Mineralys Therapeutics Q1 2024 Earnings Call Transcript

Quartr
Provided by Quartr
May 9, 2024

There are 11 speakers on the call.

Operator

Good morning, ladies and gentlemen, and welcome to the Mineralist First Quarter 2024 Earnings Conference Call. At this time, all lines are in a listen only mode. Following the presentation, we will conduct a question and answer session. This call is being recorded on Thursday, May 9, 2024. I would now like to turn the conference over to Garth Russell of LifeSci Advisors.

Operator

Please go ahead.

Speaker 1

Thank you, operator. Good morning, everyone, and welcome to our Q1 2024 conference call. Earlier this morning, we issued a press release providing our Q1 2024 financial results and business updates. A replay of today's call will be available on the Investors section of our website approximately 1 hour after its completion. After our prepared remarks, we will open up the call for Q and A.

Speaker 1

Before we begin, I would like to remind everyone that this conference call and webcast will contain certain forward looking statements about the company. Actual results could differ materially from those stated or implied by these forward looking statements due to risks and uncertainties associated with the company's business. These forward looking statements are qualified by the cautionary statements contained in today's press release and our SEC filings, including our Annual Report on Form 10 ks and subsequent filings. Please note that these forward looking statements reflect our opinions only as of today, May 9. Except as required by law, we disclaim any obligation to update or revise these forward looking statements in light of new information or future events.

Speaker 1

I would now like to turn the call over to John Congleton, Chief Executive Officer of Mineralis. John?

Speaker 2

Thank you, Garth. Good morning, everyone. Welcome to our Q1 2024 financial results and Corporate Update Conference Call. I'm joined today by Adam Levy, our Chief Financial Officer and Doctor. David Rodman, our Chief Medical Officer.

Speaker 2

Considering the relatively short period of time between this call and our Q4 call, we're going to keep our prepared remarks today fairly brief. I'll begin with an overview of the business and recent milestones, followed by Adam, who will review our Q1 financial results before we open up the call for your questions. Let me start now by stating that we continue to make great progress with our clinical trials and reaffirm our previously stated guidance on the timing of our top line data readouts, which I will review in a moment. Before getting into each trial in detail, let me take a moment to touch on our overall strategy and basis for our pipeline, which is focused on targeting dysregulated aldosterone. Aldosterone is known to be a significant driver of cardiorenal metabolic diseases.

Speaker 2

And thus, we're developing an aldosterone targeted treatment approach with lorondrastat. We believe lorondristat has the potential to benefit millions of patients who are impacted by hypertension, kidney disease and heart disease. For example, dysregulated aldosterone levels are a key factor in driving hypertension in approximately 25% of all hypertension patients. This is a significant population as there are an estimated 115,000,000 patients in the United States who have hypertension and of the 60,000,000 treated patients more than half failed to achieve their blood pressure goal. The outcome can be severe for these patients.

Speaker 2

As according to the World Health Organization, there are 7,500,000 deaths attributable to hypertension per year globally. Given the impact of uncontrolled hypertension on cardiorenal outcomes, we made hypertension our lead indication for the development of lorondristat. In addition to hypertension, we're currently investigating the benefits of lorondristat in subjects with hypertension in CKD. We entered 2024 with clear goals for our registration program in hypertension, which is comprised of 2 pivotal clinical trials, titled ADVANCE H10 and LAUNCH H10. An open label extension trial called Transform HCN to capture long term safety and efficacy data and the proof of concept trial EXPLORER CKD evaluating loranderstat and hypertensive CKD subjects.

Speaker 2

ADVANCE H10 is the first of the 2 pivotal trials we have initiated, which started enrolling patients 1 year ago. Enrollment in the trial remains ongoing and we anticipate top line data to be available in the Q4 of this year. This is a state of the art extremely rigorous hypertension trial, which is designed and executed in collaboration with the experienced cardiovascular research team at the Cleveland Clinic. The trial is designed to demonstrate the value of lirondrastat when added to standardized, optimized guideline background treatment in patients with uncontrolled or resistant hypertension as confirmed by 24 hour ambulatory BP measurement. We believe this is the only trial of an aldosterone direct therapy that is utilizing this rigorous standardized background treatment approach.

Speaker 2

As such, this trial has the potential to generate high quality evidence that will be important for potential inclusion in the hypertension guidelines for treating physicians and for creating favorable access via payers. As you may be aware, the targeted treatment of hypertension is a major point of our strategy. Data presented last year from TARGET HTN trial laid the foundation for identifying patients who best respond to lirondristat such as those patients with an elevated BMI. The planned analysis of the ADVANCE HTN trial includes a well powered confirmatory test of the predictive value of obesity on the efficacy of lorondristat. We believe the inability of an optimized 2 or 3 drug standard antihypertensive regimen to reduce BP to goal in the setting of obesity will be a straightforward approach to identifying candidates for treatment with lorondristan.

Speaker 2

In addition, we plan to continue to explore other positive and negative predictive tools using an unbiased artificial intelligence model to expand the work repertoire of useful tools for targeting lirondersat to individuals most likely to derive long term clinical benefit. LAUNCH HDAN is our 2nd pivotal trial, which we initiated in the Q4 of 2023. We continue to anticipate top line data to be available in the second half of twenty twenty five. This Phase 3 trial, which will enroll up to approximately 1,000 adult subjects, is designed with the objective of evaluating the Runderset in a real world setting when added to subjects previously prescribed background regimen of 2 to 5 antihypertensives. Subjects who fail to achieve blood pressure control on their prescribed background treatment during the run-in period will be randomized 1 to 2 to 1 to either placebo, once daily 50 milligrams of lorondrastat or once daily 50 milligrams of lorondrastat with the option to titrate to 100 milligrams once daily as needed at week 6.

Speaker 2

The primary endpoint for this trial will be change in systolic blood pressure as measured by automated office blood pressure. We believe this endpoint reflects real world measurements that will be relevant to the primary care provider this trial targets. In addition, subjects from these two trials will be offered the opportunity to roll over into the ongoing open label extension trial called Transform HTN. In addition to the hypertension pivotal program, we're conducting the EXPLORER CKD Phase 2 clinical trial for lorondrastat in patients with hypertension in Stage 2 to 3b chronic kidney disease. We continue to anticipate top line data to be available in Q4 24 to Q1 2025.

Speaker 2

EXPLORER CKD is a within subject comparison trial designed to demonstrate the benefit of lirondristat in reducing blood pressure and provide supportive evidence for potential benefit on chronic kidney disease on the background of a stable SGLT2 inhibitor treatment. This proof of concept trial will enroll approximately 60 subjects with hypertension in Stage II to IIIb CKD. We are pleased with the steady progress the team has made in the strengthening of our clinical program for this promising new approach to treating hypertension and the associated complications like chronic kidney disease and heart disease. We look forward to keeping you apprised with the status of the lorondersat development program. Let me now turn the call over to Adam, who will provide a financial review for the Q1 of 2024.

Speaker 2

Adam?

Speaker 3

Thank you, John. Good morning, everyone. Today, I will discuss select portions of our Q1 2024 financial results. Additional details can be found in our Form 10 Q, which was filed with the SEC earlier today. We ended the quarter with cash, cash equivalents and investments of $338,600,000 compared to $239,000,000 as of December 31, 2023.

Speaker 3

In February 2024, we completed a private placement financing for net proceeds of approximately $116,000,000 We believe that our cash, cash equivalents and investments will be sufficient to allow us to fund our planned clinical trials as well as support corporate operations into 2026. R and D expenses for the quarter ended March 31, 2024 were $30,800,000 compared to $12,300,000 for the same quarter of 2023. The increase in R and D expenses was primarily due to increases of $16,800,000 in preclinical and clinical costs, dollars 3,700,000 in clinical supply, manufacturing and regulatory costs, $1,700,000 in higher compensation expenses resulting from additions to headcount and stock based compensation and $300,000 in other research and development expenses, partially offset by a decrease of $4,000,000 in license fees. G and A expenses were $4,600,000 for the quarter ended March 31, 2024 compared to $2,600,000 for the same quarter of the prior year. The increase in G and A expenses was primarily due to $1,300,000 in higher compensation expense as resulting from additions to headcount and stock based compensation, dollars 500,000 in higher professional fees associated with operating as a public company and $200,000 in higher insurance and other administrative expenses.

Speaker 3

Total other income was $3,900,000 for the quarter ended March 31, 2024 compared to $2,300,000 for the same quarter of 2023. The increase was primarily attributable to increased interest earned on our investments in money market funds and U. S. Treasuries. Net loss was $31,500,000 for the quarter ended March 31, 2024 compared to 12,600,000 dollars for the same quarter of 2023.

Speaker 3

The increase was primarily attributable to the factors I described earlier. With that, I'll ask the operator to open the call for questions. Operator?

Operator

Thank you. Ladies and gentlemen, we will now conduct the question and answer session. Your first question comes from Jeff Meakim from Bank of America. Your line is now open.

Speaker 4

Hey, thanks for the question. This is John Joy on for Jeff. So with top line data expected in 4Q 2024, what would be a positive readout for you in terms of clinical response and safety profile?

Speaker 2

Yes, John, thanks for the question. Done a fair amount of market research with payers and physicians with the target HTN data where we saw an 8 millimeter to 10 millimeter mercury placebo adjusted drop. We believe if we replicate that, that is a transformative change for subjects using loroderstat in the 3rd or the 4th line. That's based on the fact that with the currently available treatments, when you go to a 3rd and 4th line agent, you typically see a 5 to 6 millimeter mercury drop at best. And so if we replicate what we've seen in target HTN of 8 to 10 millimeters mercury placebo adjusted, We believe that will be very resonant within the market and support the opportunity that loranderstat represents in the hypertension space.

Operator

Your next question comes from Annabel Samimy from Stifel. Your line is now open.

Speaker 5

Hi, this is Jack on for Annabel. Thanks for taking our questions. So could you remind us the powering for the ADVANCE HTN trial and what magnitude of placebo response you might be expecting here acknowledging that these patients should have a truly uncontrolled hypertension? And then with launch HTN, because those background treatments are going to be variable, what kind of steps have you taken to help minimize the noise and the variability there when it comes to the top line beta generation?

Speaker 6

This is Dave Rodman, CMO. Thanks for the questions. So the first question was in the ADVANCE trial, some of the statistical questions, what's the powering and what do we expect the placebo to be? So I'll remind you in ADVANCE, we're using 24 hour ABPM as the primary. And with 24 hour ABPM, because you're averaging over the course of the day, you get much more stable averaging measurements.

Speaker 6

We saw a placebo effect of around 2 millimeters of mercury in our first trial. And I think that's about what we would expect. That's obviously a very, very quiet placebo effect. As far as powering, we're certainly sufficiently powered to detect the range that John mentioned that 8% to 10% and actually overpowered for that. Now you asked also in your second questions launch, which is more real world, what steps have we taken?

Speaker 6

Let me first say that our placebo effects when we did the target HTN trial on that population was about 4 millimeters of mercury. And so all of the steps we took in that trial to get essentially a best placebo effect and lowest variability are incorporated into this trial. We've made a few other steps to look at things further. But probably the most important one is we do use a home an app based AI interpreted adherence tool. And as you probably know, a great proportion of the reason why people don't respond to their antihypertensive regimen is in fact that they don't take it.

Speaker 6

A great contributor to placebo effect is that people do start taking it on trials. We get rid of that problem because we in the run-in, we do the adherence already and we use a placebo in the run-in. So we already have a baseline taking that big variable out of the picture. We piloted a number of different adherence tools in Target. This was the one that has the best performance and it's really proven itself to be a remarkable way to get better data.

Speaker 6

There are other things, but that's really what I would emphasize.

Speaker 5

Got it. And then, if I could just sneak in one more maybe, so now that you mentioned the differences in the placebo effect of maybe 2 millimeters, 4 millimeters. About how much variance is there between the ABPM and AOBP measures? Basically, trying to ask here if you're expecting to see like vastly different result ranges in advance versus launch?

Speaker 6

Well, that's a great question. And when John mentioned 8 to 10 millimeters of mercury earlier, the primary was AOBP in the target HTN trial and the primary in the LAUNCH trial is also AOBP. So in that trial, we expect things to be pretty comparable to 8 to 10. Now when you in a person with normal blood pressure control, when you go to sleep, your blood pressure goes down. And so when you average 24 hours, you end up with a lower value for blood pressure and a proportionately lower response.

Speaker 6

The primary in the ADVANCE trial is 24 hour average ABPM. And typically you will see about a 1 to 1.5 millimeter lower systolic blood pressure change in trials when you compare the 2. We also have the ability, however, to look at 24 hour daytime and that will be closer to what you see with AOBP. Does that answer your question?

Speaker 5

Yes. That was very helpful. Thank you.

Operator

Your next question comes from Seamus Fernandez from Guggenheim Securities. Your line is now open.

Speaker 7

Hey guys, thanks for the question. So, just wanted to clarify, Dave, a couple of those last points. So, when we're thinking about the difference between 24 hour ABPM and the AOBP measures, I think that 8 millimeter to 10 millimeter threshold, I just wanted to clarify a couple of things. Number 1, we do know that the half life is a bit shorter and with lorondestat. So just trying to get a better characterization of how much you would anticipate that overnight average to change And how you're actually measuring blood pressure overnight?

Speaker 7

Is that a continuous monitor that you're using to average over time? And then when you've looked at other studies in terms of that comparison, as you look at comparisons of the design of ADVANCE versus other programs, Just trying to get a more complete understanding of what typically happens during that overnight period, for placebo as well as for a full kind of long acting once a day versus a program that has a shorter half life in that regard? Thanks.

Speaker 2

Yes, Seamus. I'll start and have Dave add some thoughts. And if we miss any of your points there, let me know. But I want to address the question on the half life because the point I do want to reiterate from Target HTN, the primary endpoint was AOBP that was in office. And those measurements were taken in the morning before that day's dose.

Speaker 2

So we were looking at nadir within the office and we actually saw that 8 millimeter to 10 millimeter mercury reduction that was also replicated within the 24 hour ABPM. So we're very confident in the once daily dose. And we actually think it the 10 to 12 hour half life creates kind of an ideal mix of efficacy and safety based on what we've seen and we'll continue to evaluate that. Now to some of your deeper questions on the 24 hour monitoring, I'll have Dave address those.

Speaker 6

Thanks Seamus. We split a lot of thought into what pharmacology would be optimum. And as John mentioned, we like this idea of having a time for some release in the sort of the pre dawn hours so that Aldo can do its job in terms of excreting potassium. But if you think about the mechanism of action, this is a diuretic. It lowers your web volume.

Speaker 6

And overnight, you don't really take on more volume, you're asleep. In the morning, when you get up, you take our drug and within 1 hour, you've gotten rid of aldosterone. And so essentially during the period of time when you need the sodium loss, the maturesis, you get it from our drug. During the amount of time when you can switch out and lose potassium, you get that window with our drug. And so the other thing that I'll mention is that when we measure aldosterone levels in blood before the dose in the morning, the median value is a 70% reduction from the baseline value that you get without drug.

Speaker 6

So we still have a substantial reduction even though we have the shorter half life, it's just not 0. We get complete suppression of Aldosterone an hour after a dose 70% in the morning. So don't think of it as a switch that's on and off. I like to think of it as restoring normal circadian rhythm. This is what you should be doing.

Speaker 6

You should have a lower algo, which is what we produce, but it should be highest in the morning and then go down during the day, which is exactly what happens.

Speaker 2

Davis, did we get to your all of your questions?

Speaker 7

I think that covered majority of it. But just as you look at other clinical studies and the performance of placebo versus an active, whether it be with an ACE or an ARB or mineralocorticoid targeted agents, MRAs, What do you typically see during that overnight period?

Speaker 6

Yes. So good question. So let me start with the placebo piece. So first of all, as I said, in our study, the first study, even with the relatively small numbers of 30 per arm, we saw a 2 millimeter of mercury placebo effect. And so that's de minimis.

Speaker 6

It's not going to change over the course of the day because that's really not a treatment effect. That's just a measurement variability. And to answer your question that I completely forgot to answer, people wear a cuff in a recorder 24 hours, whether they're awake or asleep. The only difference is we do measurements around every 20 minutes during the day and we space them out a little bit more at night because it can tend to disturb sleep a little bit, which can raise your blood pressure. So that's how we do it.

Speaker 6

We don't expect to see a difference in placebo effect overnight. We do expect to see a reduction in blood pressure. In fact, we will often see what's called restoration of nighttime dipping. So for you and I without sleep apnea, without untreated hypertension, our blood pressure will dip at night. It will go down as I mentioned.

Speaker 6

Hypertensive patients will first just lose the dipping then get actually hypertensive overnight. So that's what we expect to see at night.

Speaker 7

Great. And as we think about the this is just my last question, the importance of having a diuretic onboard like HCT, as we think about the differences between your 2 programs, how do you expect the sort of diuretics to come into play? Is that consistently baseline therapy across the board for all patients and then add on therapy from there in both trials? Just trying to get a sense of how that sequencing is likely to incorporate standard thiazide based diuretics?

Speaker 6

Yes. Thanks for letting me clarify that. Everyone in both trials needs to be on a thiazide or a thiazide like diuretic. And I'll mention also that in the United States at least, the first line drug now is recommended to be a fixed dose combination between an ACE or an arm and a thiazide diuretic. And so this mimics what guidelines would say.

Speaker 6

You come in on 2 drugs, but they're in the same pill and there's always a thiazide in that. So we're following to the letter the way we expect patients to show up in the doctor's office. And therefore, when we give them guidelines and say, if they don't respond, if they're on that regimen, if they're obese, you should think about our drug as a next step. Our data are going to exactly support that sort of practice pattern.

Speaker 2

And Seamus, as you're well aware, in target H10, we had a little over half of the subjects on a diuretic, a little under half not on a diuretic. And we saw a clear additive benefit of lorondristat with the diuretic. So when we think about what we hope to see from an effect size in advance and in launch of that 8 millimeter to 10 millimeter mercury, which is replicating target that doesn't take into account the potential additivity of the diuretic, which as Dave said, will be part of the background medication in both ADVANCE and launch HTN. Great. Thanks so much guys.

Speaker 2

Appreciate it. Seamus, good talking to you.

Operator

Your next question comes from Michael DiFiori from Evercore. Your line is now open.

Speaker 8

Hey guys, thanks so much for taking my question. Just a general one for me. It's regarding, just any preliminary thoughts you may share on how MINERALIS may proceed in cardio or renal metabolic syndrome if the CKD trial is successful, just given that the people are starting to look at the CV field more holistically nowadays?

Speaker 2

Yes, Mike. Thanks for the question. I appreciate it. I think you're right. We're seeing this shift from treating hypertension and CKD and heart failure and OSA as these independent standalone conditions, but really looking at the inter play between them, can we find benefits from a single agent across that spectrum.

Speaker 2

That's really kind of the basis of how we've been advancing for us. Hypertension is really kind of the beachhead indication. It's really in a lot of ways the genesis of these conditions. So you have hypertension that leads to CKD, heart disease, stroke. And so from our standpoint, the first step forward into that broader cardiorenal metabolic syndrome is the EXPLORER CKD study that's going to give us a perspective on not only addressing hypertension, but also the renal insufficiency within those patients.

Speaker 2

We also believe that that's a white space for us. There are a lot of agents for hypertension. There are a lot of agents for kidney disease, but to have a benefit on both is a little bit unique and distinct and that's something that we think lorondrastat can point out. As we continue to learn more information about lorondrastat through our development program, We'll continue to contemplate where else can we extend the value of an aldosterone synthase inhibitor that has best in class selectivity like lorondristat. And it could be some of these other areas that begin to get into heart disease, heart failure.

Speaker 2

There are a variety of places we can go. And I think as we're seeing a renaissance within research and in the pipelines right now, we're seeing more and more focus on Aldosterone, which we believe is an important thing to do given the rising prevalence of dysregulated Aldosterone, which Mike you've heard us say before, we believe at least 25% of all hypertension patients are dealing with this and that probably extends into full cardiorenal metabolic syndrome as well.

Speaker 8

Great. Very helpful. Thanks again.

Speaker 6

Thanks, Mike.

Operator

Your next question comes from Rami Khadla from LifeSci Capital. Your line is now open.

Speaker 9

Hey guys, thanks for taking my questions as well. I guess first, is there any risk that the 3 week run-in period in advanced HTN is not long enough to have patients get to stable blood pressure on the standardized background regimen?

Speaker 6

So good question. Many of the people who come in will already be on most or not all components of that given the type of patients we're screening for and screening out. And so I think the risk is relatively modest. It's taken care of though in the design because the placebo group stays on that regimen. So let's just say over 12 weeks in the run-in period, let's just say their blood pressure dropped by 8 millimeters of mercury, but it drops another 3 from the regimen over those 12 weeks.

Speaker 6

That will then be in the placebo effect, but it will also be in the treatment arms and it will just get subtracted out. So in the placebo adjusted, there's no risk.

Speaker 9

Got it. That makes a lot of sense. And then I guess with BI's ASI, it was recently shown to have a selectivity of 250 to 1, but they still saw a number of cases of adrenal insufficiency in their CKD study. I guess, does this change your view at all on the selectivity threshold that's needed to kind of avoid the off target suppression of cortisol?

Speaker 6

Well, it's a really good question. I'm going to point out that when we had LCI-six ninety nine at Novartis when I was there, that's essentially what killed the drug and that's why it actually is sold now as a treatment for hypercortisolism, not hyperaldosteronism. So the regulators are extremely, if not super sensitive about this issue. When we do those selectivities, what we do is we take recombinant human enzyme and test it. But once you're in a patient, there are other variables.

Speaker 6

So I don't think I can answer your question and say, we know an exact cutoff in vitro. Proof is in humans. We haven't seen this so far and it hasn't been a close call for us, but we're continuing to look at that. The YBI saw it, I can't say. We're very careful about not including people who've been using high strength steroid creams or taking inhalers for asthma and things like that and confounding the data, we will look at that in profiling later because the real world is people do that.

Speaker 6

So it's possible they're taking people who are predisposed and showing that their drug can suppress them. We're going to take that more carefully in our development program so that when we eventually have guidance for physicians, they know exactly what our drug does and doesn't do.

Speaker 9

Got it. Thanks so much.

Operator

Your next question comes from Rich Law from Goldman Sachs. Your line is now open.

Speaker 4

Hey guys, good to be back and congrats on the progress so far. For ADVANCE HTN, can you discuss how the patients are enrolled and randomized due to 3 week background standardizing period since you're taking patients off to 2 to 5 meds and then putting them on the background of 2 to 3, how do you think that change in treatment from the sanitization could affect the results in the study? And then how do you mitigate against that?

Speaker 2

Rich, the way ADVANCE is built is really to address the question of is somebody truly uncontrolled or truly resistant. And we really have 4 main vectors that we address that during that run-in period before subjects ever get randomized to either placebo or active. And the first is following prescribed guidelines for what subjects should be on. So if patients are on 2 meds coming into the trial, we take them off of those 2 meds and put them on olmesartan and ARB in a diuretic. If they're on 3, 4 or 5 meds, we put them on olmesartan and diuretic and emlodipine and calcium channel blocker.

Speaker 2

So we're putting them on the right drugs according to the guidelines. Secondly, we ensure that they're on the proper dose of those medications. So in the case of ulmicarin, it's 40 milligrams. In the case of the diuretic, it's in DAP minus 2.5 milligrams. If it's HCTZ, it's 25 and amlodipine, it's 10 milligrams.

Speaker 2

So now we've got the right drugs at the right dose. The 3rd piece that we do is we ensure compliance. We know compliance is a factor in patients' inability to get to goal. We're working with a firm called AI CURE that's done, I think, up to 300 different registrational studies with this technology and it's smartphone technology that captures their consumption of these standardized medications during the run-in and then we use it during the randomization period as well for background meds as well as placebo and active. During that run-in period, this allows us to have daily confirmation that subjects have taken their medications.

Speaker 2

This is Bluetooth cloud enabled, so we get daily feedback, our subjects being compliant or not. It goes to the site, it goes to our CRO and it comes to us as far as that information and we're able to actively reach out to these subjects if they're missing doses and reinforce the importance of taking this study drug. So now we have them on the right drug at the right dose and we're ensuring they're compliant. And then at the end of that 3 week period, which as you heard Dave said, when it gets sufficient to get subjects to peak plasma and probably maximal effect with that background regimen, we do 24 hour ambulatory blood pressure measurement. That's the gold standard measurement.

Speaker 2

As you heard Dave say earlier, it has a very de minimis placebo response, takes out a lot of noise in what can sometimes be a noisy measurement in the office. If after that measurement, they continue to be hypertensive, so they have not achieved goal, then we randomize. If they do achieve goal, we don't randomize them and they're not included in the study.

Speaker 4

Great. And then for patients who are treatment resistant on 4 or 5 MET coming into the trial and you take them down to 3 background MET and then adding lorongelstat.

Speaker 10

Do you think these patients

Speaker 4

are more difficult to treat compared to others since they are already treatment resistant on 4 or 5 and then take them back down to 4?

Speaker 6

Yes. So this is Dave Rudman. So traditionally, the definition of resistant is having not reached goal on 3 medications, an acerinarb, a thiazide or a thiazide like diuretic and then either a beta blocker or a calcium channel blocker. And so they may be on 4 or 5 drugs, but once you get to 3 without a drug like ours, you can expect maybe a 3 or 4 or maybe best case 5 millimeter mercury fall with adding any one of those as a 4th drug. But once you add the more you add, the less the benefit generally.

Speaker 6

And the reason for that is you're not going after the main reason that they have this problem. That's the reason why guidelines say go after aldosterone is your 4th line. The problem is there isn't a great drug to do that. Aperinone just simply is too weak. Spironolactone, you can't dose up to the maximum efficacious dose of 100 milligrams to 200 milligrams without running into problems.

Speaker 6

And so the reason why we think we're actually going to be very effective in that population where we cut them down to 3 is that we're going to be the 1st drug that really can go after that guideline of going after Aldo as 4th line because we can dose up to maximum efficacious dose with our drug and get a robust blood pressure response. So I don't think it's a bug. I think it's a feature of cutting them down to 3 and then giving them the drug they really need, which is what we anticipate we're going to

Speaker 4

see. I see. And then one more question from me. So looking at the data you guys presented at ASN last year, where you show BMI versus the SBP reduction, and we see around like 20% of patients who did not respond to treatment across the BMI spectrum, meaning that their SPP actually went up in the study. Have you characterized these patients further on why they did not respond?

Speaker 4

And was there any difference of non responder rate between the 50 mg and 100 mg pills in targeted CTN? And going forward, what do you expect is the non responder rate for your pivotal studies?

Speaker 6

Thanks. So that's a really good question. What we actually and so and I'm going to I hope we don't give you a wonky answer because I'm a wonky guy. But when we do a frequency histogram and ask the question, what's the distribution? On the right side of no response, it's a perfect it's nearly a perfect normal distribution.

Speaker 6

In other words, it's just statistics. They didn't respond on that day, but they might respond a simple similar amount on the next time they're measured. It's just noise in the measurement when you do AOBP. On the left hand side, it's a less skewed distribution, meaning we see responders and we see super responders. And so we really don't think it's a confounder.

Speaker 6

Sure, there will be people in a general population that don't respond to our drug more than an average drug. But it's not really responder, non responder, it's really the normal distribution on the right hand side and this really interesting less skewed distribution where we see people with 30 millimeter mercury falls in blood pressure. The higher their blood pressure, the bigger the fall essentially And that's because they're aldosterone dependent. So it's a really good question. It's easily controlled in our placebo controlled design and the use of our statistics.

Speaker 6

So it doesn't introduce any kind of a confounder.

Speaker 2

And Rich, I'll just add, and you're well aware of this. Our whole intent is to really identify those positive and negative predictors for response to lirondristat. BMI clearly was a pre specified analysis that we did in target HTN. We saw a very tight correlation as far as response magnitude relative to BMI. That's something that we're going to continue to analyze in advance and launch HTN.

Speaker 2

But as I noted in my opening comments, we're partnering with an AI firm to continue to really identify those predictive values that would say this is the type of patient that's going to respond to lirondristat very exquisitely. Dave made the point, the data is out there that as you get into that resistance state, we are on 3 or more background meds. There is an enrichment of an aldosterone dependent form of hypertension in that population because fundamentally those patients aren't being addressed with an Aldosterone directed therapeutic. And so all of those I think are really going to enable us in this development program to come forward with a really clear toolkit of who should be on lirondristat and the kind of benefits that they can derive from

Speaker 4

it. Got it. And then just following up based on what you guys said, is there like a certain percentage of patients who are just not aldo driven in that 4th that third and fourth line? Have you guys thought about there could be other drivers of hypertension?

Speaker 2

I think the literature would say that there are going to be other drivers. Our interest has always been on where aldosterone is driving it. Hypertension is a multifactorial disease. We're not developing lorondristat as a monotherapy. We actually think an ideal combination would probably be an ARB, a diuretic and lorondrastat for those patients who have aldosterone dependent hypertension.

Speaker 2

So there are definitely other factors driving this condition, but that's where frankly we're taking advantage point of let's bring a level of precision to the treatment of hypertension and acknowledge those different variables. And in our case very specifically let's identify those subjects that have dysregulated aldosterone and will benefit extremely well from where I understand.

Speaker 4

That makes sense. And then just another final follow-up. And if are you able to quantify how much of those patients are just not elder driven at that point and may not respond to an ASI?

Speaker 6

So it's a great question. Just to embellish one statement that we've made. If you look at the classical teaching, the most common cause of hypertension beyond what we used to call essential hypertension or primary hypertension is too much aldosterone. Previously that was called hyperaldosteronism and it had a very specific and complex way of diagnosing it. We now call it inappropriate aldosterone.

Speaker 6

The field recognizes that you can have a low aldosterone, but be aldosterone dependent. And so while we will be measuring blood aldosterone, urinary aldosterone, at the end of the day, the gold standard is does your blood pressure go down when you reduce that aldosterone. And so we'll be looking at that, and saying, do we have people who didn't reduce their aldosterone? And is that why they didn't respond? And if that's the case, we will see that in the 50 to 100 dose escalation arm of the trials.

Speaker 6

Or are they truly, truly, truly resistant? Aldo doesn't go down blood pressure Aldo does down blood pressure doesn't. And then we'll be able to answer your question with data and we'll have those data.

Speaker 4

Great. Thank you so much.

Speaker 2

Thanks, Rich.

Operator

Your last question comes from Mohit Bansal from Westwagro. Your line is now open.

Speaker 10

Thank you very much for taking my question. I have a question regarding the CKD proof of concept trial.

Speaker 2

So Mohit,

Speaker 10

can you hear me?

Speaker 2

It was a little bit difficult to hear you. I just wondered if you could reorient the phone.

Speaker 10

Can you hear me better now? Yes.

Speaker 2

Thank you.

Speaker 10

Hello? Yes. So I just wanted to ask, yes, sorry. Can you hear me?

Speaker 6

Yes.

Speaker 10

Okay. Sorry about that. So I just wanted to ask about the kind of magnitude of benefit you want to see in the CKD proof of concept trials here, given the shortened treatment period here, Because I think in the past, you talked about AGLT2 inhibitors could have 30% to 40% improvement in proteinuria. So can you talk a little bit about that and how would you compare and contrast when the data come with what is out there and how would you make the co novo decision here? Thank you.

Speaker 2

I think what we would anticipate Mohit and thank you for your question. In target HTN, again, we saw the 8 millimeter to 10 millimeter mercury placebo adjusted drop in blood pressure with a really nice safety profile. The majority of that response was seen in about 2 weeks, or with 2 weeks we saw the beginning of the drop and the majority of it was at 4 weeks.

Speaker 10

So I think we're comfortable that we'll see

Speaker 2

that level of drop. Renal benefit, I'd hate to extrapolate at this point in time. We know that the kidney benefit to a large degree is derisked with an ASI based on what the Boehringer Ingelheim data that was presented last fall. We wanted to confirm that we see the same benefit with lorondrastat. We think that that UACR effect is likely driven from the reduction in blood pressure.

Speaker 2

And so that's what we anticipate seeing from a BP standpoint of 8% to 10% and then we'll be evaluating what we're seeing from a UACR reduction standpoint. But again, our perspective is ASIs within CKD have been significantly derisked based on some of the other work with the class.

Speaker 6

John, can I just add a little bit to that? Sure. Thanks for the question. It's really a good question. First of all, we made blood pressure the primary because we have a very effective blood pressure drug.

Speaker 6

And if you just treat the metabolic piece of this and you don't treat the hypertension piece of it, you're still going to lose your kidney. And so you have to treat both. And we think our drug is going to be particularly effective there. But flipping over to your question about proteinuria, which is a UACR is what we're measuring. It leads through to decreased decline in GFR over a year or 2, but you can't measure that in a short study.

Speaker 6

And your point is, well, can you really measure something in 4 weeks? The answer is yes. We've talked to many experts about it. Will it be the maximum? It will be most of it.

Speaker 6

It won't be necessarily all of it, but enough. But I want to caution you, everybody is going to come in on SGLT2. This is going to be the benefit of our drug above SGLT2. We don't think we need to do a monotherapy trial anymore because that's already been questions been asked and answered by BI and also AC is doing that. And so we just want to know what's that increment above standard of care.

Speaker 6

So when you compare it, it's got to be apples to apples. Make sure it's not our addition of orondrostat compared to the combination product, say, with BI or AZ, which starts from a lower baseline, it is only the comparison to what they get above the SGLT-two. And we expect to see a similar magnitude what they've reported in their prior trials for that increment.

Speaker 10

Got it. This is super helpful. If I may ask one more, I know I understand that you are approaching CKD or chronic kidney disease as it with hypertension angle, But there is a lot of activity in rare kidney disease space as well. And I mean, the relationship between hypertension and kidney diseases is very much intertwined. Is there an angle which a lot of stat can play in those rare kidney diseases as well?

Speaker 10

Or I'm just too like it's more of a visual thinking right now?

Speaker 6

So that's a really good question. We've been excited to see for instance the IgA nephropathy data. That's a group of it's often children. It's a bad disease and now it has multiple treatments. We expect we can play in that space not against IGA.

Speaker 6

We do have some ideas right now. We're not at liberty to discuss them. But yes, the answer is, I think there is an opportunity there for

Speaker 2

Thanks, Mohit.

Operator

There are no further questions at this time. Mr. John Congolten, please proceed with your closing remarks.

Speaker 2

Thank you, operator, and thank you to everyone for joining us today. We're very excited about the progress we've made thus far in 2024 and advancing our clinical programs and remain enthusiastic about the upcoming milestones for the rest of the year. We look forward to updating you as our pivotal program for loranderstat continues to advance. With that, we'll close the call.

Operator

Ladies and gentlemen, this concludes today's conference call. Thank you for participating. You may now disconnect.

Powered by Quartr
Earnings Conference Call
Mineralys Therapeutics Q1 2024
00:00 / 00:00