Ironwood Pharmaceuticals, Inc.

My name is Kathleen and I will be your conference operator today. At this time I would like to welcome everyone to the Ironwood Pharmaceuticals 4th quarter 2024 Investor Update Conference call. All lines have been placed on mute to prevent any background noise. After the speakers remarks there will be a question and answer session. Thank you. I would now like to turn the call over to Greg Martini, Chief Financial Officer. Please go ahead.

Good morning and thanks for joining us for our 4th quarter and full year 2024 Investor Update. Our press release issue this morning can be found on our website. Today's call and accompanying slides include forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such statements involve risks and uncertainties that may cause actual results to differ materially. A discussion of these statements and risk factors is available in our current Safe Harbor Statement slide as well as under the heading Risk Factors in our annual report on Form 10K for the year ended December 31, 2023 and in our subsequent SEC filings. All forward-looking statements speak as of the date of this presentation and we undertake no obligation to update such statements. Also included are non-GAAP financial measures which should be considered only as a supplement to and not a substitute for or superior to GAAP measures. To the extent applicable, please refer to the tables at the end of our press release for reconciliations of these measures to the most directly comparable GAAP measures. During today's call, Tom McCord, our Chief Executive Officer, will begin with a brief overview. Mike Schetzlein, our Chief Medical Officer, will discuss our pipeline and I will provide a commercial update and review of our financial results and guidance. Today's webcast includes slides, so for those of you dialing in, please go to the events section of our website to access the accompanying slides separately. With that, I'll turn the call over to Tom.

Good morning everyone and thanks for joining us today to review the fourth quarter and full year 2024 financial results and business updates. We're entering 2025 with a streamlined focus on advancing apric glutide and realizing its potential to significantly expand the market in GLP-2 treated patients with short bowel syndrome who are dependent on parental support. Recent data from our open label extension study, which is called STARS Extend, further reinforce and strengthen our confidence in apric glutide's potential to become Ironwood's blockbuster therapy. Last month, we shared an analysis showing that 27 total patients achieved enteral autonomy, or in other words, achieved independence from parental support while on apric glutide. These data are important when thinking about the impact apric glutide can have in this patient population and demonstrate apric glutide's potential to provide patients with either longer periods away from or complete freedom from parental support. Building on these promising results, we're planning to include additional analysis based on exposure time from the long-term extension study into our NDA submission package to support an even more robust, clinically differentiated, and comprehensive data package to the FDA. As we recently announced, we have initiated the rolling submission of our NDA and expect a complete submission in the third quarter of 2025. If approved, apric glutide will become the first long-acting GLP-2 to market for short bowel syndrome patients who are dependent on parental support, providing a new treatment option with the convenience of once-weekly dosing. Aligned with this next phase of growth, we have restructured our business to focus on bringing apric glutide to market, strengthening our commitment to advance the advancing care for patients with short bowel syndrome. We believe these changes may position us for future growth, long-term value creation, and ultimately reinforce our commitment to bringing new medicines to patients with rare disease. We have a strong team in place to drive the success of apric glutide if approved. Our commercial efforts, led by Tammy Gaskin, our newly appointed Chief Commercial Officer, and she is supported by an experienced team with expertise in key functional areas of commercialization in both GI and rare disease. And we're actively preparing for a potential commercial launch. Unlike LenzS, launching a treatment for rare disease like short bowel syndrome requires a targeted approach. And through our extensive market assessment, we now know that this is a much smaller, rare disease-focused prescriber base primarily located in short bowel syndrome centers of excellence where the majority of patients are managed. With these insights in mind, we plan to implement a robust patient support service model, one that ensures seamless care from the point of prescription to treatment authorization, delivery, initiation, and ongoing utilization of apric glutide. While apric glutide is our focus for the future, LenzS remains a critical part of our portfolio, helping millions of adults with IBSC and chronic constipation. Even after 12 years, demand continues to grow, further solidifying LenzS as the prescription market leader. In the fourth quarter of 2024, we saw a 12% increase in prescription demand growth compared to the fourth quarter of 2023 per IQVIA and 11% prescription demand growth for 2024 year over year. New to brand volume growth was 11% for the fourth quarter of 2024 and 14% for the full year. This marks the eighth consecutive quarter for double-digit, new to brand volume growth, demonstrating that patients and providers continue to choose LenzS. For the full year of 2024, we achieved our latest 2024 financial guidance, delivering $916 million in net sales. And based on IQVIA script data, we are starting to see Medicare utilization, a headwind in 2024, stabilize as a percent of our book of business in the second half of 2024. As we look ahead to 2025, we expect to see continued strong demand growth with LenzS while also anticipating pricing headwinds and therefore have a focused investment to continue to drive profits. We expect the cash flows from LenzS will continue to sustain future capital needs to fund the next stage of growth for Ironwood, namely the commercial approval and launch of apoglutide for short bowel syndrome patients who are dependent on parental support. Before I turn the call over to Mike to talk about apoglutide and short bowel syndrome in more detail, I want to take a moment to express our gratitude to our colleagues and partners in the physician, healthcare provider, and patient community. February is Rare Disease Month, and as we work towards our goal of developing and commercializing life-changing therapies for patients with GI and rare diseases, we also seek to increase awareness for the people we serve who are at the center of our work year-round. Without their commitment and your commitment and engagement, we would not have been able to run the largest ever short bowel syndrome intestinal failure trial with apoglutide. Short bowel syndrome is a devastating condition that we thank you for your trust in us as we work urgently to deliver this important medicine to short bowel syndrome patients who are dependent on parental support. With that, I'll turn it over to Mike.

Thanks, Tom, and good morning, everyone. We're pleased to have initiated our rolling NDA submission earlier this year, which we expect to be completed in the third quarter of 2025. I wanted to dive a bit deeper into the opportunity around apoglutide and the compelling data generated from the STARS Phase III clinical trial, including additional data from the open-label extension study, STARS Extend. Short bowel syndrome with intestinal failure results from severe organ failure due to a reduction in intestinal function below the minimum necessary for adequate nutrition and fluid absorption, leading to a dependence on parental support for the IV administration of fluid and nutrients to maintain health, growth, and survival. Approximately 18,000 adult patients are impacted by this disorder across the U.S., Europe, and Japan. This condition is associated with increased mortality, significant morbidity, high economic burden, and reduced quality of life. Intervention with parental support comes with its own challenges affecting quality of life. Parental support can be required for 10 hours a day and six days a week on average. Due to the significant patient burden, reducing the number of days and or the hours a day per week on parental support is extremely important to patients and their health care providers. Aproglutide is uniquely designed to accelerate intestinal growth for improved gut function and intestinal absorption. Aproglutide is the only GLP-2 analog to achieve a statistically significant reduction in weekly parental support volume with once-weekly dosing. In the STARS Phase III study, patients also achieved clinically meaningful parental support volume reductions as early as week eight. Additionally, as previously presented, some patients achieved two and three days off of parental support per week, and a portion of patients achieved enteral autonomy in the STARS Phase III study. Enteral autonomy is when individuals no longer require parental support, a significant life-changing milestone for patients and their families in their treatment journey. We're now seeing even more patients achieving enteral autonomy in our extension study. Further reinforcing aproglutide's clinical profile. As Tom mentioned, based on an analysis we shared in January, 27 total patients treated with aproglutide achieved enteral autonomy. Beyond that, we continue to see encouraging trends in parental support volume reduction more broadly with longer exposure to aproglutide. We're excited by this growing body of clinical evidence that we believe supports aproglutide's potential, if approved, to become the first long-acting once-weekly GLP-2 therapy for the treatment of short bowel syndrome. With that, I'll turn it over to Greg to review our financials.

Greg? Thanks, Mike. We ended 2024 in a strong financial position, achieving our 2024 full-year guidance. Our business continues to be supported by strong linsest prescription demand. We saw 11% full-year 2024 prescription demand growth. Recognized $223 million in linsest US net sales in the fourth quarter. $916 million for the full year. Ironwood recorded $88.4 million in collaborative arrangements revenue in the fourth quarter of 2024. $340.4 million for the full year. As you can see on slide 11, in 2024 linsest continued to deliver strong double-digit extended unit and new to brand prescription demand growth. The continued strong prescription demand growth bolsters our confidence in the strength of linsest over time and the expectation that linsest will drive meaningful cash flows moving forward to fund the next stage of growth through the advancement of aproglutide. Turning to slide 12 to review full-year 2024 financial highlights. Total revenue was $351.4 million. Gap net income was $1.8 million. Adjusted EBITDA was $100.6 million which includes stock-based compensation. As a reminder, we have provided 2025 financial guidance for adjusted EBITDA excluding stock-based compensation expense. And we'll be moving to this new definition beginning in the first quarter of 2025. We ended the full year 2024 with $88.6 million of cash and cash equivalents on the balance sheet. In the fourth quarter, Ironwood repaid $15 million of debt ending the year with $385 million drawn on our credit facility. Over the past 12 months, in the midst of pricing headwinds in 2024, Ironwood reduced its total debt balance outstanding by roughly $115 million. As of December 31, 2024, Ironwood had access to roughly $254 million in liquidity between the $88.6 million of cash on hand and $165 million undrawn revolver capacity. In 2025, we remain focused on delivering sustained profits and cash flows to fund the advancement of Afro-Glutide and repay debt to strengthen our balance sheet. Moving to financial guidance on slide 13. We are reiterating our 2025 guidance at this time. This includes U.S. Linses net sales between $800 and $850 million. We expect Linses prescription demand to remain strong with high single-digit prescription demand growth. This strong demand growth is expected to be more than offset by pricing headwinds associated with the Medicare Part B redesign that went into effect earlier this year. We expect Ironwood revenue between $260 and $290 million. As a reminder, Ironwood recognizes collaborative arrangement revenues from Linses as a portion of commercial profits, which includes an add back for Ironwood's selling and marketing expenses. And we expect adjusted EBITDA, excluding stock-based compensation of greater than $85 million, which reflects a roughly $55 million decrease from 2024 operating expenses, primarily within SGA, driven by the reorganization actions announced last month. In summary, we have taken actions to continue to generate profits and cash flows, pay down debt, strengthen our balance sheet, and support the advancement of Afro-Glutide in 2025, and to position the company for long-term growth. We are increasingly encouraged by the positive body of clinical evidence that we believe supports Afro-Glutide's potential to meaningfully change the treatment paradigm for short bowel syndrome and become our second blockbuster therapy. We are working diligently to complete our NDA submission by the third quarter of 2025, and pre-launch planning is well underway to support the commercialization of Afro-Glutide upon approval by the FDA. I want to close by thanking all of our employees, patients, caregivers, and advocates for their shared dedication to advancing life-changing therapies for patients with GI and rare diseases. Operator, you may now open the line for questions.

Thank you. We will now begin the question and answer session. If you have dialed in and would like to ask a question, please press star 1 on your telephone keypad to raise your hand and join the queue. And if you would like to withdraw your question, simply press star 1 again. If you're called upon to ask your question and listening by a loudspeaker on your device, please pick up your headset and ensure that your phone is not on mute when asking your question. Again, please press star 1 to join the queue. And your first question comes from the line of Chase Nickerbacher of Quay Callum. Your line is now open.

Oh, good morning. Thanks for taking our questions. Just first from me, I get it's kind of early after kind of just taking these kind of headcount changes. But can you kind of just speak to the confidence you have in any kind of initial kind of learnings now that you've kind of went to more virtual-based marketing, at least personally with yourselves, around kind of the confidence you have on high single-digit volume growth this year without that in-person promotion from the Ironwood side?

Thanks. Tom, do you want to take that? Yeah, sure. Thanks, Chase. As you know, we still have a very solid marketing mix supporting and driving the growth of Lindsys. We still have a number of ABI sales personnel in really the key offices. And at this point, it's a lot of the consumer advertising that's probably driving the ongoing growth. Certainly, when we look at ROIs, it sends a look very, very positive. And this is something that we've continued to refine over time. If you we've basically cut our selling effort more than by half. And we've also pulled back on the media buy to increase the bottom line profit of the drug. And we have not seen any evidence that demand is slowing down. And we're seeing that so far out of the gate. It's early. The numbers, as you know, don't always line up year over year. But we're still seeing very, very strong momentum on the I think as long as we can maintain broad payer access, I don't see that slowing down. When you have a brand in a market that has almost 50% market share, it's really hard for an emerging competitor to really capture share around you and away from you. And we're actually continuing to see either maintaining or increasing our market share, even in the face of multiple competitors over the last four or five years. So I think we feel very confident in the single digit demand growth. And we'll be certainly watching, you know, what's going on with our payer mix, to really better understand what kind of exposure we have as the year goes on. But I think, you know, we feel very confident in the guidance we've got we've given that, you know, it's very achievable. And hopefully, you know, we'll do everything we can to exceed it.

That's great, Tom. Thanks. And Greg, maybe just a couple on the model. First, if we think about kind of the cadence of cost savings, should we be kind of assuming that, you know, Q1 has a fairly full kind of recognition of at least on a run rate basis of kind of those cost savings? And then just second on the R&D line, as these kind of, you know, trial activities start to roll off, I mean, should we be kind of modeling a decrease in R&D? Is it, you know, back up at 25? Is it in 26? Just help us think about expenses.

Yeah, thanks, Chase. In terms of the cost savings actions that were taken last month, first quarter, we won't see the full impact, because these actions were taken at the end of January. So you'll really start seeing that full run rate in Q2 for the rest of the year. And then as you think about R&D, really R&D for 2025 would not expect to see a decline, really, year over year, specifically with apriclutide and the ongoing extension study, and also some of the CMC activities that we're continuing to complete as we move forward and prepare for a commercial launch. The 2026 is where we would start to see some of that inflection in terms of overall R&D will provide more details on that as we get closer to 26.

I think it's important to mention, Chase, too, on the long-term extension. As Mike mentioned earlier, I mean, as we continue to actively follow these patients, we're seeing ongoing reduction in parental support and even enteral autonomy. So, you know, I think this is a really solid investment for us to really further understand the potential benefit that these patients can occur over time. And certainly, you know, that obviously strengthens the overall profile of the drug.

Got it. And then just last thing from me, Greg, and I'll hop back in queue. But can you just kind of speak to the confidence around, you know, maintaining compliance on the covenants around the revolver? And it gets, you know, a little bit complex. I think it would be kind of helpful to kind of walk through a little bit of the kind of add-backs if you'd oblige us. Thank you.

Yeah, absolutely. Thanks, Chase. I think just broadly speaking, we have a high degree of confidence in our outlook of 2025. With our financial guidance, we will be able to continue to maintain covenant compliance throughout the year and have a very high degree of confidence there. We did adjust the adjusted EBITDA definition, as I noted in the prepared remarks, to give a little bit more clarity about some of the key adjustments we have with debt covenants, specifically with stock-based compensation. But there are other add-backs, and I can't necessarily go through all of them in detail, but there are other add-backs that do give us additional room and comfort with being able to achieve those covenants amounts for our debt throughout 2025. And it's something we're very much focused on and very focused on disciplined expense management to continue to drive profits and cash flows with those covenants in mind.

Thanks, guys.

Your next question comes from the line of Jason Butler of CitizensJMP. Please go ahead.

Hi, thanks for taking the question. Just had one on the long-term data for apoglutide. Can you maybe speak to the patient characteristics of those patients reaching or achieving -to-end autonomy? I guess, were you seeing this from both CIC and STOMA patients? And then how does this compare to the double-blind period of study where you, I think it was about seven patients, achieved -to-end autonomy? Have any of those patients, you know, maintained -to-end autonomy for the entire period? Thank you.

Yeah, thanks, Jason. Thanks for your question. So in terms of the achieving -to-end autonomy, we really benefit from the fact that we have completed the largest ever done phase three program in SPSIF. So it's SPSIF, as you know, is a very heterogeneous, you know, syndrome patient disease. So having that large patient population really gives us an opportunity to look at a broad spectrum of the patients and their outcomes. And if you, to direct your question to the -to-end autonomy, we certainly are seeing patients achieve -to-end autonomy on both STOMA and CIC. We'll actually roll out the details on the whole population. That's one of the things we're putting together for this submission, because we know that's an important question for all of us in terms of understanding the critical benefit to this patient population. And it's fair to say that it is in all of the secondaries, we presented some of this data last year too, in all the secondaries to look at cell populations across SPSIF, we really do always see a numerical benefit with apoglutide. So we really do think this patient population that we're targeting is the right one, meaning the broad patient population with short bowel syndrome and intestinal failure. In terms of the double blind data, you probably recall that initially we saw -to-end autonomy achieved at 24 weeks, and that actually included STOMA patients as well. And then by the end of 48 weeks, we had roughly 10 patients achieve -to-end autonomy. The 27 comes from adding in the STARS extend data, which is the O12 study, which is the extension study. And that brought that number up obviously to a very meaningful number of 27, which really in aggregate is a pretty robust outcome, if you look at other comparator products in terms of how many patients are achieving -to-end autonomy. And the patients who achieved -to-end autonomy in the double blind period carry on into the extension program. So we're really seeing good fidelity, and once patients achieve -to-end autonomy, they maintain it.

Great. Thank you for taking the question.

Your next question comes from the line of Amy Lee of Jeffreys. Please go ahead.

Hi, this is Kathy. On for Amy. Congrats on the quarter. So I guess I was wondering, as we think about the timing of the Medicare Part D redesign impact, is it fair to assume that impact to Linses revenues won't be until the second half of 2025, since Linses is low cost and it takes time for patients to get into catastrophic coverage?

Yeah, thanks Kathy for the question. I think the key for us is our full year guidance obviously takes into account our expectations for this redesign for the full year. I think there is an element of timing here where we will have to see how prescription demand trends and ultimately the tiering within Medicare Part D plays out over the course of the year. So I do think each quarter we move forward, we'll have better insights into what the potential price exposure is, but we feel very confident that our guidance range appropriately accounts for the trends and the expectations we have for the year.

Okay, great. Thank you. Your next question comes from the line of Faisal Kherseed of Learing Partners. Please go ahead.

Hi guys, this is Matt Calperon for Faisal. Thanks for taking my questions. Just a couple from me. How should we be thinking about the launch expenses for Appalooza both in terms of magnitude and timing and what levels are contemplated in the 2025 adjusted EBITDA guide? And then second question, just what options exist around the 2026 convert and how is the company thinking about managing that? Thank you.

Thanks, Matt. I can take both of those. In terms of the commercial launch expenses, we have been working on commercial planning activities from 2024 and we'll continue that into 2025. I would say at this point, they are not significant expenses within the overall P&L and we would expect to see a bit of a ramp up as we get closer to launch in 2026. And we'll provide additional details on exactly what that spend looks like as we get closer to that timing. And then in terms of the 2026 convertible notes, this is something that we continually evaluate our capital structure in the context of our overall forecast and outlook. And we are very much focused throughout 2025 on strengthening our balance sheet with the intent on driving profits and cash flows to repay our existing debt. And so we'll provide additional details as we make decisions on any further actions on our balance sheet. But at this point, I really want to focus on driving cash flows to repay our outstanding debt. Got it. Thank you.

Your next question comes from the line of David Amselman of Piper Sandler. Please go ahead.

Hey, thanks. I joined late, so maybe you already addressed this. But can you just talk more broadly about the cost structure? It's not so much about your ability to launch app or Glutide, but the extent to which you can extract more savings. I know you had the recent restructuring, but maybe talk more about how you're thinking about further streamlining just given the state of the capital structure.

Thanks. Yeah, thanks, David. In terms of cost structure, I think we feel very good about our outlook, as I mentioned, in terms of 2025 and the actions we've taken to really focus on profits and cash flows in 2025. As we move forward, we'll continue to evaluate other alternatives to really prioritize investments focused on those investments we think will drive the best long-term value. And that includes the Ironwood P&L, as well as the overall Linz S brand investment in conjunction with that base. So at this point, I think we've communicated everything that we can at this time on what we plan to do for 2025. And we'll continue to evolve as we move forward in 2026 and beyond.

Okay, thank you.

Ladies and gentlemen, that concludes our Q&A session and today's call. Thank you, everyone, for joining. You may now disconnect.