Good day and thank you for joining us for the Travere Therapeutics' Fourth Quarter and Full Year 2021 Financial Results and Corporate Update. At this moment, all participants are in a listen-only mode. I would now like to hand the conference over to your speaker today, Mr. Chris Cline. Thank you, please proceed.

Thank you, Vienna. Good afternoon and welcome to Travere Therapeutics fourth quarter and full year 2021 financial results and corporate update call. Thank you all for joining us. Today's call will be led by our Chief Executive Officer, Dr. Eric Dube. Eric will be joined for the prepared remarks by our Dr. Jula Inrig, our Chief Medical Officer; Peter Heerma, our Chief Commercial Officer; and our Chief Financial Officer, Laura Clague. Dr. Bill Rote, Senior Vice President of Research & Development will join us for the Q&A session. Before we begin, I would like to remind everyone that statements made during this call regarding matters that are not historical facts are forward-looking statements within the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are not guarantees of performance. They involve known and unknown risks, uncertainties and assumptions that may cause actual results, performance, and achievements to differ materially from those expressed or implied by the statement. Please see the forward-looking statement disclaimer on the company’s press release issued earlier today, as well as the risk factors section in our Forms 10-Q and 10-K filed with the SEC. In addition, any forward-looking statements represent our views only as of the date such statements are made, February 24, 2022 and Travere specifically disclaims any obligation to update such statements to reflect future information, events or circumstances. Let me now turn the call over to Eric. Eric?

Thank you, Chris and good afternoon everyone. 2021 was an outstanding year for Travere. Our pipeline of potential first in class rare disease treatments delivered three positive top line readouts from our ongoing studies. We made significant regulatory progress and established pathways to potential accelerated approvals for our lead candidates for sparsentan in both IgA nephropathy and focal segmental glomerulosclerosis or FSGS. We delivered 6% growth in net product sales from our commercial products, despite the ongoing challenges from COVID and a generic entrant for Thiola. And we continue to strengthen our ability to successfully deliver our treatments to the rare disease community in the future. I’ll touch on each of these areas briefly. First, regarding the pipeline, we are incredibly pleased with the outcomes from both of our Phase 3 studies of sparsentan, DUPLEX in FSGS, and protect in IgA nephropathy. With positive top line interim readouts from both studies, sparsentan has established a robust body of evidence around its ability to reduce proteinuria in patients with rare kidney diseases. Importantly, the sparsentan readouts have positioned us for three potential regulatory submissions this year. I am pleased to report that we remain on track to submit an application for accelerated approval under subpart H for IgA nephropathy during this quarter. If that application is accepted and granted priority review, we would anticipate a PDUFA date for sparsentan and IgA nephropathy towards the end of this year. We are also on track to submit to the FDA additional EGFR data from the ongoing DUPLEX study in the first half of this year. If at that time, the data further strengthens the prediction of long-term benefits in the study as we expect they should. We anticipate submitting an NDA for accelerated approval for FSGS around the middle of this year. Together with our European partner Vifor Pharma, we also remain on track to submit a combined IgA nephropathy and FSGS MAA submission for conditional approval for sparsentan in Europe, pending additional support of EGFR data from DUPLEX. As you can see, we have a very exciting year ahead for sparsentan. Also from the pipeline, in December, we reported positive top line data from the ongoing Phase 1/2 COMPOSE study of pegtibatinase in classical homocystinuria or HCU, a rare and devastating metabolic disorder. We believe these data support the potential for pegtibatinase to become the first therapy targeting the underlying cause of HCU for the more than 7,000 people in the US and Europe, who are not able to adequately control their HCU with the available treatment options today. Having achieved this milestone also reinforces confidence in our strategy of bringing in external programs to further address the unmet needs of rare disease patients while diversifying and building our growth potential. This year, we look forward to engaging with regulators to establish next steps for a pivotal development program while we also gain experience with formulation enhancements and further explore the dose response curve in the final plan cohort at the study. On the commercial side of the business, we continued our track record of strong execution. Our results in 2021 marked the sixth straight year of organic growth. We believe this illustrates the strength of our commercial capabilities and our ability to identify, treat, and support patients living with rare kidney and liver conditions. For 2022, we currently expect to see continued growth of our bile acid products. But we do expect pressure from the Thiola business. As a result, our consecutive growth streak in total net product sales is not likely to continue this year. But with the potential for sparsentan to launch as early as the end of this year, we look forward to returning to growth again in the future. Importantly, our business planning has been accounting for this. Peter and his team are continuing to build upon our commercial strength to translate our experience and establish relationships for successful launches for sparsentan in the US. Finally, I’d like to introduce Dr. Jula Inrig, our new Chief Medical Officer. Jula joined us in January and has taken over for Noah following his planned transition. Jula is a nephrologist who brings to Travere more than 15 years of expertise in drug development, clinical trial planning and execution, global regulatory engagement and medical oversight. She has a clear passion for championing positive change for patients, and a deep history of advancing new treatment options for rare diseases, specifically in rare nephrology. She joins our team at an exciting time, as we approach the next inflection point on the path to bringing innovation to patients living with IgA nephropathy and FSGS. With that, let me turn the call over to Jula for the clinical update.

Thank you, Eric and good afternoon. I’m honored to be here and partnering with our team members at Travere to advance new therapies for people living with rare diseases. Over the course of my career, I’ve experienced the challenges that patients and their families have encountered as a result of having few options available to slow the progression of their kidney disorders toward end stage kidney disease. That has shaped my own personal mission to help the nephrology field advance new treatments that may be able to delay the time to transplant or dialysis. This has taken the form of working with FDA, EMA and community leaders to further establish proteinuria as an acceptable regulatory endpoint for clinical trials in nephrology, and it has taken the form of helping strategize and execute nearly 50 clinical trials in the space. I was incredibly motivated to join the Travere team because of the patient inspired leadership that has been established over the last several years, and the exciting potential to continue working at the forefront of advancements in rare nephrology, ultimately by helping physicians understand the foundational role sparsentan may be able to play for their patients if approved. To that end, I’m pleased with the continued progression of sparsentan programs. Both the DUPLEX study and FSGS and the Protect study in IgA nephropathy are progressing according to expectations and are well positioned for their confirmatory EGFR endpoint readouts next year. To-date sparsentan has consistently shown the ability to meaningfully reduce proteinuria versus the current standard of care. And proteinuria is a key measure by which nephrologists determine treatment for patients with proteinuric kidney diseases. And the combined treatment groups in the Phase 2 study in FSGS, sparsentan more than doubled the reduction of proteinuria compared to the active control irbesartan. In the top line interim results from the Phase 3 DUPLEX study and FSGS treatment with sparsentan resulted in a 60% greater relative likelihood of achieving the clinically relevant FSGS partial remission of proteinuric endpoint or SPRE when compared to the active control irbesartan. And in the Phase 3 protect study and IgA nephropathy, sparsentan demonstrated a greater than threefold reduction in proteinuria from baseline compared to the active control irbesartan. The first time a single non-immunosuppressive therapy demonstrated this magnitude of effect on proteinuria reduction in a large, well controlled study in IgA nephropathy. These results are exciting for the nephrology community, and are providing great motivation for our medical teams. As Eric outlined earlier, we are on track for all of our regulatory milestones planned for this year. Of note, we were encouraged to see FDA recently grant the first accelerated approval based on proteinuric reduction in IgA nephropathy. This precedent is in clear alignment with our approach. For IgA nephropathy, we anticipate submitting our application for accelerated approval in the US before the end of this quarter. We would anticipate hearing a response on that application in the second quarter with a potential PDUFA date as early as the fourth quarter if accepted for priority review. And for FSGS, we are on track to provide the FDA with additional EGFR data from the ongoing DUPLEX study in the first half of this year. As many of you will recall, at the time of the Interim Assessment for DUPLEX, a high proportion of the available EGFR data were weighted to early study visits. This is the period in which acute reductions in EGFR are likely to be most prominent from RAS and ETA blockade. Following our pre NDA interactions for FSGS last year, we aligned with the FDA on a plan to provide the agency with additional EGFR data from the ongoing DUPLEX study to provide a more mature dataset and enable us to continue on the accelerated approval pathway for FSGS. At the time of the plant EGFR data cut later this year, all patients in the DUPLEX study will have completed at least one year of treatment, and approximately 50% of patients will have completed two years of treatment. Based upon our understanding of sparsentan and its mechanism of action, we believe at this time point in the DUPLEX study, the data will have sufficiently matured to strengthen the prediction for long-term EGFR benefit. If the EGFR data continued to progress as planned, we expect to submit for accelerated approval in the US mid this year. Finally, I’ll touch on our pegtibatinase program which reported positive top line results from the ongoing Phase 1/2 COMPOSE study in December. From a safety perspective, we were pleased to see that pegtibatinase has been generally well tolerated to-date in the study. From an efficacy perspective, pegtibatinase demonstrated dose dependent reductions in total homocysteine during the 12 weeks of treatment. And we were very pleased to see that in the highest dose cohort to-date of 1.5 milligrams per kilogram dose twice weekly. Treatment with pegtibatinase resulted in rapid and sustained reductions in total homocysteine beginning at week two and continuing through 12 weeks of treatment, resulting in a 55.1% reduction from baseline and maintenance of total homocysteine below a clinically meaningful threshold of 100 micromoles. Additionally, the data demonstrated a substantial reduction in assigning and increase in cyst assigning in a dose dependent manner following treatment with pegtibatinase, which supports our mechanistic approach. These data provide proof-of-concept supporting the potential for pegtibatinase to become the first disease-modifying therapy for HCU and gives us confidence in moving toward aligning with regulators on a pivotal program. As we do that, the program this year will be focused on three areas. The first is engaging with regulators to align on total homocysteine as a biomarker endpoint. And with that, a Phase 3 program design that can support approvals in the US and abroad. The second is completing the sixth cohort in the COMPOSE study to further build our knowledge of the dose treatment response of pegtibatinase and to explore potential formulation advancements. Enrollment activities here are already underway. The third is working through the global supply constraints, suppliers in the industry are currently facing to scale CMC and manufacturing for the pivotal phase of development and commercial access. Overall, I have inherited a great set of programs with real potential to make a meaningful difference in patients’ lives and an extremely talented team to help advance them. We are well positioned to deliver sparsentan if approved as the first non-immunosuppressive therapy for the treatment of IgA nephropathy, and to continue the advancement of our other programs this year. Let me now turn the call over to Peter for the commercial update.

Thank you, Jula. As Eric said, our commercial organization continues to execute incredibly well under challenging conditions in 2021. Despite fewer patients seeing their physicians as a result of COVID and a generic entrance for the original formulation of Thiola, we identified and treated new patients with all of our commercial products and achieved our targets for the year. In the fourth quarter specifically, net product sales grew by 7%. This was driven by organic year-over-year growth across Thiola and the bile acid products. We finished the year with approximately $211 million in net product sales, more than a 6% organic increase over 2020. As we look to 2022, we are expecting continued growth of our bile acid products with increasing pressure on our Thiola business as a result of generic competition. This has been factored into our business planning for some time and allows a natural pivot to our preparation for launching sparsentan. The results from this past year further bolster my confidence in our team’s commercial execution and their established relationships in the rare nephrology community. We are building upon this established infrastructure and expertise as we prepare our organization to position sparsentan as the new treatment standard for IgA nephropathy if approved. We are currently doing this by focusing on three areas. The first is further educating the scientific community by leveraging the deep understanding and long-held belief in the utility of proteinuria reduction amongst nephrologists in the sparsentan, if approved may substantially lower proteinuria for their patients. We know from syndicated market research that nephrologists consider the emerging product profile of sparsentan as one of the most desirable programs in development. So we are building and educating upon that. The second is furthering our work to instill a strong understanding of the burden of disease amongst payers. The value that sparsentan may be able to provide and progressing our strategy that will allow for broad access to become new treatment standards if approved. Many of you will recall the 2019 publication of the kidney health initiative project team, where proteinuria was identified as the most widely recognized and well-studied risk factor for the progression to end stage kidney disease in IgA nephropathy. Following this risk prediction analysis, the patient level risk assessment was presented, describing that a 30% reduction in proteinuria could result in a greater than 10-year delay in dialysis for IgA nephropathy patients. With the proteinuria reduction demonstrated in the recent protect data, we have a strong foundation to build upon. Lastly, now that we have line of sight of the regulatory milestones this year, we have plans to expand our commercial organization for launch readiness. This includes adding to our field force to reach more nephrologists, building upon our best practices for future engagement with healthcare providers and readying our distribution and patient support services infrastructure all ahead of launches. So we can hit the ground running if approved. With an anticipated addressable US IgA nephropathy patient population of 30,000 to 50,000 people at launch, we recognize the significant potential for this market if sparsentan is approved. We have started early and are investing and building appropriately to position ourselves for success. Most importantly, we are doing it from a differentiated position of strengths. We are not starting from scratch, but instead building upon a team that has leadership experience in rare nephrology and has demonstrated for more than six years that it can successfully identify, treat, and support patients living with rare diseases. Let me now turn the call over to Laura for financial updates.

Thank you, Peter. For the fourth quarter of 2021, we reported net product sales of $54.6 million from our commercial portfolio compared to $51 million for the same period in 2020. For the full year 2021, we reported $210.8 million in net product sales. Total revenue for the full year 2021 was $227.5 million, consisting of $210.8 million in net product sales and $16.7 million in licensing and collaboration revenue from our European partnership with Vifor Pharma. We reported a GAAP net loss of $51.6 million for the fourth quarter of 2021. For the full year 2021, GAAP net loss was $180.1 million. After adjusting for non-cash expenses and income tax, we reported a non-GAAP net loss of $37.6 million for the fourth quarter and $100 million for the full year 2021. On a GAAP basis, R&D expenses were $62.2 million for the fourth quarter and $210.3 million for the full year 2021. The increase compared to 2020 is largely attributable to increased patient enrollment and the ongoing studies of sparsentan as well as the advancement of the pegtibatinase program in HCU. On an adjusted basis, R&D expenses were $57.7 million for the fourth quarter and $196.2 million for the full year 2021. Relevant non-cash expenses for the fourth quarter included $4.4 million of stock-based compensation and amortization. On a GAAP basis, selling general and administrative expenses for the fourth quarter were $42.1 million and $149.9 million for the full year 2021. The increase compared to 2020 is largely attributable to increased headcount and professional fees as a result of the company’s operational growth as we prepare for potential commercial launches. On an adjusted basis, SG&A expenses for the fourth quarter were $30.9 million and $106.6 million for the full year 2021. Significant non-cash adjustments for the quarter consisted of $11.2 million in stock-based compensation and depreciation and amortization. As we look ahead to 2022, we are not providing specific net product sales guidance, as this is a transitional year with the expected impact on Thiola sales from generic competition, and a potential launch of sparsentan in the fourth quarter. As has been typical for us in past years, we do anticipate higher growth to net discounts in the first quarter driven by insurance coverage changes in the beginning of the new year. From an OpEx perspective, we anticipate that our R&D expenses will continue to run at a rate slightly higher than in the fourth quarter. This is representative of the ongoing DUPLEX and protect studies that will continue into 2023 as well as the ongoing COMPOSE study of pegtibatinase and foundational work including scaling CMC to prepare for a pivotal program. We also expect meaningful increases in SG&A, particularly in the second half of this year as we look to continue the commercial build out, including additions to our field team for the potential launch of sparsentan in IgA nephropathy. Importantly, we continue to be in a strong financial position to execute in 2022 and beyond. We ended the year with $552.9 million in cash and cash equivalents. This balance includes $30.8 million in net proceeds from our aftermarket facility during the fourth quarter. Taking into account the potential impact of a more competitive Thiola market, but not yet factoring in the full pivotal program for pegtibatinase, we anticipate this cash balance will support our planned operations through 2023. Let me now hand the call to Eric for his closing comments.

Thank you, Laura. Our execution in 2021 has enabled us to enter this new year with great momentum and an incredibly bright outlook. Our priorities for 2022 are clear. We will remain focused on positioning sparsentan to become a new treatment standard for IgA nephropathy and FSGS if approved. This includes achieving on time and high quality regulatory submissions, the first of which could enable an approval of sparsentan for IgA nephropathy by the end of this year. We will also focus on continuing to advance our pegtibatinase program following the exciting proof of concept data in HCU reported in December. And in parallel to focusing on the advancement of our pipeline, we will further prepare our organization for the potential upcoming launches of sparsentan by building upon our proven commercialization capabilities in rare nephrology. Let me now turn the call over to Chris for Q&A.

Great, thank you, Eric. Can we please go ahead and open up the lines for Q&A?

Your first question is from Greg Harrison of Bank of America. Your line is open.

Hi, good afternoon and thanks for taking our questions. On FSGS, what would you consider to be supportive EGFR data in your opinion? And if that were not considered to be sufficient for filing, what would be required for filing? Would you have to complete the entire study or could there be another interim analysis performed?

Greg, thanks so much for the question. Bill, why don’t you speak to the regulatory expectations with the FSGS data and Jula perhaps you can speak a bit to what might be supportive from a nephrologist perspective?

Certainly, I’ll start with the construct of the trial. The primary endpoint for approval under subpart H accelerated approval is proteinuria. And we’ve met that milestone with a very robust superiority of sparsentan over irbesartan. But in that accelerated approval rubric for the FDA, their criteria is that the totality of the data are generally supportive or reasonably likely to support or to predict success at the two-year endpoint. So in that case, the agency is going to be looking to see, are the trends there that are consistent with the hypothesis that this level of proteinuria reduction should yield preservation of renal function and in this case, that would be shown by a separation in the EGFR slopes at two years. I’ll hand over to Jula for the nephrologist viewpoint.

Certainly, thanks. Well recall and do that there was an early acute EGFR decline, and then a flattening with sparsentan. And this is consistent with the protective agents such as SGLT 2 inhibitors and RAF inhibitors. And the key is to understand the nature of the curve as the reduction in proteinuria should flatten the EGFR curve, and then provide long-term nephro protection. So for DUPLEX, it’ll be a matter of having enough EGFR data that is mature enough to predict the two-year EGFR slope endpoint.

Thank you, Bill and Jula. And Greg, just to complete out the last part of your question around if FDA does not deem the additional EGFR data sufficient for subpart H submission, what next? Well, I think we first believe that the profile sparsentan will, it’s behaving like we expect, it should support the longer-term two-year difference that we expect. And we are candidates to completing this trial out to two years. So if for some reason, FDA says, we wouldn’t support a Subpart H, we would evaluate, but our plan certainly would be to complete the trial, and then submit for full approval at that point. And just a reminder, we would expect the last patient last visit for the two year endpoint to occur in the first half of next year.

Great, that’s helpful. Thanks again, and congrats on the progress. It’s exciting to see guys getting close to the finish line.

Your next question is from Carter Gould of Barclays, your line is open.

Yes, this is just Justin on for Carter, congrats on all the progress this year. Another one on the interim readout for DUPLEX, sort of how long after discussing those data with FDA, do you expect to be ready to file for approval? And then sort of related to that. Do you expect to file the combo MAA in Europe around the same time as the NDA or is one of those kind of precede the other?

Yes, so great questions. Justin, thank you for them. Bill, would you like to talk about the timing, just as a reminder, overall, we would expect those filings assuming the regulators are supportive of the additional EGFR data. And we look to do that in the middle of this year. Bill, perhaps can provide a little bit more color on the timing and sequence.

Yes, I think the preparation is well underway. Justin, working on those filings now, so that once we do have that supplemental look at the EGFR data, we can tuck those additional data in and submit very quickly. So we’ve guided midyear for both of those filings. They’re going to be very close to one another because they’re both essentially waiting for that additional data to be available. And then we’ll have the conversation with the agency. And in the scenario where they are, as we expect and supportive that will be the last elements to drop in so that we’re ready to file quickly.

Awesome. Thanks so much.

Your next question is from Joseph Schwartz of SVB Leerink, your line is open.

Thanks very much. To what extent will you be scrutinizing the merit of the proteinuria and EGFR effects in the next look at the DUPLEX data in order to determine whether it makes sense to show to the FDA? In other words, is there a scenario where you would not submit the data to the FDA? If it were not supportive? However remote? And if so, how much would the data have to be worse and beyond what you’ve already seen? In order to lead you to not submit the data to the FDA?

So thank you for the question. I think first, I’ll just reinforce that our view is that sparsentan overall has performed very consistently throughout our clinical program. And so, we do believe that sparsentan does behave the way that it has, and that we expect that there will be continued improvement over time. But I’ll ask Jula to comment on, what type of assessment would be looking with these? And what’s that limited kind of evaluation that will be done?

Certainly, so the only evaluation is EGFR. We’ve already seen the magnitude of the proteinuria reduction from the top line results. So we are just looking at EGFR and the additional maturity of the data to be predictive of the long-term EGFR benefit. And we believe that the proteinuria reduction is meaningful. And then really, as I said, it’s just looking at the EGFR data at that point in time.

Okay, great. That’s very helpful. Thank you. I have another question regarding IgA nephropathy, considering the recent approval and pricing of another therapy. I'm curious about how the pricing for that agent compares to the work you've been doing in setting a price for sparsentan in IgA nephropathy.

Yes, Joe, thank you for the question. I think first, we were quite pleased now to see a precedent from a regulatory approval and the use of proteinuria with the approval of Budesonide. And so, we think it further bolsters our confidence. I’ll ask Peter to talk a little bit about how we think about pricing, and as you say, the economic evidence to support pricing and access for sparsentan.

Certainly, Eric, and thanks for the question. So I think it’s good to start with like, what is your unmet need, and we know the unmet need, and particularly in IgA nephropathy, but also in FSGS, is among the most difficult patients to treat for nephrologists and in particular, for the current standard of care. Because patients are not being treated well to the targets that physician want with ACE inhibitors and ARB. And that’s where we see the sweet spot for sparsentan. We hear it from patients, as well as from nephrologist that are very excited about the profile because they see this as a new set of their potentially replacing aging arms, without having the need to go to the steroid bath. And so our work, our planning, our positioning will be to take that foundational position and our pricing will be consequently. With regards to the pricing your reference, I think there are now multiple products in the rare nephrology space in the last year in particular, including the decimate that you were referencing. And I think that allows us a certain level of flexibility, but again, like we see sparsentan as a new potential of care and as a new standard of care and we will be pricing accordingly.

Thanks for taking my questions.

Next question is from Maury Raycroft of Jefferies, your line is open. Your next question is from Michelle Gilson of Canaccord Genuity. Your line is open.

Hi, can you guys hear me?

Yes, we can, Michelle.

Hi, thank you for taking my question. I guess a couple on pegtibatinase, you indicated when you presented the data in December, that you’re planning to meet with the FDA in the first quarter of this year to get aligned on potential profit. I was just curious if you guys have had that meeting, and then when it comes to total homocysteine as a surrogate endpoint, or as a biomarker, can you maybe discuss how established the link is with homocysteine and clinical outcomes in homocystinuria? And just if the FDA does ask you to run a trial with a clinical outcome endpoint, what kind of options do you have?

Michelle, thank you so much for the question. Bill, would you like to take those?

Sure, I’d be happy to. And clearly the FDA is a big fan of pegtibatinase. Remember, with respect to the FDA and the discussions around endpoints for Phase 3, remember that we’ve made the comments in the past that this is an iterative process. There are multiple elements to that agreement around the assay, establishing the biomarker according to guidance, Phase 3 clinical trial design. So it’s more than just a one step process. We’ve begun that process with the agency. We’re not in a position where we can comment on it beyond the fact that we’re pleased with the directions that it’s going and we’ll update as we get to a point of completion. And we have more certainty around what that path looks like.

The second part of your question was about the connection between reductions in homocystinuria and their clinical impacts. The existing guidance suggests that physicians aim to lower total homocysteine levels below 100. This guidance was established based on observations of patients, their homocysteine levels, and the occurrence of clinical events, including eye problems, bone thrombotic events, and cognitive issues. The conclusion drawn was that when homocysteine levels fall below 120 micromolar, these clinical events become quite rare. The guidance was set at 100 micromolar to provide some leeway and for ease of recall. There is retrospective data showing the connection between clinical outcomes and overall homocysteine levels. Additionally, we have natural history study data from our ongoing research that supports the link between clinical events and total homocysteine. We will compile this information to strengthen your arguments. Looks like can you hear me it looks like we might have lost Bill’s connection. So Michelle, the last question.

To realize that we will be making clinical measurements, they just won’t be primary endpoints, we will look at ocular.

Bill, I think we’re having some audio difficulties. Maybe if I can frame. Michelle, the last part of your question, which is do we believe that there would be a need for clinical outcomes in a Phase 3 program? And I think, certainly as Bill has mentioned, we’ll be looking at that as secondary measures, both for the ongoing Phase 1/2 COMPOSE study as well as likely in any Phase 3, although we haven’t yet reached agreement on what that trial design could look like. Homocystinuria is certainly one of those diseases that is heterogeneous both in the presentation of the disease as well as the kind of time to onset of some of those. And so that heterogeneity that would make it very difficult to select a particular clinical outcome in a development program, which is why we’re so focused on ensuring that total homocysteine or biomarker can be used for further development given again, that this is an ultra-rare condition that that would be a challenge to have a Phase 3 with a clinical endpoint. So more to come on that. And I think what’s important is, you know, there is more engagement and work that will be done this year to ensure that we have that alignment with regulators and can move forward with the next phase of development. And, Bill, I’m not sure if we have you back. Okay, Michelle, hopefully that answers your question. And I think hopefully, we’ll have a resident expert back here soon.

Your next question is from Liisa Bayko of Evercore ISI, your line is open.

Hi, thanks for taking the question. I just wanted to give us a little color. Maybe we’ve talked about this before, but we just wanted to confirm on the data that you’re going to deliver to FDA on FSGS. Is that like one year, estimated EGFR? Is that what it is that all the patients have been through one year? Could you just kind of give us some sense of that. Thanks.

Sure. Jula, would you like to say that? Lisa, thank you very much for the question.

So the additional data 50% of the patients will be at two years and 100% of the patients will be at one year for the EGFR data. And so it’ll be a much more mature data set with regards to EGFR. And that’s the data that we’re going to be providing.

Your next question is from Maury Raycroft of Jefferies. Your line is open.

Hi, thanks for taking my question and congrats on the progress. I was going to ask a question just based on the tar pail launch. Do you have an updated view on how you see the treatment paradigm shaping up? And if you have any feedback from pairs on replacing traditional RAS inhibitors? Or will you have to step through traditional RAS inhibitors? I guess, how are you guys thinking about that?

Maury, thanks so much for the questions. Jula, maybe I’ll start with you, you can talk about how you might see the landscape evolving. And then Peter, if you can add anything further as we think about commercialization and any feedback from payers?

Sure, there remains a huge unmet need for patients with partner kidney diseases. And we basically treat patients who have proteinuria above 0.75 grams per day or 0.5 with RAS inhibitors. And that’s our foundation and we envision sparsentan to be the initial therapy or foundational therapy, if approved. The utilization of steroid therapy historically, and likely going forward is outlined in the guidelines, which we only use in a subset of patients who are really at high risk of progression and those who have either a rapid decline in EGFR or very high proteinuria. And I don’t really envision that changing based on our guidelines and based on what we know and it’s really a risk-benefit ratio that we do and patients and when we decide to use that therapy or pull that in.

Yes, and building on that Maury. So the introduction of the new therapy is not changing the way we think about the introduction of sparsentan and the potential it has to become a new standard of care. But we are hearing from our physicians, as well as from patients societies is that they’re feeling very comfortable on the position of sparsentan to replace the current standard of care, ACE inhibitors and ARBS. And so positioning it before the use of steroids and allowing that additional option later on in a pathway. So to your question. It doesn’t change the way we’re thinking about it. On your second part of the question with regards to payers, I think we’re pleased with the interest of payers have, we are building the value proposition we’re building the burden of disease and the natural history of the disease to have a meaningful conversation with the payers but we are pleased with where we are. And again, the introduction of new therapies is not changing the way we position sparsentan.

Yes, I think you know, specifically. Thank you, Peter, for that. Maybe just one other thing that I’ll add more to your question around, do we think that we need to step through an ACE or an ARB? I think given in nephropathy, that the patients that are currently being treated, nearly all of them are on an ACE or an ARB, it’s highly likely that those patients would if still having elevated proteinuria would likely be, stepped up to or switch to sparsentan. And so, as Jula highlighted that in the future patients may start on sparsentan or on an ACE or ARB and then are stepped up, we actually don’t see that as an issue or a barrier for us, particularly given that so many of these patients still have elevated proteinuria and are at great risk of progression. So I think it underscores the role that we believe sparsentan will play as becoming a foundational treatment within this disease.

Next question is from Laura Chico of Wedbush, your line is open.

Good afternoon, guys. Thanks for taking the question. I apologize, because this is going to be pretty naive one, but I wanted to ask them DUPLEX. I’m wondering if you could just kind of walk me through the communication strategy, essentially, what level of detail should investors be anticipating with respect to the interim analysis here that’s coming up? And I guess I’m asking, because I’m not really clear, I just want to make sure that we’re all clear on terms of what data should be anticipated. I know you’ve been cautioned by the FDA on certain disclosures. So just trying to understand what visibility we as investors will have with respect to the update. Thanks.

Laura, thank you very much for the question. Certainly not naive, it’s a very important one is we can help provide as much clarity in the coming months, I think what’s important is that we are on track for the additional data on EGFR that we will provide to FDA and EMA. Those data to date have not been extracted, but we’re on track to do that in the first half of this year. And at that point, we really will not be commenting on any of the process for any of the data. You will hear from us once we’ve had the meetings with regulators, and that we have that direction from the FDA on the potential submission, timing and process, but nothing incremental before that happens. And so we’re going to remain quiet on that front. But you can expect to hear from us, once we do have that agreement. And then of course, related to sparse sets and expect to hear from us on the submission of our NdA this quarter, as well as when we would receive an acceptance from the FDA of that NDA. So there will be quite a bit of communication. But as you point out, we are going to remain very vigilant in the integrity of that trial and not disclosing anything on EGFR. Does that answer your question?

Yes, it does. Thanks, Eric.

Your next question is from Tim Lugo of William Blair, your line is open.

Hi, this is John for Tim, thanks so much for taking our question. Just wondering if you could give us any more details on what additional data from the COMPOSE study you’re planning to share at a medical meeting? What meeting might see that data at and how we should be looking at or is there anything that we should be looking for in that additional data?

John, thank you so much for the question. Jula, would you like to take this one?

So we do expect to have additional detail from COMPOSE at a medical meeting this spring and it’ll be detailed from the first five cohorts and as we do with participation, any medical meeting will provide the details at an appropriate time.

No more questions. I would like to turn the call back to the presenters for final remarks.

Great, thank you, Vienna. And thank you all for joining us. This concludes our update for today. As you can tell we have many exciting milestones ahead and we look forward to keeping you updated throughout the year. Have a great rest of your evening.

This concludes today’s conference call. Thank you for participating, you may now disconnect.