Good day, everyone, and welcome to today's EDAP TMS Third Quarter 2024 Earnings Conference Call. At this time all participants are in a listen-only mode. Later you will have the opportunity to ask questions during the question-and-answer session. Please note, this call is being recorded and I will be standing by if you need any assistance. It is now my pleasure to turn today's program over to John Fraunces of LifeSci Advisors.

Good morning. Thank you for joining us for the EDAP TMS third quarter 2024 financial and operating results conference call. Joining me on today's call are Ryan Rhodes, Chief Executive Officer; Ken Mobeck, Chief Financial Officer; and Francois Dietsch, Chief Accounting Officer. Before we begin, I would like to remind everyone that management's remarks today may contain forward-looking statements which include statements regarding the company's growth and expansion plans. Such statements are based on management's current expectations and are subject to a number of risks and uncertainties that could cause actual results to differ materially from those described in such forward-looking statements. Factors that may cause such a difference include, but are not limited to, those described in the company's filings with the Securities and Exchange Commission. I would now like to turn the call over to EDAP's Chief Executive Officer, Ryan Rhodes. Ryan?

Thank you, John, and good morning, everyone. In the third quarter, we reported total worldwide revenue in U.S. dollars of $14.4 million, representing currency-adjusted growth of 11.6% on a year-over-year basis. Our core Focal One HIFU business continues to experience strong growth with a 48.2% year-over-year increase in revenues, reflecting continued adoption of Focal One by the global urology community. We placed three Focal One systems in the third quarter, which included a system placement at Virginia Commonwealth University, as well as placements in Italy and Spain. All three placements were cash sales, and the Focal One sale to Virginia Commonwealth University was our first placement in the State of Virginia. Virginia Commonwealth University is also one of only two National Cancer Institute-designated comprehensive cancer centers in Virginia. As noted on our second quarter earnings call, a growing number of leading U.S. cancer treatment centers are now using Focal One based on our technology's proprietary robotic platform that targets cancer cells in the prostate while sparing surrounding healthy tissue. As a reminder, last year in the third quarter, we saw several engaged customers delay their purchase of Focal One to the fourth quarter. We are experiencing a similar pattern of purchasing behavior this year. As such, we expect to finish 2024 with a strong fourth quarter performance. Positively, we have already closed a Focal One sale in the U.S. early in the fourth quarter with St. David's Hospital in Austin, Texas. St. David's is part of HCA Healthcare, the nation's leading provider of healthcare services, comprising 186 hospitals and approximately 2,400 care sites in 20 states and the United Kingdom. The cash sale at St. David's Hospital came at the conclusion of a successful evaluation period that demonstrated positive clinical outcomes, high procedure volumes, and favorable reimbursement while also meeting the hospital's strategic business objectives. This first sale in an HCA hospital has the potential to facilitate and accelerate the closing of future sales, as we are currently in discussions with multiple hospitals within the HCA Group. We also continue to experience strong growth in U.S. Focal One HIFU procedures. During the quarter, U.S. procedures grew 34% on a year-over-year basis, reflecting continued adoption by urologists who view Focal One as an important treatment option for delivering targeted focal therapy in earlier-stage prostate cancer patients. As mentioned during our last call, we believe that as the results from the groundbreaking HIFI study become more widely disseminated, demand for the Focal One platform will continue to grow. The HIFI study presents clear and compelling evidence that robotic HIFU therapy delivered by EDAP's proprietary technology is as effective as radical prostatectomy as a frontline treatment for localized prostate cancer management while additionally offering patients better functional outcomes concerning urinary continence and sexual function. As a reminder, EDAP technology was used exclusively to treat all patients receiving HIFU therapy in this study, including 90% with the Focal One platform. We anticipate the publication of the HIFI study results in a high-impact, peer-reviewed medical journal, which will provide Focal One HIFU with important visibility to aid in accelerating market adoption. I will now provide a brief update on Focal One reimbursement. The Center for Medicare and Medicaid Services, CMS, just released the final payment rules for 2025 on November 2. The HIFU procedure continues to be supported with favorable reimbursement with CMS finalizing a Medicare hospital payment rate of $9,247 as a national average per the adjusted corresponding local wage index factor. This rate will become effective on January 1, 2025, and represents a 5.4% increase over the 2024 payment. These reimbursement levels continue to support the favorable strategic business case for hospitals to both invest in and integrate Focal One HIFU while providing greater patient access to this valuable non-invasive treatment option. CMS also released the physician fee schedule for 2025, which continues to provide strong physician reimbursement for HIFU with 17.73 work relative value units or work RVUs and 29.41 total RVUs. These figures are significantly higher than any other prostate ablation procedure. Additionally, it provides physicians with a level of reimbursement that is more than 80% of the payment for performing surgery, including robotic radical prostatectomy. In conclusion, we are pleased with the continued support of the defined reimbursement levels for using HIFU, which provides a financially sound and sustainable economic offering for both the hospital and the physician. I would now like to briefly discuss some of our recent strategic collaborative activities. On September 19, we announced a very exciting collaboration with Avenda Health for the purpose of launching the world's first AI-assisted Focal One robotic HIFU procedures. Avenda's FDA-cleared unfold AI technology builds 3D patient-specific cancer maps that reveal the extent of the tumor boundaries while enabling physicians to deliver more precise and tailored treatments. By leveraging unfold AI's planning with the Focal One robotic HIFU platform, we believe that urologists can provide a more customized, patient-specific HIFU ablation procedure for treating prostate cancer. The first series of these Focal One AI-assisted procedures have already been conducted by Dr. Wayne Brisbane, Assistant Professor of Urology at the University of California, Los Angeles David Geffen School of Medicine. Thus far, we have received overwhelmingly positive feedback regarding the combination of these two groundbreaking technologies. AI represents an important and strategic next step in the evolution of the Focal One platform and will help us remain at the forefront of delivering the most advanced focal therapy treatment solutions for patients diagnosed with prostate cancer. During the quarter, we had a notable presence at several strategically important urology-focused scientific meetings. We conducted numerous Focal One simulated procedures at the 2024 joint meeting of the Focal Therapy Society and Society of Urologic Robotic Surgeons, which took place from September 19 through the 21st in Washington, D.C. During this scientific meeting, there was significant interest surrounding our Focal One technology, and this meeting served as an important venue for building our relationships with leading urologists in the United States. We also had a major presence at the 2024 Focal Plus Annual Meeting, which took place from October 17 through the 19th in San Diego, California. The Focal Plus meeting is particularly relevant to our business as the majority of attendees have a growing interest in utilizing focal therapy for prostate cancer. There were numerous presentations highlighting Focal One HIFU at the meeting, and we continue to see strong interest amongst urologists who recognize the need to offer a suitable treatment option between active surveillance and radical therapy. Early in the third quarter, we attended the 41st World Congress of Endourology in Uro-Technology meeting, which took place in Seoul, South Korea from August 12 through the 16. During this meeting, we provided dozens of hands-on Focal One simulations, which garnered strong engagement from the attending urologists. To quote Dr. Inderbir Gill addressing a large audience of urologists at the meeting, he said, 'Going forward, if you don't offer focal therapy, your prostate cancer practice will start shrinking.' Dr. Gill is a pioneer in robotic surgery and a world-renowned expert on urological disease and Chairman of Urology at the University of Southern California Keck School of Medicine. The WCET scientific meeting also featured a semi-live moderated Focal One clinical procedure conducted by Dr. Tarik Benidir, Clinical Assistant Professor at the University of Florida, which demonstrated numerous benefits of the Focal One robotic platform. I will now briefly touch on our clinical development programs in BPH and endometriosis. On October 1, we announced that the first patients were treated in our combined Phase I/II study evaluating Focal One robotic HIFU for treating benign prostatic hyperplasia (BPH). As a reminder, BPH represents an enormous market opportunity for Focal One. Globally, 94 million prevalent cases of BPH were estimated in 2019, and in the U.S. alone, as many as 15 million men currently have BPH symptoms. The Phase I/II study is a company-sponsored prospective multicenter clinical trial and is designed in two parts. The first part of the study is taking place at three leading institutions in France with recognized expertise in treating BPH as well as in using Focal One HIFU technology. Part one is designed to define the treatment parameters per protocol to effectively treat BPH with the goal of achieving optimal patient outcomes. Part two of the study will expand patient enrollment across a larger number of clinical sites to validate the safety and efficacy of the parameters defined in part one of the study. We are particularly excited about this program as the Focal One approach, compared to other treatment options, has the potential to better protect the integrity of the urethra and other critical structures. We believe that Focal One could become an important effective and less invasive treatment approach for addressing BPH. The ongoing Phase I/II study will also serve as a foundation for initiating a clinical trial in the United States next year. I'll now provide a brief update on our endometriosis program. As previously announced in July, interim results from our Phase III study evaluating robotic HIFU technology for the treatment of deep infiltrating endometriosis showed that robotic HIFU therapy maintained an excellent safety profile while demonstrating greater reductions in endometriosis lesion volumes compared to patients in the Sham arm of the study. Both arms of the study also showed significant improvements in pelvic pain reduction at three months from baseline as measured by the standardized visual analog scale. As previously reported, the primary endpoint of superior reduction in acute pelvic pain in the HIFU arm compared to the Sham arm was not reached. However, upon further review by the clinical investigators, this outcome was likely attributed to comparing differences in pain scores between the two arms of the study after only three months following the procedure. In our view, a therapeutic benefit favoring robotic HIFU is more likely to be confirmed over a longer period of time post-procedure, as suggested by the stabilization of pain scores at six and 12 months from our published peer-reviewed Phase II study. At present, the study is now unblinded, and patients have been allowed to cross over to the HIFU arm protocol. I'm pleased to report now that 85% of the patients from the Sham arm have already elected to cross over into the open-label extension arm of the study and receive treatment with robotic HIFU. This is not surprising, as the pain symptoms for these Sham patients returned to their high baseline levels after one year post-procedure. In contrast, the patients from the HIFU arm who were evaluated one year following robotic HIFU treatment maintained a similar level of improvement over their baseline pain symptoms as measured at three months post-procedure. Importantly, these findings are consistent with the significant reduction in lesion volume as measured by MRI, which was observed in the HIFU arm, only following the unblinding of the study. This additional data continues to suggest that HIFU therapy is a safe, non-invasive treatment with significant potential to reduce pain for women suffering from this debilitating condition. Between now and year-end, we anticipate meeting with the FDA to discuss this additional data while determining the next steps for this program. Before handing the call over to Ken to review our third-quarter financial results, I want to briefly mention a change to our Board of Directors. Following the departure of Marc Oczachowski, we appointed our existing Board member, Dr. Lance Willsey, to serve as Interim Board Chair effective September 30. Dr. Willsey is playing an active role assisting the executive team while we continue to search for a permanent replacement. Dr. Willsey was first appointed to the EDAP Board of Directors in December 2023 and has since made valuable contributions to help guide our strategic planning as we expand the Focal One platform across the global urology market. Dr. Willsey is a trained urologist with over 35 years of private and public board experience focused on cancer diagnostics and therapeutics. He completed his surgical and urology training at the Massachusetts General Hospital and additional postgraduate training in the Steele Lab at Harvard University and the Dana-Farber Cancer Institute. I will now turn the call over to Ken to review our third-quarter financial results.

Thanks, Ryan, and good morning, everyone. Please note that all figures except for percentages are in euros. For conversion purposes, our average euro-dollar exchange rate was 1.101 for the third quarter of 2024. Total worldwide revenue for the third quarter of 2024 was €13.1 million, an increase of 11.6% compared to total worldwide revenue of €11.7 million for the comparable period of 2023. This was a record for third-quarter revenue performance. Looking at revenue by division, total revenue in the HIFU business for the third quarter of 2024 was €4.5 million compared to €3 million for the third quarter of 2023, which represents growth of 48.2% year-over-year. We placed three Focal One systems in the third quarter, and all three placements were cash sales. Third-quarter worldwide HIFU disposable revenue grew 35.3% on a year-over-year basis, reflecting strong U.S. procedure growth. Total revenue in the distribution business for the third quarter of 2024 was €6.6 million compared to €6 million for the third quarter of 2023. Distribution revenue was driven primarily by recurring revenues from laser sales. Total revenue in the LITHO business for the third quarter of 2024 was €2 million compared to €2.7 million for the same period in 2023. The decrease in LITHO revenue was due to selling three lithotripsy units in the third quarter compared to seven units sold in the third quarter of 2023. Gross profit for the third quarter of 2024 was €5.2 million compared to €4.2 million for the year-ago period. Gross profit margin on net sales was 39.4% in the third quarter compared to 35.5% in the year-ago period. The increase in gross profit margin year-over-year was due to a favorable shift in Focal One product mix and positive absorption in the factory. Operating expenses were €11 million for the third quarter compared to €9.7 million for the same period in 2023. Operating expenses increased primarily due to investments made to support Focal One commercial operations globally. Operating loss for the third quarter of 2024 was €5.8 million, which was relatively flat compared to an operating loss of €5.6 million in the third quarter of 2023. Net loss for the third quarter of 2024 was €6.4 million or €0.17 per diluted share, compared to net loss of €3.9 million or €0.11 per diluted share in the year-ago period. Turning to the balance sheet, ending inventory was €21 million in the third quarter of 2024 compared to €15.1 million at the end of the fourth quarter of 2023. As I mentioned last quarter, we have made advanced purchasing decisions related to ultrasound technology, and we have built additional Focal One and ExactVu inventory in anticipation of higher demand. Also, as a result of new medical device requirements under CE Mark, multiple ESWL units had to be manufactured in advance of these new requirements becoming effective. We anticipate selling the ESWL inventory down by the first half of calendar year 2025. Total cash and cash equivalents at the end of the third quarter was €25.5 million compared to €43.5 million at the end of the fourth quarter of 2023. The €18 million decrease in cash and cash equivalents on a year-to-date basis was attributed to spending on operating activities, including inventory investments, as I described earlier, capital investments to help grow the HIFU business, and the paydown of long-term borrowings. We remain focused on optimizing our investments from both an operating and cash resource perspective to effectively manage and grow our Focal One business in the long term. Those are our key financial highlights for the third quarter of 2024. And with that, I would like to turn the call back to Ryan.

Thanks, Ken. As we look outward, we are making significant investments to capitalize on the growing focal therapy market opportunity with the most advanced technology platform and a growing installed base of Focal One systems at leading institutions and hospitals. We are achieving this strategic objective as we build an important new treatment category for prostate cancer that lies between active surveillance and radical therapy. While building a new treatment category takes time and effort, there is no question that this paradigm shift in the treatment of prostate cancer is taking place. We believe Focal One is fast becoming the leading technology platform that will dominate this new treatment category for years to come. As we grow, we continue to deploy our talent and capital in a highly strategic manner to build relationships across a continuum of stakeholders, including all the urology majors, large hospital networks, and urology fellowship programs. Through these efforts, we are creating world-class robotic HIFU treatment programs to ensure that Focal One is being fully utilized and that more urologists are trained early in their careers to use this important technology. As discussed in my prior comments, we are also attending the most relevant urology-focused scientific conferences around the world and integrating cutting-edge technologies such as AI to further extend our market and technology-leading position. These combined efforts are translating into commercial success, demonstrated not only by our consistently strong year-over-year procedure growth in the U.S. but also by the strong Focal One adoption among the most well-recognized cancer treatment centers. In fact, Focal One is now installed in over one-third of the National Cancer Institute-designated comprehensive cancer centers, and we expect that percentage will continue to grow. As more urologists embrace Focal One, higher utilization will lead to more clinical data, and this data will gain more attention at upcoming urology meetings. This data will also lead to more peer-reviewed publications, which further validates the technology and will provide a basis for expanding robotic HIFU in the treatment guidelines for prostate cancer. As urologists' enthusiasm and adoption for Focal One continues to grow, we also see increasing demand coming directly from patients, who will increasingly seek effective less invasive treatment options that fall between active surveillance and radical therapy. Patients and their doctors want to address cancer earlier in the course of the disease while maximizing quality of life outcomes. Focal One, as a non-invasive therapy providing excellent oncologic control, represents an important treatment option for many of these patients. As we have discussed on past earnings calls, I believe we are in the early stages of an important and positive shift in how prostate cancer is being managed. We are executing on our strategic goal of establishing Focal One as the premier robotic HIFU therapy for prostate cancer, which we believe will generate significant value for our shareholders. With that, I would now like to turn the call back over to the operator for questions.

And we will take our first question from Michael Sarcone with Jefferies. Please go ahead, your line is open.

Good morning and thanks for taking the question. I guess just to start – can you elaborate a little more on what you're seeing just in the – among the hospital customers and the Focal One pipeline, three placements this quarter. I think last quarter you said you were expecting second-half placements to exceed the first half. Is that still the case? So yes, basically, the pipeline, what you're seeing in the hospital environment and then 2H versus 1H placement? Thank you.

Yes, Michael. We saw good activity in the third quarter. Of course, we're always building our pipelines. We had a few sales that slipped into Q4, as noted. We are still planning on having a stronger back half of the year, the second half of the year. We continue to see momentum and high-level engagement in many of our pipeline customers. Coming off a number of very key scientific meetings, there has been strong clinical interest from many urologists in attendance at those events. So yes, we do continue to see strong growth in the second half of the year.

Got it. Thank you. And you're still seeing nice Focal One procedure growth in the U.S. year-over-year. Ryan, I was wondering if you could just maybe elaborate somewhat on how utilization per customer or account has been trending and maybe where that stands today?

Yes. So as we're adding really a new treatment service line when we launch our Focal One program, there's a ramp period. We view our accounts objectively as programs. So we build these programs, launch them, and then there's typically a ramp and training period. We continue to see hospitals increasing their procedures, some faster than others. But the commitment is there. As noted, we made an announcement regarding reimbursement. Reimbursement continues to be strong. So the economics support the activity. The key thing we observe is increased clinical value demonstrated by a number of our installed users. The data presented at several local and national scientific meetings has been very positive. Additionally, some hospitals are now turning on more marketing activities to attract a broader patient population. So, again, good healthy growth in procedures. It's something we pay a lot of attention to. We have a bifurcated sales force, one focusing on capital and the other on clinical. We continue to monitor adoption at each account and utilization by each urologist trained on using Focal One.

Great. Thank you, Ryan.

Hi. Good morning, guys. This is Sean here for RK. And thanks for taking my questions. I just have two quick ones on the clinical programs. So regarding the BPH study, when can we expect the initial results from that? And what kind of data would that entail?

Well, as noted, we're on the journey of a Phase I, Phase II study. So results we would not see until sometime later next year. Again, we are combining these two parts of the study to accelerate our scientific findings around treatment parameters, etc. We have three sites now that are active and have the ability to add additional sites. Once we get through some of the early work we're doing now, we will expand to other sites. So it won't be until later next year. We'll be excited to present some of that data and those findings accordingly.

Great. One quick follow-up on that. How many patients are expected in the first two parts?

Yes. Well, it's truncated per the protocol. It's broken down into various numbers. We have a subset of 30 to expand above 30 to 60. It's called out directly in the protocol. The key to understand in this study is that we combined both parts of the study, right, the Phase I and Phase II parts. As we look at that, our goal is to accelerate to more sites. Once we look at treatment parameters, including volume, treatment location, and really setting up the procedure for a wider group of participants, we'll be able to adjust those numbers accordingly as we move forward and develop additional new study protocols.

Great. Thank you for that. In the prepared remarks, you mentioned that the company expects to initiate a BPH study in the U.S. next year as well. Would that mirror this French study? Or would you modify it based on what you see in the first study?

Yes. So we want to take the results of the combined Phase I/II study to expand to multiple sites. While doing that, we'll be looking at protocol design to get in front of the FDA sometime next year. So again, we're accelerating this process and looking to expand into additional sites. We would work closely with our investigators to develop the right protocol that would suit the needs for the FDA.

Thank you for that clarification. And my final question on the endometriosis program. You mentioned that the longer-term effects are more likely to be seen. How long are you continuing to follow these patients for longer? And when do you expect to release these longer-term results sometime down the line?

We have the ability to follow these patients, and we can continue for up to 12 months and beyond. We're monitoring these patients closely. We've shown a high safety and use of the technology. We've demonstrated a reduction in size of the lesions under MRI visualization in the HIFU arm. We've also shown a crossover rate of 85%, meaning that patients who were followed in the original study, once unblinded, returned to their baseline pain scores. This indicates that the follow-up time at three months was probably not adequate to prove the data endpoints we needed post-treatment. Our goal will be to use the latest data analysis and follow-up for discussions with the FDA soon. We're excited about these recent findings as we've uncovered more. We have high belief in the procedure, and we will continue to look positively outward.

Great. Thanks for taking my questions.

Thank you.

Thank you. It seems there are no more questions on the phone. I will now hand the program back to Ryan Rhodes for any additional or closing remarks.

I want to thank everyone again for joining us on today's call, and we look forward to seeing you at the upcoming Jefferies London Healthcare Conference on November 19 and the following month at the Piper Sandler Health Care Conference in New York City. Thank you.