Jeff Dunn
Analyst · Morgan Stanley. Your line is now open
Thanks, Lynn. Good afternoon, and thank you for joining us. I'm pleased to welcome you to SI-BONE's second quarter 2019 earnings call. Before we get started, I'd like to announce that Laura Francis has been promoted and will now serve as both Chief Operating Officer and Chief Financial Officer for SI-BONE. Across these roles, she is responsible for finance, accounting, treasury, supply chain operations, quality, IT, facilities and human resources. During her time at SI-BONE, Laura has demonstrated exemplary leadership, integrity, problem-solving acumen and dedication. We look forward to her continued contributions. Turning to our business results. We made important progress during the second quarter. Total revenue was $16.3 million, growing 19% over 2018. U.S. revenue was $15 million, representing 24% growth over the same period last year. And international revenue for the quarter was $1.3 million. Our second quarter results demonstrated momentum as we expanded our commercial footprint for providing differentiated surgical devices in the sacropelvic space. This was particularly evident in the U.S. where we have seen accelerating growth since the end of 2018. We are starting to see the impact from growing payer coverage and sales force expansion. We expect further productivity gains in the back half of this year as our newer sales reps ramp toward full productivity. As a result of this momentum, we recently reached a very important milestone. iFuse has now been used in more than 40,000 procedures by more than 1,900 surgeons worldwide. This achievement confirms the growing attention and focus on sacroiliac joint dysfunction and its role in lower back pain as well as the joint's importance as part of our musculoskeletal system. It is gratifying that so many patients who have suffered for years are now able to regain [Technical difficulty] who become potential candidates for surgery, due to their debilitating SI joint dysfunction, we believe we are still just at the beginning of this journey. On the sales and marketing front, we ended the second quarter of 2019 with 50 direct sales reps and 37 clinical support specialists. We're encouraged by these quality additions to our growing sales team and are firmly on track to reach our goal of adding 10 to 15 direct sales reps and 25 to 30 new CSSs by the end of the year. As a reminder, these expected additions will bring us close to a 1:1 ratio for direct sales reps to clinical support specialists in the U.S. And we will get our total count to over 100 reps in the field by the end of the year. In addition to our U.S. sales force expansion, our medical affairs team remains focused on training, educating and supporting new surgeons, we are on track to increase the number of active surgeons from 450 during the fourth quarter of 2018 to 550 by the fourth quarter of 2019. Turning to our international opportunity, we experienced some residual weakness in Germany related to our previous revenue issues from the second half of 2018. As we mentioned on our last call, we have made important investments to improve our situation in Germany. In line with these efforts, our new head of sales has made significant changes in the field personnel that were necessary to drive the business forward. This transition resulted in a few open territories during the second quarter, which impacted the region's performance. Outside of Germany, our operations in the U.K., France, and Italy are driving growth in-line with our expectations. Looking ahead, we expect international Q3 revenue to be relatively in-line with the second quarter, and we anticipate incremental improvement over the next 12 months as the new German team ramps to full capacity, while other countries continue to execute. Turning to clinical evidence. SI-BONE has always been a company grounded in robust and high quality, long-term data and we remain committed to building on our vast body of clinical evidence. In line with this commitment, five-year follow-up results from LOIS, a long-term prospective study, were recently submitted for publication. At five years, the data demonstrates durability of the clinical benefit related to the procedure and further supports the benefits of minimally invasive sacroiliac joint fusion with iFuse. We believe our superior clinical data is a key component of growing positive support from clinical evaluation organizations and garnering payer wins, many of which are exclusive to iFuse based on our clinical evidence. We will leverage the extended results from LOIS with our existing data to drive progress on the reimbursement front and pick up the remaining U.S. commercial payers that currently do not cover iFuse. From a reimbursement perspective, there has been a draft update on the surgeon payment for minimally invasive sacroiliac joint fusion under CPT code 27279. In July 2017, the code was identified as mis-valued by the CMS in the Federal Register. On July 29, 2019, CMS proposed to maintain the current work RVU of 9.03 as recommended by the RUC, resulting in a surgeon payment of $720 for Medicare. U.S. commercial payers generally follow this recommendation, although they pay 20% to 30% more on average than Medicare. Following this proposal, CMS solicited public comment on whether an alternative valuation would be more appropriate. That said, we're confident in our ability to grow in the U.S. with the current and proposed surgeon payment and will continue our efforts to improve the reimbursement landscape for hospitals, physicians and patients. We are also continuing to see increasing interest in our iFuse Bedrock technique, which we believe is an important advancement in how surgeons treat adult deformity patients. As a reminder, in November of 2018, the Bedrock technique was cleared by the FDA for use in adult deformity surgeries in patients with SI joint dysfunction. In April, we received an additional FDA clearance to expand the indication to cover any long construct procedure in which the surgeon wants to stabilize the SI joint. The Bedrock technique allows the surgeon to place one iFuse implant on each side of the sacrum with a posterior approach or up to three implants on each side with a lateral approach in conjunction with a multi-level spinal fusion. Biomechanical testing data shows that the addition of iFuse implants placed using the posterior Bedrock technique reduces SI joint motion by 30% more than an S2AI screw alone. Adult deformity surgery represents one of the fastest-growing segments of the spine market with an estimated 50,000 procedures last year, of which 25,000 involved fusions down to the sacrum. Acknowledgment of the SI joint as a pain generator by key opinion leaders is foundationally important to the adoption of this technique. Following our U.S. surgeon summit this past May, we hosted a Bedrock symposium in Amsterdam in early July at the International Meeting on Advanced Spine Techniques. Presenters included Dr. David Polly from the University of Minnesota, Dr. Chris Shaffrey from Duke, Dr. Isador Lieberman from Texas Back Institute and Dr. Juan Uribe, from Barrow Neurological Institute. The symposium was attended by surgeons representing leading academic institutions from around the world, including the Netherlands, Germany, Switzerland, Italy, Hong Kong, and the U.S. The key opinion leaders discussed tactics for increasing awareness of the SI joint as a pain generator and the value of the Bedrock technique and technology. Long construct deformity surgery was also a key area of focus at the 16th Annual State of Spine Surgery Think Tank meeting in late June. Presentations were given by Dr. Frank Phillips from Rush on the effects of long construct fusions on the SI joint, Dr. Juan Uribe from Barrow on the biomechanical effects of long construct fusion on the SI joint, Dr. Rush Fisher from Christiana Spine on why he fuses the SI joint in adult deformity patients, Dr. Josh Heller from Jefferson University on a single center study showing rates of SI joint pain in adult deformity patients and Dr. Robert Eastlack from Scripps on the technique for the Bedrock approach. We are encouraged by this growing interest in the Bedrock technique at leading academic institutions where the majority of long construct deformity surgeries are performed. We have a fantastic team of passionate and dedicated individuals focused on transforming sacropelvic treatment. To that end, we were thrilled to welcome Mark Foley and Heyward Donigan to the SI-BONE team as new members of our Board of Directors. Mark brings more than 25 years of operational and investment experience in health care, including having been Chairman, President, and CEO of ZELTIQ Aesthetics from 2012 through the company's acquisition in 2017 by Allergan. Heyward brings more than 30 years of payer and digital health experience, including executive leadership positions at Cigna, Premera Blue Cross Blue Shield and Empire Blue Cross Blue Shield. I'm delighted that SI-BONE can benefit from their respective leadership experiences, which span multiple technology and health care companies as well as the private payer landscape. Finally, I'd like to take the opportunity to congratulate Laura on her expanded role. I will now turn the call over to her for details on our financial performance then will return with closing comments.