Sera Prognostics, Inc. (NASDAQ:SERA) Q1 2024 Earnings Call Transcript May 8, 2024
Sera Prognostics, Inc. isn’t one of the 30 most popular stocks among hedge funds at the end of the third quarter (see the details here).
Operator: Good afternoon and welcome to the Sera Prognostics Conference Call to Review First Quarter Fiscal Year 2024 Results. At this time, all participants are in a listen-only mode. We will be facilitating a question-and-answer session toward the end of today’s call. As a reminder, this call is being recorded for replay purposes. I would now like to turn the call over to Peter DeNardo of CapComm Partners for a few introductory comments.
Peter DeNardo: Thank you, operator. Good afternoon everyone. Welcome to Sera Prognostics’ first quarter fiscal year 2024 earnings conference call. At the close of the market today, Sera Prognostics released its financial results for the quarter ended March 31, 2024. Presenting for the company today will be Zhenya Lindgardt, President and CEO; and Austin Aerts, our CFO. During the call, we will review the financial results we released today, after which we will host a question-and-answer session. If you’ve not had a chance to review our quarterly earnings release, it can be found on our website at seraprognostics.com. This call can be heard live via webcast at seraprognostics.com and a recording will be archived in the Investors’ section of our website.
Please note that some of the information presented today may contain projections or other forward-looking statements about events and circumstances that have not yet occurred, including plans and projections for our business, future financial results, and market trends and opportunities. These statements are based on management’s current expectations and the actual events or results may differ materially and adversely from these expectations for a variety of reasons. We refer you to the documents the company files from time-to-time with the Securities and Exchange Commission, specifically the company’s annual report on Form 10-K, its quarterly reports on Form 10-Q, and its current reports on Form 8-K. These documents identify important risk factors that could cause the actual results to differ materially from those contained in our projections and other forward-looking statements.
As a reminder, a webcast replay of this call will be available on the Investors’ section of our website. I will now turn the call over to Zhenya, Sera Prognostics’ President and CEO. Zhenya?
Zhenya Lindgardt: Thank you, Peter and good afternoon everyone. We continue to make progress in putting keeper requisites in place for inflection in test volumes and revenue growth, coupled with improved margins. As Austin will detail, we believe 2024 is a foundational year of development for Sera with strategic goals we are pursuing to position the company for increased test adoption in the quarters ahead, while diligently preserving our strong balance sheet and cash position as we manage the business for future growth. These strategic goals include publication of our important AVERT and PRIME clinical study results to showcase the health and economic benefits of the PreTRM test, building awareness of our capabilities to help improve patient care and outcomes.
Continuing our strong focus on R&D to bring new products in our pipeline and new collection method to market, all the while improving access to our products to afford better health equity, scalability for our lab, once demand inflection occurs as well as increased product margins and profitability. Since the beginning of the year, we’ve made progress across these strategic priorities, including submission of PRIME study interim findings for publication; first whole blood collection kits to our customers; shifted to a more cost-effective laboratory test analysis process, resulting in an estimated 60% COGS savings at scale; prepared two television programs, which will air on public and network stations later this year to increase awareness surrounding PreTRM birth.
Deliveries of PRIME study participants, the remaining 2,200 who were enrolled before the enrollment stopped for DSMB recommendation in December 2023 are also now complete, and we’re now planning analysis and data for the final PRIME study publication. We’re pleased to report that we’ve validated ambient whole blood collection and have begun shipping our new kits to customers. We expect to see whole blood collection kits start running through our laboratory in the coming weeks. This, together with our laboratory enhancements are expected to yield several distinct advantages primarily, ease of collection, increased lab capacity and decreased turnaround time and reduced cost of goods. By improving and simplifying the collection method, we expect to enable greater patient access to our test, which should really allow us to reach more mothers across the country.
Simplified collection also means an improved user experience for the patient and provider. We believe less friction for the physician ordering process will lead to more repeat orders by providers. The processing of whole blood samples is coupled with the rollout of our newly validated laboratory process that leverages Sera proprietary antibodies used in mass spectrometry. In addition to enabling the processing of whole blood specimens, this new technology affords an approximate bifold improvement in sample processing capacity for laboratory technician, an approximate tenfold increase in throughput and cuts our turnaround time by about 50%. In addition to capacity and scalability enhancements, a faster and simpler laboratory process reduces material and labor costs, while whole blood ambient samples can be drawn and shipped at a much reduced cost when compared to frozen serum.
Overall, we expect an estimated cost of goods reduction of up to 60%, possibly higher beyond certain scale milestones. These improvements to our margins should serve to increase access to our technology, a key prerequisite to our growth strategy. While we work to communicate data from our AVERT and PRIME studies, we believe this will provide strong validation of the benefit of utilizing the PreTRM test for guideline development and adoption. A recent ACOG note on guidelines on biomarker testing for Preeclampsia points to the attention from guideline-setting bodies to PreTRM birth complications. For now, we’re continuing engagement with various stakeholders to increase adoption of our tests in order to improve pregnancy and maternal outcomes.
These stakeholders include providers we’re teaming up with to target the state’s hit-hardest by spontaneous premature birth rates. Our plans include working with payers and providers in collaboration with other stakeholders on targeted state implementation programs to promote health equity to address spontaneous premature births and improve pregnancy care, particularly among undisturbed populations and communities. This could provide a way to resolve a big problem and broaden awareness and increase adoption of PreTRM by patients, physicians, and the medical community overall. There has been a lot of interest in the potential impact of the FDA’s review of laboratory-developed tests, often called LDTs. The FDA published its final LDT rule last week on April 29th, and while there may be subsequent changes given pushback from certain industry stakeholders, we share the goal of keeping patients safe with a reasonable oversight of LDTs. A higher level of review and approval for new tests, whether under FDA’s final LDT rule or the valid act that has been pending in Congress for a while could set a new and higher bar for new entrants into the space reserve.
There’s always uncertainty whether a new regulation may be challenged, but we believe we are well-placed to work within the FDA’s proposed LDT framework to continue bringing our test to patients. For example, the FDA’s new LDT rule, includes continued enforcement discretion, the pre-existing status quo for LDTs approved by the New York State Clinical Laboratory Evaluation Program, which includes our PreTRM Test. Given our strong long-term R&D-driven history and extensive clinical study data, we believe the higher bar set by stronger regulations could serve as a source of advantage for Sera by requiring competitors dedicated years of work and significant investments. FDA states that increased oversight may help promote adequate representation in validation studies, which would help advance health equity and which lines up nicely with our mission.
As a reminder, about one in 10 babies is born prematurely in the United States at a rate of 10.4% according to CDC for 2022, while racial and ethnic differences in preterm birth rates remain. For 2022, the rate of preterm birth among African-American women of 14.6% was about 50% higher than the rate of preterm birth among white or Hispanic women at 9.4% and 10.1%, respectively. We need to do more, and we can with PreTRM. Sera was recently invited to support broadening awareness of innovative solutions available to expectant mothers and their physicians to understand the risk of preterm birth. Later this year, Sera will be featured on two television programs, Viewpoint with Dennis Quaid and Empowered with Meg Ryan. Distribution of these programs is expected to reach over 100 million people in the United States.
This will be a strong awareness building tool for Sera in 2024 to follow the physician education campaigns, we’re launching this summer. Outside of our current core market in the United States, we’re exploring attractive international markets. This process is expected to involve engaging with regulators in countries with a significant number of premature births where the addressable market for the Sera PreTRM Test is compelling. Upon publication of our pivotal, AVERT and PRIME studies, we plan to share the data with regulators. We also plan to engage with multiple potential partners to assess what may be needed to enter key international markets. If we ultimately enter this markets, our ambient whole blood kit collection methods are expected to ease market access, promote accessibility to address healthcare equity, and have optionality on test cost to promote adoption, while still leveraging healthy product margins.
Developing test processing via ELISA would also make it easier for Sera to go to market internationally. In conclusion, we’re pursuing multiple shots on goal to build awareness and adoption and believe our pathway will not only become easier upon publication of the study, as I mentioned, but such validated and compelling data in regard to PreTRM will also bolster and embolden the pursuit of our mission. Now over to you, Austin.
Austin Aerts: Thanks, Zhenya, and good afternoon, everyone. Let me review our financial results for the quarter and then briefly review our thinking on commercial investment. Net revenue for the first quarter of 2024 was nailed due to revenue adjustments made as part of our normal revenue recognition process, updating our expected collection amounts through periodic refinement of revenue estimates as described in detail in our 10-K. Gross revenues before adjustments were approximately $39,000 compared to $100,000 for the first quarter of 2023. This reduction in our revenue is an expected outcome of optimizing our investment in commercial activities and preserving capital to deploy for future commercial investments once we have built our evidence portfolio and executed on other prerequisites for success.
Our decision to rightsize our cost structure last year has materially improved our cash runway. As we previously noted, it was highly uncertain that we would achieve all of the key requirements that could foster an immediate revenue ramp, such as publications validating our preterm test, insurance coverage and consumer and physician awareness and adoption during the first half of 2024. As Zhenya mentioned in this call, we are working diligently to execute each of these prerequisites in the first half of this year and hope to share exciting news with you in the coming quarters. Total operating expenses for the first quarter of $9.1 million were down 20% from $11.4 million for the same period a year ago due to steps we took to streamline commercial operations, better focus our commercial strategy and reduce overall operating expenses.
Net loss for the first quarter of 2024 was $8.1 million, down 24% from $10.6 million for the first quarter of 2023. Research and development expenses were $3.7 million and down 10% from $4.1 million for the first quarter of 2023, due primarily to lower clinical study costs. Selling, general and administrative expenses for the first quarter were $5.4 million, down 26% from $7.3 million for the same period a year ago due to the steps we’ve taken to reduce expenses, while focusing on the most efficient means to build revenue in the quarters ahead. We have begun planning for a prudent expansion of our commercial operations and while we are not expecting an immediate return to previous expense levels, we are prepared to invest quickly into any commercial opportunities generated by study publications and increased market awareness when appropriate.
As of March 31, 2024, the company had cash, cash equivalents and available-for-sale securities of approximately $85.4 million. This was an improvement of about $5.5 million over $79.9 million at December 31, 2023, and resulted primarily from a payment received from our strategic partner in January, offset by regular cash operating expenses. We continue to be mindful of our cash burn rate and understand the uncertainties of the current and future capital markets environment. We will remain diligent in our strong fiduciary management of cash, balancing this with strategic investment and execution that we believe will position the company for commercial progress in the quarters and years ahead. Operator, we can now please open the call for questions.
Operator: Thank you. Ladies and gentlemen, we will now begin the question-and-answer session. [Operator Instructions] One moment, please, for your first question. Our first question comes from the line of Andrew Brackmann from William Blair. Go ahead please.
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