Q3 2024 Xenon Pharmaceuticals Inc Earnings Call
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Speaker Change: Good afternoon and thank you for standing by. At this time, I'd like to welcome everyone to Zenon Pharmaceuticals, Inc. third quarter 2024 earnings conference call. All lines have been placed on mute to prevent any background noise.
Speaker Change: After the speaker's remarks, there will be a question and answer session. If you would like to ask a question during this time, simply press star followed by the number 1 on your telephone keypad. If you would like to withdraw your question, press star 1 again. Thank you.
Speaker Change: I will now turn the conference over to Chad Fugere, Vice President of Investor Relations. Please go ahead, sir.
Chad Fugere: Good afternoon. Thank you for joining us on our call and webcast to discuss Xenon's third quarter 2024 Financial and Operating Results. Joining me today are Ian Mortimer, Xenon's President and Chief Executive Officer, Dr. Chris Kenney,
Chad Fugere: I'm just going to jump in for Chad, so Ian will begin with a summary of our recent progress
Chad Fugere: Chris Kenney will provide an overview of our clinical stage programs and ongoing outreach to the medical community. And I will close with a summary of our financial results and anticipated milestones. We will then open the call up for your questions.
Chad Fugere: Please be advised that during this call, we will make a number of statements that are forward-looking, including statements regarding the timing of and potential results from clinical trials.
Chad Fugere: The potential efficacy, safety profile, future development plans, and current and anticipated indications, addressable market, regulatory success, and commercial potential of our and our partners' product candidates, the efficacy of our clinical trial designs,
Chad Fugere: our ability to successfully develop and achieve milestones in our clinical development programs,
The timing and results of our interactions with regulators.
Chad Fugere: our ability to successfully obtain regulatory approvals, anticipated timing of the top-line data readout for our clinical trials of Azetu-Kellner, and our expectation that we will have sufficient cash to fund operations into 2027.
Today's press release summarizing Xenon's third quarter 2024 financial results.
Chad Fugere: and the accompanying quarterly report on Form 10-Q will be made available under the investor section of our website at xenon-pharma-dot-com and filed with the SEC and on CDAR Plus. Now I'd like to turn the call over to Ian.
Ian Mortimer: Thank you, Sherry, and good afternoon, everyone, and thanks for joining us on our call today. We have made significant progress over the past quarter, consistent with our overall strategy of being at the forefront of discovery and development of eye and channel therapeutics.
Ian Mortimer: And our focus hasn't changed. To maximize the full potential of our lead products is that to counter, to build upon our leadership position in the KV7 space, and to continue to mature our promising ion channel pipeline.
Ian Mortimer: Xenon's leadership position in the KV7 field is unmatched, as the ZETU calendar represents the only highly potent and selective KV7 potassium channel opener in clinical development for multiple indications.
Ian Mortimer: that is backed by long-term efficacy and safety data in patients living with epilepsy and encouraging proof of concept data in patients with major depressive disorder.
Within our portfolio, we remain focused on three key areas.
Ian Mortimer: Continuing the execution of our Phase 3 Zetucalendar Epilepsy Program while raising the profile of Zetucalendar with both physician and patient communities.
Ian Mortimer: Advancing our Phase 3 ZETU Calendar MDD program with a focus on XNOVA2 which is expected to initiate before the end of this year and expanding our pipeline.
Ian Mortimer: both through the advancement of our portfolio of next-generation ion channel modulators, as well as further potential indication expansion of a ZETU counter.
Ian Mortimer: As I said earlier, Xenon's leadership in the KV7 landscape is unmatched. The ZETU calendar represents the most advanced clinically validated potassium channel modulator in late-stage clinical development.
Ian Mortimer: Our substantial clinical experience with the Zetu calendar includes robust long-term efficacy and safety data with over 600 patient years of exposure in focal epilepsy patients.
Ian Mortimer: Importantly, we have generated highly compelling double-blind efficacy data from our X-Toll study that we believe demonstrates the best placebo-adjusted results ever seen in a clinical study in patients with focal onset seizures.
Ian Mortimer: In our EXTOL Open Label Extension Study, we are seeing patients experience the long-term benefits of seizure freedom and improved quality of life.
Ian Mortimer: as well as a favorable safety profile. We believe that azethucalonar represents a potentially best-in-class anti-seizure medication that could be paradigm shifting in the treatment of epilepsy.
Ian Mortimer: In addition to the impressive efficacy data generated to date, Zetu Calendar has other important attributes.
Ian Mortimer: such as once-daily dosing without the need for titration, rapid onset of effect, novel mechanism of action, and potential mood benefit.
Ian Mortimer: The body of compelling clinical evidence that we have amassed to date continues to generate significant excitement from physicians and key opinion leaders as they see the potential of what a ZETU counter could mean to the epilepsy community.
Ian Mortimer: As we continue to educate key stakeholders around the benefits of the ZETU calendar, Xenon will have an increased presence at the upcoming American Epilepsy Society meeting, or AES, taking place December 6th through the 10th in Los Angeles.
Ian Mortimer: We'll have new data presentations and updated results from our ongoing XTOL Open Label Extension Study.
Ian Mortimer: Patients in the X-Tool OLE have now been on drug for at least three years, with some patients in the OLE having more than five years of exposure to a Zetu calendar.
Ian Mortimer: We continue to see better efficacy in the open label extension the longer patients are on drug and many patients are experiencing the long-term benefits of seizure freedom and improved quality of life and we're excited to present this new 36-month data at AES next month.
Ian Mortimer: We believe this long-term data package will support our regulatory filings on the pathway towards commercialization and is a key differentiator when compared to other molecules in earlier stage clinical development.
Ian Mortimer: Further, we are in an incredibly fortunate position in that EZETU calendar's attributes enable significant potential across both epilepsy and neuropsychiatry, including MDD and potential other indications.
Ian Mortimer: Physicians who treat MDD are looking for medications with novel mechanisms and favorable product profiles, such as the ability to address anhedonia, demonstrate a rapid onset of effect, or avoid adverse effects that are seen with standard of care agents.
such as sexual dysfunction or weight gain.
Ian Mortimer: As we shared last quarter, clinical site planning is well underway, and we expect to initiate our Phase 3 MDD program before the end of this year.
15 years beyond the Zachu calendar to our broader pipeline.
Ian Mortimer: Our discovery team has applied its many years of experience in ion channels to advance multiple KV7 product candidates that are chemically diverse from a set to counter, so that we can leverage the target's pipeline in a mechanism potential, providing us with numerous clinical development opportunities.
Ian Mortimer: across a broad range of therapeutic indications, including seizure disorders, pain, and neuropsych conditions, and ultimately extending the reach of this differentiated mechanism to even more patients in need of better therapeutic options.
Ian Mortimer: Staying on the topic of our early stage pipeline, we continue to make meaningful progress within our NAV 1.7 sodium channel program as well.
Ian Mortimer: We are proud of Xenon's pioneering work to identifying promising genetic targets associated with rare phenotypes.
Ian Mortimer: It was through these efforts that the connection was made between individuals who had the inability to perceive pain and the complete loss of function mutations in the gene encoding for NAV1.7.
Ian Mortimer: Conversely, individuals who experience non-precipitated spontaneous severe pain correlated with NAV1.7 gain-of-function mutation.
Ian Mortimer: This identification of NAV1.7 as an important pain-related target also offered the possibility of a new class of pain medications that are not burdened by the liabilities of opioids.
Ian Mortimer: Importantly, we believe that NAV1.7 has by far the strongest genetic validation amongst pain targets, and we continue to pursue the development of novel non-opioid-based pain medications.
Ian Mortimer: And while the development of ion channel therapeutics is certainly a complex challenge, we are applying all of the knowledge gained from the past molecules to advance novel selective NAV1.7 inhibitors within our portfolio of next generation modulators.
Ian Mortimer: Currently, IMD enabling work is underway with a lead NAV 1.7 development candidate in support of our goal of filing an IMD or equivalent in 2025, enabling us to generate important de-risking proof-of-concept data.
Ian Mortimer: In addition to NAV 1.7 and KV7, we are also advancing potentiators of NAV 1.1.
Ian Mortimer: with the aim of addressing the underlying etiology of Dravet syndrome.
Ian Mortimer: and delivering a disease-modifying therapy in support of our hypothesis that a precision medicine therapy for Dravet syndrome should restore NAV1.1 activity specifically without impacting other neuronal functions or proteins.
Ian Mortimer: We look forward to presenting some of our preclinical NAV1.1 data, including protection against spontaneous seizures and SUDEP, as well as strengthening long-term potentiation at the upcoming AES meeting.
Ian Mortimer: These data support an incredibly compelling profile for a small molecule NAV1.1 potentiator when compared to other drugs available and in development to treat Dravet syndrome.
Ian Mortimer: Finally, as I continue to reiterate, it's an exciting time for Xenon due to the advancement of our clinical programs and our progress towards commercialization.
Ian Mortimer: In August of this year, Dr. Matthew Ronsheim joined our senior executive team as chief operating officer based in Boston.
Ian Mortimer: overseeing our R&D operations and providing strategic and operational leadership for our pipeline of small molecule programs and preparation for the anticipated commercial launch of a Z2 Calendar.
Ian Mortimer: Matt's extensive operational, pharmaceutical development, and manufacturing expertise are important as we expand our Phase III programs, plan for regulatory submissions and commercialization, as well as progressing our broad portfolio of early-stage assets.
Ian Mortimer: Matt has already made a positive impact and we look forward to his continued leadership.
Speaker Change: With that, I'll now turn the call over to Chris Kenney to provide a brief overview of our clinical stage programs and our ongoing outreach with healthcare providers at key medical congresses. Chris, over to you.
Chris Kenney: Okay, thanks a lot Ian. I'm pleased to report that our late-stage clinical development programs for azethucalonur are progressing as planned.
Chris Kenney: Our Phase III Epilepsy Program includes XTOL-2 and XTOL-3 in focal onset seizures and EXACT in primary generalized tonic-clonic seizures.
Chris Kenney: Importantly, the first top-line focal onset seizure data readout from XTOL-2 is anticipated in the second half of 2025.
Chris Kenney: In support of an anticipated NDA filing, we plan to submit the results from XTOL-2 along with the existing data package from XTOL and additional safety data from other clinical trials.
Chris Kenney: In parallel with the significant progress made across our Phase III Zetu-Kalna programs,
Chris Kenney: our medical affairs team continues to engage with the broader medical community to highlight the robust scientific evidence generated to date.
Chris Kenney: We're in an enviable position as not only can we showcase the positive results from our completed XTOL trial, but we have our ongoing seven-year open label extension study.
Chris Kenney: providing further long-term data from patients living with epilepsy, which we believe is a key differentiator from other molecules currently in development.
Chris Kenney: To give you a sense of some of these interactions, in September we attended the European Epilepsy Congress.
Chris Kenney: which attracted more than 3,600 delegates from around the globe. Xenon had a strong presence, presenting three posters and hosting a scientific exhibit.
Chris Kenney: We successfully engage with key opinion leaders, prescribing clinicians, and principal investigators from our study sites.
Chris Kenney: Many of our discussions centered around the X-toll data, which we believe demonstrate the best placebo-adjusted clinical efficacy in the most refractory patient population trialed.
Chris Kenney: as well as a favorable tolerability profile in adult patients with focal onset seizures.
Furthermore,
Chris Kenney: We continue to receive strong feedback from the epilepsy community on the long-term efficacy data from our XTOL open label extension study, which shows increased seizure reductions.
Chris Kenney: with patients on a ZETU calendar out to 30 months experiencing a greater than 90% reduction.
and median monthly seizure frequency.
Chris Kenney: Additionally, approximately one in four patients on a ZETU calendar for at least two years in the extol open label trial have been seizure free for a full year or longer.
Chris Kenney: giving both us and the epilepsy community tremendous confidence in Ezetu-Caliner's potential to address the significant need for new anti-seizure medications.
Chris Kenney: These data are particularly impressive given that the literature concludes the likelihood of achieving seizure control once a patient has failed three anti-seizure medications is less than 5%.
Chris Kenney: and we believe that future Open Label Extension data updates, including our upcoming 36-month data set at AES, will continue to strengthen our leadership position.
Chris Kenney: Physicians regularly treating epilepsy patients are impressed by the Azetu calendar data gathered to date, noting that it sets an incredibly high bar, not just for other KV7 drugs in earlier stage clinical development, but other anti-seizure medications within the current treatment landscape.
Chris Kenney: This is especially true when considering some of a Z2 calendar's potentially differentiating attributes such as its positive impact on mood.
Chris Kenney: Our outreach to the medical community is not limited to epilepsy. We're also engaging with prescribing physicians in the MDD space.
Chris Kenney: With our Phase III MDD program, the first of three planned Phase III clinical trials examining azethucalonarin major depressive disorder is anticipated to initiate before year-end.
Chris Kenney: At the end of October, we attended the Psych Congress in Boston, giving us another key opportunity to interact with physicians in the MDD space and present our Phase II ex nova data.
Chris Kenney: discuss the potential use of a Z2 calendar as a treatment for MDD, and outline our near-term plans to initiate a Phase III program in major depressive disorder.
We continue to emphasize the Z2 Calendar's potentially differentiated profile.
Chris Kenney: versus standard of care agents in MDD as physicians continue to have a particular interest in a Z2 calendar's novel, selective KB7 mechanism of action and its potential benefit on anhedonia, rapid onset of effect, as well as its potentially favorable tolerability profile.
Chris Kenney: with no notable adverse effects on sexual function or weight gain.
Chris Kenney: We have the benefit of being able to reference not just the ex nova data for efficacy but also the long-term tolerability data gathered from our ongoing XTOL open label extension study.
Chris Kenney: We're excited to be advancing another late-stage clinical development program for a ZETU calendar with the hope of addressing the needs of patients diagnosed with MDD who are still struggling to find effective treatments.
Chris Kenney: We also continue to support the investigator-led MDD study conducted by Dr. James Murrow of Mount Sinai School of Medicine and Dr. Sanjay Mathew at the Baylor College of Medicine.
Chris Kenney: This 60-patient placebo-controlled Phase 2 trial has a functional primary endpoint.
Chris Kenney: with the objective of evaluating the effect of a ZETU counter on brain measures of reward as measured by the change in activation within the bilateral ventral striatum from baseline to end of treatment at week eight as assessed by functional MRI.
Chris Kenney: Also, the study is evaluating secondary endpoints that include madras and shaps. Patient enrollment was recently completed and results anticipated in the first half of 2025.
Chris Kenney: Now, looking ahead, we're incredibly excited to expand our presence at AES this year as part of our ongoing outreach to the medical community.
Chris Kenney: As the premier epilepsy conference, AES is an important venue for us as we continue to strengthen our profile and reputation as a leader in epilepsy, laying the foundational framework for a successful future potential launch in epilepsy.
Chris Kenney: We have scheduled numerous meetings with physicians, key opinion leaders, academic leaders, and patient advocacy groups.
Chris Kenney: I'm extremely proud that we have five accepted abstracts at this medical meeting and look forward to presenting these posters, including an update to our ex-toll open label extension study.
Chris Kenney: We have expanded our presence in the exhibit hall and are eager to welcome all visitors to the Xenon booth who are interested in learning more about a Z2 calendar and our broader pipeline.
Speaker Change: I'll now turn the call over to Sherry, who will provide an overview of our third quarter financial results and upcoming milestones. Sherry?
Sherry: Thanks, Chris. Looking briefly at our third quarter financial results, as of September 30, 2024, we had cash and cash equivalents and marketable securities of $803.3 million, compared to $930.9 million as of December 31, 2023.
Sherry: based on current operating plans, including the completion of the AZETU calendar phase 3 epilepsy studies.
Sherry: and fully supporting late-stage clinical development of a ZETU calendar and MDD, we anticipate having sufficient cash to fund operations into 2027. I'd refer you to our news release and 10Q report for further details around our financial results.
Sherry: We anticipate that 2025 will be a pivotal and transformational year for Xenon with several important milestones on the horizon.
Sherry: First and foremost, we're driving towards the highly significant data readout for Mextel-2, expected in the second half of 2025. Importantly, positive results from Mextel-2 will enable the submission of our NDA, with the goal of advancing a ZETU calendar towards commercialization.
Sherry: In the MDD program, we're anticipating results from the investigator-sponsored Phase 2 proof-of-concept study of Izetu Kellner in MDD in the first half of 2025.
Sherry: In addition, our company-sponsored, broad Phase III MDD program will be well underway with the initiation of Ex Nova II anticipated before this year-end.
Sherry: As we continue to advance our early-stage preclinical pipeline, we anticipate filing multiple INDs or equivalent in 2025, with the goal of initiating first-in-human trials across multiple targets.
Sherry: while also exploring other potential indications for azethucalonar that may be well-suited for late-stage clinical development.
Sherry: With this in mind, we have built a foundation of strong, thoughtful fiscal management, which positions us to execute on our planned strategies to advance Zetu-Kelner through late-stage clinical development in both epilepsy and MDD, while at the same time supporting a robust pipeline of next-generation ion-channel therapeutic candidates.
to summarize some of the key takeaways from today's call.
Sherry: We believe strongly in the Z2 Calendar's compelling clinical profile, which is built on its unique mechanism of action and supported by the meaningful body of clinical data we've generated thus far.
Sherry: We're excited to engage with key patient and physician communities to raise further awareness about the potential of azethucaloner in the future treatment of epilepsy at the upcoming AES meeting, where we will also present the latest data from our ongoing X-Toll OLE study.
Sherry: For those of you on the call attending AES, we look forward to connecting with you in Los Angeles.
Sherry: And looking slightly further out, we look forward to connecting at the upcoming J.P. Morgan conference.
Sherry: which will give us an opportunity to kick off the year and outline our key goals for 2025 in more detail. I hope you share our excitement as we continue to execute our clinical development plans and anticipate these key events next year. Thank you for your attention today and we look forward to sharing more in the coming months.
Speaker Change: I'll now ask the operator to open the line for any questions.
Speaker Change: Thank you. We will now begin the question and answer session. If you would like to ask a question, please press star 1 on your telephone keypad to raise your hand and join the queue.
Speaker Change: If you would like to withdraw your question, simply press star 1 again.
Speaker Change: If you are called upon to ask your question and are listening via loudspeaker on your device, please pick up your handset and ensure that your phone is not on mute when asking your question.
Speaker Change: Your first question comes from the line of Paul Mathis with Stifle. Your line is open.
Speaker Change: Hi there, this is Julian for Paul. Thanks so much for taking our question and congrats on the progress.
Speaker Change: just wondering if you could provide a little bit of color again on on enrollment dynamics and and whether things are tracking according to your expectations any other details or learnings perhaps since you know our last quarterly update
Speaker Change: And then secondly, quickly, just on the NDD investigator-sponsored study, I'm just curious on how you perceive that study.
Speaker Change: either reading on to or not reading on to your Phase 3 Pivotal program and thus confidence in execution of your own study. Thank you.
Speaker Change: Thanks very much for the questions. So I'm happy to take the first one and maybe start on the second one. And Chris Kenney, you can...
Chris Kenney: provide your perspective on the on the IST and MDD as well. Yeah, obviously we get a lot of questions on just how we're doing in the phase 3 epilepsy program. We're really comfortable where we are. I'm not sure anything's changed in the last quarter to your very specific question.
Chris Kenney: You know, I would always remind people that I think we have more experience, kind of, in the contemporary.
Chris Kenney: clinical trial environment of executing large focal epilepsy studies, so we're very comfortable on where we are.
Chris Kenney: you know obviously we always give the best information we can and currently the guidance for XTOL 2.
Chris Kenney: is to have top-line data in the second half of next year. So I don't think there's.
Chris Kenney: anything specific that you haven't heard from us and seen from us that I need to add to that answer. In terms of MDD, yeah, I'll give maybe a perspective on the read-through to what we're thinking about, and then Chris can just remind the group, you know, what we expect to see from that study, because the end points to
Chris Kenney: Chris mentioned in his prepared remarks, but they are slightly different than what we would look at on the sponsor side. We've always said that, you know, these are two really important KOLs in terms of the group at Mount Sinai and at Baylor.
Chris Kenney: with Dr. Murrow and Dr. Matthew, and they had done a lot of the early and pioneering work around this mechanism in major depression, and so we're very happy to support them in terms of drug supply and collaborate with them. They're key collaborators.
with us.
Chris Kenney: That said, you know, it's a small IST at two medical centers.
Chris Kenney: And it's not something that we're reading through to our own MDD program. We've committed to running three phase three clinical trials in major depression with the 20 milligram dose of azethucalonin, as we mentioned, the first of those studies.
Chris Kenney: Xnova 2. We've made really nice progress and that'll be up and running shortly. So, really no read-through in terms of what that study may show. It looks like we'll have top-line data from that study in the first half of 2025. Chris, do you want to add your perspective?
Chris Kenney: Sure, just as a reminder, the investigator-initiated trial has enrolled 60 patients.
Speaker Change: One arm in placebo and one arm in active. And as a reminder, our ex-NOVA study had like 168 patients.
Speaker Change: and as we go forward into phase three, our phase three studies are gonna have 450 patients. So I'm just trying to make the point that the investigator-initiated trial is relatively small in size, 30 patients per treatment arm.
Speaker Change: And so it's underpowered from the standpoint of the clinical outcomes like Madras and SHAPs.
Speaker Change: What it is powered for is to show improvements in fMRI based upon the fMRI work that was done with the zogabine in moderate to severe depression. And so it will be interesting, I think two things will be interesting from that study.
Speaker Change: One is, you know, is there a readout on fMRI, which is, it's a bit academic, but it's still be quite interesting to, you know, to understand why this mechanism is helpful in major depressive disorder. The hypothesis is that it helps out with the reward circuit. So that'll be interesting. But to Ian's point, it's not going to gate our phase three plans. And the other thing that, you know, I think this study will be interesting is, you know, we saw great tolerability.
Speaker Change: in our phase two study. And so it'll be nice to confirm that in, or confirm or refute that in the, you know, when we see those results next year.
Thank you, operator. We can go to the next question.
Speaker Change: Next question comes from the line of Tessa Romero with J.P. Morgan. Your line is open.
Speaker Change: Hi team, this is Caroline Poacher. I'm for Tessa Romero with JPMorgan. Thanks for taking our questions.
Speaker Change: So first from us, when can we expect to learn more about the clinical profile of the lead NAV 1.7 candidate, including the level of receptor occupancy?
Speaker Change: potentially a signing site. And then if I could just sneak another one in. Based on your prepared remarks, it sounds like a proof of concept study is in the cards for next year. Could you just frame what such a study could look like for NAV 1.7? Thank you.
Speaker Change: Great, thanks very much. I'm happy to take that one. Yeah, we've we've been we've I think a lot of the overall properties you've
You've...
Speaker Change: hit a couple, receptor occupancy and binding site. I mean, it's even broader than that in terms of just the selectivity profile, the biodistribution. There's a number of things that we track that I think we've learned a ton from the field.
Speaker Change: We haven't provided a lot of that information publicly, and I don't think you're going to hear a lot from us. I think that's really important learnings that we've made.
Speaker Change: that were incorporated into our program that we're not sharing broadly.
But needless to say, we believe we have.
Speaker Change: the right profile of molecules to really run the correct human experiment to see whether selective
Speaker Change: NAV1.7 sodium channel inhibition with, you know, high receptor occupancy can provide analgesia. So I think we're very comfortable that we have the right profile to test the hypothesis in humans, which what we're really excited about.
Speaker Change: In terms of the clinical development plan, so the initial study will be a standard, you know, first in human study, SADMAD. And then when we talk about proof of concept, not fully designed yet, but probably is no surprise, we're really thinking about running a proof of concept study in bunionectomy. So we're starting to bring all of that planning together. But first step would be to get through GLP toxicology and file an IND and get into the first in human studies.
Speaker Change: Next question comes from the line of Andrew Chai with Jeffries. Your line is open.
Speaker Change: Hey, good afternoon. Thanks for the updates. Thanks for taking my question. Maybe a brief question is just for the ongoing extral studies, extral two and three. What are you assuming for the placebo rate on seizure reduction? Is it similar to what you saw in the phase 2b? And how are you controlling for a placebo risk if there is one? Thanks.
Thanks, Andrew.
Speaker Change: Chris, maybe I'll start because I might take the question and a little bit of a
Speaker Change: in a different direction, Andrew, just to give you a, provide a little bit of context and perspective that I think would be helpful. And then Chris, maybe you can just weigh in on controlling the placebo rate.
Speaker Change: in epilepsy studies in terms of the jurisdiction and quality of sites that we're working with.
Speaker Change: But Andrew, in terms of our modeling, I think the question really comes down to what are we comfortable with in terms of the study design.
Speaker Change: and the powering and the statistical analysis. So what we've done is we've looked at all of the data we generated in the X-Toll study. Obviously that was a large.
So we've used the actual placebo rates.
Speaker Change: which, if you recall from our EXTOL study, but just as a reminder, that was kind of in the high teens in terms of the placebo rate. And that's kind of what we expected going into the phase.
Speaker Change: to study. So I think it was really, you know, well executed and what we would expect and then we can take those actual data in terms of the placebo rate, the active rate, the standard deviation into our model for phase three. And as I think what we said
Speaker Change: previously is that the high dose of 25 milligrams we have more than 99% power and we have around 90% power for the lower dose of 15 milligrams and so in terms of the sizing of the studies we really went off that lower dose because we have considerable power.
Chris Kenney: at the high dose. Chris, maybe just you can comment on the execution of phase 3 in terms of placebo rate.
Chris Kenney: Yeah, I mean one of the luxuries of epilepsy compared to other areas of neurology or psychiatry is the translatability of the data going from phase 2 to phase 3.
Thank you.
Chris Kenney: So, but that said, there are several things that we're doing to try to mitigate the risk of an increasing placebo effect.
Chris Kenney: And it largely has to do with geography. So there are known geographical regions where the placebo effect in epilepsy is higher relative to others.
Chris Kenney: and the other thing that we've used is to target experienced sites, not just experienced sites.
Chris Kenney: based upon other drugs but actually sites that have had experience working with the Zetu calendar. And then we've also been fairly picky about the sites that in general that we allow into the study in terms of their experience with
with epilepsy. So you could, you know, potentially open up...
Chris Kenney: study like this to many other sites and we've been quite choosy and most all of our sites have.
Chris Kenney: dedicated expertise within epilepsy. So those are the main ways in which we're working on mitigating the placebo effect going from phase two to phase three.
Awesome. And Chris, I'll...
Speaker Change: I'll add, and Andrew, I'll add one more which I think is really interesting is
Speaker Change: is the use of electronic diaries. And, you know, when we were initiating the X-Toll study, that was a real conversation internally because it was where it seemed to be a transition between companies using and sponsors using paper diaries or electronic diaries. And obviously we can't run the experiment twice, but I think we do have a feeling internally that the electronic diary
Speaker Change: and the technology that we used in phase two that we're, and we're using electronic diaries in phase three as well, has helped on that side because we're continuously reminding patients to enter in their seizure data.
Speaker Change: And we can track that real time in the cloud to make sure that there's not missing data. I think that's also beneficial.
Speaker Change: Next question comes from the line of Brian Abrahams with RBC Capital Markets. Your line is open.
Brian Abrahams: Hi there, thanks for taking my question and congrats on the continued progress.
Brian Abrahams: As we head into AES, I'm wondering if you could talk a little bit more about what some of the highest focus elements of the 36-month data will be relative to prior cuts, your level of confidence in the continued safety profile, and then some of the key aspects that you're going to be highlighting and seeking input on there as you ramp up your presence and engagement. Thanks.
Speaker Change: Thanks, Brian. Yeah, really important questions. I think this AES is really the most important medical Congress.
Speaker Change: in epilepsy and it's a huge amount of planning for our team going into it. We're gonna have an incredible presence there. We're really excited about showcasing all of the work we're doing across the portfolio. So maybe I'll start and both Chris Kenney and Chris von Seggern.
Speaker Change: to provide their perspective as well because both of their teams are going to have a really large presence there.
Speaker Change: both as we continue on our medical communication side as well as the preparation on the commercial side of the business.
Speaker Change: But I'll give my perspective initially on the 36-month data. So, the nice thing is, Brian, you've seen the OLE data cuts from us before, so you're going to see consistency there. You're going to see, you know, all of the patients have gone through 36 months. We have a cut of those data where we can show what the population looks like in terms of the seizure reduction. And as we've mentioned, we've seen, you know, improved seizure reduction over time for those that stay on drug, just as a reminder.
Speaker Change: The second thing we'll see is just what the seizure freedom rate is. And that number, you know, continues to go up because patients are on the drug for longer. And so for that 12-month seizure freedom rate, which is really kind of the focus.
Speaker Change: of the clinical and medical community is that more patients have the opportunity to have that 12 months of seizure freedom, so we're excited to be able to communicate that. I don't want to lose the point that Chris Kenney made in his prepared remarks. You shouldn't, you know, if we look at the literature that this patient population, given the number of drugs that they have failed,
Speaker Change: and kind of the refractory nature of them. We really shouldn't be seeing seizure freedom or the literature would suggest it should be less than 5%, but we've seen considerably higher seizure freedom in our 24 month cut of the data last year and we'll be updating it for 36 months this year.
Speaker Change: And on the safety side, you know, one of the things, again, that gives us a lot of confidence is we've seen a real consistency in the safety profile. So, we will provide a safety update, but the types of adverse events that we're seeing in the double blind period is consistent with what we're seeing in open label extension as well. So, as we mentioned, now that we have patients over five years of dosing and we have over 600 patient years of exposure, we're really, really understanding the adverse event and safety profile overall of the molecule and have real comfort and confidence around that.
Speaker Change: But Chris Kenney, why don't you start with your perspective, and then Chris von Seggern. I know this is a big meeting for your team as well.
Chris Kenney: Yeah, it's our Super Bowl. We have a lot going on at AES above and beyond the open label extension poster, but that's what, Brian, you focused the question on that. I think Ian covered it pretty thoroughly. The only thing that I'll add is that we'll also have
Chris Kenney: retention rates out for a longer period of time, not just at one year and two year but up to three years.
Chris Kenney: And I think what we're seeing is that patients who, once they reach two years, they really tend to stay in the study for a long time. And just to build on what Ian said about seizure freedom, just the longer that study goes, the longer we're able to look at seizure freedom over longer periods of time.
I think you'll be impressed with the data. Chris?
Chris Kenney: Yeah, then beyond just the data platform itself, which we're really excited about, AES represents a phenomenal opportunity for us to engage with potential future prescribers in this marketplace. And we think about AES as a high concentration of epileptologists and broader neurologists with a focus on epilepsy. And our team is going en masse in order to have the opportunity to interact with as many potential, both key opinion leaders as well as potential future prescribers in this marketplace as possible to hear feedback on its F2 calendar, the profile, and how it could potentially fit into a marketplace.
Speaker Change: Next question comes from the line of Brian Skorney with Beard. Your line is open.
Speaker Change: Hi, this is Luke on for Brian. Thanks for taking the question. On FOS, can you share your current thinking on bringing azethicolinor into development for pediatric patients?
Speaker Change: and is this something that could commence ahead of XTOL2 data and is there anything unique from XTOL2 in how you would conduct a study in these patients?
Thanks.
Speaker Change: Thanks, Luke. Yeah, good questions. We haven't actually talked about the pediatric development probably for a few quarters now, so a nice reminder. So yes, we have agreed upon pediatric plans with both FDA as well as EMA, so we know exactly what we need to do.
Speaker Change: to bring the molecule into younger patients. So just as a reminder, in FOS, XL2 and XL3 are focused on adults. Actually, in our primary generalized tonic-clonic seizure study, we're going down to 12-year-olds. So that was based on some FDA feedback. So that study is looking at 12 and above.
Speaker Change: But we have an agreed upon plan and essentially you go through younger cohorts.
Speaker Change: of patients over time. There's nothing specific in the XTOL2 data that we're looking for that necessarily informs there. A lot of the work we're doing is really the pediatric formulation.
Speaker Change: Juvenile Toxicology, the other work that we need to do to get into younger patients. So a lot of that work is happening in parallel. And then over time, you'll see kind of these age groups of cohorts as we step down, all the way into very, very young patients over time. So the pediatric plan is ongoing, kind of in parallel in the background. And you'll start to see some clinical development over the next couple of years in younger FOS patients. And then as I mentioned, on the primary generalized side, we're already down to age 12.
Thank you.
Speaker Change: Yeah, the only thing I'll add to that is that you asked a question about, Luca, you asked about the unique take on the pediatric. The only other thing that we need to take into account is that, of course, those patients are lighter in weight, so we have to to make dose adjustments, but that's it. Otherwise, Ian covered everything. Thanks.
Speaker Change: Next question comes from the line of Jason Gerberi with Bank of America. Your line is open.
Speaker Change: Hey guys, thanks for taking my question. Mine just is a patent question actually. So specifically your food effect patent.
Speaker Change: My understanding is the strength of these patents tends to be, you know, can you get
some sort of incorporation in the product labeling.
Speaker Change: around the food effects such that generics wouldn't be able to eventually one day carve it out in their own inserts. So just wanted to get your confidence when you think about the phase 3 study protocol, you know, in getting label language around a recommendation for dosing close to mealtime, which I think is sort of
Speaker Change: key to that bioavailability argument with that patent and just wanted to understand kind of how you're thinking about that and the strength of that patent. Thanks.
Speaker Change: Yeah, thanks, Jason. I think you framed it really well. Sherry can go into the details on our approach.
Speaker Change: Yeah, well, I won't get into too much detail on this, Jason, as I'm sure you can appreciate there's some sensitivities around this. But look, overall, we're very comfortable in this food effect patent, but more broadly in our patent portfolio, which takes us out to
Speaker Change: 2039-40 absent extension of term. But on the food effect point specifically, so we do have a food effect with this molecule which is unique.
Speaker Change: calendar. So it's not something that is seen broadly with the mechanism. So it wasn't
Speaker Change: for example, seen with the Zogabine, and we understand it's not seen with other KB modulators in development.
not something that was therefore predicted by us.
Speaker Change: But yes, we have been dosing azethucalonar with food in proximity with the evening meal through our Phase 2 study, extol, as well as in Phase 3 development, both in our epilepsy program as well as in MDD. So we do reasonably expect that that will be on label at the end of the day.
Speaker Change: given that's how the drug has been dosed and not doing so would potentially have implications on both or either of efficacy and tolerability.
Speaker Change: Next question comes from the line of Saira Shram with William Blair. Your line is open.
Saira Shram: Hi, yeah, congrats on another great quarter and thanks for taking my questions.
Saira Shram: Would you expect to pursue both acute and chronic pain indications, or do you anticipate a little bit more of a narrow focus? I know you mentioned bunionectomy studies earlier, but is there kind of anything specific to NAV1.7 that would be more well-suited to, you know, one pain setting or the other? And relatedly, give your expertise an eye on channel chemistry, would you ever look to develop a NAV1.8 inhibitor, or do you see that space is increasingly crowded here? Thanks.
Thanks, Sarah. I'm happy to answer those questions.
Speaker Change: are neuropathic. So, as we sit today, and with the caveat that it's still early days, this is still a preclinical asset, I think we want to do a proof of concept study like bunionectomy to show, you know, target engagement and that we can get an analgesic effect. But as we think about the mid and later stage clinical development, nothing's off the table right now. So, I think we would be looking at all of those things because, as I mentioned, kind of going into this.
Speaker Change: were not guided one way or another based on the genetics or based on the target.
Speaker Change: In terms of, you know, Nat 1.7 versus 1.8, that's a question we often get. You know, we like 1.7 as a target, a number of reasons. We think the genetics are stronger. I think you mentioned it's a less competitive space. I think it's been harder chemistries. And I think we have a real leadership position there that we can capitalize on.
Speaker Change: You know, we have some other ideas on where we may want to go, which we haven't really talked about publicly, but we don't have.
Speaker Change: a formal NAV1A program just to address that question head on. We've really focused on NAV1.7 because I think it is a target where we're uniquely suited to be able to run the human clinical experiment.
Bye-bye.
Speaker Change: Next question comes from the line of Paul Choi with Goldman Sachs. Your line is open.
Speaker Change: Hi, thanks for taking our questions. ClinicalTrials.gov is currently showing that the extol-3 study
will reach primary completion just four months after X-Toll 2.
Speaker Change: So, presumably, the top-line results should be available roughly or concurrently with
Speaker Change: your planned NDA filing for Azteca-Colonel following Ex-Toll 2. So can you maybe just update us on your latest thinking of how Ex-Toll 3 might figure as part of your data strategy for your filing? Will it be primarily included in the NDA or is it primarily for the European filing? Just your latest thoughts there would be great. Thank you.
Speaker Change: Yeah, thanks Paul. I'm happy to start Chris. If you've got comments, please please add in.
Chris Kenney: Yeah, I mean we've said for some time that we've prioritized
Chris Kenney: XTOL2 over XTOL3 and that's being pulled through a couple of different ways. One, XTOL2 was just initiated before XTOL3 in terms of those first clinical sites up and running. We also prioritized a number of the sites that had experience with the molecule into XTOL2 and we did have a bias in jurisdiction as well.
Chris Kenney: where, you know, these studies get up and running generally quicker in the U.S. than they do in some other jurisdictions, and so we've biased.
Chris Kenney: a number of those sites into XTool2. So, and the priority and the focus on XTool2 is really because that's on the critical path, as you've mentioned, to filing the NDA and commercialization in the U.S.
Chris Kenney: In terms of xTool3, yes, we think it's important for filing in jurisdictions outside of the U.S., so you're absolutely right there. And it's really important for our overall safety database.
Chris Kenney: So, you know, obviously we think about safety in terms of the requirements under under ICH, but also just
Chris Kenney: exposures in in the labeled population so you know I think we're gonna have a huge we've talked a lot this this afternoon about our long-term exposure we're gonna have lots of long-term exposure but I think we're gonna have you know a lot of unique exposures as well both with XTOL, XTOL2, XTOL3
Chris Kenney: and Zach in all of the open label work. So I think that kind of provides the perspective in terms of how the interplay between the two studies. Chris Kenney, anything that I missed?
Chris Kenney: No, you didn't miss it, but I just think it's really worth emphasizing that we are positioning the XTOL study as our first pivotal trial in focal onset seizures.
Chris Kenney: Once we get the second trial, presumably ex-tol 2, we will submit the NDA. So there will be no hold-up waiting for ex-tol 3 to submit the NDA. I just want to make sure that's absolutely clear.
[inaudible]
Thanks, guys. Thanks, Paul.
Speaker Change: Next question comes from the line of Daniel Brill with Raymond James. Your line is open.
Speaker Change: Hi guys, thanks so much for the question. Chris, you commented during the prepared remarks that in XTOL a Z2 calendar demonstrated the best
Speaker Change: placebo-controlled efficacy to date. If the effect size happens to diminish in X-Tol2 relative to X-Tol, what impact might that have, if any, on its value proposition? Thanks so much.
Thank you.
Speaker Change: You want me to go in? Chris, do you want me to start and then you carry on?
Chris Kenney: Okay, cool. Thanks, Danielle. Yeah, I mean, the message really is that I think we've set an incredibly high bar here, right? So, in terms of our review of the literature with all the caveats of cross-trial comparisons,
we believe is at your counter, has the best...
Chris Kenney: efficacy on a placebo-adjusted basis so looking at 25 milligrams the MPC primary endpoint in X-toll minus the placebo rate
Chris Kenney: has the highest number that we can see in the literature. And just as a reminder, in the most severe or refractory population ever trialed, at least based on our review of the literature. So I know we're doing cross trial comparisons, but I think it's a very impressive.
Chris Kenney: efficacy outcome and has set a very, very high bar. Because, as we've just talked about in the last question, because we're filing on XTOL and XTOL2, that doesn't change, right? We, you know, no one is going to, those data are completed, that double blind is unblinded, we have those data already.
Chris Kenney: So, you know, the nice thing about epilepsy is we see this reproducibility and consistency study to study, but there's always going to be differences, and I think there's always going to be a different rate.
Chris Kenney: And so to your very specific question, Danielle, if the XTOL-2 data aren't quite as robust as XTOL, I still think we have the XTOL data and XTOL-2, we believe.
Chris Kenney: are gonna be confirmatory that this is an efficacious agent and an important molecule, and there's all of the other attributes as well. So we actually don't anchor too much on exactly what the efficacy readout is gonna be in X-Tool2 and what the implications may be.
Chris Kenney: And I think Chris Kenney should provide his perspective, but Chris von Seggern as well, because ultimately, you know, I think you're asking a commercial question, if we see something different in in XTOL2 than in XTOL. So Chris Kenney, maybe you want to add and then Chris von Seggern.
Chris Kenney: I'll just say one thing quickly, I mean, we really emphasize the X-toll data because
Chris Kenney: It's what we have, and because we think it's quite compelling. It's not that we're looking at extol two or three and saying, I think the data's going to be better or worse or the same. It's sort of hard to predict these things. So we're just making that emphasis because it's the actual data that we have in hand. But ultimately, what we need is for the trial to be positive, and then we can submit the NDA.
Chris
Speaker Change: Yeah, and then if we if we think about the positioning of Zephyr Calendar in a potential future commercial environment,
Speaker Change: Clearly what we've said in the past is that physicians are looking for new medicines to address
Speaker Change: continued seizures in this patient population. And efficacy is an important value attribute.
Speaker Change: But when we think about efficacy, there are multiple dimensions beyond just the top-line data. We're going to share the updated open-label data, which are going to show continued durable response and impressive seizure freedom data over time.
Speaker Change: That's the totality of the efficacy story in addition to potential rapidity of onset as demonstrated by week one efficacy. And then there are a whole host of other ease of use attributes that consistently are identified by physicians as a reason to turn to a Zetecaliner for a patient who's continuing to suffer from residual seizures. So while efficacy is important, the totality of the data package associated with this molecule, we consistently hear time and time again, it's compelling. And therefore, we believe it will offer a really important treatment alternative to patients in this marketplace.
Speaker Change: Next question comes from the line of Mark Goodman with Leering Partners. Your line is open.
Speaker Change: Ian, can you just talk about the strategy for MDD program just in total with respect to when are we going to get the second trial started and the third trial started and how you're thinking about that, how to stagger it, and you know, just in the same light as the way you talk about the epilepsy program, just so we have an update. Thanks.
Speaker Change: Yeah, thanks Mark. Yeah, very consistent with with the epilepsy program. So essentially we want to run the phase three studies in MDD in parallel, but they just never practically start at the same time.
Speaker Change: So, we're not gating, you know, Ex Nova 3 on an outcome on Ex Nova 2, but there will be a natural stagger. It's usually kind of in, you know, a couple of quarters between, you know, we're right now focused on Ex Nova 2 and getting that up and running, and then there'll be a bit of a natural delay before Ex Nova 3 is run. But both of those studies and then Ex Nova 4, those studies will be run essentially in parallel. You know, as you know, the MDD studies are a little quicker to enroll than our epilepsy studies. And so…
Speaker Change: you know maybe I'll kind of zoom out a little bit and if we think about over the next couple of years 2025, 2026, 2027 there's going to be a huge amount of clinical data coming from Xenon with a ZETU calendar kind of across the entire portfolio.
Speaker Change: Next question comes from the line of Joseph Thome with Tilly Cowen. Your line is open.
Joseph Thome: Hi there. Good afternoon, and thank you for taking my question. Maybe as we think about the KV7 development candidates that you have in the early pipeline, how are those differentiated from a ZEPTA calendar?
Joseph Thome: Do they have different selectivity, different PK, or sort of what will you be looking for for those assets? And then, related to an earlier question, would all of these have, I guess, a new IP portfolio around it? Can you talk a little bit about that as well?
Yeah, thanks Joe.
Speaker Change: Yeah, to answer your last question first, yes, these are all, this is all, these are all novel structures.
Speaker Change: Novel Marcouche. So yes, all different intellectual property when compared to a Zetsu calendar.
Speaker Change: You know, one of the interesting things in discussions we have internally when we think about the KV7 molecules and maybe franchise is there's nothing specific in the profile of a Z2 calendar that we're trying to...
Speaker Change: change or improve on. So, you know, as you can understand, these things are multifactorial, right? We're looking at a whole bunch of different properties.
on these molecules, but we haven't really zeroed in.
Speaker Change: on any one specific thing, you know, you mentioned PK or selectivity, there's nothing one thing that we're really focused in on because I think the profile
Speaker Change: you know as as as Chris and Chris just mentioned is so compelling of a Z2 calendar.
Speaker Change: That said, we absolutely have chemical diversity, and so these are novel, but we do have chemical diversity. And in terms of really what some of those properties are going to be, I mean, I think we're really excited about the properties preclinically, but I think the proof's really as we transition those into the clinic.
Speaker Change: and we start to learn about the PK in a human and also making sure, you know, one of the nice things about epilepsy, and I know we're going to go broader than epilepsy for our KV portfolio, but we also know kind of the exposure levels that we're looking for in a human because
Speaker Change: the translatability in terms of some of the preclinical work. We know that we're in the we'll be in the right range. We also know with a Zetucaliner at a certain
Speaker Change: exposure in the plasma. We're seeing an anti-seizure effect. We're also seeing an antidepressant effect.
Speaker Change: And so we know we can look at that translatability from animals into humans as well. So yeah, it's a real exciting time for the early stage portfolio, you know, in addition to KV with the 1.7 program and the 1.1 program, but I think you're gonna see multiple molecules on KV7, you know, mature and head into human clinical development over the next couple of years.
Speaker Change: and some of them will look, we expect will look more like a Zecchia calendar and some I think will probably have some different properties which we'll learn about in the development.
[inaudible]
Speaker Change: And our last question comes from the line of Laura Chico with Wedbush Securities. Your line is open.
Speaker Change: Hello. Thank you for taking our question. This is Dylan on for Laura Chico. We're just wondering, so how should we think about the cadence of readouts for the Ion Channel portfolio and should we be looking for data in the 2025 time frame?
Speaker Change: So thanks for the question, Dylan. We haven't got to that level of granularity yet. I think from the prepared remarks and what you've seen in our press release and in our queue, the KV7 molecules and the 1.7 molecules are a little bit ahead of where we are with NAV1.1. So what we've said is we're, you know, we're in IND enabling studies for KV7 and for
Speaker Change: and for NAV1.7. So those molecules are going to transition, you know, if everything goes well in the remaining non-clinical studies, those will transition into human clinical development next year.
Speaker Change: I think depending, and we'll give updates during 2025 as those transition, and depending on the timing of that transition is when, you know, we'll have a better idea of when we're going to see some human PK data, as well as our SADMAD data, and then we can start talking about some of the properties of those molecules, like we talked about on the last question, you know, the earlier question in terms of exposure, as it relates to receptor occupancy, in terms of our NAV 1.7 program. So I think we're going to learn a lot.
Speaker Change: in those first in human studies, and then we'd move into the proof-of-concept studies thereafter. So, stay tuned for further updates in 2025.
Thank you. Thank you. Thank you.
Speaker Change: If there are no further questions at this time, I will turn the call back over to Sherry Aulin for closing remarks.
Sherry Aulin: Great, thanks everyone for joining us today. If we didn't manage to get to your question during the allotted time, we'll reach out directly to Connect. Operator, we can now end the call.
And this concludes this conference call. You may now disconnect.
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