Good day, and welcome to the Biote Second Quarter 2024 Earnings Conference Call. All participants will be in listen-only mode. After today’s presentation, there will be an opportunity to ask questions. Please note this event is being recorded. I would now like to turn the conference over to Szymon Serowiecki, Investor Relations. Please go ahead.

Thank you for joining us today. This afternoon, Biote published financial results for the second quarter ended June 30, 2024. This news release is available on the Investor Relations section of the company’s website. Terry Weber, Chief Executive Officer; and Bob Peterson, Chief Financial Officer, will host today’s call. Before we get started, I’d like to remind everyone that management will make statements during this call that include forward-looking statements regarding, among other things, the company’s financial results, future performance and growth opportunities, business outlook, strategies, goals, business development, manufacturing and commercialization activities, regulatory process operations, the impact of macroeconomic conditions on its business, results of operations, financial conditions and other matters. These statements are not guarantees of future performance. They are subject to a variety of risks and uncertainties, some of which are beyond the Company’s control. Actual results could differ materially from expectations reflected in any forward-looking statements. These statements are subject to risks, uncertainties and assumptions that are based on management’s current expectations as of today. Biote undertakes no obligation to update them in the future. Therefore, these statements should not be relied upon as representative of the company’s views as of any subsequent date. For a discussion of risks and other important factors that could affect our actual results, please refer to our SEC filings available on the SEC’s website and the Investor Relations section of our website as well as risks and other important factors discussed in the earnings release. Management will also refer to adjusted EBITDA, which is a non-GAAP financial measure to provide additional information to investors. Reconciliation of the non-GAAP to GAAP measure is provided in our earnings release with the primary differences being stock-based compensation, fair value adjustments of certain liabilities, transaction-related expenses and other non-operating expenses. Please refer to our second quarter 2024 earnings release for a reconciliation of adjusted EBITDA to net income, the closest comparable GAAP measure. I’ll now turn the call over to Terry Weber.

Thank you, Szymon, and thank you all for joining us. On the call with me today is Bob Peterson, our Chief Financial Officer, who will review our financial results and discuss our outlook for 2024. Marc Beer, our Executive Chairman, is also on today’s call to help answer your questions during the Q&A session following our prepared remarks. Biote generated solid financial performance in the second quarter, highlighted by a sequential increase in procedure revenue growth. This improvement reflected our strategic focus on driving growth from our top-tier accounts, expanding our practitioner network, and optimizing new clinic success through our quick-start program. In the first half of 2024, we added approximately 30% more new clinics on a year-over-year basis, with significant growth in new clinics achieving quick starts. We have found that the early success generated by clinics that achieve quick-start status translates into stronger clinic performance over time. As a result, we continue to work closely with our new providers to optimize the launch of their hormone and therapeutic wellness practices. We also achieved solid gross profit and adjusted EBITDA, even as we selectively increased our investments in key marketing and sales initiatives to enhance our long-term growth opportunities. These investments included our annual provider conference where we strengthened engagement with our top practitioners. We spent 2.5 days with over 500 practitioners teaching advanced concepts and therapeutic wellness. Even with these strategic investments, we remain on track to achieve our 2024 financial guidance. The phased launch of BioteRx across our network continues to progress well, with approximately 600 clinics now enrolled. We believe our BioteRx platform represents a unique and differentiated approach to care in the hormone and therapeutic wellness market. In addition to an expanded range of products and treatments, BioteRx supports practitioners with a comprehensive portfolio of advanced technical tools, support, training, and educational resources, which we believe separates us from our competitors. Over the next several weeks, we will introduce several major enhancements to the Biote method, expanding our science-based approach to care. With these enhancements, we’re confident that Biote will enable practitioners to deliver an even higher level of holistic, personalized medicine for their patients. First, we’ll expand our wellness lab panels to utilize the latest technology, liquid chromatography, and mass spectrometry for blood sample analysis. These additional lab panels broaden our testing capabilities while providing greater testing sensitivity and accuracy. These advantages will enable practitioners to provide more precise dosing that addresses a wider range of treatments and delivers better health outcomes for patients. To further enhance clinical decision-making, we will update our proprietary software with new functionality to deliver even more individualized precision patient care. For example, our updated clinical decision support software features enhanced algorithms for ongoing patient management, continuously adapting to a patient’s evolving health needs. We are also broadening our BioteRx offerings across key therapeutic categories. We will introduce new offerings in the areas of body composition, sexual wellness, non-pellet hormone optimization, and thyroid and autoimmune conditions. These new products complement our existing therapies, elevating our value proposition and enabling more comprehensive patient care. Finally, we will further bolster our support for practitioners with enhanced tools and procedures, including a new trocar for pellet delivery and new techniques for pellet insertion. As always, Biote will continue to provide an unmatched level of education and training, covering a broad spectrum of hormone and therapeutic wellness. The integration of Asteria Health into our operations continues to progress smoothly. We’ve been pleased with the positive feedback we’re hearing from our practitioners, who value the capabilities that Asteria Health adds to our business. As we continue the integration process, we remain focused on expanding Asteria Health’s licenses to additional states, as well as driving long-term manufacturing cost efficiencies. During the second quarter, we were pleased to conclude outstanding litigation with two large shareholders. These agreements eliminate the time and expense associated with litigation and build long-term shareholder value through significant share repurchases. Bob will provide more information in his remarks. In summary, Biote continues to make solid progress in advancing our strategic objectives, and we remain on track to deliver our 2024 financial guidance. I’ll now turn the call over to Bob to discuss our second quarter financial results and provide our outlook for 2024.

Thank you, Terry, and good afternoon, everyone. Total revenue in the second quarter was $49.2 million, essentially flat year-over-year, and consistent with our expectations. Procedure revenue growth increased 7.8%, increasing sequentially from the 6.6% growth rate reported in the first quarter of 2024. Second-quarter procedure revenue growth was broad-based across our network and primarily driven by growth from our top-tier clinics. Our performance also benefited from approximately 30% growth in new clinics over the past 12 months. As Terry mentioned previously, many of these newly added clinics have successfully implemented our quick start program that accelerates new procedure revenue streams. As expected, second-quarter dietary supplement revenue decreased 32.2% year-over-year as we continued the transition of our e-commerce business and lapped a significant seasonal promotion in last year’s second quarter. Consistent with our timeline, we began managing distribution of several key products previously delivered from our former distributor at the end of the second quarter. While we continue to work down the inventory of certain nutraceuticals from our prior distributor, we expect overall nutraceutical revenue to resume year-over-year growth in the second half of this year. Second-quarter gross profit margin was 68.9%, a 100 basis point increase from the second quarter of 2023. Gross profit of $33.9 million in the second quarter of 2024 included a $1.2 million step-up in inventory value related to the acquisition of Asteria Health. Excluding this inventory revaluation, second quarter 2024 gross profit margin would have been 70.9%. The year-over-year improvement in gross profit margin reflected product mix and effective cost management. As expected, we anticipate consolidated gross profit margin will revert to historical levels as nutraceutical sales resume year-over-year growth in the second half. Consistent with our expectations, selling, general and administrative costs were $27.6 million compared to $25.8 million in the second quarter of 2023. Operating expenses increased from the prior year, primarily due to planned strategic investments in sales and marketing, including our annual provider event. As a result, second-quarter operating income was $6.2 million compared to $7.7 million in the prior year quarter. Net loss in the second quarter was $10.5 million, inclusive of a $13.9 million loss due to a change in the fair value of the earnout liability. This compares to a net loss of $13.1 million in the second quarter of 2023, which included a $6.4 million loss due to the net change in fair value of the earnout liability and an $11.8 million loss due to the net change in fair value of the warrant liability. During the second quarter, we selectively increased our investments in sales and marketing to strengthen engagement with our top providers, expand our therapeutic wellness offerings, and further our geographic expansion. Largely due to these investments, second-quarter adjusted EBITDA decreased 12.4% from the prior year to $12.7 million with an adjusted EBITDA margin of 25.9%. This compares to adjusted EBITDA of $14.5 million with an adjusted EBITDA margin of 29.5% in the prior year period. While we continue to make investments aligned with our growth strategy, we anticipate our overall operating expenses will moderate in the second half of this year compared to the first half. Second-quarter operating cash flow was approximately $17.3 million. As Terry noted and as previously announced, Biote concluded litigation with two large shareholders during the second quarter. These settlements include significant share repurchases and the release and cancellation of earn-out shares for no additional consideration. Under the terms of these settlements, Biote repurchased the first tranche shares from Dr. Gary Donovitz for $32.2 million in April. Subsequently, in June, Biote repurchased the first tranche of shares from Marci Donovitz for $30 million. After the repurchase of the first tranches, Biote has agreed to repurchase the remaining 14.4 million shares over the next three years. Largely because of these share repurchases, cash and cash equivalents at the end of the second quarter of 2024 were $26.4 million, down from $78.8 million at the end of the first quarter of 2024. Moving forward, we will continue to prudently manage our operating cash flow to assist in funding settlement-related share repurchases while maintaining our capital allocation discipline. Turning to our financial outlook for fiscal 2024. We reiterate our previously reported guidance with revenue of $200 million to $204 million and adjusted EBITDA of $60 million to $63 million. At a high level, our 2024 sales guidance reflects our expectations for improving procedure revenue growth in the second half and a return to year-over-year growth in nutraceutical sales. On the expense side, we anticipate moderation in the second half operating expenses compared to the first half. Strengthening procedure revenue growth in the second half of 2024 relative to the first half is expected to be driven by three factors: one, improving performance from our top-tier clinics; two, the continued expansion of our existing practitioner network; and three, a growing contribution from new clinics, including continued growth in clinics implementing quick starts. Now I’ll turn the call back to Terry for her closing comments.

Thank you, Bob. Biote generated solid financial performance in the second quarter, and we are on track to achieve our financial and strategic objectives for the year. We continue to progressively roll out BioteRx across our network with plans to add new capabilities to better serve both patients and practitioners. We also continue to integrate Asteria Health, which improves our manufacturing efficiency and offers new opportunities for growth over time. Finally, we have enhanced long-term shareholder value by concluding outstanding litigations and committing to significant share repurchases on favorable terms. We remain focused on driving profitable growth as we strive to become the leading single-source provider of evidence-based therapeutic wellness solutions. And now I’d like to open the call for questions. Operator, please begin the question-and-answer session.

We will now begin the question-and-answer session. Our first question comes from Les Sulewski with Truist Securities. Please go ahead.

Yes. Good evening, guys. Thank you for taking my questions. So Terry, I didn’t hear much commentary around your weight loss program and your strategy. Can you just perhaps highlight now that we’ve heard some of the brand GLP-1s coming off of the shortage list? Essentially, how does that impact your compounded GLP-1 strategy? And how do you confirm with regulations if there are restrictions from the FDA or if there are limitations since products will no longer be available?

Wow, Les, that is a lot. So I’ll break it into pieces. So let me give you some context of a framework for our BioteRx and our use of the GLP-1s. So we have launched this therapeutic wellness platform, BioteRx. It has a full complement of therapeutic wellness products, which includes the GLP-1s. It includes both Tirzepatide and Semaglutide that are both being produced by compounders because of the shortage list. For us, it’s a part of a formula with a lot of other products that allows for a one-stop shop at Biote. We have a platform that allows those providers to order the product easily and delivered on very short timelines. It’s part of a performance piece on therapeutic wellness, and it’s just some of the products. We’re not concerned about this. The platform is working well, and there’s a lot of adoption. Right now, if you look at the shortage and why compounders can manufacture, it’s the shortage list, and the FDA considers several criteria before removing a drug from the shortage list. First, whether the manufacturer is able to meet total national historical demand, and you can report on the amount of that national demand even within the last year for both formulations. The second part is whether the manufacturer can verify that it has built enough safety stock for the drugs. Other considerations include whether prescribers or patients have the availability under the drug or if there’s still that type of a shortage. So it’s a long process, and the only person that determines whether it goes off the shortage is the FDA. If our audience has listened to both Eli Lilly and Novo Nordisk regarding their two branded products, Tirzepatide and Semaglutide, both companies have addressed the fact that they had difficulties with leading demand, and that these certain dosages of their drugs come in and out of supply. Lilly announced there would be intermittent supply disruptions for a drug such as Zepbound and Mounjaro, while supply and demand are better in balance; they noted they expect increases in demand may result in periodic supply tightness at different dosage levels. When we look at this, it appears that, certainly for Novo Nordisk, they announced they would continue restricting supplies of their starter doses in the U.S. market to ensure patients who start the treatment can continue this treatment. Therefore, we believe these drugs will remain on shortage for a while, but there are many options available. New drugs are being developed in the GLP-1 space as we speak. These compounders will be allowed to continue producing the ones that are on shortage. For us, we’re not concerned about it in our model. We just want to ensure that our doctors have easy access to it and a consistent supply. Our platform offers that, and I hope I’ve given you some insights into why that is not a big concern for us. I’d also remind you that we get paid a tech platform fee for accessing our platform, which offers the other formulations as well in therapeutic wellness. So this is just part of our long-term therapeutic wellness focus.

Excellent color. I mean, very helpful. Perhaps just to maybe build on that, you mentioned the Asteria facility. You said you’re looking to add a production line on the compounded GLP-1. Is that still in the works? When can we kind of expect that to be operational? And I guess my last question is what percentage of your physicians are in the medical spa setting? And how many operate in a virtual setting? Thank you.

Good questions, three parts there. So number one, on Asteria. We are looking to expand our space at Asteria and after we’re sure that we can meet all the production needs in our integration, we’re very focused on manufacturing the other GLP-1 products. I’d be looking to 2025 for that manufacturing impact. Your second question, could you repeat that real quick?

What percentage of physicians are in the medical spa setting and how many operate virtually?

So our practitioners in the medical spa setting have all supervising practitioners. They’re usually an arm of an OB/GYN or an internist who has a wellness practice next to their traditional practice. The structure allows us to have very good supervising practitioners. I would certainly say less than 10% and on the virtual end, we have very few – they have a virtual component of their practice, but they’re all practitioners with clinics. So we don’t, at this point, service just any completely virtual group.

Great. Thank you.

And the next question comes from Jonna Kim with TD Cowen. Please go ahead.

Hi, thank you for taking my questions. Curious about the marketing and investments that you’ve made this quarter just like a step-up there. Should we expect a similar level of marketing and investments for the remainder of the year? As a follow-up to that, how are you measuring the success of the spend? And going forward, how should we think about your investment plan? Thank you so much.

What Biote looks to do is really engage long-term with these practitioners so they keep decades of involvement with us. What we invested in this year is the enhancement to our clinical decision support software. Not only will you have that clinical decision support software doing an excellent job of hormone optimization, but it also includes therapeutic wellness products from our BioteRx. That was an investment in growing engagement with those providers. This is innovative science. The large meeting we had with so many of our key providers; we spent 2.5 days educating them off-site on these new therapeutic wellness products and where the science is going. That was a large investment in Q2, but all of this should yield a very solid ROI on both the enhancement in the Tier 1 clinics and our largest providers as well as taking us into the next generation, where we remain differentiated from the competition.

And Jonna, just to add a little bit to that. As we look at our operating expenses, typically, it’s higher in Q2. Several of the expenses to support sales, marketing, and other customer-related expenditures were planned for Q2, as Terry mentioned. When we think about the investments that we’re looking to continue to deploy, whether it’s practitioner engagement, modernization of our data systems and data analytics, all those really support what Terry is saying about reviewing ROI on the spends we deploy.

And just one follow-up, have you seen any notable changes or anything to call out quarter-to-date trends versus second quarter? And what gives you confidence in the second half of inflection embedded in your guidance? Thank you.

Yes. So right now, when we look at Q2 revenue, the improved growth from a sequential perspective on procedure revenue was consistent with our year-to-date guidance. We’re expecting that uptick. We don’t provide quarterly guidance. We continue to anticipate second-half performance will strengthen compared to the first half. However, we’re really focused on our key trends: growth in our top-tier accounts, new customer growth, and particularly improving the quick starts and neutral growth in the second half, which should show positive momentum.

All right. Thank you.

And the next question comes from Jeff Van Sinderen with B. Riley Securities.

Hello, this is Richard Magnusen in for Jeff Van Sinderen. Thanks for taking our call. First off, you did mention quickly state licenses. I was wondering if you could provide more color on where you are exactly with obtaining all the various state licenses?

Yes. So we’ve made pretty good progress. As you look at the entirety of Asteria, we keep applying for new licenses; it’s constantly in flux. We’re obtaining those licenses as planned, and we continue to work with our teams to diligently progress in that area. I would say we’re approaching about the halfway mark of the licenses we are looking to obtain, with a handful coming over the next quarter or so.

Okay. And then my next question is, previously you talked about how the doctors were a bit stubborn to migrate towards your new platform. Some of it was because they had inventory from previous sources. My question is have they depleted that inventory as far as you know, or a lot of it? And have they been reluctant to move away from the legacy sources, testing Biote as a source with smaller orders until they felt comfortable?

Yes, it’s meaningfully improved. We’ve been adding new doctors because new state licenses are coming in for our BioteRx. So we’ve been adding practitioners; they’ve been increasing their orders, and they’re seeing the consistency of the delivery time and the quality of the product. All that’s going very well. What I’m excited about is these new clinics that we’ve got have become dependent on us for all of their BioteRx products. It’s a good mix; it’s not just GLP-1s. They’re not just shopping GLP-1s, but they’re learning the business and depending on us for their supply and used to our platforms. The strategy is working very well.

All right. Thank you.

The next question comes from George Kelly with ROTH Capital. Please go ahead.

Hey everyone, thanks for taking my questions. Just a couple for you. First, on Asteria, I'm curious how much of your production is running through there, and what is your expectation for year-end?

Yes. The way I would look at this, George, as we’ve discussed the state licenses, we are at a point now where from a production perspective, we built the capabilities to meet needs in the short-term and now, probably in the medium-term by building additional machinery. I think we are at a point now where we’ve scaled up well and are building the inventory to ensure we can meet our future demand.

So I guess the next part of that question is, are you anticipating a meaningful step up in gross margin in the back half just based on that production point for Asteria?

Here’s the way we look at this. As mentioned earlier, you need to focus on doing each facet well. We’ve discussed the state licenses, the conversion of additional states we get access to, and we’re finding we’re working well with our commercial teams to ensure a successful transition. Asteria is an important piece and a strategic part of our overall capabilities within Biote. As we progress operationally, we’ll begin to integrate and operationalize pellets into the different clinics. These procedures in the second half of the year will provide a phased approach with a financial impact on gross margin factored into our 2024 adjusted EBITDA guidance range.

Okay. And then two other quick ones. In your prepared remarks, you mentioned that you expect SG&A to moderate in the back half versus what you reported in the first half. Can you be more specific? Does that mean that you expect absolute SG&A dollars to decline in the back half versus the first half, or what does that mean?

Here’s the way we look at it. We expect our core expenses to remain flat. We don’t see any significant shifts in the business. However, we’re going to continue to spend additional funds on revenue-generating activities. We don’t have any big expenses like the Sun and Sea event that Terry mentioned we had in Q2, but we’re going to spend on new customer trainings, Amazon and demand-generation activities. So the moderation is baked into that guidance.

Okay.

Did that answer your question?

Yes, I think so. I’m just trying to triangulate your EBITDA guidance, which implies a significant step-up in EBITDA margin in the back half. What’s driving that? Is that a gross margin issue or an SG&A issue? I don’t know if there’s a way to clarify that.

No, I would just say we expect that moderation and as we look at gross margin in the second half, we expect to be guiding towards the higher end of our historical range, in the upper 60s. That should give you a sense of where we’re going.

Okay. Understood. Thank you.

And the next question comes from Kaumil Gajrawala with Jefferies. Please go ahead.

Hey guys, good evening. A couple of follow-ups from some of your answers to other questions. On the state licensing, can you give an idea of how many states are left and if any particularly large states are ones where you recently became licensed?

I would tell you that the state licenses we have been approved match up fairly well with our existing footprint. We’ve applied for nearly all states; they’re in varying phases of the approval process.

Okay, got it. On the step-up in marketing, was the increase simply due to the big event, or were there additional investments that stepped up the dollars?

The Sun, Sea event is a pretty significant event, and that is likely one of the largest drivers. There’s a combination of optimizing our sales force, engaging with practitioners, and improving our data systems. There are smaller items, but you hit the major one.

Yes, Kaumil, one thing I’d like to emphasize is investing in educators. We’re moving toward therapeutic wellness and ensuring that all of our providers have a much more evidence-based science approach. We invested in our educators, the materials, and the whole education process to ensure a strong interactive experience for our new providers and those returning for additional training.

Got it. Sounds like a good time. We’ll look out for an invite. Thanks, guys. We’ll talk soon.

Thanks, Kaumil.

This concludes our question-and-answer session. I would like to turn the conference back over to Terry Weber for any closing remarks.

Thank you, everyone, for joining us today. We appreciate the interest in Biote, and we look forward to updating you on our progress in therapeutic wellness on our next conference call.

The conference has now concluded. Thank you for attending today’s presentation. You may now disconnect.