Cognition Therapeutics, Inc.

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Hello and welcome everyone joining today's Cognition Therapeutics fourth quarter and full year 2025 earnings call. At this time, all participants are in a listen-only mode. Later, you will have the opportunity to ask questions during the question and answer session. To register to ask a question at any time, please press star 1 on your telephone keypad. Please note this call is being recorded. We are standing by if you should need any assistance. It is now my pleasure to turn the meeting over to Mike Moyer with LifeSci Advisors. Please go ahead.

Thank you, operator, and good morning, everyone. Welcome to Cognitions Therapeutics' fourth quarter and year-end 2025 results conference call. With me today are Lisa Ricciardi, President and Chief Executive Officer, John Doyle, Chief Financial Officer, and Dr. Tony Caggiano, Chief Medical Officer. This morning the company issued a press release detailing its 2025 fourth quarter and year-end results. We encourage everyone to read this morning's press release as well as Cognition's annual report on Form 10-K, which is now filed with the SEC and available on our website. In addition, this conference call is being webcast through the company's website and will be archived for 30 days. Please note that certain information discussed on the call today is covered under the safe harbor provisions of the Private Securities Litigation Reform Act. We caution listeners that during this call, management will be making forward-looking statements. Actual results could differ materially from those stated or implied by those forward-looking statements due to the risks and uncertainties associated with the company's business. These forward-looking statements are qualified by the cautionary statements contained in Cognition's press releases and SEC filings, including its annual report on Form 10-K and previous filings. This conference call contains time-sensitive information that is accurate only as of the date of this live broadcast. Cognition undertakes an obligation to revise or update any forward-looking statements to reflect events or circumstances after the date of this conference call. With that, I would like to turn the call over to CEO Lisa Ricciardi.

Lisa Ricciardi Thank you. Good morning, everyone. Cognition's primary focus since its inception has been on the development of Xervimicine for patients with debilitating neurodegenerative diseases. Zurimacine is the USAN name for CT1812. Over the past 18 months, we've reported data from two phase two studies, one in dementia with Lewy body and a second one in mild to moderate Alzheimer's disease. Finally, we concluded enrollment in our 18-month START trial. This is a 545-patient study in early Alzheimer's disease, and we've held meetings with both U.S. and European regulators. With data in hand and feedback from regulators, we've made the decision to prioritize development of zirvimicine for the treatment of DLB psychosis. I'll turn the call over now to Tony Caggiano, our chief medical officer, to walk you through the rationale.

Thank you. We recently published results from our phase two shimmer study in DLB and show that zirvimicine has a meaningful impact across DLB symptom domains, specifically movement, cognition, function, and behavior, including psychosis. These behavioral symptoms were the subject of our recent presentation at the Alzheimer's and Parkinson's disease conference last week in Copenhagen. These symptoms were measured in the Phase II trial using an assessment called the MPI-12, which is a 12-item index of neuropsychiatric symptoms. Zervimicine showed a strong impact on the neuropsychiatric symptoms with an 86% slowing of progression relative to placebo. Within the MPI-12 behavioral symptoms, the effects of zervimicine were particularly notable for hallucinations and delusions, which collectively we refer to as psychosis. This is an important finding and one of the topics that we discussed both with the FDA in our FDA Type C meeting in January as well as with our peers during the ADPD meeting. We are very encouraged by the response to this plan from our KOLs and expert consultations and expert consultants at ADPD. In our conversations with the FDA team, they agreed that the effects on psychosis were compelling and directed us to the Division of Psychiatry in order to define a path towards registration. The Division of Psychiatry has familiarity with trials designed to measure psychosis associated with neurologic disease. They have recently overseen registration studies and new drug applications for Rixalti for Alzheimer's agitation and Nuplazib for Parkinson's disease psychosis. We look forward to meeting with the Division of Psychiatry to discuss a registrational plan for the treatment of DLB psychosis. A meter request for the division has already been filed. Many of you who follow this space know that psychosis is commonly associated with neurodegenerative diseases like Alzheimer's disease, frontotemporal dementia, Parkinson's disease dementia, and DLB. In DLB, psychosis is more prevalent than in other dementias and often occurs early in the course of the disease. As many as 80% of DLB patients experience psychosis. The presence of hallucinations is one of the core clinical criteria for a diagnosis of DLB. Unlike psychiatric conditions like schizophrenia, some DLB patients recognize that these images, sensations, or sounds that they are experiencing are actually hallucinations. This is understandably very stressful, both to patients and to their families, and can lead to withdrawal from social activities and isolation negatively impacting the entire family unit. Delusions are also common in DLB. These are often imposter delusions, where patients believe their friends and family members have been replaced by others pretending to be their family members. These delusions are difficult to manage and can accelerate the family's decision to move their loved ones into core care facilities. As you can see, psychosis is extremely debilitating for DLB patients. There are no approved medications for DLB patients with psychosis. Neurologists and psychiatrists have few treatment options for hallucinations and delusions, as most patients cannot tolerate traditional antipsychotics. Few clinical trials for patients with DLB psychosis have been conducted, and none have been successful to date. Most drugs in development for DLB psychosis are acute treatments, as they modulate specific receptors involved in psychosis. The difference between the acute treatment and cognitions approach is the mechanism. Acute treatment acts rapidly to impact specific symptoms but does not change the course of the disease. Patients' disease continues to progress, their symptoms will worsen, and these acute treatments may become less effective over time. Zervimicine works differently by interrupting the basic pathophysiology of the disease. It has shown robust efficacy over six months in certain symptom domains of DLD, most notably behavioral symptoms including psychosis. In the Phase II shimmer study, patients with psychosis, anxiety, aggression, and aggression with zerimethane were stable compared to these same symptoms that worsened in placebo-treated participants. As we mentioned, these data were presented last week at the ADPD meeting, and the posters are available on our website. Given the strength of psychosis data, we expect registrational studies focused on psychosis to be smaller and shorter in studies that focus on cognition and general symptomatology. Therefore, we believe that our decision to develop Dervimicine for DLB psychosis will allow us to expedite this path to market. After completing our meeting with the Division of Psychiatry and receiving the official meeting minutes mid-year, we will issue an update in a press release.

Thank you, Tony. Before I move on, I'll add that one of the factors that led us to decide to pursue DLD psychosis was the anecdotal feedback from our expanded access program, or as we refer to it, our EAP program. We started this program in mid-2025 after we received a philanthropic donation from a patient's family. The patient had been in our Phase II Schumer study. This family was driven to find a way to maintain access to zirvimicine because of the impact they believe it had on the patient with DLB. They were focused not only on their mental health needs, but that of the broader shimmer trial population. Once the EAP started, it quickly filled to capacity. The level of interest from DLB patients and their physicians was and is astounding. We still get queries from patients and families about gaining access or extending access to the drug. Now, since the EAP is open label, we're in a unique position to hear directly from patients and their loved ones. And the response has been consistent, that people believe zirvimicine is making a tangible difference in their daily lives. These experiences fuel our desire to complete our development work, and if approved, see this drug available all over the world. Right now, we have funding to continue the EAP program for another 9 to 12 months. Now, moving on to Alzheimer's disease. As you may recall, we completed the Phase 2 SHINE study in mild to moderate Alzheimer's disease in 2024. We saw a reduction in cognitive decline of 38%, and that is on the ATIS-COG-11 scale, in treated versus placebo patients. This was comparable to the effects observed in Phase III trials with the immunotherapeutics Kisumla and Likimbi. In SHINE, the treatment effect was most pronounced in patients with lower levels of a protein called PTAU-217 in their blood. These participants experienced a 95% reduction in cognitive decline. When we met with the FDA during an end of phase two meeting in 2025, the FDA agreed with our proposal to screen for participants with lower levels of P tau 217. This strategy could expedite patient recruitment. Importantly, it will also enrich the study with patients who are most likely to benefit from zirvimicine treatment. Gerimicine currently is being studied in a Phase II trial called START in patients with mild cognitive impairment, or MCI, and early Alzheimer's disease. This study met its enrollment goal at the end of 2025 with a total of 545 participants. Top-line results are expected in 2027 after the last participants complete the 18-month treatment period. Given the strong results we observed with Zervimicine in the mild to moderate AD trial, we remain committed to developing Zervimicine for Alzheimer's disease, and we look forward to the results of our START trial. With that, John Doyle will review our financial results and provide more color around our cash position and capital requirements. John?

Thank you, Lisa. Cash, cash equivalents, and restricted cash equivalents as of December 31st, 2025 were approximately $37 million. And total grant funds remaining from the NIA were $35.7 million. We estimate that the company has sufficient cash to fund operations and capital expenditures through the second quarter of 2027. Research and development expenses were $37.2 million for the year ended December 31st, 2025, compared to $41.7 million for 2024. The change in R&D expenses was driven by the completion of Shine and Shimmer clinical trials and associated professional fees. General and administrative expenses were $10.6 million for the year ended December 31st, 2025, compared to $12.3 million for 2024. This change in G&A expenses was driven primarily by reduced stock-based compensation expenses. The company reported a net loss of $23.5 million, or $0.32 per basic and diluted share, for the year ended December 31, 2025. This is compared to a net loss of $34 million, or $0.86 per basic and diluted share, for 2024. Lisa?

Thank you, John. I'll now turn the call back to our operator who can open this up to questions. Nikki?

Thank you. And if you would like to ask a question, please press star 1 on your keypad. To leave the queue at any time, press star two. Once again, that is star two to ask a question. And we will pause for a moment to allow everyone a chance to join the queue. I will take our first question from Talia Guru with HC Wainwright. Please go ahead, your line is open.

Hi, this is Katie on for ROM. Do you guys plan to seek a partner for further exploration with derma medicine, particularly in ocular conditions? If so, when?

Hi, good morning. Nice to talk to you. Right now, our priority is on, excuse me, developing Zervimicine for DLB. And so we're not looking at an ophthalmology program at the moment. Thank you for the question.

Great. Thank you.

Thank you. We will move next with William Wood with B. Reilly Securities. Please go ahead. Your line is open.

All right. Thanks for taking our questions, and congratulations on the very nice ending of the year. Just trying to sort of think about in terms of the DLB program, maybe you could walk us through what you see as the big regulatory path forward. Should we expect your next trial? I believe you said in the past it might be a Phase IIb. Would that be expected to be registrational, or do you think you could go to phase three directly? And then what are your current thinkings on your DLB trial, both in terms of size and duration, but also primary endpoint? And then I have a follow-up.

Yeah. Yeah, thank you for the question. As we mentioned, our intent is to develop this now for a label relating to psychosis in DLB, like we saw, as was mentioned, with Nuplasid and Rixalti. and Alzheimer's disease and Parkinson's disease dementia. Now, you know, we have not completed, you know, the FDA meetings yet to comment on exactly what the outcome measure will be. We have to work on that, but you can imagine they'll be very similar to what we've done here before. And certainly our intent is to move as expeditiously as possible through registrational trials. But again, until we have the meeting with FDA and have minutes, it would be premature to comment exactly what that would look like.

Okay, got it. And then in terms of you, you also had reported that you had a numerous other additional trials, including pharmacology and healthy volunteers, availability food. And then I believe also you're switching from a capsule to a tablet formation. Is there any update on any of these additional trials that could aid in in your moving forward quickly? into your DLB psychosis? And then additionally, what other remaining gating steps do you sort of see in getting that DLB psychosis trial underway once you have the regulatory feedback?

Yeah, you're correct. Those are the studies that we'd want to complete before starting those trials. Again, you know, based on the nature of these studies, these are very low-risk studies, right? They're really informing us. on things such as do we need to add any instructions as to whether people should take drugs with or without food or have no instructions whatsoever. So these are extremely low risks that we just need to get behind us. And as you mentioned, you're correct, we're moving from a capsule form to a tablet form, which we think will be better as this is eventually, right, hopefully once approved, commercialized. So those are all moving along, and we look to accomplish this all in this year, 2026.

Okay, got it. Helpful. Thank you very much. I'll hop back into queue.

Thank you. We will move next with Daniel Gatellin with Chardon. Please go ahead. Your line is open.

Hey, good morning, guys. Thank you for taking my question. First, how does the effect of surveillance on behavioral domains in DLB affect your thinking about pursuing also behavioral domains in Alzheimer's disease, or is the current focus still on an overall slowing of the disease progression?

Thanks for the question, Daniel. We want to see the results of our START trial, big trial, important trial. We hope it builds on the SHINE results, which we've already seen, particularly those impressive effects in patients with low PTAL. With that kind of data, we can then prioritize in the out years, what do we do next? Right now on the fairway is the DLD study as a first priority. And then while that study is recruiting and getting underway, we anticipate seeing the results of START. which is the early AD trial. We find no means given up on AD. It's a question of prioritization. As a small company, we've chosen DLB psychosis, and we'll get such great information sometime next year from start in AD.

Got it. Okay. Makes sense. And then for DLB, so you will be having the meeting with the FDA. What about alignment on psychosis with the EMA? Where are you in those meetings? And do you anticipate the trial to be including sites both in the United States and Europe to support global approval?

Yeah, thank you. So we haven't really announce exactly where the trial will be. Certainly, once we have agreement with FDA, you know, as we've done with AD, we'll want to seek alignment with EMA before launching trials there. But it's a little premature to talk about exactly what those plans are.

Got it. All right. Thank you for taking my questions.

Thank you. We do have a follow-up from Rem. with HC Wainwright. Please go ahead. Your line is open.

Thank you. Which existing approved CNS medications might the medicine exhibit synergy? Do you guys plan to explore any of those synergies clinically in the foreseeable future?

Well, so we have a bit, right? So most of our studies are done on CNS. standard of care background medications. So obviously in Alzheimer's disease and our mild to moderate study, this was acetylcholine esterase inhibitors and memantine. Interestingly now, most people with DLB are also on acetylcholine esterase inhibitors. And in our trial, and this is all published information, about 80 or 85% of individuals were on acetylcholine esterase inhibitors. So the effects of our drug have been on top of these standard of care. Similarly, in our START trial in early AD, we've allowed people to be on and have been on, provided they were on a stable maintenance course of the immunotherapies, right, lacanumab and tenanumab. And the intent there, as much as you suggested, to begin to collect data not only on zurbimicin alone, but is there any indication that there might be an additional benefit of using the drugs in combination? So that's the information that we have and will be getting in the near future.

Perfect.

Thank you so much. Thank you. We will move next with Sumant Kulkarni with Canaccord. Please go ahead. Your line is open.

Good morning. Thanks for taking my questions. I have a couple questions. First, what's the state of the art in terms of the hypothesis behind Zerva-Messing's mechanism of action on psychosis? And do you have any similar anecdotes from patients in your SHINE study?

What was the second part of your second question?

The second part was, just like you had some anecdotes that led you to explore psychosis in DLB, did you have any similar anecdotes on the Alzheimer's study?

Got it.

Tony, do you want to take the first question? Sure. You know, we mentioned briefly, but obviously we didn't get into too much detail in our discussion. So, you're right. So, we don't believe that we are impacting the receptors, particularly, you know, known to be responsible for psychosis. What we believe, much like the global state of the disease, is that we're interrupting the basic pathophysiology by, just like in Alzheimer's disease, blocking the ability of a beta oligomer to interact with neurons. We have similar data showing that. We prevent the interaction of alpha-synuclein from interacting with their receptors, thereby preventing, right, the basic damage to neurons. And now the symptomatology in DLB from alpha-synuclein toxicity, right, is based on where that toxicity is occurring. And so, again, we believe that we are able to impact the broad symptomatology of the disease and that those effects, as we noted, were most notable or most measurable within the psychosis. So that's what we're pursuing.

Got it. And then my follow-up, in your DLB, I guess in your proposed DLB psychosis trial, what would the time point be to the primary endpoint on psychosis? And do you expect to have secondary endpoints involving cognition? I'm asking because with reference to your potential to eventually attain a disease-modifying label.

Yeah, so we have not announced exactly what the study looks like and the duration and so forth. That'll certainly be a topic of our discussion with FDA. You know, obviously, you've seen the results of our SHIMR trial, and we won't want to stray too much from that design. And absolutely, we will have other measures, secondary measures, which, you know, are ranked and protected, looking at, you know, cognition and motor function and sleep and so forth. Again, because as you saw with the results of the SHIMR trial, you know, we were very impressed by the global impact of the drug on the disease. And certainly eventually we'll walk to study those other impacts as well. The reason we're focusing right now on psychosis is because the impact of the drug on psychosis is really quite strong. And that gives us the ability to do smaller, faster trials and hopefully a much more efficient path to markets.

Got it. Thank you.

Thank you. And at this time, there are no further questions in queue. I will now turn the meeting back to CEO Lisa Ricciardi for closing comments.

All right, Nikki. We are looking forward to meeting with the FDA Psychiatry Division shortly. So as Tony said, we can finalize our plans and timing for study in DLB psychosis. This is an important indication. It's currently unaddressed by any approved or unapproved medications. Based on our phase two findings and anecdotal feedback as we discussed in participants in our EAP program, we believe zirvimicine has the potential to be a first-in-class treatment option for DLB patients with psychosis. With that, thank you all for joining us today.

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