Evolus, Inc. (NASDAQ:EOLS) Q2 2024 Earnings Call Transcript

Evolus, Inc. (NASDAQ:EOLS) Q2 2024 Earnings Call Transcript July 31, 2024

Evolus, Inc. misses on earnings expectations. Reported EPS is $-0.18095 EPS, expectations were $-0.14702.

Operator: Good afternoon, everyone and thank you for standing by. Welcome to Evolus’ Second Quarter 2024 Earnings Conference Call. As a reminder, today’s conference is being recorded and webcast live. All participants are on a listen-only mode. After the speakers’ remarks, there will be a question-and-answer session. I would now like to turn the conference over to your host, Nareg Sagherian, Vice President and Head of Global Investor Relations and Corporate Communications. Please go ahead.

Nareg Sagherian: Thank you, operator, and welcome to everyone joining us on today’s call to review Evolus’ second quarter 2024 financial results. Our second quarter 2024 press release is now on our website at evolus.com. With me today are David Moatazedi, President and Chief Executive Officer and Sandra Beaver, Chief Financial Officer, Rui Avelar, Chief Medical Officer and Head of R&D is also with us for the Q&A portion of the call. Before we begin our discussion, I’d like to note that during our call, our prepared remarks will include forward-looking statements within the meaning of United States Securities Laws and management may make additional forward-looking statements in response to your questions. Forward-looking statements are based on management’s current assumptions and expectations of future events and trends, which may affect the company’s business, strategy, operations or financial performance.

Listeners are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this call and the company undertakes no obligation to update or review any estimates, projections or forward-looking statements except as required by law. These forward-looking statements are based on estimates and assumptions that although believed to be reasonable are inherently uncertain and subject to a number of risks and uncertainties. A detailed discussion of the risks and uncertainties that the company faces is contained in its annual report on Form 10-K, quarterly reports on Form 10-Q and current reports on Form 8-K. Additionally, today’s discussion will include non-GAAP financial measures, which should be considered in addition to and not as a substitute for or in isolation from our GAAP results.

A reconciliation of GAAP to non-GAAP results maybe found in our earnings release, which was furnished with our Form 8-K filed today with the SEC and on our Investor Relations website at evolus.com. Following the conclusion of today’s call, a replay will be available on our website at evolus.com. With that, I’ll turn the call over to our CEO, David Moatazedi.

David Moatazedi: Thank you, Nareg. Good afternoon, everyone. Thank you for joining us on our second quarter 2024 earnings conference call. This is a very exciting time for Evolus as we’ve now completed the first half of 2024 and have demonstrated continued market share gains with Jeuveau. This year is focused on our flagship product, while we prepare to expand our portfolio. We are incredibly pleased with the continued momentum in our business, which is clearly reflected in our second quarter results announced earlier today. In the second quarter, we achieved an important milestone, profitability. And Jeuveau’s market share increased to 13%. We accomplished this with a single product, while investing in the launch of our filler line.

Our focus is delivering exceptional results and our unique structure and value proposition are operating at a high level. Our reported revenue of $66.9 million in the second quarter represents 36% growth over the prior year. The combination of the continued strength of our execution and the momentum we have built during the first half of the year give us the confidence to raise our full-year 2024 net revenue guidance to between $260 million and $270 million. This updated guidance equates to 34% growth at the top end and is several degrees of magnitude above the estimated growth rate for our category. Importantly, this is a brand that continues to grow at over 30% in its fifth year on the market, signaling the quality of the Jeuveau brand and the strength of our unique business model.

We continue to build loyalty and trust with our customers. We have a unique position as the only dedicated cash pay aesthetic toxin company and a differentiated approach to building a performance beauty brand. We remain focused on the younger generations and helping practices grow. Our differentiation is evident in the continued growth in new purchasing accounts, increasing by 770 in the quarter. This brings our total number of customers purchasing since launch to approximately 14,000, which is approaching 50% penetration of the market. Our Evolus consumer loyalty program is also thriving and on track to surpass 1 million consumers in the program by year end. The underlying strength of our business and our strategic focus are just part of the story.

Internally, we are preparing for transformative year in 2025. This preparation starts with the commercialization of our novel dermal filler line. In June, we submitted our premarket approval application to the FDA for Evolysse Lift and Evolysse Smooth. In Europe, regulatory approvals for the Athene [ph] dermal filler products are anticipated later this year. And we remain on track for U.S. and international launch in 2025. Our commercialization plans are well underway and we will share more details at our Investor Day in September. Internationally, we continue to make significant progress with Nuceiva. We continue to expand our international business with a focus on deeper penetration in the U.K., Germany and Italy, while broadening our global footprint by commercially launching in Spain and Australia.

A patient in a medical aesthetics clinic smiling joyfully, showing the temporary improvement in appearance from the botulinum toxin type A formulation.

With these recent launches, we are now operating in all the major markets needed to deliver our 2028 guidance. The toxin market remains strong and we are well positioned to benefit from the growing shift towards Evolus and the Jeuveau brand. Jeuveau’s brand recognition, clinical performance and high satisfaction profile are well positioned for new consumers entering the category. This positioning will allow us to continue capturing demand, while we actively prepare to integrate our novel dermal filler line, Evolysse. These efforts collectively keep us on pace to our long-term revenue target of at least $700 million by 2028. Our differentiated go-to-market strategy continues to set us apart and I look forward to sharing more updates as we progress.

Now I’ll turn it over to Sandra, who will cover the financials.

Sandra Beaver: Thank you, David. I would like to congratulate the Evolus team on another quarter of above market sales growth and prudent management of our operating expenses that enabled us to achieve profitability two quarters earlier than anticipated. These above market Q2 results represent a meaningful step towards achieving our guidance in 2024, delivering full-year profitability for 2025 and positive cash generation. Turning to the results. Global net revenues for the second quarter were $66.9 million, up 36% compared to net revenue in the second quarter of 2023. Sales in the U.S. comprise more than 95% of revenues this quarter. International revenue contribution will continue to increase as international toxin growth will outpace the U.S. In the U.S., where our price remains strong, our customer reorder rate was approximately 70% and our sales were driven primarily by higher volumes.

Our reported gross margin for the second quarter was 70.3% and our adjusted gross margin, which excludes the amortization of intangibles was 71.5% and above the top end of our full-year guidance. Our GAAP operating expenses for the second quarter were $74.6 million compared to $68.3 million in the first quarter. Non-GAAP operating expenses for the second quarter were $46.7 million compared to $42.1 million in the prior quarter. Reported selling, general and administrative expenses for the second quarter were $50.2 million compared to $45.1 million recorded in the first quarter. This quarter, SG&A expenses included $5.8 million of non-cash stock based compensation compared to $5.1 million in the first quarter. Operating expenses saw a modest increase this quarter, a trend we expect to continue as we prepare for the 2025 filler launch.

For the first time and two quarters ahead of our expectations, we achieved profitability in the second quarter. Our non-GAAP income from operations in the second quarter was $1.1 million, this represents a $2 million sequential improvement in non-GAAP income from operations as compared to our Q1 non-GAAP operating loss of $0.9 million and represents meaningful continued progress on our path towards profitability for the full-year 2025 and positive cash generation. As a reminder, Q3 is seasonally lower revenue as compared to Q2. Considering this expected seasonal revenue decrease, it is likely we will not be profitable in the third quarter. Both non-GAAP operating expenses and non-GAAP operating income excludes stock based compensation expense, revaluation of the contingent royalty obligation and depreciation and amortization.

Turning to the balance sheet. With our consistent operating performance, we continue to be efficient with our use of cash. We had a low single-digit cash burn with our second quarter cash use of $3.3 million. We ended the second quarter with $93.7 million in cash compared to $97 million at March 31, 2024. The cash balance includes $4.2 million of remaining net proceeds from the $50 million underwritten offering of common stock in March 2024. Net cash used for operating activities was $6.5 million which improved $6.8 million as compared to Q2 2023. We expect that our existing liquidity will fully fund us to positive cash generation and the repayment of our $125 million debt facility in 2026 and 2027. We continue to target total net revenues of at least $700 million by 2028, driven by continued growth and share gains in our neurotoxin business in the U.S. and international markets along with the growing contribution from our novel line of fillers that begins in 2025.

This equates to a compound annual growth rate of 28% since 2023, on a total addressable market of approximately $6 billion today growing to approximately $10 billion by 2028. With that context in mind, I’d like to summarize our guidance. Based on our strong year-to-date performance, we have raised our total net revenues to between $260 million and $270 million. Over 95% of which will come from the sales in the U.S. and the balance from international market. Our quarterly revenue assumes typical industry seasonality. In addition, it is worth noting that we expect first half growth rate to exceed second half growth rate, primarily driven by the 2023 compare period and adjusted gross profit margin in the range of 68% to 71%. Non-GAAP operating expense guidance is between $185 million and $190 million driven by the increase in our revenue guidance range, we expect to be at the top end of our operating expense guidance range.

We expect to achieve positive non-GAAP operating income on a consolidated basis for the fourth quarter of 2024 and the full-year 2025. It is worth noting that within the year 2025, profitability may not be sustained every quarter due to the filler launch. Finally, the company projects its total net revenue can reach at least $700 million by 2028. Now let me turn the call back to the operator to begin Q&A.

Q&A Session

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Operator: Thank you. We will now be conducting a question-and-answer session. [Operator Instructions]. Our first question comes from Jack Padovano with Stifel. Please proceed with your question.

Jack Padovano: Hi, this is Jack on for Annabel. Thanks for taking our questions. So how are you seeing the state of play in the filler field? Because I know that this has been a little thorn in the side for aesthetics companies recently. AbbVie specifically did see some recovery there, but it wasn’t quite as much as anticipated. So did you have a pulse on that market yet? And what state of affairs will you be seeing as you approach launch?

David Moatazedi: Great. Thanks for the question. What we’re seeing, as you know, it’s always hard to parse out procedural growth as you look at different companies reporting. You have companies that are newer into their launch and companies that are more mature. Overall, we’re seeing a filler market on the full-year that is growing. Clearly, there’s some share shifts happening within the category. But also a market that is growing at a lower rate relative to the historical trends that we’ve seen. So we do see sort of a low- to mid-single-digit growth rate on the filler market in U.S. this year. And we do anticipate that filler market wrapping around on this depressed growth rate and benefiting from the boon of the patients coming in for GLPs, achieving their optimal weight and looking at on a filler.

We have multiple data points that confirm that the market should benefit from the GLP trends and we should start to see that in the coming quarters. So we feel very good about the market we’re entering. Keep in mind, the filler market is a $1.8 billion category. We expect it will grow in this mid- to high-single-digit over the five year horizon through 2028, where we’ve given our guidance outlook. And it’s a favorable market in the sense that there’s really three families of fillers that command roughly 80% to 90% of the U.S. market and the Evolysse line is clearly differentiated in the way that it’s manufactured and the clinical data that we shared relative to one of the market leading fillers. And of course, putting it into our cash-pay platform, we think there’ll be a tremendous amount of value.

We shared it with our advisors in a number of advisory board meetings and in research, and they’re very excited to see a product come in with a profile of the product, I believe that we’re going to be bringing. So, we’ll look forward to sharing more color on that at our upcoming Investor Day.

Jack Padovano: Great. And then just one more, if I may. On the toxin side, are there any additional competitor programs that you’re seeing out there whether it be loyalty programs or promotional programs that you expect to have to adapt to? Or in other words, do you sense the need for any shift in your marketing strategies as the field starts to get a little bit more crowded?

David Moatazedi: Yes. We continue to maintain our marketing strategy, which is really at a strategic level. It’s our cash pay advantage that’s enabled us to create a different experience for these practices. And we’ve leaned more heavily into that, whether you think about our consumer loyalty program or the way we engage with practices in co-branded media in the sense that both of them, the co-branded media and the rewards are growing at a very healthy clip and they remain our areas of focus. We stay really disciplined and a lot of credit to the team for continuing to build our scale and presence in the market. I do believe that’s why you’re continuing to see a business down its fifth year growing at 36%, which is effectively the growth rate we had on the full-year last year.

It’s because of that continued operating discipline that we’ve had as a company. As it relates to promotions in the market, look these markets, there’s a lot of promotions each quarter. Every manufacturer has their own set that they introduced into the category. But as you point out, nothing that changes the way that we’ve approached, Jeuveau and how we bring into the market.

Jack Padovano: Great. Thanks so much and congrats on the quarter.

David Moatazedi: Thank you.

Operator: Our next question comes from Marc Goodman with Leerink Partners. Please proceed with your question.

Unidentified Analyst: Hi. This is Madhu on the line for Marc. Just piggybacking off of that, could you talk a little bit more about your fillers and the differentiation from other products on the market and sort of how you’re thinking about — talking about those filler lines once they’re launching and comparing them to what’s already out there? Thanks.

David Moatazedi: Sure. Hi, Madhu. I’ll briefly touch on it. I think, there’s a section in our investor deck that highlights the scientific differentiation, and you can expect a lot more color from Rui at our upcoming Investor Day. But clearly, this product is the first one manufactured under freezing cold temperatures. Every other hyaluronic acid is heated in the manufacturing process and that preserves the natural HA trend. And clearly, the word natural is a significant term in the world of aesthetics. And the manufacturers of this technology have developed one of the leading hyaluronic acid currently available on the market. So there’s a lot of credibility in the technology and the science behind it. And then, of course, the clinical data that we shared from our trials now supports the science that we saw in the data.

So I think we have a clear story in terms of the product and the data, it still the early innings what you’re seeing is, as you know, multiple products under clinical development in different areas of the phase where this line was designed specifically for each area and we’ll be sharing more clinical data as we get closer to commercialization.

Unidentified Analyst: Thank you.

Operator: Our next question comes from the Navann Ty with BNP. Please proceed with your question.

Navann Ty: Hi, thanks for taking my questions. First, can you discuss the appointment of Cooper, current CEO to the Board and what he will bring to Evolus? And also, if you have any timing updates on Hugel, Letybo and Galderma QM1114, please? Thank you.

David Moatazedi: Great. Thanks, Navann for the question. I’ll start with the addition of Al White. We did a search and we are very selective about who we brought on to the Board. And I’d tell you, Al White clearly stood out for a number of reasons. One is, obviously, his background with a tremendous track record of success, having moved built the Cooper company, which now, of course, cover a number of therapeutic areas. And he moved his way into the CEO role, which he’s been in for about as long as I have now. But he’s played a significant role in building that company and that was important to us as we look at geographic expansion, profitability, building out our portfolio, a lot of the same elements that Al has faced as Cooper has grown.

And so having his experience around the table is invaluable for us as a company entering this next stage of our growth. And so it’s — I’ve really enjoyed the time I’ve spent with Al. I know he’s very excited about the story. He knows the aesthetic market well, and he’s also excited to see what we’ve been able to do and help contribute to our future growth story. And then, we actually had him on a Board call earlier this week for the first time. So it’s been great to have Al. On the competitive front, as you saw, placebo received approval earlier this year. They most recently announced a partner in the U.S. And they plan to commercialize sometime here in the back half of the year. At this point, as you know, we’re competing with Letybo in Europe, and we’re aware of the product and the dimensions of that brand as it enters the market.

We’ll be prepared as well when they enter the U.S. And I’ll just remind you that as we’ve had entrants that have entered since we launched, the market continues to grow at a very healthy clip. Our growth wasn’t impacted by the latest entrant. If anything, we accelerated a bit. I think the focus on toxins only increases with new entrant. And our value proposition is clearly defined in this space. And so, the entrants, whether that’s placebo or Galderma, which I believe, they did receive the CRL for the liquid, but they do plan to refile sometime next year, which could put them on the market towards the end of next year the following, not clear. I think it ultimately leads to continued focus on this category and growth, which is significant in the end.

It was nice to see this quarter all the significant players in the space reported positive growth despite an increasing competitive environment. And I think that just speaks to the backdrop that we have very low consumer penetration in this market, and there’s a lot of growth ahead of us. And as the new player comes in, they can carve out an opportunity for themselves just as we’ve done successfully in this younger generation of consumers.

Navann Ty: Thank you. That’s very helpful. And can I add one? Do you have a recent breakdown of facial injectables used by age range? Is the share of Millennials and Gen Z users, is it increasing? Thank you.

David Moatazedi: Yes. So the question is around Millennials in younger and what percentage of our patient base that represents? I can’t answer for the category at this time. But in terms of when we look at our consumer loyalty program, and it’s a sizable base, as you know, approaching 1 million consumers, We have over 50% or the majority, our millennial patients are younger. So we’re really pleased with that younger demographic. It’s been our focus and it’s worked. We do believe — we over index relative to the overall market, and it continues to be the growth driver for this space that this younger generation is more likely to get treated. They view this product as a beauty treatment and we think we’re incredibly well positioned to capitalize on next shift towards the younger movement.

Navann Ty: Thank you.

Operator: [Operator Instructions]. Our next question comes from Uy Ear with Mizuho Securities. Please proceed with your question.

Unidentified Analyst: Hi, this is Charles on for Uy. I just had one question about kind of the fillers. So in the U.S., I believe you said that the lips filler would be kind of the workforce. And I guess I was just kind of curious how ex U.S. those fillers would be like with a lips or also be the workhorse or would the lips filler kind of take over ex U.S.? So just trying to get a better sense of those dynamics. Yes. Thank you.

David Moatazedi: That’s a great question, Charles. The dynamics with filler use in the U.S. and abroad are actually quite similar. There’s obviously more choices in Europe than there are here in the U.S. But in the end, we do believe that the lips product that we’ll introduce here in the United States will be the workhorse in the line regardless of which market you’re in. But clearly, areas like the cheeks are an area of high use as are the lips. But keep in mind, when you’re going to areas like the lips, the volumes are lower than they are — when they’re treating areas like the nasolabial folds and highest in areas like the cheeks even though maybe the percentage of patients getting it in the cheeks are the lowest. So I think we’ll give you a lot more color around the market during our Investor Day.

We received a lot of questions around the growth of the category going forward, the impact of GLPs as well as the utility of the different products and what we’ve learned from them in the real world. You can expect to get a lot more color around that in September.

Unidentified Analyst: Great. Thank you and congrats on the quarter.

Operator: Our next question comes from Serge Belanger with Needham & Company. Please proceed with your question.

Serge Belanger: Hi, good afternoon. Thanks for taking my questions. I guess the first one for David. Both of the large aesthetic bellwethers reported last week and both kind of reported some softness in U.S. market across both fillers and toxins, especially in terms of procedure volumes. Just curious if you’ve — what you have noticed over the second quarter regarding the growth of those volumes? And then secondly, can you just remind us of the PMA process for the fillers? So both of them have now been filed. Is this a 12-month process? And should we expect radio silence until approval here or there’ll be some updates along the way before the second half 2025 when you expect approval launch? Thanks.

David Moatazedi: Great. I’ll ask Rui to take the second question in just a moment, and I’ll take your first one. What’s interesting is the messaging across the Board on toxins is that — it’s a very resilient category. We’re seeing healthy growth. I think you heard that from all the bigger players in the space and we’ve seen the same thing. And even though we continue to hear, there’s sort of this backdrop of, is there softness in the market that continues to persist, we’ve heard it now for almost two years. The reality of it is, having spent a lot of time in market, these practices are growing. The groups that have multiple facilities that we’re planning to expand are continuing with their expansion plan. And we’re seeing healthy growth all around, as far as toxins.

They’re very affordable, the $300 to $500 procedures and this movement with this younger generation is clearly a meaningful catalyst for this market. I think fillers have not had as much as the same level of consistency as toxins and we’re hearing that fairly consistency, but it continues to remain a healthy business. It is growing, we believe, in terms of procedural volume year-to-date, and we expect the market to wrap around on what happened depressed growth rates throughout the historical and potentially start to benefit from the GLP use as we turn the corner into next year. So our timing for the launch, we’re excited about. We think we’ll be launching into a healthy market environment and one that’s going to continue to benefit from a backdrop of more consumers going into weight loss treatment.

And when they achieve that optimal weight, that opens the door for the filler. I’ll turn it over to Rui to talk a little bit about the FDA and the timeline.

Rui Avelar: Sure. Thank you. Your question about PDUFA and devices versus drugs is a great one. When you’re dealing with a drug, we all hear about that PDUFA timeline. And what happens is industry pays a user fee and then the FDA gets back to you and they give you a specific PDUFA date and you hear about a year timeline. PMA is different. There is no PDUFA date that’s given. And they basically follow what’s called the MDUFA, and that’s Medical Device User Fee Modernization Act. And the way that works is they have a “180-day clock.” And what happens during that process is they work, then they stop the clock, ask you questions and you respond and it’s a back and forth process, very different from the drug. So as such, it can take a while for it to get done.

It’s not uncommon for it to be a year or longer. And that’s why we’ve conservatively said that in the back half of 2025, we’d expect approval as we take into consideration that this is a new technology, these are new facilities and usually they’re audits and visits. And then your other part of your questions, you’re absolutely right. We as a rule of thumb, we will announce when we filed and then we will announce when we get the approval.

Serge Belanger: Thank you.

Operator: Thank you for all your questions. At this time, I’d like to turn the call back over to David Moatazedi, President and Chief Executive Officer for closing comments.

David Moatazedi: Thank you. It’s an incredibly exciting time at Evolus, and I want to take a moment to acknowledge the exceptional execution by our team this quarter. The dedication and hard work has been instrumental in achieving these milestones. Evolus’ continued above market performance in the second quarter marked by record revenue and achieving profitability ahead of expectations showcase the unique difference we bring to the market as an innovator in the industry. Our flagship product Jeuveau continues to drive strong demand and our strategic initiatives have successfully expanded our customer base. The results from this quarter show our ability to consistently build and maintain momentum. As we evolve from a single product to a multi-product company, we expect to expand our leadership position in this category.

With the U.S. and EU filings well into the approval process, we are actively preparing for 2025 launch of the new filler product. These near term milestones will enable Evolus to continue to outpace the market. Looking ahead, we remain on track to achieve profitability in the fourth quarter of 2024 and are confident in our strategy to continue to gain market share. Our commitment to financial performance, operating expense discipline and capital efficient investments will drive us to sustain profitability, while achieving our long-term goal of at least $700 million in revenue by 2028. We are dedicated to building a sustainable leading performance beauty company and are grateful for the continued support and confidence of our customers and shareholders.

Thank you for joining us today and for your ongoing commitment to Evolus. We’re looking forward to seeing you on September 12th at our Investor Day in New York City.

Operator: Thank you. This concludes today’s call. You may now disconnect your lines.

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