Mirum Pharmaceuticals (ticker: NASDAQ:) has reported a significant increase in financial results for the first quarter of 2024, with net product sales soaring to $68.9 million, marking a 137% rise from the prior year.
The company’s flagship product, LIVMARLI, has been approved in the US for PFIC treatment, contributing to the positive performance. Mirum forecasts a full-year revenue guidance between $310 million and $320 million.
Additionally, the company is preparing for an NDA submission for CHENODAL and advancing volixibat for PSC and PBC, with promising interim analysis expected in June.
Total revenue for the quarter was $69.2 million, and Mirum’s financial position is strengthened with $302.8 million in cash and investments.
Key Takeaways
- Mirum’s net product sales reached $68.9 million in Q1 2024, a 137% increase year-over-year.
- US approval of LIVMARLI for PFIC treatment marks a significant milestone.
- Full-year revenue guidance set at $310 million to $320 million.
- NDA submission for CHENODAL and advancement of volixibat for PSC and PBC are underway.
- Total Q1 revenue stood at $69.2 million, with a solid financial position of $302.8 million in cash and investments.
Company Outlook
- On track to meet full-year revenue guidance.
- Focused on label expansion opportunities and upcoming volixibat interim results.
- Dialogue with European regulators for orphan drug status for PFIC in the EU is ongoing.
- Preparing for potential LIVMARLI launch in Europe upon approval.
Bearish Highlights
- A $3 million impact in the quarter due to a healthcare issue, considered a one-time event.
- Slight quarter-to-quarter decrease in bile acid product sales, partly due to the Change Healthcare (NASDAQ:) cyberattack.
Bullish Highlights
- Consistent growth in product demand expected throughout the year.
- Positive feedback on LIVMARLI in PFIC and productive payer conversations.
- Anticipation of mid-single-digit year-on-year growth for bile acid products.
- Excitement for potential FDA approval for CHENODAL and CTX next year.
Misses
- Minimal revenue contribution expected from PFIC in the next quarter or two.
Q&A Highlights
- The company plans to continue enrollment in PBC and PSC studies.
- Patients on the expanded access program for PFIC will transition to paid drug in coming quarters.
- The company remains disciplined in its business development, focusing on rare disease settings.
- Safety, serum bile acids, and pruritus will be the focus of the PBC interim data readout.
Mirum Pharmaceuticals is poised for continued growth, with strategic plans for its product pipeline and market expansion. The company’s strong financial position supports its research and development efforts, as well as its commercial business.
With the US approval of LIVMARLI and the anticipation of further regulatory successes in Europe, Mirum is strategically advancing its presence in the treatment of rare diseases.
InvestingPro Insights
Mirum Pharmaceuticals (ticker: MIRM) has been making headlines with its impressive revenue growth and strategic advancements in the rare disease treatment space. As the company continues to develop its product pipeline and expand its market reach, here are some insights from InvestingPro that could be particularly relevant to investors and analysts following Mirum’s journey.
InvestingPro Data indicates that Mirum’s revenue for the last twelve months as of Q1 2024 stands at $224.0M USD, which represents a substantial growth rate of 133.9%. This aligns with the company’s reported increase in net product sales and underscores the financial momentum Mirum is experiencing. Additionally, the Gross Profit Margin for the same period is a robust 73.26%, reflecting the company’s ability to maintain profitability in its core operations despite the challenges of the biopharmaceutical industry.
From the perspective of InvestingPro Tips, it’s noteworthy that Mirum’s liquid assets exceed its short-term obligations, suggesting a solid financial foundation for ongoing and future projects. This is a crucial factor for investors considering the company’s ability to fund its research and development without compromising financial stability. However, it’s also important to note that analysts do not anticipate the company will be profitable this year, and the company has been trading near its 52-week low, which could present a buying opportunity for value investors.
For those interested in a deeper dive into the financial health and future prospects of Mirum Pharmaceuticals, there are additional InvestingPro Tips available at With the use of the coupon code PRONEWS24, readers can get an additional 10% off a yearly or biyearly Pro and Pro+ subscription, unlocking access to a wealth of investment insights. Currently, there are 6 additional InvestingPro Tips listed for MIRM, which could further inform investment decisions and strategies.
Full transcript – Mirum Pharmaceuticals Inc (MIRM) Q1 2024:
Operator: Hello, and welcome to the Mirum Pharmaceuticals First Quarter 2024 Financial Results and Business Update. My name is Terry, and I will be the conference operator today. All lines have been placed on mute to prevent any background noise. [Operator Instructions] I will now hand the call over to Andrew McKibben, Vice President of Investor Relations, to begin. Please go ahead.
Andrew McKibben: Thanks, Terry, and good afternoon, everyone. I’d like to welcome you to Mirum Pharmaceuticals first quarter 2024 conference call. I’m joined today by our CEO, Chris Peetz; our President and Chief Operating Officer, Peter Radovich; Chief Medical Officer, Joanne Quan; and Eric Bjerkholt, our Chief Financial Officer. Earlier today, Mirum issued a news release announcing the company’s results for the first quarter 2024. Copies of this news release and SEC filings can be found in the Investors section of our website. Before we begin, I’d like to remind you that during the course of this conference call, we will be making certain forward-looking statements about Mirum and our programs based on management’s current expectations, including statements regarding Mirum’s current and future business plans, development programs and regulatory expectations, strategies, prospects, market opportunities and financial expectations. Mirum is under no duty to update these statements, and they are subject to numerous risks and uncertainties, and actual results could differ materially from the results anticipated by these statements. Investors should read the risk factors set forth in Mirum’s 10-Q for the quarter ended March 31, 2024, and any subsequent reports filed with the SEC. With that said, I’d like to turn the call over to Chris. Chris?
Chris Peetz: Thanks, Andrew, and good afternoon to everyone. 2024 is tracking to be another year of significant growth for us. And I’m very pleased to highlight our progress across key strategic objectives to grow the commercial business, expand the indications of our commercial medicines and advanced volixibat to market. We continue to build value while delivering on our commitment to create and commercialize life-changing medicines for rare disease. Now, first, driving growth across our commercial medicines. Total net product sales this past quarter were $68.9 million, representing a 137% increase from the first quarter of 2023. LIVMARLI continues its strong performance. Newly diagnosed and prevalent patients continue to come to treatment in both the U.S. and internationally, and we are well positioned to meet our full year revenue guidance of $310 million to $320 million, driven by continued demand increases across all medicines, internal — international launches and contribution from the PFIC approval. Second, we are also making significant progress towards expanding the impact of our potentially life-changing medicines through new approvals and label expansions. In March, we announced the U.S. approval of LIVMARLI and PFIC, an important milestone for Mirum in the PFIC patient community. This approval represents the culmination of years of dedication from patients, researchers and our team. We are excited to be able to bring LIVMARLI to this community, particularly those patients with rare genetic types of PFIC. The pivotal data was also just published this week in the Lancet, highlighting the improvements in itch, bile acids, bilirubin and growth seen with LIVMARLI treatment. And we’re off to a great start with positive reception post approval. We’ve also made great progress preparing our upcoming NDA submission for CHENODAL for the treatment of CTX. And third, we are advancing volixibat in PSC and PBC, which are more common adult cholestatic setting, where we can apply the scientific and regulatory insights from the LIVMARLI program to address bile acid accumulation in patients suffering from these diseases. This quarter, we will be taking an important step in advancing the program with our interim analysis of volixibat in the VISTAS PSC and VANTAGE PBC studies, which are scheduled in June. We see both indications as significant opportunities as there are no approved therapies for PSC and no approved therapies to treat cholestatic pruritus in PBC. In summary, we continue to make excellent progress across our core strategic objectives, supported by a strong underlying financial position that will allow us to further execute on upcoming opportunities. And with that, I’ll turn the call over to Peter to discuss our commercial business. Peter?
Peter Radovich: Thanks, Chris. Our commercial teams delivered another strong quarter with continued demand growth for LIVMARLI across all geographies. Underlying growth dynamics remain strong across our medicines and geographies, and we are tracking well towards achieving our full year revenue guidance of $310 million to $320 million. For LIVMARLI, total global net product sales grew to $42.8 million in the first quarter, up from $41.4 million in the fourth quarter of 2023 and $29.1 million a year ago. U.S. LIVMARLI sales were $30.8 million, and international LIVMARLI sales were $12.1 million. Our U.S. Alagille business continues to benefit from durable demand expansion in total LIVMARLI prescriptions, with a mix of older and newly diagnosed patients starting treatment. Internationally, we are also seeing sustained demand growth from our core markets, and we continue to launch in new countries, most recently in Italy. Our U.S. business was impacted by the changed healthcare cybersecurity incident affecting our specialty pharmacy. This resulted in a temporary disruption to insurance claims processing during the quarter, which we estimate had approximately a $3 million impact on Q1 sales across our products. Turning to the recent approval of LIVMARLI for cholestatic pruritus in PFIC patients, this is an important step forward for the business, and I’m happy to say that our approval has been well received by the physician and patient community, and discussions with payers are progressing well. We continue to anticipate reimbursement and pay dispenses to materialize over the next few quarters. Turning to CHOLBAM and CHENODAL, we recognized net product sales of $26.1 million in the first quarter of this year. Overall, I’m pleased with the strong demand we have seen year-to-date and how this positions us towards achieving our full year guidance of $310 million to $320 million. I look forward to continued growth in the coming quarters and years to come. And with that, I’ll turn it over to Joanne. Joanne?
Joanne Quan: Thanks, Peter. We have a lot to look forward to this quarter as we continue to advance our pipeline. First, I would like to take a few minutes to talk about our upcoming interim analysis in June for our volixibat VISTAS PSC study and VANTAGE PBC study. Starting with the VISTAS PSC study, a blinded interim analysis will be conducted to support dose selection. We have prespecified and efficacy threshold for continuation, which is based on prior experience with IBAT inhibitors and cholestatic pruritus. Using these criteria, the independent data monitoring committee will review the data and recommend whether to continue the study with a selected dose or to unblind if the thresholds for safety or efficacy are not met. The starting point for the study design assumed a treatment difference of 1.75 points in pruritus and standard deviation of 3. As a reminder, pruritus is assessed on a 10-point numerical rating scale. This approach allows us to accomplish three key objectives: first, we want to confirm a meaningful treatment effect; second, we want to select the best dose; and third, by keeping ourselves blinded to the interim results, patients from the interim will be included in the potentially pivotal data set. This gets us to pivotal data faster, and at the same time, we have reassurance of a meaningful treatment effect. We will also be sharing top line data from the interim analysis of the VANTAGE study in PBC. As a reminder, this study allows patients with both normal and elevated alphos who are on ursodiol. The interim data set included 32 patients across three arms with two active doses and placebo. The objective of the interim is to select the appropriate dose to take forward to the pivotal portion of the study. Given the historical data with IBAT inhibitors in PBC, we believe this is adequately sized to select the dose and show a trend on efficacy. The interim is not designed to show statistical significance. At the interim, we expect to show topline data on pruritus improvement, safety and other biomarkers such as serum bile acids. Both of these are seamless adaptive study designs, and we continue to enroll the goal of supporting registration. Enrollment in both studies is progressing well. These studies represent an important step towards addressing the accumulation of bile acids in broader patient groups with adult cholestasis where a significant portion of patients lack adequate treatment options for cholestasis and a severe symptomatic burden. We’ll provide an update on projections for completion of enrollment for both studies when we announced the interims in June. 2024 is off to a great start, and I look forward to sharing our progress with you this year. With that, I’ll now turn the call over to Eric to discuss our financial results. Eric?
Eric Bjerkholt: Thanks, Joanne. Earlier today, we issued a press release that included financial results for the first quarter, which I’ll briefly summarize. Total revenue in the first quarter of 2024 was $69.2 million compared to total revenue of $31.6 million in the first quarter last year. Total operating expenses for the quarter ended March 31 were $95.7 million, which includes R&D expenses of $32.2 million, SG&A expenses of $45.6 million, and cost of sales of $17.8 million. The total operating expense for the quarter included approximately $17.1 million of non-cash charges. For the quarter ended March 31, net loss was $25.3 million or $0.53 per share. Our cash, cash equivalents and investments increased to $302.8 million as of March 31, 2024, up from $286.3 million at the end of last year, primarily due to a reduction in working capital. We expect that our working capital balances will vary from quarter-to-quarter depending on timing of payments and inventory investments. So, in summary, our business continues to be well funded, and we are in an excellent position to support the advancement of our pipeline and expansion of our global commercial business. Now, I’ll turn the call back over to Chris for final comments.
Chris Peetz: Thanks, Eric. It’s been a great start to the year, and our business continues to grow. We remain on track for our full year revenue guidance. We are executing across our label expansion opportunity [indiscernible] launches and are very much looking forward to the volixibat interims ahead. And with that, operator, please open the call for questions.
Operator: Thank you. [Operator Instructions] Your first question on the line comes from Jessica Fye of JPMorgan. Please go ahead. Your line is open.
Jessica Fye: Great. Good afternoon. Thanks for taking my questions. For the two volixibat studies, can you remind us what background medications patients are allowed to be on that may also address pruritus? And how that kind of factors into your expectations for the results, if at all?
Chris Peetz: Thanks, Jess, for the question. I’ll ask Joanne to jump in and talk a little bit about the background setting.
Joanne Quan: Yeah. Thanks Chris, and thanks Jess for the question. We think actually that the way that we designed the studies actually make it really broadly applicable for both of these populations. So for instance, in PBC, we’re allowing patients who are either on or not on ursodiol and we’re allowing patients with varying — with any level of alphos. So, a little bit different than some of the other trials that have been for the other agents kind of in this area. So, we really think this translates to use in first-line [indiscernible] ultimately for PBC. For PSC, as you know, there’s no other therapies and we know that a majority of patients with both these diseases, PSC and PBC do have pruritus. So, we think this — the way we’ve designed the studies with a very broad inclusion criteria do allow us to translate kind of a very real world issue into our studies and therefore, give us useful information.
Jessica Fye: Great. And maybe just one more, if I could. Can you remind us what to expect from a tolerability standpoint for volixibat?
Joanne Quan: Yeah. Well, thanks for the follow-up, Jessica. So we know IBAT inhibitors quite well. And I will say, so far, volixibat kind of tracks in what we know and we know exactly how to dose these and we know exactly what to look for. So, we don’t expect really any surprises in this way.
Jessica Fye: Great. Thank you.
Chris Peetz: Thanks, Jess.
Operator: Thank you. Your next question comes from Mani Foroohar from Leerink Partners. Your line is now open.
Mani Foroohar: Thanks for taking the question, guys. A quick one. You mentioned about a $3 million impact this quarter, it sounds like, some changed healthcare issue. To what extent is that sort of a one-time loss revenue as opposed to revenue might pop up in sort of a recognition function next quarter? And separately, when you think about that $3 million, as we try and back that out and think about kind of underlying demand metrics, how is that separated between your products this quarter in terms of the split between LIVMARLI versus the acquired TBTX assets?
Chris Peetz: Thanks for the question, Mani. I’ll let Peter kind of dive into the details. I mean short answer to this, it’s a one-time effect, but Peter can give a little color on the background here.
Peter Radovich: Yeah, one-time effect that is concluded by the end of the quarter. So I don’t expect to see any lingering effects from this in future quarters. And the overall demand for all of our products grew. Total prescriptions grew over the quarter. So not really — that’s why we’re very confident in the $310 million to $320 million. I think — and you also asked about the $3 million. I think assigning $3 million by individual product is kind of probably a false precision here. I mean we kind of think about $3 million as an impact across the U.S. business.
Mani Foroohar: Okay. But is it reasonable to assume the great majority of it was driven by LIVMARLI given the geographics of those products?
Peter Radovich: I think it’s probably balanced. It’s — you could think about it generally in proportion to the size of the products.
Mani Foroohar: Okay. That’s helpful. And as we think about between now and the end of the year, staying on commercial questions, obviously, you maintained your guidance. Should we think about the tempo between now and reaching somewhere in $310 million to $320 million as fairly consistent is more of the growth back end weighted until like 3Q into 4Q, how should we think about that from a modeling perspective now that we’re sort of deeper into the year?
Peter Radovich: Yes. I think — I mean, the way we think about it is generally consistent. I mean the cadence of demand is strong, and we see it growing quarter-to-quarter. You will have PFIC coming on, although as we’ve commented, most of 2024, we expect many of the PFIC dispensers to be pre-drug and they’re probably contributing more in 2025. That might be the one dynamic that comes into play more later in the year. But generally, I think it’s a pretty consistent build towards the $310 million to $320 million.
Mani Foroohar: Okay. That’s helpful. Thanks, guys.
Chris Peetz: Thanks for the question.
Operator: The next question on the line comes from Gavin Clark-Gartner of Evercore ISI. Please go ahead. Your line is now open.
Gavin Clark-Gartner: Hey, congrats on the progress, and thanks for taking my questions. First, on the PSC, I believe you noted there was a 1.75 point expected pruritus benefit in 3 standard deviation that was informing your powering assumptions. Was that 1.75 point absolute or placebo adjusted? And maybe just remind us your expectations for the placebo arm for this trial?
Joanne Quan: Yeah. So yeah, thanks for the question, Gavin. So by 1.75 point, we mean the treatment difference, so active compared to placebo. And we took some fairly conservative assumptions by putting that together. And as you know, those are always kind of a starting point for where you kind of put the study. But we did want to share at least our starting point for looking at the study design.
Gavin Clark-Gartner: Yeah, that’s helpful. And are you able to share the baseline pruritus scores for either trial for volixibat?
Joanne Quan: Not at this point. When we — we’ll be happy to share information when we show the interims in June with you. So I think that would be — we look forward to that along with you folks.
Gavin Clark-Gartner: That sounds good. Just the last one. Any updates on the potential for orphan drug status for PFIC in the EU?
Chris Peetz: Yeah. Thanks for the follow-up there. This is one that we are continuing in dialogue with the European regulators and hope to have an update soon. But still come back to really strong conviction in our data for the LIVMARLI program in PFIC, providing some real advantages for patients. So hoping to have an update on that one soon.
Gavin Clark-Gartner: Sounds good. Thanks, guys.
Chris Peetz: Yeah, thanks for the questions.
Operator: The next question on the line comes from Dae Gon Ha from Stifel. Please go ahead. Your line is open.
Dae Gon Ha: Hey, good afternoon, guys. Thanks for taking my questions. Maybe a two-part question. On the PFIC side of the story, I was wondering if you can comment on your dialogue with the physicians given the label disparity between this and Bylvay the time being. And when you think about the reimbursement dialogue, will there need to be subsequent dialogues to be had once you get the label expansion done? And switching over to volixibat, bearing in mind the interim update in June for both VISTAS and VANTAGE, how are you guys thinking about sort of the Glaxo’s drug towards the back end of this year? And how might that impact your PBC strategy if both come out positive? Thanks so much.
Chris Peetz: Yeah. Thanks for the questions. Maybe I’ll just make a quick comment on the volixibat competition briefly and then pass over to Peter to talk about PFIC. And what we’re seeing and kind of how we’ve approached the dosing for volixibat, I think provides the potential for a real advantage in terms of activity level. It’s something we’ve learned across all of the IBAT programs, in particular, all the work we’ve done with LIVMARLI and volixibat on understanding where we’re at on the dose response curve, I think provides the potential to have really strong activity here. Of course, this is something we’ll see play out with the actual data sets as they come forward but excited about the dosing regimens that we’re evaluating in the VANTAGE study and what that can mean for patients. Maybe Peter can speak to the PFIC questions.
Peter Radovich: Sure. Yeah, thanks for the questions. Feedback on the LIVMARLI profile and PFIC has been very positive. I think, a lot of favorable feedback on the efficacy profile that was observed in the March study is reflected in the label as well as the broader genetic types of PFIC that are included in the labeling, which can sometimes make a difference in market access, depending on the payers’ policies. So, we really, really favorable feedback from clinicians and patients happy to have LIVMARLI available for those patients. And yes, payer conversations so far are going well. It’s kind of early days still, but have had really happy with the policies that have emerged. And then in terms of updated policies after, as you mentioned, a potential label update for younger than five years of age. I’d expect that those — I mean, there’s a lot of payers in the U.S., it’s heterogeneous, but generally, those would occur pretty quickly. We saw that with Alagille when the initial label is one year of age and older and then lowered the age. Those subsequent follow-up conversations generally occur pretty quickly to update policies.
Dae Gon Ha: Great. Thanks for taking our questions.
Chris Peetz: Yeah, thanks for the questions.
Operator: The next question on the line comes from Steven Seedhouse of Raymond James. Please go ahead.
Steven Seedhouse: Hey, good afternoon. Thanks for taking the questions. Two separate questions. I’ll just ask them both now as they’re pretty straightforward. First, on the PBC readout, you mentioned price improvement, safety and serum bile acids would be the focus of that data release. And I’m just curious if you’ll also be sharing liver function tests, alphos, ALT, AST, bilirubin, just to get a sense of — even from a safety standpoint, what’s happening there? If there’s any impact of de novo bile acid synthesis on any of those parameters? And then the second one is just on business development. I would be curious your comments or thoughts on just the overall view of that or priorities for Mirum over the next, call it, 12 to 18 months, are you thinking about expanding the pipeline or focusing on volixibat primarily? Thank you.
Chris Peetz: Thanks, Steve, for the questions. I’ll speak to and comment on kind of our business development efforts and let Joanne come back on the PBC interims. And for our strategy and approach to business development remains consistent with what we’ve done over the course of Mirum. It’s very much in our DNA. It’s how the company came to be and started and its approach of being disciplined about making sure anything that we look to bring on is something that we can add value to that’s at terms and something that helps grow the company and really across a number of different rare disease settings is where we’re looking. I think we’re in a position where we’re quite lucky in that there’s a lot of growth in the commercial business, label expansion opportunities, the volixibat developments that there’s no urgency to do something so we can remain disciplined in looking at ways to grow the company. And then maybe Joanne can speak to the PBC question.
Joanne Quan: Yeah. Thanks, Chris, and thanks for the question. As I mentioned, this is an interim analysis. So it’s pretty limited in terms of scope. We’re mainly looking at it to ensure safety and to select the dose moving forward. So with that, we’ll look at pruritis, we’ll look at serum bile acids and safety, in particular. The data set is going to be pretty limited. So, we think it will be quite limited in terms of making any conclusions, certainly about any other parameters. I think we’d look to the final data set for that.
Steven Seedhouse: Thanks so much.
Chris Peetz: Thanks for the questions.
Operator: The next question on the line comes from Brian Skorney of Baird. Please go ahead. Your line is open.
Unidentified Analyst: Hi. This is Luke on for Brian. As we set expectations for VANTAGE in particular thinking about a comp to the seladelpar response study, do you think the subgroup in that study with baseline NRS greater than 4 is a reasonable comp for pruritus benefit? And then are you aware of the 11-point NRS scale they used in that study is the same as the itch reported outcome scale that you’re using?
Chris Peetz: Thanks, Luke, for the questions. Yes. I mean the scale used — it is similar. I mean there’s some very minor differences. But for adult pruritus measurements in registrational studies that kind of — this is all in line with FDA guidance. It uses 10 scale. That’s what we’re using in our study. So there is some — definitely some similarity there. And the treatment effect in that subset that they looked at, it’s not too far off with how we look at our change from placebo assumptions and powering, right, where we looked at the 1.75 point difference from placebo. So kind of looking at potentially a little bit more effect from an IBAT. But in general, it’s really not too far off if you’re thinking about study design assumptions. Of course, we’re quite excited about getting this data and seeing what that looks like. particular change from baseline, which is really what the patient experience is and what you’re doing to address the burden of disease.
Unidentified Analyst: Great. Thank you.
Chris Peetz: Thanks for the question.
Operator: The next question on the line comes from David Lebowitz of Citi. Please go ahead. Your line is open.
David Lebowitz: Thank you very much for taking my question. On the 1.75 point difference on pruritus, could you just elaborate as to whether you’re talking about through the blinded portion or through the actual pivotal portion at a subsequent time point? And perhaps give us some view of what that point and how you will use it to consider upsizing if that is needed, what type of thresholds we could expect?
Joanne Quan: Yeah. Thanks for the question. We’re not going to get into the details of the study design, but I just provided some of the number so that you could get a sense of what kind of treatment effect we’re looking at. The 1.75 point treatment difference and the 3 in terms of standard deviation is just a general number that we’re looking for the overall design of the study. So, we won’t be sharing any specifics in terms of kind of where we are with the interim. Obviously, we’ll share the results of the interim since we’ll be blinded. We certainly hope that we’d be continuing the study. So that’s what we hope to be in to see in June.
Chris Peetz: And I want to add to that, David, is that the measurement is actually looking at over time, right? It’s the month three, four, five — sorry, four, five and six actually of the treatment effect for the final analysis. That does allow to add power and try to deal with any potential for placebo response because you’re looking at multiple time points and how they roll into the analysis. That’s another kind of factor to the study design. Applying what we used from the PFIC study and the adult settings.
David Lebowitz: Got it. Thank you very much for taking my question.
Chris Peetz: Yeah. Thanks for the question.
Operator: The next question on the line comes from Jon Wolleben of Citizens JMP. Please go ahead. Your line is open.
Jon Wolleben: Hey. Thanks for taking the question. Just logistic one for me on PBC and PSC. When you select the dose, the patients on higher dose get to roll back in at either placebo or the new dose, or do you have to re-enroll patients? And can you comment on how long enrollment could take to complete in both those studies? Thanks.
Chris Peetz: Thanks, Jon, for the question. Just on timelines, we’ll give a more formal update on what we expect to see for the — to get to the full data set in June when we have the interim. I’ll let Joanne speak to a little bit of mechanics of how patients flow through the study.
Joanne Quan: Yeah. So we’re going to be continuing — we are continuing enrollment in the study at this point. And then, we’ll be continuing with one active dose and placebo. So we expect to include all the patients ultimately in the analysis when we ultimately unblind the whole data set.
Chris Peetz: Thanks for the question, Jon.
Operator: The next question on the line comes from Mike Ulz of Morgan Stanley. Please go ahead. Your line is open.
Unidentified Analyst: Hi. This is [Rohit] (ph) on for Mike. Can you just provide any color on the ongoing launch prep for PFIC? And when do you expect patients on the expanded access program to get on paid drug? Thanks.
Chris Peetz: Yeah. Thanks for the question, Rohit. In U.S., obviously, launch is underway, seeing prescriptions come in for LIVMARLI, PFIC patients now. We have talked about — we have about 25 patients in the U.S. who are on clinical drug. Most of those are eligible to roll over at this time, and we’d expect them to come over to commercial drug in the coming quarters throughout this year. So that’s how we see the cadence playing forward.
Unidentified Analyst: Thank you.
Operator: The next question on the line comes from Ed Arce from H.C. Wainwright. Please go ahead. Your line is open.
Thomas Yip: Hi. Good afternoon, everyone. This is Thomas Yip asking a couple of questions for Ed. Thank you for taking our questions. So first, following up on U.S. performance for the LIVMARLI PFIC. Just wonder of the $42.8 million net sales in the first quarter, how much was it from PFIC approximately? And then also what are some early launch metrics that investors came up to?
Chris Peetz: Thanks, Thomas, for the question. In Q1, there really — there’s no PFIC contribution in there yet. And we’re just — the approval came in March and just now kind of rolling over those clinical patients. So, expect that revenue contribution to be pretty minimal from PFIC over the next quarter or two as we get into the back half of the year where we expect more reimbursement.
Thomas Yip: Got it. And then switching gears to the European front. Have you any interaction with EMA or CHMP recently given your expectation on a recommendation in the first half of this year? And if positive, any ongoing commercial preparations for European market for PFIC?
Chris Peetz: Yeah. Thanks for the follow-up there. On the EMA discussion, you have over the — we have been active in discussing with EMA. As I mentioned, feel confident in our arguments and hope to have an update on that soon. Som no formal determination yet. And maybe Peter can speak a little bit to the launch prep in Europe for PFIC.
Peter Radovich: Yeah, certainly, upon a potential approval, it would be ready to launch LIVMARLI in Europe. Prescribers for PFIC are essentially identical to the prescribers of LIVMARLI for Alagille syndrome. So you’ll be ready to go with dossier submissions to help technology agencies, et cetera, to work with pricing and reimbursement and [indiscernible] level as well.
Thomas Yip: Okay. And then one last question from us. Can you discuss some of the main drivers for the bile acid product sales that’s slightly by $2 million quarter-to-quarter? Can you provide some major factors?
Peter Radovich: Yeah. I mean we mentioned the Change Healthcare cyberattack was kind of in play for our entire portfolio. I think if you look back over time in the bile acid product sales, there are — there’s quarter-to-quarter volatility given the ultra-rare nature of the disease in small number of patients over time. But do see an opportunity to continue to build on those products this year, mid-single-digit year-on-year growth, consistent with historically is our expectation. And going forward, really excited about potential approval by FDA next year for CHENODAL and CTX and the chance to go out and find more patients there.
Thomas Yip: Understood. Thank you, again, for taking our questions. We look forward to CHMP recommendation soon and also your June presentation for volixibat.
Chris Peetz: Sounds good. Thanks, Thomas.
Operator: We have no further questions. Therefore, I will hand back the call to Chris Peetz, CEO, for final remarks.
Chris Peetz: Great. Thank you all for joining us today. Really appreciate the interest in Mirum and our programs. Have a good evening. Goodbye.
Operator: This concludes today’s conference call. Thank you all for joining. You may now disconnect your lines.
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