Zevra Therapeutics, Inc. (NASDAQ:ZVRA) Q4 2023 Earnings Call Transcript

Zevra Therapeutics, Inc. (NASDAQ:ZVRA) Q4 2023 Earnings Call Transcript March 28, 2024

Zevra Therapeutics, Inc. misses on earnings expectations. Reported EPS is $-0.4 EPS, expectations were $-0.2. ZVRA isn’t one of the 30 most popular stocks among hedge funds at the end of the third quarter (see the details here).

Operator: Good afternoon, everyone. Thank you for joining the Zevra Therapeutics’ Q4 2023 Corporate Updates and Financial Results Call. Today’s call is being recorded. It will be made available the company’s website following the conclusion of the call. With that, I will now turn the call over to Nichol Ochsner, Vice President of Investor Relations and Corporate Communications for Zevra Therapeutics.

Nichol Ochsner: Good afternoon, and thank you for joining us today to review Zevra Therapeutics’ progress in the fourth quarter and full year of 2023, outlining our clinical advances, operational achievements and financial results. Before we get started, let me take a moment to provide some important information. I encourage you to access the news release which was just published and available in the Investor Release section of Zevra’s website. As we proceed with this call, it’s important to highlight that today’s discussion will include forward-looking statements. Forward-looking statements are not promises or guarantees and are inherently subject to risks, uncertainties and other significant factors that may to actual results differing materially from the projections made.

Please refer to the Risk Factors section in our most recent quarterly reports on Form 10-Q and our other filings with the SEC and annual report on Form 10-K. I’m pleased to welcome Zevra’s management team members participating in today’s call. I’m joined by Neil McFarlane, President and Chief Executive Officer; LaDuane Clifton, our Chief Financial Officer, Joshua Schafer, our Chief Commercial Officer and EVP of Business Development; Christal Mickle, our Chief Development Officer; and Adrian Quartel, our Chief Medical Officer. Now I’ll turn the call over to Neil.

Neil McFarlane: Thank you, Nichol. And thank you all for making the time to join us today. During the fourth quarter and into 2024, we made solid progress transforming Zevra into a commercial stage company. On our last call, we announced that we were focused on 3 key priorities: First, to close the Acer acquisition and deliver value to patients by commercializing OLPRUVA. Second, to resubmit the arimoclomol NDA. Third, to complete the Phase II trial in idiopathic hypersomnia and prepare to advance KP1077 into Phase III. I’m happy to report that we executed on all of these objectives, and I would like to take the opportunity to recognize the extraordinary effort from our entire team to deliver for people living with rare diseases.

Before discussing our results, it’s important to note that our financial statements for fiscal year ’22 including all interim periods and the interim periods of 2023 will be restated due to a change in our warrant accounting. LaDuane will provide more details later on the call, but we believe the restatements will have no impact on the company’s cash or ability to execute on our strategic priorities. Turning to the fourth quarter corporate highlights, let me start with the completion of the Acer acquisition, which propelled us into becoming a commercial stage company, diversifying our revenue potential and providing scale. The acquisition was a natural fit with Zevra’s mission, bolstering the talent on our team and bringing complementary rare disease assets, including commercially available OLPRUVA.

OLPRUVA is indicated for the treatment of certain urea cycle disorders, UCDs, which are a group of rare genetic disorders that can cause harmful levels of ammonia to build up in the blood, potentially resulting in new kind of impairments, brain damage and in some cases, coma or death. We estimate that there are approximately 2,000 people in the U.S. with UCDs of which roughly half have been diagnosed and treated. The UCD market in the U.S. is estimated at approximately $350 million annually. Despite the available therapies, unmet needs for people living with UCD persist. We believe that OLPRUVA is well suited to address these needs as it provides personalized dosage for each patient’s requirements, it’s portable and easy for patients to take.

And most importantly, it is powder, as it was formulated to overcome the challenging taste and smell that is associated with other formulations of sodium phenylbutyrate. Our commercial launch strategy is comprised of 2 major ones. One, establishing a customer-facing team; and two, building awareness. Since the completion of the Acer acquisition in mid-November, we have made significant progress towards executing on these priorities, ensuring that people who suffer from UCDs have access to and are aware of the benefits of OLPRUVA. As of the end of January, we have a customer-facing team with decades of rare disease experience to support the launch of OLPRUVA. This team was built to be targeted and able to reach the needs of our customers and partners, most of whom are located in approximately 40 centers of excellence across the country.

In addition to the sales specialists, we have marketers, patient services and market access professionals as well medical science liaisons and patient advocates for engaging with key customers. While initially built to support the launch of OLPRUVA, this same group of professionals will launch arimoclomol, if approved. We’ve initiated several strategies that are being utilized to build awareness of OLPRUVA, which is currently quite low. For example, we have established Quick Start, which is a 30-day free trial to allow patients and physicians to gain experience with OLPRUVA. We’re working with patient advocacy groups, the patient community and UCDs centers of excellence to drive brand recognition. We’re also working with payors to ensure broad market access for patients.

We’ve seen a meaningful growth in reimbursement coverage, which was approximately 55% at the time of acquisition to now more than 70% of covered lives. While it’s too early in the launch to provide data on today’s call, we’re monitoring key launch indicators, including new patient enrollments, number of covered lives and net revenue. As previously mentioned, the commercial footprint we established provides a high strategic fit for arimoclomol as the majority of prescribers for both products work within the same centers of excellence. If arimoclomol is approved, we believe its close proximity and overlap in patient care will allow us to realign synergies and scale with the infrastructure that we built. As a reminder, arimoclomol is our drug candidate in development for the treatment of Niemann-Pick type C or NPC.

NPC is a rare genetic, aggressive and potentially fatal neurologic disease. Earlier this month, the FDA has signed a new PDUFA date of September 21, 2024, and reaffirmed its intent to present the resubmission for discussion at an adviser committee meeting. If approved, we intend to utilize our clinical data as well real-world evidence and the data from our expanded access program to support market access, reimbursement and treatment decisions to establish arimoclomol as the foundation of treatment for people with NPC. We will continue to work closely with key opinion leaders to educate on arimoclomol’s clinical profile and raise awareness of the heterogeneous presentation of NPC, which may include neurological and psychiatric symptoms, all of which make MPC difficult to identify and diagnose.

Because of this, the time to diagnosis remains a significant unmet need in the NPC community. Therefore, we’re working with patient advocates to drive early diagnosis and supporting efforts for NPC to be included in newborn screening. Together with an approved indication, these initiatives will help drive the evolution of treatment guidelines and accelerate the time to diagnosis and treatment initiation. We will continue to work with all stakeholders to develop patient services that will provide access and a positive experience. We applaud the NPC patient advocacy community, who united and submitted a compelling response to an informal petition to the FDA in support of arimoclomol’s approval. We have received nearly 1,000 signatures fromo 47 states vouching their support.

As the FDA review continues, Zevra will maintain our expanded access program for arimoclomol and continue working tirelessly to bring this potential therapy to patients as soon as possible. Now I’d like to turn your attention to KP1077, our clinical candidate being developed as a treatment for idiopathic hypersomnia or IH. IH is a rare chronic sleep disorder characterized by excessive daytime sleepiness and uncontrollable need to sleep and difficulty waking up from sleep in most instances despite average or longer amounts of narcolepsy. As you may recall, KP1077, serdexmethylphenidate or SDX was designed to steadily [indiscernible] active ingredients. This unique pharmacokinetic profile allows for flexible dosing to overcome these primary IH symptoms.

The design also ensures that patients receive a high strength concentration when they need it most. SDX is designated as a Schedule 4 controlled substance Drug Enforcement Administration. Earlier this week, we announced positive top line data from our placebo control double blind proof of concept Phase II study, evaluating the safety and tolerability KP1077 in patients with IH. Consistent with the interim data that we previously reported in Q4, KP1077 was well tolerated at all dose levels evaluated in the study, including the highest dose of 320 milligrams daily and a dosing regimen of either once or twice daily. The most common adverse events were insomnia, headache, anxiety, nausea and decreased appetite. Due to KP1077’s unique pharmacokinetic profile, adverse events were mostly mild in severity, despite higher overall exposure levels.

These data support the study’s primary endpoint of safety and tolerability. Top line results from the Phase II study also showed that KP1077 produced critical meaningful improvement in excessive daytime sleepiness or EDS as assessed by change from baseline in the Epworth Sleepiness Scale during the 5-week open-label titration period, which was maintained throughout the two-week double blind withdrawal period for both those. Additionally, patients administered KP1077 showed benefit and change from baseline at the end of the open-label titration. And at the end of double line withdrawal period for the IH severity scale, the sleep inertia visual analog scale and brain severity scale. The study successfully fulfilled the objectives by providing key information for the design of a potentially pivotal efficacy trial and the results of the secondary efficacy endpoints are supportive of initiating a Phase III trial of KP1077.

We plan to request an end of Phase II meeting with the FDA to seek guidance on Phase III clinical trial design. We are pleased with the top line data and believe that KP1077 can provide a significant benefit to the estimated 37,000 people in the U.S., who are currently diagnosed with IH. With only 1 FDA approved treatment for IH, there remains an unmet need for therapies with different mechanisms of action to address symptoms including sleep inertia, excessive daytime sleepiness and cognitive dysfunction. We look forward to present in the results from our Phase II study at the upcoming SLEEP 2024 conference this fall. And in summary, we’re pleased with our progress in the fourth quarter. As we enter 2024, we have 3 areas of focus: First, to successfully launch OLPRUVA and ensure access for patients.

Second, to prepare for the potential launch of arimoclomol. And third, to advance KP1077 in sleep disorders. We believe that we are — we believe that we are well positioned to continue to execute and deliver on these key strategic objectives. Now I’ll hand the call over to LaDuane, who will provide an update on our financial results and outlook.

LaDuane Clifton: Thank you, and good afternoon. 2023 was a time of incredible progress as we seek to make therapies available to people living with rare diseases. Our financial results for the quarter and full year reflect our continued investment in advancing our development programs and building out our commercial capabilities. As Neil pointed out at the beginning of the call, we are restating our previously issued financial statements for the fiscal year ended 2022, including all interim periods and the interim period in 2023 due to a change in the accounting with certain cash settlement features. Warrants from 2021 has been classified as equity and are now accounted for as a liability, resulting in noncash fair value adjustments that will be recognized at the end of each reporting period.

This change and the related noncash adjustments are expected to have no direct impact on the company’s cash, cash equivalents and investments, our forecasted runway or our business operations. Now on our financial results for Q4 2023. We reported net revenue of $13.2 million. This was a solid quarter in which we met the milestone of $10 million under the AZSTARYS license agreement as annual net sales for that product surpassed $50 million for the year. Revenue also included royalties under the license, which rose to $1.3 million for the period comparing to $900,000 in Q3 2023. Net reimbursements from the French expanded access program for arimoclomol was $1.8 million, and there was recognition of some initial sales of approval. R&D expenses for the quarter were $1.4 million which was primarily driven by the Phase III study in KP1077 that has since been completed.

Along with to compare the FDA for resubmission. General and administrative expenses were $14.7 million. The period-over-period increase was primarily related to personnel costs and professional fees associated with our investments and our commercial infrastructure as well as our business develops activities, which included the closing of the Acer acquisition. Net loss Q4 2023 was $19.6 million or $0.51 per basic and diluted share. Our full year 2023 loss included net revenue of $27.5 million, which was primarily driven by the $15 million in total net sales milestones earned under the AZSTARYS license agreement, royalties of $3.8 million and net reimbursements from the French early access program for arimoclomol, totaling $8.6 million for the year.

Total R&D expenses of $39.8 million and G&A expenses of $34.3 million, we reported a net loss of $46 million or $1.30 per basic and diluted share for 2023, which includes the noncash impact of the change in fair value adjustment for the liability of $1.4 million or $0.04 per basic and diluted share. As of year-end, total cash, cash equivalents and securities were $67.7 million, which was a decrease of $15.7 million compared to September 30, 2023. Total shares of common stock outstanding were 41.5 million and fully diluted shares outstanding were 38.2 million, which includes approximately 5.6 million shares issuable upon exercise awareness. Looking ahead, our available resources are expected to support our forecasted operating cash runway into 2026, and we intend to evaluate optimization of our debt structure.

Our forecast includes commercial revenue from sales of OLPRUVA and ongoing reimbursements from the French EAP for arimoclomol, but it does not include commercial revenue from sales of arimoclomol or the sale of the priority review voucher, which will follow potential FDA approval. We remain optimistic about the opportunities we have in store during 2024 and our focus is on creating long-term value for shareholders by consistently executing against our plan and support our mission to becoming a leading rare disease company. Now our colleagues, Josh, Christal and Adrian will join us for our Q&A session. Operator, please open for questions.

See also 20 States with the Most Fluoridated Water in the US and 15 Best Smelling Essential Oils and Their Superpowers.

Q&A Session

Operator: [Operator Instructions] We’ll take our first question from Oren Livnat with H.C. Wainwright.

Oren Livnat: I have a couple. Really curious about this OLPRUVA launch. It sounds like you’ve got your infrastructure in place and maybe are just now trying to build awareness. I know you’re not giving guidance is certainly not a product-specific basis, but should we expect material revenue growth for that product this year? Or is this more about just like a sampling and awareness building year and just getting all the processes worked out, especially ahead of arimoclomol? And on arimoclomol, can you just talk about what, if anything you can say about your expectations around an ADCOM as far as what areas of focus you are most preparing for, where do you think the agency might be most interested, whether it be the connection between real-world data and your clinical data or validation and statistical issues? Anything you can provide on that would be really helpful.

Joshua Schafer: Oren, it’s Josh. Thanks for the question. With regards to the OLPRUVA performance, as you noted, we are in full launch. And as Neil just mentioned, effective at the end of January, we had the entire commercial and medical team out engaging with our customers. We knew at the beginning of all this that awareness for OLPRUVA and Zevra was quite low. But OLPRUVA in particular, if you’ll recall, it was a true through a 505(b)(2) pathway, which meant that it had very clinical experience. And so our priorities have really been around driving awareness and ensuring that patients have access to OLPRUVA. And to do that, our team is working with physicians to identify the appropriate patients. We have a Quick Start program in place to make sure that patients can experience the benefits of OLPRUVA.

And our reimbursement is increasing from 55% to over 70%. So it is too early for us to give any guidance on performance and revenue. We will be watching new patient enrollments, covered lives and net sales as we go, and we’ll be providing updates on a quarterly basis. I will ask Adrian on the agency and the potential focus of the ADCOM.

Adrian Quartel: So the FDA has currently not confirmed the ADCOM. So there is an to hold the ADCOM, nobody has been said preparing for ADCOM. As far as the — there is a submission and kind of know what the questions were that the agency were looking for. We’re focusing on addressing those as important though is focusing on telling the story that data shows a significant pain benefit for patients. Some additional information that we got during the 2 B meetings prior to our resubmission we also move to the we mostly looking forward about what we consider clear efficacy in these patients and a clear benefit of this profile.

Operator: Next question from Jonathan Aschoff with ROTH MKM.

Jonathan Aschoff: I haven’t had a chance to read the press release. It came out a little late and there’s a whole bunch of calls. But can you help us better understand the magnitude of benefits in IH and thus optimism for an end of Phase II meeting that so well and inform Phase III design?

Unidentified Company Representative: Absolutely. First, we just really focus on what the Phase II trial is trying to Achieve. This is a trial that was designed to demonstrate safety and tolerability inform us for what the data be saying into how to design development in IH. Part of the secondary endpoints was looking at the and have some of your insomnia scoring scale. We saw clinically meaningful improvements, not only in the taxation phase, but also line phase. As said, these trial’s to design a statistical significance. We are planning to present this data at 324 meeting and that we’re on data embargo. So we will discuss the data there with the feedback for that will attend think.

Jonathan Aschoff: Okay, so when you did this trial, you optimized these people to any one of the 4 different doses. So it’s a complete random smattering like it’s not 16 patients per dose. It’s it’s whatever was their optimum dose, that’s where they land. There’s no balance among those 4 groups.

Joshua Schafer: That is correct.

Jonathan Aschoff: Okay. So after seeing the Phase II press release, are you still contemplating a narcolepsy trial, because the word narcolepsy is not in that press release on Tuesday, I was just curious why that was.

Neil McFarlane: Thanks, Josh, it’s Neil. We’re taking this data that we’ve got now on our Phase II to inform a Phase III in IH. But we’re also understanding our Phase I data — some of our Phase I data data to understand how to unlock the value of the broader sleep disorder opportunities. So we’re evaluating that, but we have no further comments today on it, if we’re going to move forward into narcolepsy.

Joshua Schafer: Okay. And just a answer now. OLPRUVA is going to until you see how you track with the first indication, correct? Or you have development plans for MSA such you could even give us a time line?

LaDuane Clifton: So you are correct. We’re waiting to do a full evaluation of our portfolio and strategic plan before we make any decisions on narcolepsy.

Jonathan Aschoff: Okay. Lastly, when it comes to AdCom, do companies typically have any sort of back and forth with the patient as it gets the strategized in any way? And if so, do you intend anything like that? Or is it just everyone shows up?

Christal Mickle: Yes, we — this is Christal. It is very important the company to engage with Innovation MC Group, and that we are doing that. One as to the patient physicians that came through Certainly, that was something that we were very happy to see and will continue to engage and make sure that the voices of the patients that are being incurred at the AdCom in their own way.

Jonathan Aschoff: I think that will be an important part of an ADCOM. So that’s good to hear.

Operator: We will take our next question from Sumant Kulkarni with Canaccord.

Sumant Kulkarni: I have two. First 1 is, have you had any interactions with the FDA on pending arimoclomol filing announced the 3 months short of the action date and how those discussions gone?