis in Acute Ischemic Stroke. There are four key updates I would like to highlight. First, with respect to the IST being conducted by Professor Kluver, enrollment has been completed in the first cohort of the Phase 2 Early Onset Fetal Growth Restriction Study. The cohort consists of six participants treated at the five microgram per kg dose level. This is important as it expands the clinical use of DM-19 into a second serious women's health disorder for which there are no approved therapies. We plan to host a Key Opinion Leader event in September with Professor Kathy Kluver, the study's principal investigator, and other experts to discuss the potential of DM-19 in fetal growth restriction and share top line results for the completed first cohort open label phase two trial. Second, The extension cohort from the Part 1a of the IST has been completed. This was the initial dose escalation cohort treating women with late-stage preeclampsia. The combined results from the dose escalation and extension groups were important, as noted in the earnings press release, as they provide the clinical support driving the selection of the mid-dose range for the evaluation both for early-onset fetal growth restriction and early-onset preeclampsia studies. Julie will review the data later in the call. We continue to advance our early onset preeclampsia programs on the regulatory and operational fronts, which I will discuss in a moment. And fourth, Remedy 2, our Phase 2-3 acute ischemic stroke study, is approaching the 200th patient required to trigger the pre-specified interim efficacy analysis. Although enrollment slowed somewhat in July, we now have surpassed 85% of the enrollment target, and we anticipate the interim analysis readout in the first quarter of 2027. As a reminder, DM-19 is a recombinant form of the naturally occurring human KLK1 protein. KLK1 is a serum protease that acts through the BK2 receptors present in the enthalial blood vessels to restore the body's natural ability to increase levels of nitric oxide, prostacyclin, and end-of-field-derived hyperpolarizing factors. We believe that this novel mechanism improves vascular biology, makes DM-19 both unique and well-suited to address the endothelial and perfusion-related dysfunction common in preeclampsia, fetal growth restriction, and acute ischemic stroke. As I mentioned, we are pleased to report today that enrollment has been completed in the first cohort of the open-label Phase II IST fetal growth restriction study. The first cohort consisted of six participants treated at the 5 microgram per kg dose level. This study is enrolling early-onset fetal growth restriction patients with or without concurrent preeclampsia. This expansion of our development program allows us to evaluate FGR, a related yet distinct clinical indication to preeclampsia. Early onset FGR is a serious complication of pregnancy associated with inadequate utero placental blood flow. There are currently no therapies approved to treat FGR, just early delivery which can have very serious consequences for the babies. This study is evaluating three dose levels. With the first cohort now fully enrolled, enrollment in the second cohort at 10 micrograms per kg should begin shortly. The dose for the third cohort will be between 1 and 15 micrograms per kg and will be based on the results from the first two cohorts. Key FGR study endpoints include safety and tolerability, prolongation of gestation, flow-mediated dilation, among other measures. This is an important study. It's the first time that DM-19 has been used in early-onset patients. We plan to host a Key Opinion Leader event in September featuring Professor Kuhler, the study's principal investigator, where rationale for DM-19 in treating fetal growth restriction will be discussed, along with top-line results from the completed first cohort. We are excited about this indication because it represents an expansion of DM-19's potential reach based upon the demonstrated improvement in the pulsatility or the resistance index observed in the initial preeclampsia part 1A study. We also anticipate the first patients to be dosed shortly in the IST early onset preeclampsia and continuous IV infusion preeclampsia studies. Based on the results of the recently completed late onset preeclampsia study, a protocol amendment was filed in July to adjust the dosing regimen to provide more flexibility on dosing at the mid to lower level range. Dosing will start shortly after the acceptance of the protocol amendment is completed in coming weeks. Moving to the Global Phase II Early-Onset Preeclampsia Program, Health Canada authorized initiation of our open-label Phase II dose-ranging study in early-onset preeclampsia patients earlier this year. The study is also designed to enroll approximately 30 patients at three dose levels. We are working with SISEN Canada and anticipate to dose the first patient in Q4 of this year. We're also working to expand the study to the United Kingdom later this year, subject to regulatory authorization and site readiness. The results of the multi-preclampsia and FGR studies will be important in defining the dosing for the phase three registrational trial in one or both indications. Turning to expanding the early onset preclampsia trial into U.S. sites, as we announced in June, we believe that based on the FDA feedback, our previously completed RET reproductive toxicology study may be acceptable to support a US IND application, provided that we can demonstrate sufficient evidence of DM-09 exposure and enzymatic activity throughout the previously completed rat study, as well as the adequate pharmacologic effects in rats to support their use as an appropriate toxicology species. To address FDA's request, we are conducting a pharmacokinetic and pharmacologic activity study of DM-09 in rats. following completion of the study anticipated in September and reports in October. We plan to present results to the FDA and work with the agency towards initiating clinical development in the US. Finally, turning to the remedy two, our ongoing phase two slash three acute ischemic stroke trial. Enrollment has now surpassed 85% of the 200 patients required to trigger the pre-specified interim analysis, which is expected in Q1 of 2027. We currently have approximately 70 active sites across the US, Canada, the UK, and six countries in Europe. Site activation in Europe are adding meaningful enrollment capacity. The interim efficacy analysis, which occurs after completion of the protocol-defined 90-day follow-up, will be conducted by the Independent Data Safety Monitoring Board, or the DSMB, and is intended to assess whether a sample size re-estimate is warranted. The final size may range between 300 and 728 patients or futility. Diomedica will remain blinded to data and treatment effect estimates reviewed by the independent DSMB. I'll now turn the call over to Julie to walk through the late-onset preeclampsia Phase 2 Part 1A clinical update in more detail.

Thank you, Rick. As Rick notes, the Part 1A Extension Cohort has been completed with the dosing of the final 12 patients at Stellenbosch University site in South Africa. The cohort enrolled women with late-stage preeclampsia who had severe hypertension and were expected to deliver within 72 hours under the current treatment protocol. The purpose of the Extension Cohort was to more fully characterize the highest dose of DM-199 and provide additional dose response and Dr. Kahn. Thank you for joining us today. At the pre-specified assessment five minutes after completion of the IV infusion, mean systolic blood pressure decreased by 29.1 millimeters of mercury from a baseline of 169.3 millimeters of mercury with a p-value less than 0.001. Mean diastolic blood pressure decreased by 17 millimeters of mercury from a baseline mean of 103.7 millimeters of mercury with a p-value less than 0.01. Mean systolic blood pressure remained below 160 at all measured time points over 24 hours, an important threshold systolic blood pressure for required delivery to reduce the risk of brain hemorrhage in the mother. These findings were consistent with the previously reported dose-responsive reductions in systolic and diastolic blood pressure. Across the dose-ranging cohorts, the most clinically meaningful pharmacodynamic effects observed in part 1a of the study were produced in the mid-dose range cohorts 4 through 8. These participants showed clinically meaningful reductions in both maternal blood pressure and the uterine artery pulsatility index. Note that reductions in the pulsatile index are consistent with reduced uteroplacental vascular resistance, suggesting improved blood flow to the baby, which we believe is key to potentially modifying the underlying disease process in these patient populations. These findings support setting dose levels from the mid-dose range for further clinical evaluation as we move to the early-onset preeclampsia and fetal growth restriction studies. The dose levels for the next studies will begin at 5 micrograms per kilogram and advance to 10 micrograms per kilogram in the second cohort. The dose level for the third cohorts will be selected based on results from the first two cohorts and will range somewhere between 1 and 15 micrograms per kilogram. This is intended to provide flexibility to further define the optimal dose range based on the emerging data. Taken together, we believe these findings provide evidence of a mechanistically on-target pharmacodynamic response for DM-199 and preeclampsia. The study investigators plan to present the full data set including safety, pharmacokinetic, and pharmacodynamic analyses at an upcoming medical conference and submit the results for publication in a peer-reviewed journal later this year. Let me now turn the call back to Rick.

Thanks, Julie. I'd like to now ask Scott to review the financial results for the quarter.

Thank you, Rick, and good morning, everyone. So in walking through the financial results for the second quarter, As of June 30, 2026, our cash, cash equivalents, and short-term investments were $43.5 million. Current liabilities were $6.6 million, and working capital was $37.7 million. Compared to cash and investments of $59.9 million, current liabilities of $5.1 million, and working capital of $55.5 million as of December 31, 2025. We continue to believe that our current cash position will fund our planned clinical studies and corporate operations through 2027. Net cash used in operating activities for the six months ended June 30, 2026 was 17.2 million compared to 14.7 million for the same period in 2025. The increase resulted primarily from the increased net loss in the current year. Turning to the income statement, R&D expenses were $8.2 million and $16.1 million for the three- and six-month time periods ending June 30, 2026. This was an increase from $5.8 million and $11.5 million for the same time periods in the prior year. The increases are primarily due to the expansion of our clinical team, continuation of our Remedy 2 clinical trial, including its global expansion, Costs related to additional reproductive toxicity testing being performed in support of our PE program in the United States, increased manufacturing and development activities, and increases in non-cash share-based compensation. We expect that our R&D expenses will moderately increase in future periods relative to recent prior periods as we continue both our Remedy 2 trial and continue the expansion of our DM-199 clinical development program in preeclampsia. Our general and administrative expenses were $2.3 million and $4.8 million for the three and six-month time periods ending June 30, 2026. These expenses increased slightly compared to the same time periods in 2025, which were $2.2 million and $4.7 million, respectively. The increase for the three-month period was driven primarily by increased non-cash share-based compensation and professional fees, while the increase for the six-month period resulted primarily from increased personnel costs incurred in conjunction with expanding our team, partially offset by a reduction in current year legal and other professional fees. We expect G&A expenses to remain relatively consistent in future periods as compared to recent prior periods. In summary, we remain well-funded with a cash runway through 2027. This covers through our major upcoming milestones, including the Remedy 2 interim analysis, Planned Data Readouts from our Preeclampsia and Fetal Growth Restriction Programs, and Continued Advancement of our Phase 2 Preeclampsia Program in Canada and the United Kingdom. With that, let me ask the operator to open lines for questions.

Thank you. We will now begin the question and answer session. If you would like to ask a question, please press star then the number one on your telephone keypad to raise your hand and join the queue. If you would like to withdraw your question, simply press star 1 again. Your first question comes from Josh Shimmer with Cantor. Your line is open.

Great. Thanks for taking the questions, two quick ones. First, just trying to understand the commentary around dosing while you're focusing on the 4 to 8 microgram per kilogram cohort, so not the higher doses for the late onset preeclampsia program, but then you are exploring higher doses. The early onset preeclampsia program, so maybe you can kind of square that and help us understand that strategy. And then for the fetal growth restriction program, are there any inclusion criteria that you're using to try to focus on patients who you might think might be most likely to respond and or have evidence of impaired placental perfusion at baseline? Thank you.

Sure, thanks. Thanks, Josh. Yeah, so what we're seeing from the Part 1a As we've seen in other clinical trials, there's really a sweet spot for dosing DM-199. And we believe KLK1 selectively improves uterine blood flow while also controlling blood pressure. But what we see is happening if we go too high, we think we're still controlling blood pressure, but we think that we run into receptor desensitization. And because of that, we see less of the dilation. And so this is consistent to actually what we've seen in Glucose studies for type 2 diabetics, we've seen the same effect. In kidney disease studies, we're looking at EGFR and UACR, where we see a greater clinical effect at the 3 microgram compared to the 15. And then in addition, we also have an issued patent as well on this nonlinear dose response curve. So I think for us it's important that we've got some flexibility here that we can adjust the dose, but really more targeting this mid-range. In regards to your second question, in terms of FGR, so these are very severe patients. So these are FGR between weeks 27 and 32, and they'll be patients that earn the 3% or less percentile in terms of body weight. So they're very severe. So we think that these babies typically, if they were not being treated, that they would be delivering between one and six days. And so we think extending the gestational days, dilating the interuterine arteries and other factors, we think this could be very exciting. So this really is focusing on the dilation. And then we also believe that if we do see positive signals, this will be encouraging ahead of early onset preeclampsia because there we think we can also be controlling blood pressure in addition to the dilation. We're really excited to have this KOL event in September.

Your next question comes from Stacy Koo with TD Cowen. Your line is open.

Hi, good morning. Thanks so much for taking your questions and congratulations on all the progress. So first, on the fetal growth restriction, let's say cohort one data that we're going to get in September, maybe just help us understand The importance of maybe that chronic dosing that we're going to see. How many doses do you think you might disclose? Again, I know very early days, so just help us understand kind of that dynamic. And then as we think to maybe the growth restriction and what's maybe clinically meaningful, is it a week of extension before delivery? Is it longer than that? Just help us understand. for the type of dynamics or maybe even a little sneak peek for the KOL event when it comes to the unmet need. So that's the first question on FGR. The second is on maybe your learnings for early onset preeclampsia. Just remind us, what are the, I guess, ongoing thoughts around IV versus subcutaneous administration? maybe what kind of refinements you might be applying as you think about the different cohorts. I know you just talked about the receptor desensitization, but just help us understand what's the most up-to-date thinking on the frequency of dosing, et cetera. And then the last question is a clarification on the FDA IND submission. Is it fair to assume after we finish this enzymatic study, sounds like it's gonna be completed in October, that you'll be able to kind of submit the R&D to the FDA. Thanks so much.

Yeah, sure. So starting with the first question. So for FGR, I think what's important here is that, you know, we think we've got very encouraging data thus far with the late-onset patients where the patient's got one dose IV and then one dose subcutaneous. But this is really going to be the first time that we've actually dosed early-onset patients. And the premise is the patients will come in, they're getting... Subcutaneous dosing every three days until delivery. And as I mentioned, we think that standard of care, which basically is really limited, we were anticipating somewhere between one and six days. So from our perspective, we had indicated earlier that if we could get another five, six days, that could have a profound impact in terms of outcomes for these babies. Hopefully we'll get a few weeks on that front. In terms of the early onset preeclampsia, one of the changes as well we've made is that we're dropping the IV infusion and focusing on subcutaneous dosing every three days until delivery. One of the cohorts coming up for preeclampsia is a continuous IV infusion, and that'll be in late onset patients. And the premise there is that We believe by adjusting the dose, we can dial in the blood pressure to the targeted range. And so if we see positive effects there, what we would then anticipate for phase three for preeclampsia is that we're dosing every three days until systolic blood pressure approaches 160. And then at what point we would switch over to continuous IV infusion that can hopefully get us even a few extra days. And then turning to your third question with the IND. Yeah, assuming all goes well with the rat study that's already been initiated, it's ongoing. We should be completing that in the early part of September. The plan would be then to submit for a US IND. When we did meet with the FDA to discuss this topic, the last comment they had indicated to us that this was the last piece that they thought we needed to open up the IND.

Thank you so much.

Your next question comes from Thomas Flavin with Lake Street.

Your line is open.

Good morning. Thanks for taking the questions. Rick, just following up on the FTR, you know, what's clinically meaningful, what's not. So you mentioned days of gestation. Is there going to be an endpoint looking at what percentile the baby grows to? I know you said these are, you know, third percentile or less. Are you trying to get the baby up to fifth, tenth percentile? I don't really know what the number would be, or is this simply and others.

We'll be looking for changes to that. The two main ones we're looking at initially is the gestational days because we do believe keeping baby and mom longer should result in larger, healthier babies. We'll also be looking at the dilation of interuterine arteries. Typically, if a mother is not getting a treatment. There's no fact that that dilation should be worsening with time. So if we can even see a stabilization to an improvement, that would be super encouraging. Yeah, and there will be a series of other endpoints that we'll be looking at as well for the study.

And then just for the part 1a data that you shared today, I'm assuming you tracked the same endpoints that you did in prior cohorts around placental transfer, uterine dilation, and intrauterine artery dilation. Will that be presented at some point, or how do you think about disclosing those other endpoints?

Yeah, so our collaborators are preparing to submit for publication in a peer-reviewed journal and sharing the full data set there.

Got it. And then one final one on Remedy2. Assuming enrollment pace picks up from July, Once you hit the 200 and get past the endpoint for the data to get to the DSMB, how close will you be to that initial target of total enrollment, do you think, at that point when you do the interim analysis readout?

Yeah, so after patient 200 is dosed, there'll be a 90-day follow-up for the primary endpoint, and then there'll be another, you know, four to six weeks for the data analysis, and then at one point we'll provide a public update. and during that period of time we will continue to be dosing patients. So hopefully we'll be getting closer and closer to 300 patients that we think would be potential the base case in terms of the study.

Got it, thank you.

Your next question comes from Matthew Caulfield with HC Wainwright. Your line is open.

Hi, thank you. Hi Rick and team, congrats on the interim data set. So for the Phase 2-3 remedy trial, the interim analysis looks like it's slightly shifted from fourth quarter to early 27. You've noted the 85% enrolled towards the interim analysis. Have there been any nuances for the recruitment process to date, or how that could possibly translate to the ease of real-world patient selection in the future? Thanks a lot.

Yeah, I mean, this trial's been very interesting. We'll get one month where we get very significant enrollment and then the following drops up substantially. And so it's odd in terms of how it goes. But in terms of practical, in terms of real world use, I think the big benefit of this drug here is the safety profile. So we think this drug will be able to be used in community hospitals. And so because of that, I think we're very excited about the prospects of Your next question comes from Chase Knickerbocker with Craig Hallam. Your line is open. Morning, everyone. Thanks for taking the questions.

This is Jay Kahn for Chase.

I was wondering for the company sponsored phase two, can you just walk us through the timelines to be in the clinic in both the UK and the US?

Yes, so we are for the company sponsored trial for the early onset preeclampsia, we're targeting late this year. And then for the UK, we're just going through the regulatory process. hopefully a similar time, maybe that's into early 2027.

Okay, and is there any more detail on the regulatory process in the UK that we could get?

No, we're just going through the process we've identified. To the submission process, we have identified three great sites, and we're working through them in terms of getting the study to launch. So in total, we've got five sites, So we've got three in the UK and two in Canada. And again, in total, we're targeting 30 patients. And the protocol is very similar to the IST that's also running concurrently.

Thank you. Appreciate that, Keller.

That concludes our Q&A session. I will now turn the conference back over to Rick Pauls for any closing remarks.

All right. Thank you, operator. Before we close today's call, I want to say to please keep an eye out for a press release announcing the date of our KOL event focusing on early onset fetal growth restriction. At that event, we look forward to sharing the scientific rationale for using DM-19 to treat FGR along with top line results from the first patient cohort in our open label phase two trial. We believe DM-19 represents an important opportunity in treating pregnant mothers with FGR. We're really excited to share more details with you soon. Thank you again for joining us today and for your continued interest and support. We look forward to updating you on the progress in the coming months. Operator, you may now close the call.

This concludes today's call. Thank you for attending. You may now disconnect and have a wonderful rest of your day.