Marc Oczachowski
Analyst · Lake Street Capital Market. Please proceed with your question
Thank you, Philippe. Good morning and thank you for joining our call. As Philippe highlighted, we have had a strong first half of the year. It was indeed very strong and positive not only by the numbers we produced, but also with the quality of the progress in major projects on which we continue to focus our time and efforts. We have high expectations thanks to this great and solid momentum in our overall performance and we look forward to continuing this trend. Since the beginning of the year, we have sold six HIFU devices in the US, including three in the second quarter. Let me provide you with a couple of specific examples in the quarter that demonstrate how our differentiated sales model can help us serve a larger portion of the addressable market in many different contexts. Rochester Regional Health in Upstate New York is an existing EDAP customer and user of our Ablatherm HIFU device which they utilized by a relationship with American HIFU, a mobile medical equipment provider. Rochester Urology Group then decided to purchase a Focal One machine outright from EDAP and use it in their prostate cancer treatment protocol. Being one of the pioneers in using HIFU in the US, Dr. John Valvo wanted to continue in his innovative vision of treating prostate cancer by upgrading his practice to requiring the latest innovation of HIFU device and continuing to lead the trend of non-invasive and focal ablation of prostate tissue. The University of Chicago medicine surgical team, on the other hand, did not have a lot of experience with HIFU technology. The team performed its first HIFU test using the Ablatherm device in 2017 and has since acquired a Focal One device for their prostate cancer program. Dr. Shalhav, chief of urology surgery, explained that Focal HIFU is bridging a significant void between i-sys surveillance, or a watch and wait approach, which can be stressful, and radical treatments like code 9 removal or radiation. It's indeed bridging the gaps and allows patients to maintain their quality of life. Focal one and its ability to deliver highly targeted treatment to the prostate was the perfect solution. The level of accuracy and safety of Focal One as the latest generation of HIFU device made a clear difference in the decision process. Finally, Houston Methodist Hospital was one of the first hospitals in the US to offer Ablatherm robotic HIFU in early 2016. They wanted to upgrade to a Focal One and upgrading [ph] the Ablatherm. However, the hospital later decided that they wanted to offer a broader HIFU program using both Focal One and an Ablatherm. Houston Methodist wound up buying back the Ablatherm for another of their hospitals and are now one of our biggest customers, and they use both our Ablatherm and Focal One on a very regular basis. They not only upgraded to Focal One technology in their HIFU practice, but they clearly extended their HIFU operations by having two HIFU devices in their group of hospitals in Houston, Texas. We are very excited and pleased to report continued strong growth in HIFU revenues during the second quarter of 2019 compared to the same quarter of last year. This growth is mostly driven from US HIFU revenues, which reflects the continued enthusiasm and momentum that our latest generation, state-of-the-art HIFU technology is receiving in the US since clearance from the FDA in June of last year. Based on this positive feedback, we are optimistic that this could be the beginning of an inflection point in terms of greater Focal One adoption and market penetration. Going forward, our communication strategy is not to continue to announce each and every US sale of Focal One, but we will definitely keep the market updated on our sales and placement advances regularly during the quarterly calls. As a reminder, our HIFU business generates a higher gross margin which has led to significant expansion of our overall gross margin. The gross margin leverage has dropped to our bottom line and driven our third consecutive quarter of profitability for EDAP. Our goal is to continue to improve these metrics and further enhance our profitability as the mix of HIFU to overall revenues continues to grow. We had a very productive presence at the AUA meeting in May, which helped to fill our pipeline of potential customers. We look forward to updating you on this momentum going forward. We also reported a major development that occurred during the second quarter of 2019, which was the very positive update on the reimbursement front. The American Medical Association's CPT editorial panel, at its May 2019 meeting, accepted our request to establish a new Category 1 CPT code that will facilitate the reimbursement of the ablation of malignant prostate tissue with HIFU technology. The CPT-specific code description selected by the panel is ablation of malignant prostate tissue, transrectal, with high-intensity focused ultrasound. The establishment of the CPT code is significant because it allows for reimbursement of for both the technical fee as well as additional reimbursements to the surgeon. In contrast, the C-code only provides for reimbursement of the technical fee [indiscernible]. We believe the additional reimbursement afforded by the new CPT code will serve to further accelerate adoption of this technology within the urology domain. This is a significant milestone for EDAP as it now gives us a line of sight to definitive reimbursement and provides confidence and visibility to the marketplace about the clinical effectiveness and financial viability of the use of HIFU technology. As part of the process of developing specific reimbursement guidelines, the American Urology Association and the American Medical Association has commenced a survey of the market in order to determine the value level of this procedure code. The survey is ongoing and should be completed shortly and presented at a panel before the end of the year. We look forward to specific reimbursement details in mid-2020. To the extent that we are able, we will communicate these to our analysts and investors as they evolve. The code will be included in the next CPT code group in 2020 and will be effective on January 1, 2021. Beyond the US market, we continued to experience strong momentum with Focal One, in particular we're continuing to focus on expanding our presence in large markets such as Brazil where we completed one Focal One sale in the second quarter and now have an installed base of six machines in the country. Mirroring what we're seeing in the US, our sales pipeline continues to grow in key ex-US territories and we look forward to announcing future deals and placements. HIFU is the most advanced ablation technology available and we remain focused on developing this technology. With HIFU continuing to get recognition among surgeons and with the enhanced awareness of the Focal One system since gaining FDA approval for prostate tissue ablation, we are focused on developing a HIFU platform [indiscernible] ablation indication. In terms of our ongoing development activities, we continue to refine plans for both the multicenter Phase II study of Focal One for the treatment of rectal endometriosis and a Phase II study using [indiscernible] HIFU prototype to treat liver metastasis. These are both high need indications. And if we're successful, these activities will further expand our position as the global leader in minimally invasive therapeutic Ablatherm. In summary, we're very pleased with every aspect of our second quarter results. The reported revenue growth and the gross margin expansion speak to the significant unmet medical need that we are able to address with Focal One. We are excited with our current growth trajectory. And with further clarity on reimbursement, we anticipate good things to come. And now, our CFO, François Dietsch, will provide a review of our financial results. François?
François Dietsch: Thank you, Marc. 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 $1.1241 for the second quarter of 2019 and $1.1297 for the first half of 2019. Total revenue for the second quarter was €12.5 million, an increase of 45.1% versus €8.6 million in Q2 2018, reaching a new record level for second quarter. Our HIFU division generated sales of €12.6 million, representing an increase of 98.3% versus Q2 2018 HIFU sales of €2.3 million. During the quarter, EDAP sold five HIFU devices, including three in the US versus one Focal One during the same period of 2018, and we recorded a 60.9% increase in HIFU treatment revenue. Our UDS business bounced back nicely from the first quarter, with €7.9 million of revenue, which is a 25.9% year-over-year increase. We sold 8 lithotripsy devices in the quarter versus 10 in the same period last year. The growth was driven by a 43.7% increase in sales of distribution product. Gross profit for the second quarter of 2019 was up 78.3% to €6.3 million from €3.6 million for Q2 2018. Gross profit margin on net sales was 60.7% in Q2 2019 compared to 41.3% in the year-on-year period. The increase of 9.4 percentage points was driven mainly by the increase of HIFU activity which has better margin. The strong increase in the gross profit drove the third consecutive quarter of global profitability. The operating profit for the second quarter of 2019 was then €1.7 million compared to an operating loss of €1.1 million in the year-ago period. Net income for the quarter was €1.4 million or €0.05 per diluted share.