Glen French
Analyst · Stifel. Go ahead Rick
Thank you, Laine. Good afternoon everyone and welcome to our third quarter 2022 earnings call. Here with me is Derrick Sung, our Chief Financial Officer. We remain excited about the $12 billion opportunity to establish our clinically proven Zephyr valve therapy as standard of care for the over 1 million patients around the world who suffer from severe emphysema and are profoundly short of breath, despite high-dose medications. Over the past 2.5 years, our business has been severely impacted by COVID surges, filling ICU beds and negatively impacting our procedure volumes. Thus, we are pleased to see that looking forward, despite the continued prevalence of COVID, healthcare systems in most places are adapting to the new normal, and we are moving into a more predictable macro environment for our business. Reflecting on the third quarter, we generated worldwide sales of $13.5 million, representing growth of 2% year-over-year and 7% on a constant currency basis, with $8.4 million coming from the United States, representing growth of 22% compared to the same period last year. While we feel we are moving into a more favorable steady state, our business in the third quarter was negatively impacted by continued foreign exchange headwinds, in addition to two key dynamics, which we’ve mentioned on our last call, hospital staffing constraints and seasonality. Hospital labor constraints, while not getting any worse, continue to limit procedure capacity and reduce patient screening across the geographies we work in, and we expect this dynamic to persist into next year. Meanwhile, summer seasonality was more pronounced than we have seen in the past, particularly in Europe. Looking ahead, we remain focused on creating the market for our Zephyr valve therapy, which addresses an unmet need for over 1 million severe emphysema patients globally, who have very few alternatives available to them and is backed by unparalleled clinical evidence. Specifically, we will focus on the 3-pronged commercial approach, which we have previously discussed to drive growth and penetration of our solution. First, training and launching new accounts that we believe have the potential to be strong Zephyr Valve centers; second, increasing the efficiency and scalability of our base, particularly among our newest accounts, by working hand in hand with our physician and administrative champions, to expand procedural capacity; and finally, increasing center utilization by building local awareness of the benefits of Zephyr Valves with patients and physicians, thereby developing a strong referral network. In terms of account openings, we added 13 new accounts in the U.S. in Q3, bringing the total number of U.S. treatment centers that are performing Zephyr valve procedures to 261. Even with the seasonal impact from the third quarter, we anticipate ending the year, with about 275 total U.S. treatment centers. Meanwhile, we gained greater visibility into the state of our treating centers, as pandemic-related pressure has subsided and staffing-related constraints have become clearer. It has become evident that we need to continue to focus driving efficiency and scalability across our account base, and that we will – and that it will take longer to bring accounts up to maturity. Over the past two quarters, we have seen a strong recovery in procedure volumes at our well-established sites, but utilization across our less developed accounts was more intermittent than we had expected. With many respiratory care programs thinly staffed and overstretched, we see opportunity to improve program efficiency and scalability, by taking all of our accounts through a series of training and site readiness processes that we have found to be effective at our more developed accounts. In support of these efforts, we have allocated additional field marketing, sales and patient access resources, to support account development and have adopted a new tracking system, to measure our success in implementing best practices with our customers. We expect the impact of these programs to be increasingly evident over the next few quarters, and we have confidence that these efforts, combined with a more normalized operating environment for our customers, will allow us to further enhance procedure rates across all our accounts. Meanwhile, within our more developed accounts, we are also seeing early returns from our efforts to educate referring physicians who manage large populations of COPD patients. We know who these folks are, and we are working to both provide information on our treatment and introduction to the treating physicians in area hospitals. Remarkably, when we meet with a referring physician and educate them on our therapy, more than half the time, that physician refers a patient to a treating physician within 6 months. We believe we have a strong playbook that will drive penetration across accounts while expanding our base of more developed accounts. However, given the increased time needed to fully develop our accounts, coupled with the ongoing hospital staffing dynamics and foreign exchange pressure, we are moderating our full year 2022 revenue expectations to now be in the range of $51.5 million to $52.5 million, and we expect global revenue to grow approximately 20% in 2023. In the third quarter, we continued to make significant progress on expanding our addressable market as we grow our commercial footprint and introduce our treatment to new patient populations around the world. We are celebrating a major milestone in our strategic initiative to expand our global footprint. The Japanese Ministry of Health, Labor and Welfare, MHLW agreed to approve Zephyr valves to treat severe COPD emphysema patients in Japan, following a special panel meeting on October 3, 2022. We look forward to bringing our treatment to patients in Japan following the establishment of reimbursement, which we expect in late 2023. As a reminder, we estimate Japan to be a $1 billion market opportunity with approximately 100,000 patients who stand to potentially benefit from our treatment. Also in the third quarter, we saw two very encouraging data readouts associated with our AeriSeal clinical development program. As a reminder, we are developing AeriSeal to expand the addressable market of our Zephyr valve solution to severe emphysema patients not currently eligible due to the presence of a gap in the fissure, separating lobes of the lungs, which results in collateral ventilation or air flow between these lobes. This collateral ventilation prevents the target lobe from deflating when Zephyr valves are inserted. Approximately 1 out of every 5 patients who undergoes our Chartis assessment is deemed ineligible to receive Zephyr valves due to the presence of collateral ventilation. AeriSeal is a polymeric foam that is delivered via a bronchoscope to seal the airways leading to the fissure gaps between lobes of the lung, potentially enabling treatment of patients who were previously ineligible for valves, due to collateral ventilation. At the European Respiratory Society International Congress in Barcelona, Spain, interim findings from our CONVERT multi-center trial, showed that treatment with AeriSeal in the first 40 patients of the study successfully converted 78% of patients to having little to no collateral ventilation, and these patients were subsequently treated with Zephyr valves with successful volume reduction in the target lobe of the lung. The CONVERT trial is ongoing, and we expect it to complete enrollment next year with final data presented in 2024. Learnings from the CONVERT trial continue to inform the design of our U.S. IDE protocol, which we are discussing with FDA and expect to initiate sometime next year. Also in the third quarter, the full data set from a single center feasibility study in Australia was published in the Journal of Respirology, Results demonstrated that AeriSeal not only successfully closed collateral air channels to allow patients with collateral ventilation to be treated with Zephyr valves, but that these treated patients showed clinical outcomes comparable to patients without collateral ventilation who are treated with Zephyr valves. Both the preliminary CONVERT trial data presented at ERS and the published Australian study data bolster our belief that AeriSeal could offer a compelling solution to expand our Zephyr valve therapy to patients who are today not candidates. In summary, we have taken steps forward on multiple market development initiatives, expansion of our global footprint and our clinical development pipeline. We anticipate growing our market presence by driving site efficiencies across our account base, and increasing utilization in our more developed accounts by geographic expansion, and through broadening the array of patients who are – we are able to treat with our technologies. Our progress across these initiatives, along with substantial increasing patient interest in Zephyr valves, limited competition in the field and our financial strength provides us with continued optimism for our long-term growth potential With that, I will now turn the call over to Derrick to provide a more detailed review of our third quarter results.