Tom Burns
Analyst · Ravi Misra of Berenberg. Your line is open
Thank you, Chris. Good afternoon and thank you for joining us today. The coronavirus global pandemic has created an unprecedented time for all of us in different ways, both professionally and personally. I want to start by saying on behalf of everyone at Glaukos, that our hearts go out to all those affected by COVID-19 and we are especially grateful for the healthcare workers and first responders who are selflessly serving on the front lines. Before we talk about our first quarter performance in the current trends on our business. I want to provide an update on what we've been doing at Glaukos in response to this rapidly changing environment. I have been thoroughly impressed with the response and resiliency of our employees around the world, who make up the strong foundation of our disruptive franchises in glaucoma, corneal health and retinal disease. Despite negative personal and professional impacts induced by COVID-19, our employees have initiated a new fundraising campaign through the Glaukos charitable foundation that allows them to contribute money to charitable organizations providing relief for those affected by this pandemic. I want to especially thank them for their dedication and commitment to maintaining their important work to move the company, their families and their communities forward during this challenging time. I am confident we will get through this together and emerging even stronger, more efficient and more capable company. We are also building upon our longstanding mission to offer product donation and patient assistance programs providing access to our technology for those who lack access to care insurance, including those who have lost insurance benefits due to the COVID-19 pandemic. As a current situation emerged, we immediately developed and implemented, implemented business contingency and continuity plans beginning in the first half of March and executed on several key initiatives, as the current crisis began to unfold globally in mid to late March. Our response plans were guided by several key priorities. First, protect the health and safety of our employees and their families. Second, to support our customers. Third to preserve jobs globally. Fourth, to protect core research and development projects. And finally fifth to maintain our strong financial and operating position following this pandemic. As many of you know, the safety first mantra is at the core of our Company's foundation and our patient centric mission, yes these past few months have greatly expanded the importance of that commitment in really an entirely different way. Our top priority has been to protect the health and safety of our employees and their families, our customers and their patients, our clinical investigators, our suppliers in the communities in which we operate. While the majority of our employees have been required to work-from-home, we have maintained streamline manufacturing and assembly processes in order to consistently provide product to our customers who depend on us. Glaukos employees involved in such operation critical processes have been organized into a number of small shifts designed to minimize the time anyone individuals required to be on site. We've implemented numerous health and safety protocols that our sights following CDC guidance and local regulations and we'll update those as needed going forward. I'm pleased to say that both of our main sites continue to operate during this period, albeit differently. And our supply chains have experienced minimal disruption to date. In order to sustain us through this period of uncertainty and maintain jobs and our strong capital position, as we come out of this pandemic, we have implemented a number of cost-containment measures. These include substantial reductions in discretionary spending and capital expenditures, temporary salary reductions for our executive team, senior leadership and many others throughout the company as well as other employment actions. And Joe will elaborate on these later. While we are not immune from the economic impact from COVID-19, we did like -- I would like to forgo pursuing the CARES Act PPP funding, so that this important source of capital could be directed to the truly small businesses in our communities that needed for survival. We believe our cost saving initiatives paired with our strong balance sheet, leave us well positioned to ultimately provide our central ophthalmic therapies to customers and their patients who will return for treatment as we move past the peak of this current prices. We were pleased with the -- strengthening business trends experienced as we progressed until late February and early March it is health care system shifted resources to the treatment of COVID-19 and government restrictions on elective procedures and therapies were implemented throughout the world, we experienced material disruptions to our business. I think, March these restrictions led to increase in deferral of Cataract and care to [indiscernible] procedures and global sales trends that were less than 15% of levels achieved prior to the COVID-19 operate. Although our near-term sales have been temporarily disrupted, our commercial focus does not as we remain committed to deepening our customer relationships in new and creative ways. We have sponsored customer oriented webinars hosted by well-respected ophthalmic surgeons to provide our customers with value-added insights into relevant hot topics such as the CARES Act. The current state of electric procedures, key business and operational considerations for an ophthalmic practice during this time and planning guidelines for reopening. Our sales professionals remain hard at work maintaining close engagement and dialog with the customers through remote online training modules, regional conference calls, highlighting the performance of our technologies, interactive case space tutorials and various other customer support initiatives. With a market access, our team in conjunction with our customers, continues to work with providers and payers to optimize the [indiscernible] the reimbursement landscape, train office staff on claims and contractual processes and expand our arch claims program. Internally, we continue to execute on our commercial integration plans through cross-functional training, key account targeting and market segmentation deployment. While many of our customers practices have been largely shut down during this time our commercial focus and customer dedication remains strong enduring partnerships we have built over the years with our customers are more important than ever. We are proud to partner with them as they navigate through these unprecedented times. Our commercialized ophthalmic solutions address chronic diseases -- diseases that only worsen as patients are often treated. Given the medical necessity of these interventions, we believe most of these deferred procedures will ultimately be performed in the future as a COVID-19 pandemics subsides, while remains difficult to predict the specific timing and slope of this recovery curve. I'm encouraged by the recent indications of plateauing and even declining infection rates and deaths from COVID-19 in many areas of the world, along with many US states that have become the reopening process. At the same time, we recognize the challenges and risks in the potential unpredictable -- spikes in COVID-19 infection rates, that remain ahead of a vaccine or therapeutic solution. We continue to analyze, both the COVID-19 drivers of return to treatment and customer input regarding their restart plans and processes. Not surprisingly, we see a variety of potential scenarios for our business as ophthalmic practices begin to reopen and elective procedures, return. From a higher level, we currently expect to phased and deliberate return beginning slowly in May and June to increasingly more normalized levels for cataract and care to comments [ph] procedures. By later 2020 subject to any resurgence of COVID-19 in the fall on winter months. A rate of return for elective surgery may also be driven by site of service, site restrictions and type of care with the physician office and ambulatory surgery center settings, recovering before hospital based procedures. As a reminder, all of our glaucoma technologies are used in outpatient surgeries, 80% of which in the United States are estimated to be performed in ASCs. And our for [ph] solution for keratoconus is primarily performed in the physician's office. Reopening process will include heightened and safety protocols to ophthalmic practices to ensure the safety and instill patient confidence. We will close to support customers as they bring capabilities back online and follow the reopening guidelines and recommendations from the CDC, coronavirus task force, The American Academy of Ophthalmology and other key societies' detail and specifically [indiscernible] approach and manage. Some of the key decisions and reopening more normal practice in the post COVID-19. We know our customers are eager to get back to work to treat their patients and we're ready to support them. Moving onto our pipeline, which consist of 13 publicly disclosed programs and various development and clinical stages and another 10 yet to be disclosed development programs also underway. A number of these pipeline programs are in active pivotal clinical trials including iStent infinite at beyond and iDose TR. For these trials, we are actively assessing potential impacts due to COVID-19 disruption. Our top priority within clinical operations is to protect the health and safety of our clinical field personnel, investigators and participants currently enrolled in our clinical trials and in addition, we've implemented a number of measures to maintain the integrity of these trials in a manner to fully satisfy regulatory requirements. We've worked with clinical investigators to closely monitor and to help assure patient compliance with clinical trial protocols and are also planning numerous virtual investigator meetings over the coming weeks. We're encouraged with the FDA's recent communication and position on these clinical trial matters during COVID-19 pandemic and we'll continue to collaboratively work with the agency to advance our clinical programs in a safe and timely manner to ensure study by our ability. Clinical trials for iStent infinite and [ph] have already fully enrolled and although they may experience some modest delays and patient follow our plans. We continue to express confidence in our previously disclosed FDA approval targets of late 2021 and '22 respectively. For iDose where we have been rapidly progressing to patient enrollment completion, the temporary closure of ophthalmic practices and deferral of electric procedures cost like Covid-19 has led to a temporary pause on new patient enrollment, as investigator sites begin the process of reopening to more normal ophthalmic practice, we will work with our clinical partners to reignite the enrollment momentum that we'd previously built. While the situation remains fluid as of now, we believe that iDose may continue to be impacted well beyond the current shut down as doctors' focus on clearing their patient backlog over clinical trial enrollment. We plan to provide further updates on this front as we gain additional visibility in future quarters. Importantly, despite this transit disruption, we maintain a high degree of confidence in the integrity and viability of our high-dose clinical program. Given the trial's design and protocol. We also remain an early preparations for the potential US commercial launch of Santen's Pharmaceuticals' pressure flow MicroShunt and elegant AV external surgical implant for late-stage glaucoma management. During this time, we want to reassure our stakeholders that we are continuing to invest in our future. We have prioritized the investments we are making to focus on our near-term pipeline programs that we believe may drive significant value creation for our company over the coming years, balanced by earlier stage development projects where costs made be deferred. That said, we continue to advance our development efforts on our core-clinical stage development programs, as well as our dry eye and retinal R&D programs. One such investment priorities is within our expanding corneal health franchise, we're -- extremely pleased with the integration process and progress as we execute on our corporate milestones, commercial strategies and cost synergy goals. While we remain in the early stages of unlocking to the combined organizations for potential, we are encouraged with the market receptivity to our fully integrated expanded commercial organization and the customer-friendly initiatives we've introduced, which helped drive more than triple the number of capital placements in the US during the first quarter of 2020 versus the prior year period. These initiatives are also producing tangible results with end-market access, where we continue to solidify consistent payment for TREXs product specific J code which is now covered for 96% of commercial payer lives. We also making substantial progress across a number of other business fronts with key accomplishments that include high iStent inject regulatory approval in Japan, a standalone indication approval in Australia, a tariff increase in the United Kingdom and an average increase of 44% to over $300 on professional fee over 0091T [ph] professional fees from Meridian [ph]. Our Medicare administrative contractor with jurisdiction in 13 Western US states. In summary, while we continue to actively monitor COVID-19 in this business disruptions, I remain confident that the longer term fundamental prospects of our business remain strong as we seek to create a unique strategic vision care leader building thriving franchises in glaucoma, corneal health and retinal disease with novel therapies that disrupt, conventional treatment paradigms, improve patient outcomes and create new robust market and market opportunities. So with that, I'll turn the call over to Joe to discuss our first quarter 2020 financial results. Joe?