Earnings call transcript: Alpha Cognition Q2 2025 sees stock fall 20%

Alpha Cognition Inc (ACOG), with a market capitalization of $160 million, reported its Q2 2025 earnings, revealing a significant operating loss and a subsequent 20.82% drop in its stock price, closing at $9.99. According to InvestingPro data, the stock has shown significant volatility with a beta of 2.71, while maintaining a "GOOD" overall financial health score. The company highlighted the commercial launch of its Alzheimer’s treatment, Zunveil, but faced challenges with high operating expenses and a net loss of $10.5 million.

Key Takeaways

• Alpha Cognition reported a net loss of $10.5 million for Q2 2025.
• Stock price fell by 20.82% in aftermarket trading.
• The company launched Zunveil, targeting Alzheimer’s patients with swallowing difficulties.
• Operating expenses were high at $7.4 million.

Company Performance

Alpha Cognition’s Q2 2025 performance was marked by the launch of its new Alzheimer’s drug, Zunveil. Despite the launch, the company reported an operating loss of $5.7 million. The company is focusing on the long-term care Alzheimer’s market, aiming to capture patients with specific needs like swallowing difficulties. While high operating costs and a substantial net loss overshadowed these efforts, InvestingPro analysis shows the company maintains strong liquidity with a current ratio of 17.14 and more cash than debt on its balance sheet. Get access to 10+ additional ProTips and comprehensive analysis with an InvestingPro subscription.

Financial Highlights

• Revenue: $1.7 million, primarily from net product sales.
• Net product sales: $1.6 million.
• Licensing revenue: $81,000.
• Operating loss: $5.7 million.
• Net loss: $10.5 million (65¢ per share).
• Cash and equivalents: $39.4 million.
• Interest income: $425,000.

Outlook & Guidance

For the full year 2025, Alpha Cognition anticipates operating expenses between $34 million and $38 million. The company expects its monthly net revenue run rate to reach between $5.75 million and $6.25 million. InvestingPro data indicates the stock has shown strong momentum with a 69.61% YTD return, though analysts expect net income to decline this year. Additionally, Alpha Cognition is working on a sublingual formulation of its drug, anticipated for 2026, and plans to explore ex-US revenues by late 2026 or early 2027. Discover detailed Fair Value analysis and growth projections with an InvestingPro subscription, including access to comprehensive Pro Research Reports covering 1,400+ US stocks.

Executive Commentary

CEO Michael McFadden expressed enthusiasm for the initial launch of Zunveil, stating, "We are excited about the initial quarter of launch for Zunveil." COO Lauren DeAngelo added, "The majority of new patient starts are progressing through the titration period as expected," highlighting the company’s focus on building its prescriber base.

Risks and Challenges

• High operating expenses could continue to impact profitability.
• Market competition in the Alzheimer’s treatment space remains intense.
• The company’s reliance on a single product for revenue growth poses risks.
• Economic pressures and healthcare reimbursement challenges may affect future sales.
• The anticipated "hockey stick" revenue growth curve might not materialize as expected.

Alpha Cognition’s Q2 2025 results reflect the challenges of launching a new product in a competitive market. While the company is optimistic about its future prospects, the significant stock drop indicates investor concerns about its financial health and growth potential.

Full transcript - Alpha Cognition Inc (ACOG) Q2 2025:

Conference Operator: Greetings and welcome to the AlphaCognition Earnings Call. At this time, all participants are in a listen only mode. A brief question and answer session will follow the formal presentation. As a reminder, this conference is being recorded. It is now my pleasure to introduce your host, Henry Du, Interim Chief Financial Officer, Vice President of Accounting and Finance.

Thank you. You may begin.

Henry Du, Interim Chief Financial Officer, VP of Accounting and Finance, AlphaCognition: Thank you, Sachi. Good afternoon, everyone, and thank you for joining us today for AlphaCognition’s second quarter twenty twenty five financial results conference call. This morning, the company issued a press release announcing these results. On the call with me today are AlphaCognition chief executive Michael McFadden and Chief Operating Officer Lauren DeAngelo. Today’s call is being made available via the Investors section of the company’s website at www.alphacognition.com.

During the course of this call, the management may make certain forward looking statements regarding future events and the company’s future performance. These forward looking statements reflect Alpha Cognition’s current perspective on existing trends and information. Any such forward looking statements are not guarantees of future performance and involve risks and uncertainties, including those noted in the Risk Factors section of the company’s latest SEC filings. Actual results may differ materially from those projected in these forward looking statements. For the benefit of those of you who may be listening to the replay, this call is being held and recorded on 08/14/2025.

Since then, the company may have made additional announcements related to the topics discussed. Please reference the company’s most recent press releases and current filings with the SEC. AlphaCognition declines any obligation to update these forward looking statements except as required by applicable securities laws. I’ll now turn the call over to Michael.

Michael McFadden, Chief Executive Officer, AlphaCognition: Thank you, Henry. Good afternoon, everyone. Thanks for taking the time to join us on today’s call. Today marks an exciting milestone for our company as it marks our first quarter of earnings following the commercial launch of Zunveil for the treatment of mild to moderate Alzheimer’s disease. The 2025 was characterized by a successful commercial launch of Zunveil, engagement in the long term care segment of our market, advances with payers, progress with our business development partner, and the initiation of publications highlighting SunVeil data and the market opportunity before us.

During the quarter, the company made substantial progress on our commercial launch. The sales and marketing team made contacts with over 3,700 HCPs in the long term care market. We saw prescriptions written in over 300 nursing homes. We saw duplicative prescriptions written in 65% of these nursing homes, which we believe is a strong indicator of product trial. We expect new and duplicative home numbers to rise significantly in the coming quarters.

Regarding medical progress, Zunveil appears to be performing well reports of cognitive improvement, behavioral reduction, and continued limited reports of adverse events. Our medical team has five abstracts that have been accepted for publication with three presentations made at AAIC in July. Additionally, we anticipate seven additional abstracts to be submitted for publication or presentation at future medical meetings in the long term care segment. Regarding an update on research and development, we continue to advance our sublingual formulation and anticipate formulation and tasting work to be completed in 2026. The company plans to run a comparative PK study versus our tablet and intranasal formulations, and we will use this data as a basis for submission of an IND in the 2026.

The significance of this formulation is it can be used for patients with Alzheimer’s who have dysphasia or aphasia, which is difficulty swallowing, or the inability to swallow tablets or capsules. Our estimates are that twenty percent of Alzheimer’s patient population suffer from this malady, and they currently have the option of a patch formulation or their caregiver must grind a tablet or mix capsule contents in applesauce or something similar to deliver their medicine. We believe if ultimately approved, the sublequal formulation will displace the current options for majority of patients. Further in research and development, the company’s bomb blast preclinical study with alpha ten sixty two concluded in late Q2. This was a two part study funded with the Department of Defense grant and in collaboration with the US Department of Veterans Affairs and the Seattle Institute of Biomedical and Clinical Research.

The conclusions of part one of the study demonstrated that alpha ten sixty two administration reduced levels of neuroinflammation and neuropathology that occur after a blast trauma. The second part of the study concluded that alpha ten sixty administration reduced brain levels of three toxic forms of the protein tau. One of the forms, tau two seventeen, has been suggested to identify patients at greater risk of long term cognitive decline. An additional form, tau two thirty one, is elevated in early Alzheimer’s disease and in TBI. These toxic forms of tau suggest a potential role for alpha ten sixty two in the treatment of TBI.

Additional benefits were shown that alpha ten sixty two reduced numbers of myeloid cells, which play a critical role in neuroinflammation and tissue repair, as well as the number of astrocytes which regulate neurotransmitters like glutamate and GABA, which support neuronal health. These changes are consistent with reduced neuroinflammation following alpha ten sixty two administration. Regarding business development, the company made significant progress with our first ex US partner, CMS Pharmaceuticals, who’s representing Zunbel r and d and distribution in China and Greater Asia. The company heard from Chinese regulatory authorities they’ve accepted Zunbel application for review, which represents a milestone for CMS and the AlphaCognition team. Additionally, our partner is on track to file in four additional countries by the 2025, which keeps us on track to generate ex US revenues in the latter part of twenty twenty six.

The company continues to manage expenses judiciously while preparing to capitalize on emerging opportunities in the long term care market. Chief among these is optimally positioning Zunveil, which has clinically meaningful benefits across both cognitive and behavioral symptoms associated with Alzheimer’s disease. These effects are consistent with the product label as multiple studies have shown Zunveil to improve behavioral symptoms frequently observed in patients with mild to moderate Alzheimer’s disease. I’ll ask Lauren to discuss our commercial progress momentarily, but first I’ll turn the call over to Henry to speak to the financials for the company.

Henry Du, Interim Chief Financial Officer, VP of Accounting and Finance, AlphaCognition: Thank you, Michael. As I review our second quarter twenty twenty five results, please refer to today’s press release and 10 Q that were filed earlier this afternoon. Starting with our operating results, for the 2025, we generated total revenue of $1,700,000 This consisted of 1,600,000.0 in net product sales from our lead commercial product, ZYNVAIL, which launched at the ’1, an additional 81,000 in licensing revenue from our strategic collaboration with CMS. Since launch, we have reported approximately $2,000,000 in net product revenues for ZYNDAL. These results underscore initial traction in our commercialization efforts and lay the foundation for scalable growth in the quarters to come.

Total cost and expenses for the quarter were $7,400,000. This comprised of $539,000 in first year cost of revenues and operating expenses of $6,900,000 versus 2,400,000.0 in q two twenty twenty four. The change was largely attributed to initial year sales and an increase in selling, general, and administrative expenses as we invested in our commercial launch activities for ZYNDAL and related operational expansion. Correspondingly, our operating loss was 5,700,000.0 versus 2,400,000.0 during the same period in 2024. Turning to net income performance.

For the 2025, we reported a net loss of $10,500,000 or 65¢ per share compared to a net loss of 2,100,000.0 or 35¢ per share in the same quarter last year. The difference primarily reflects a $5,200,000 noncash loss from changes in fair value of warrant liabilities. Now moving on to the balance sheet where we remain well capitalized. As of 06/30/2025, the company had approximately $39,400,000 in unrestricted cash and cash equivalents, supplemented by $425,000 of interest income earned during the quarter. Lastly, a brief update on guidance.

While we are still not providing revenue projections at this time, we anticipate our full year 2025 operating expense to be in the range of $34,000,000 to $38,000,000 This is actually from previous guidance primarily reflects the successful execution of cost optimization initiatives, disciplined expense management, and a more efficient allocation of resources across the organization. We believe this range approximate appropriately reflects the level of investment required to advance our commercial efforts and support key corporate initiatives throughout the year. In summary, the 2025 was a period of continued momentum highlighted by the incremental revenue growth from Zunveil and a solid liquidity position. These outcomes demonstrate prudent financial execution and encouraging early signs of market uptake. As we look ahead, our team remains committed to executing against our strategic goals creating long term value for all our stakeholders.

I will now turn the call over to Lauren to discuss commercial progress.

Lauren DeAngelo, Chief Operating Officer, AlphaCognition: Thanks, Henry. The 2025 marked a significant acceleration of ZUNVAIL in The U. S. Long term care market. Following our late Q1 launch, we are seeing strong early indicators, including positive market signals, meaningful early adoption and encouraging engagement from both prescribers and LTC facilities.

By the end of Q2, ZunVeil had been ordered in over 300 long term care homes across our priority regions. Notably, 65% of those facilities have already placed repeat orders, a strong early indicator of both clinical confidence and operational fit within the LTC setting. Prescriber feedback remains very strong. The majority of new patient starts are progressing through the titration period as expected. We are closely tracking patient persistence and initial data trends are encouraging.

While increased demand created new payer related hurdles, particularly around prior authorizations, these challenges have not dampened prescription volume, though they have slowed the approval process. I am pleased to report though that 90% of Zunveil orders have been filled. Our team is actively adapting to the nuances of each health plan and PBM, and we expect the approval process timeline to compress with continued learning. Our sales team made substantial progress in expanding clinical reach during Q2. As of quarter end, our field force had directly engaged with fifteen sixty four unique prescribers and reached nineteen sixty nine homes.

Additionally, virtual education programs have been well attended, helping to drive ongoing brand awareness and clinical confidence. To date, approximately three seventy HCPs have written at least one Zunveil prescription during Q2, and fifty six percent of those writers have written more than one order, a strong early indicator of initial interest across our target prescriber base. Looking at the nineteen sixty nine homes reached, three thirty of those homes are productive with sixty five percent of ordering homes having repeat orders reflecting strong engagement. Additionally, twenty eight percent ordered for the first time in June. Our disciplined market access strategy continues to progress.

As of July 1, we are pleased to report the signing with a large national health plan, one of the largest pharmacy benefit managers in The U. S. This agreement opens the door to potential access for approximately 17,000,000 Medicare Part D lives. While access across downstream clients may vary, this milestone significantly strengthens our position within long term care. Additional discussions with regional payers and LTC focused plans are currently underway.

Our twenty twenty six Medicare Part D bid submissions remain on track. We remain committed to broadening access while maintaining pricing discipline. Our wholesale acquisition cost of $749 a month continues to be viewed as competitive and aligned with branded CNS therapies. Our commercial organization continues to perform at a high level. All four regional sales leaders and our full field team are now fully deployed.

Their deep CNS and long term care experience is driving effective engagements across the complex and highly regulated channel. With an average of sixteen years of industry sales experience, including ten years in LTC, our team is demonstrating a strong competitive advantage. Operationally, we’ve maintained high fulfillment rates across our distribution network, ensuring reliable product availability as demand scales. Q2 marketing efforts were highly targeted with a focus education and brand visibility. Our digital and in person initiatives were carefully crafted to reflect the unique decision making structure within LTC settings.

Early feedback on messaging and materials has been very positive. Importantly, based on direct provider feedback, we have refined our messaging to highlight Zunveil’s label consistent benefits across multiple behavioral domains measured by the neuropsychiatric inventory, or the NPI. These refinements ensure our communications remain clinically grounded, regulatory aligned, and relevant to prescribers managing a broad spectrum of behavioral symptoms in Alzheimer’s disease. NPI was a key secondary endpoint in galantamine’s registrational trial and the findings provide strong support for Zunveil’s impact on neuropsychiatric features commonly seen in long term care populations. We also introduced a clinical titration support toolkit to aid HCPs during initiation.

This resource has been well received and is reinforcing clinical confidence. Looking ahead, as we enter the 2025, our commercial focus remains on expanding Zunveil’s presence across additional long term care homes, growing our base of repeat prescribers, deepening engagement with high potential HCPs, and advancing payer access initiatives in preparation for 2026. We are encouraged by our early results and confident in our ability to sustain momentum in the quarters ahead. Thank you to our commercial team for their outstanding execution and to our investors for your continued support. With that, I’ll turn it over to Michael.

Michael McFadden, Chief Executive Officer, AlphaCognition: Thank you, Lauren. In summary, the team is focused on execution. We’re focused on executing more calls with high value HCP targets, managing current restrictions with health plans and pulling through the contracts with others, increasing prescriptions by home and by prescriber to take advantage of the opportunity we see for Zunvell in the long term care market. Our business development team has worked with our partner in Asia to file Zunvell ahead of schedule to deliver what we believe will be twenty twenty six approvals that will add additional revenues for the company. The company continues to believe we have a disruptive opportunity with Zunveil, and we’ll focus the next quarters on our selling efforts and continued financial discipline.

With that, we’ll take questions. Sachi?

Conference Operator: Thank you. We will now be conducting a question and answer session. You may press 2 if you would like to remove your question from the queue. For participants using speaker equipment, it may be necessary to pick up your handset before pressing the star keys. One moment please while we poll for questions.

The first question is from Ram Selvaraju from H. C. Wainwright. Please go ahead.

Ram Selvaraju, Analyst, H.C. Wainwright: Thanks very much for taking my questions and congratulations on all the progress so far. First, a couple of questions for Lauren. I was wondering if you could characterize for us the typical profile of what you expect to be a repeat prescriber of ZUNVAIL. You know, if there’s anything particularly distinguishable about such physicians. And also if you could perhaps comment on what you expect the state of contracting to be by the end of this year, How many additional contracts you expect to have in place?

Whether that is likely to be primarily at the GPO level? And what the scale of those contracts is likely to be based on the discussions you’re currently having? Thank you.

Lauren DeAngelo, Chief Operating Officer, AlphaCognition: Sure. No, those are great questions, Ram. Thank you so much for the questions. As far as what the typical profile looks like for a repeat prescriber, the good news is most of so we’ve got targets that we set at quarterly business reviews, and our sales representatives are really targeted in on those specific targets. And what we have seen to date with consistent messaging, with consistent frequency visits, calling on these facilities, most of them are repeat customers.

So I wouldn’t say there’s a particular specific type of profile that’s repeat, because we’ve already honed in on those really high volume nursing home facilities that have a high number of Alzheimer’s patients. And then now with our additional behavioral messaging, it broadens the opportunity even further for potential patients for Zunveil. So I hope that answers your question. It’s really about us staying super diligent and focused on our key targets that we’ve identified during our quarterly business reviews and executing to that plan. And those customers, based on all of the feedback to date that we’ve received with their experience on

We expect repeat customers. As it relates to additional contracts for the remainder of the year, as you can probably hear in my tone, we are very excited that we already have a very large plan that we have contracted with. This is very rare. When you just launch a couple of months within the first quarter to get a signed contract, I’m happy to report that we are in deep discussions with a couple more plans. I do expect to have at least one more large national plan contracted by the end of the year.

And hopefully, as the team stays diligent on our market access strategy, we could potentially announce additional plans. But I feel confident that we will have another large plan by the end of the year.

Ram Selvaraju, Analyst, H.C. Wainwright: And then just a couple more, maybe both Lauren and Michael you can address these. Firstly, with respect to the evolving picture on the prior authorization front, maybe you can give us a little bit more color on that, what in addition is being asked or put in place in terms of previous treatment history, prior experience with cholinesterase inhibitors, you know, that, you know, is different from, you know, what we saw at the previous earnings report, as well as with respect to as as as we look ahead to how the company is gonna be prioritizing capital allocation, maybe this question is a little bit more for Michael and maybe also Henry. You know, how are you thinking about the timeline for ongoing and future R and D activities, particularly clinical development as things scale on the revenue side? Thank you.

Lauren DeAngelo, Chief Operating Officer, AlphaCognition: Sure. So, I’ll take the prior authorization question and then I’ll pass it over to Michael. So when we came out of the gates in April, as you’ll probably remember, I reported to the team here that we were seeing very little prior authorizations. And of those prior authorizations, we were seeing a very simple checklist and they weren’t getting approved. What we found as we moved into May and June with increased demand, we came out pretty strong.

The plans did take notice. And so we did see the prior authorizations increase amongst across the board, among all of the prescriptions that were written. Also in the long term care setting, there’s concept called transitional fill. So when a patient is put on a new treatment, many of these patients will get a fourteen day or twenty eight day transitional fill without a prior authorization, and then they’ll get the prior authorization will kick in. So, we saw a lot of that coming into April, which is why we saw such little prior authorizations.

Now, as what the team is doing, and I’d say we are adjusting on demand daily, we’re having calls to see which plans are giving us more trouble, I will say that the prior authorization checklist or what’s required is very similar to what we’re seeing from just a smaller number in April. So, have they failed and tried a generic? And then is there a reason why they can’t use a generic? So, the prior authorizations, the ones that the team is getting to and supporting the pharmacies on guidance on how to fill out these prior authorizations, we’re able to provide support, they are all getting through. So, we are getting much better with monitoring the prior authorizations.

We now know what to expect. Our reimbursement specialists are in contact with a lot of key pharmacies. They have a relationship ongoing, and therefore we’re able to provide best case scenarios what has worked in the past. So it’s still a simple PA, there’s just more of them. So we’re not seeing the PAs not get approved.

I think as I mentioned, 90% of orders are getting filled. It’s just delaying the time to fulfillment. So we’re seeing we could see up to a three week delay before that PA actually gets through just because the volume is increasing. I hope that answers your question, Ram.

Ram Selvaraju, Analyst, H.C. Wainwright: No. That’s very helpful.

Michael McFadden, Chief Executive Officer, AlphaCognition: I’m sorry. Do you have a follow-up, Ram, on that before I answer the clinical question?

Ram Selvaraju, Analyst, H.C. Wainwright: You know, just in in in that context, I was wondering if you would care to share at this point in time what the monthly net revenue run rate looks like here in the third quarter.

Michael McFadden, Chief Executive Officer, AlphaCognition: Yeah. We anticipate a range of $5.75 to $6.25 depending on the execution of that contract. So I think that’s a good net number for everybody to model. And regarding the clinical funding for advancement with our sublingual formulation and advancement on the TBI front, We have built into the expense guidance that Henry provided the dollars required to advance those programs to IND, so we’re in good shape. The formulation and work that we’re doing is a tedious, complex work, but it’s low cost work.

And, we’ve already captured the work necessary on the TBI front as well for next steps for that program.

Ram Selvaraju, Analyst, H.C. Wainwright: Thank you.

Conference Operator: The next question is from Boris Peaker from Titan Partners. Please go ahead.

Boris Peaker, Analyst, Titan Partners: Great. My first question is, can you comment maybe anything particularly special about the initial adopters from the patient’s perspective? Do they have GI symptoms? Or are these patients just starting cholesteatase inhibitors? Or are they maybe switching from Aricept?

Just help us understand the low hanging fruit from the patient side.

Lauren DeAngelo, Chief Operating Officer, AlphaCognition: Sure. So what we’re seeing as it relates to which patient type physicians are using Zunveil on, I would say about half of them are patients who are a Denepozyl patient and we are seeing those patients being switched from Denepozyl to Zunveil. That also helps obviously with the prior authorization because right there you’ve got a recent activity that they were already on a generic. But we are also seeing a large bolus of patients who have been treated in the past, but in most cases they weren’t able to tolerate the treatment medication, as you guys know. That’s why Zunveil is here.

And so they may have been off treatment for a little bit, but they’re on nothing. And so they will initiate therapy with Zunveil. I would say those are our two most common types of patients. However, recently with the launch of our behavioral messaging, we have really, really solid data that is consistent with label, regulatory aligned that we are able to use with Sunveil on these behavioral symptoms associated with Alzheimer’s disease. I would say moving into the quarter that we’re in now, we’re seeing a little broadening there where physicians are now identifying patients who have Alzheimer’s, whether they’re on an acetylcholinesterase inhibitor or they’re not, and they see an opportunity for Zunveil to help with some of those behaviors.

I think we’re moving into a third patient type as we move forward with our new messaging on behaviors.

Boris Peaker, Analyst, Titan Partners: Great. My next question is on gross to net discounting. Can you maybe comment, on where it stands now and how you think that’s gonna evolve maybe over the next, six to twelve months?

Michael McFadden, Chief Executive Officer, AlphaCognition: Yeah. We’re we’re approximately $600 now. We think over the coming quarters, not months, but quarters, it’ll be in the $5.75 to $6.20 25 range depending on the mix of patients per health plan. So I think those are good numbers to model.

Boris Peaker, Analyst, Titan Partners: Great. And my last question is when should we be expecting that second $3,000,000 tranche from CMS?

Michael McFadden, Chief Executive Officer, AlphaCognition: We expect that the last quarter of this year based on current progress with CMS.

Boris Peaker, Analyst, Titan Partners: Great, thank you for taking my questions.

Conference Operator: The next question is from Dave Storms from Stonegate. Please go ahead.

Dave Storms, Analyst, Stonegate: Good evening and thanks for taking my questions. I just wanted to start, you’ve mentioned in the past that you’re expecting a hockey stick shaped revenue curve. I guess do you see anything changing there? Does maybe Asia run a little ahead of schedule, deepen this curve, move it to the left a little bit, anything there?

Michael McFadden, Chief Executive Officer, AlphaCognition: I think currently our expectations remain the same. We’re seeing exactly what we thought we would see in the long term care segment. The physicians are trying our drugs unveil, and a few patients. They’re monitoring those patients. They’re going through the titration process.

We anticipate in this quarter, they’re going to try a second tranche of patients and go through the same process. After they try that second tranche of patients, we anticipate physicians gain comfort if they continue to see good results with ZENVIL. Then they’re thinking about the patient type and broadening their use of the drug, either in protocol or in how they’re using it in the nursing homes. Regarding the remainder of the business, I think for the next two to three quarters, we don’t see ex US revenues changing substantially that hockey stick. I think those will become meaningful in late twenty twenty six, early twenty twenty seven.

Dave Storms, Analyst, Stonegate: That’s perfect. Thank you. And then maybe more of a modeling question. Also, kind of looking into 2026, your guidance for operating expenses anticipates a ramp up through the second half of the year. Should we expect that ramp to continue into 2026 for operating expenses?

Or do you anticipate that will maybe level out over the next couple quarters here?

Michael McFadden, Chief Executive Officer, AlphaCognition: I think it levels out. I think it I think that 2034 to ’38 range is gonna be pretty consistent over the next three to four quarters.

Henry Du, Interim Chief Financial Officer, VP of Accounting and Finance, AlphaCognition: Understood. Thank you for taking my questions.

Conference Operator: This concludes the question and answer session. I would like to turn the floor back over to Michael McFadden, Chief Executive Officer, for closing comments.

Michael McFadden, Chief Executive Officer, AlphaCognition: Thank you, operator. Thank you everyone for attending the call today. I’ll reinforce we’re excited about the initial quarter of launch for Zunveil. We’re focused on execution in this quarter and coming quarters to build our base of prescribers, to build the base of nursing homes where Zunveil can be used, and then to optimize our messaging with on label promotion. We’ll continue to be judicious with our expenses, and, we hope that these efforts reward our shareholders, and, appreciate you taking time to be on our call today.

Conference Operator: This concludes today’s teleconference. You may disconnect your lines at this time. Thank you for your participation.

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