Title

Presentation

Fulgent Genetics, Inc. beats earnings expectations. Reported EPS is $-0.22, expectations were $-0.43.

Operator: Hello and welcome to the Fulgent Genetics Q1 2023 Earnings Conference Call and Webcast. [Operator Instructions] As a reminder, this conference is being recorded. It’s now my pleasure to turn the call over to Melanie Solomon, Investor Relations. Please go ahead.

Melanie Solomon: Thanks, Kevin. Good morning and welcome to the Fulgent first quarter 2023 financial results conference call. On the call today are Ming Hsieh, Chief Executive Officer; Paul Kim, Chief Financial Officer and Brandon Perthuis, Chief Commercial Officer. The company’s press release discussing the financial results is available on the Investor Relations section of the company’s website, www.fulgent.com. A replay of this call will be available shortly after the call concludes on the Investor Relations section of the company’s website. Management’s prepared remarks and answers to your questions on today’s call will contain forward-looking statements. These forward-looking statements represent management’s estimates based on current views and assumptions which may prove to be incorrect.

As a result, matters discussed in any forward-looking statements are subject to risks, uncertainties and changes in circumstances that may cause actual results to differ from those described in the forward-looking statements. The company assumes no obligation to update any of the forward-looking statements it may make today to reflect actual results or changes in expectations. Listeners should not rely on any forward-looking statements as predictions of future events and should listen to management’s remarks today with the understanding that actual events, including the company’s actual future results may be materially different in what is described in or implied by these forward-looking statements. Please review the more detailed discussions related to these forward-looking statements, including the discussions of some of the risk factors that may cause results to differ from those described in these forward-looking statements contained in the company’s filings with the Securities and Exchange Commission, including the previously filed 10-K for the year ended December 31, 2021 and subsequently filed reports which are available on the company’s Investor Relations website.

Management’s prepared remarks, including discussions of earnings and earnings per share contain financial measures not prepared in accordance with accounting principles generally accepted in the United States or GAAP. Management has presented these non-GAAP financial measures because it believes they may be useful to investors for various reasons but they should not be viewed as a substitute for or superior to the company’s financial results prepared in accordance with GAAP. Please see the company’s press release discussing its financial results for the first quarter of 2022 for more information, including the description of how the company calculates non-GAAP income or loss earnings or loss per share and adjusted EBITDA and a reconciliation of these financial measures to income or loss and earnings or loss per share to the most directly comparable GAAP financial measures.

With that, I’d now like to turn the call over to Ming.

Ming Hsieh: Thank you very much, Melanie. Good morning. And thank you for joining our call today. I will start with some comments on the quarter. Then Brandon will review our product and go-to-market updates from the first quarter. And then Paul will conclude with the financials and outlook before we take your call. We are pleased with our results in the first quarter. Exceeding the revenue guidance we provided earlier this year on our last call, we also had $3 million in revenue from COVID-19 testing, bringing us to a cumulative $2 billion in revenue from COVID-19 testing since 2020. More importantly, revenue from our core business outperformed our expectation. This was driven by strong results from our pharma services segment and the precision diagnostic segment.

Including launch of our expanded Beacon testing, we see continuing momentum for Beacon testing, as well as other reproductive health service. According to recent report from Frost & Sullivan, it is estimated that global prenatal testing market was over $8 billion in 2021, and is forecasted to grow to over $11 billion by 2026, a 7% CAGR. Over $8 billion in 2021, 31% was carrier screening, over $2.5 billion. It is forecasted to grow to $3.2 billion by 2026, with a consolidation in the space. We now find our company as one of the top providers of carrier screening in the U.S., with a significant runway for growth. I want to make comments on Inform Diagnostics. As we have mentioned, the Inform Diagnostics business bolsters our capabilities in Anatomic Pathology, and adds significant revenue, though it has put some pressure on margins.

As we continue to integrate acquisition, our focus on the implementing improved process to increase margin and continue to grow the top line with a new kind acquisition. This will take some time. Long-term, we believe the opportunity we have is a value of thousands of customers we gain, and the potential to expand the offering to them. However, we do see significant opportunity for cross-selling in the precision diagnosis market. Given the first-quarter results, we are raising our full-year guidance to account for momentum we see with reproductive health services this year and the anticipated COVID-19 revenue. We believe we are moving to the right direction in terms of sales momentum we expect to see this year as we grow our core business across precision diagnosis, pharma service, and Anatomic Pathology.

Turning to our pharma business, Fulgent Pharma has developed and processed a novel nano-encapsulation technology which includes over 40 patents and a targeted therapy platform designed to improve therapeutic windows and pharmacokinetics profile for both new and existing cancer drugs. Our lead drug candidate, FID-007, has shown promising results for the treatment of numerous cancers, including head and neck, ampullary, and pancreatic, with reduced side effects. We will share data from the on-going Phase 1b study at the upcoming American Society of Clinical Oncology annual meeting in Chicago, June 2nd to 6th. We look forward to share additional progress and a new initiative on the pharma business as we move throughout the year. Now I’d like to thank our employees and shareholders for your loyalty during the past quarter.

We look forward to the year ahead and the momentum we are creating with our combined business. Now I will turn over the call over to Brandon Perthuis, our Chief Commercial Officer, to talk about our diagnostics business results during the quarter. Brandon?

Brandon Perthuis: Thanks Ming. We had a solid first quarter. While we are seeing [Indiscernible] across the entire organization the first quarter outperformance was led again by our offering for pharma services and reproductive health. I will cover these in detail momentarily at a high level first quarter sales with $62.7 million an increase of 150% year-over-year and 14% sequentially. This does not include any COVID-19 testing while a fraction of what it was a couple of quarters ago, we still do some COVID-19 testing. Now giving additional color on the business by breaking it out into three categories;. these include precision diagnostics, which is most of our clinical NGS business, Anatomic Pathology, and pharma services. Starting with our reproductive health business, which would fall into precision diagnostics.

We are seeing tremendous growth here. The marquee product for reproductive health is our Beacon Expanded Carrier Screening Service. We addressed the features and benefits of this product in detail on the last call, but as a reminder, Beacon is a suite of products that range from small panels of 3 to 4 genes all the way up to 787 genes, which is one of, if not the largest panels offered today. The first quarter saw triple digit percentage growth in Beacon. Clients are choosing Fulgent and Beacon based on our comprehensive and customizable panels, our detection rates, especially for those genes complicated by high sequence homology, as well as our turnaround time. In all areas of reproductive health, but especially in the fertility clinics, turnaround time is critical.

We are currently returning results within two weeks for over 90% of our patient samples, and those that take longer are usually because they require orthogonal confirmation. So even with triple digit percentage growth, our laboratory hasn’t missed a beat. We showed the power of the Fulgent platform with COVID-19 testing, and we’re now showing it again with Beacon. In addition to our organic wins, we have also entered into a long-term relationship with one of the largest national laboratories to partner up to expand access to carrier screening. This lab greatly increases our sales and contracts reach, and this relationship is already resulting in a material amount of sales. Also in the first quarter, we joined the Access to Expanded Carrier Screening Coalition, or AECS.

AECS is a multi-stakeholder coalition dedicated to ensuring all individuals of childbearing age and their partners have access to expanded carrier screening. As part of the steering committee, initial efforts are to expand patient and client education of carrier screening, as well as work with commercial and governmental payers for continued coverage improvement. While Beacon is certainly an area of focus, our reproductive health services also include single gene tests, prenatal tests, preimplantation genetic testing for aneuploidy, cytogenetics, and more. We believe our suite of services, quality, and turnaround time make us a good choice for clinicians. Other areas of focus for our Precision Diagnostics Division includes a revamped go-to-market strategy for pediatrics, including leveraging our insurance contracts, cross-selling our hereditary cancer tests to our new fulgent oncology clients, and cross-selling neurogenetic next-generation sequencing tests to our adult neurology clients, which we acquired through informed diagnostics.

Switching over to our Pharma Services Division, Pharma Services had a record quarter, growing 306% year-over-year and 149% sequentially to $7.4 million. While this area of our business tends to be a bit lumpy, depending on the timing of the contracts, the momentum is clear. Over the last several quarters, we have continually expanded our capabilities to build an impressive multi-omics product offering, covering both clinical and translational research. Most recently, we launched four new powerful and in-demand technologies for single-cell and spatial multi-omics. Notably, we became a certified and qualified service provider for the Aquoia’s Multiplex Immunofluorescence Spatial Phenotyping and for the 10X Genomics Single-Cell and Spatial Gene Expression Platforms.

Our portfolio now includes, among other things, whole genome, whole exome, RNA sequencing, proteomics, tumor profiling, epigenomics, lipid biopsy, single-cell sequencing, spatial biology, and a wide range of pathology offerings. Our client list continues to grow, and as importantly, we feel we are driving deeper relationships with our clients, which now include six of the top 10 pharma companies in the United States and three of the largest global CROs. We aim to continue to broaden our test menu for pharma services and increase our visibility with additional sales, headcount, and marketing efforts. The Fulgent Oncology launch continues to be a focus for our company. We announced last quarter that our Lumera Heme NGS, a state-of-the-art 670 gene profile for hematological malignancies, received MolDx approval with a robust coverage determination and a rate of $2,950.

We are excited to announce today that our Lumera NGS solid tumor profile has also received MolDx approval with a reimbursement rate of $3,288. The Lumera NGS solid tumor profile utilizes next-generation sequencing to cover 523 genes, including RNA sequencing of 55 genes, enabling a highly sensitive review of tumor genomics, fusions, and splice variants, all critical to precision care. Additionally, our Lumera NGS solid tumor profile results tumor mutational burden and microsatellite instability. Both critical components when assessing immunotherapy eligibility in several malignancies. Lumera NGS solid profile is a standout in this field as it relates to turnaround time and QNS ratio, which are crucial to patient care and play a central role in the deciding factors clinicians use to choose a testing laboratory.

To put it in perspective, our current turnaround time is less than two weeks, compared to the industry standard measure of three to six weeks. And perhaps most important is our current QNS rate, which stands at approximately 2%. This differentiator demonstrates our ability to provide actionable results on very small tissue or neoplastic cell content when compared to the industry standard QNS ratio of approximately 25% on solid tumor tissue. Our proprietary extraction techniques coupled with our expertise in the research and development space have led us to commercialize a comprehensive genomic profile that can deliver more actionable results with less tissue availability, thus making the Lumera NGS solid tumor profile a uniquely competitive option in the busy precision diagnostic space.

While we are still early in the stages of launching and commercializing Fulgent oncology, we believe we have taken the right steps to set us up for long-term success. We ended the fourth quarter call saying that we felt we had the wind in our sails entering the first quarter. I think we demonstrated that with a strong performance across all three business lines. As we look ahead, we are enthusiastic about the business opportunities we see, and we are confident that the steps we have taken to build a strong core business will continue to pay off. I’ll now turn the call over to our Chief Financial Officer, Paul Kim. Paul?

Paul Kim: Thanks, Brandon. Revenue in the first quarter totaled $66 million compared to $320 million in the first quarter of 2022. Roughly $3 million came from COVID-19 testing for Q1, which was not part of our guidance. Revenue from our core business totaled $63 million, which exceeded our guidance of $56 million and grew 150% year-over-year. Gross margin was 28.4%. The declining gross margin year-over-year is primarily related to the higher costs of Anatomic Pathology revenues from InformDX, which we purchased in Q2 of 2022. However, we are pleased to have achieved a 9 percentage point improvement in our gross margin sequentially over the prior quarter, as we see our efforts to create efficiencies across our acquired businesses pay off.

Turning now to operating expenses, total GAAP operating expenses were $43.6 million in the first quarter, down from $49.5 million in the fourth quarter of 2022. Non-GAAP operating expenses totaled $33.8 million, down from $38.7 million in the fourth quarter of 2022. Non-GAAP operating margin increased 15 percentage points sequentially to a negative 19%, more than offsetting the increase in R&D of $1.2 million, which was primarily related to our pharma business, was a decrease in G&A of $7 million, as we continue our integration efforts to achieve efficiencies with our recent acquisitions. Adjusted EBITDA for the first quarter was a negative $7.2 million, compared to a positive $213.5 million in the first quarter of 2022. On a non-GAAP basis, and excluding equity-based compensation expense and intangible asset amortization, loss for the quarter was $6.5 million, or $0.22 per share, based on a $29.5 million weighted average shares outstanding.

Turning over to the balance sheet, we ended the first quarter with approximately $868 million in cash, cash equivalents, and marketable securities, excluding investments pending settlement. Now moving on to our outlook for 2023. Given the outperformance in the first quarter and the momentum, we’re raising our core guidance core revenue guidance to $250 million. This number does not anticipate additional revenue from COVID-19 testing. Looking ahead, we expect our gross margin and operating margins to continue to improve as we implement efficiencies throughout our integration efforts and recent acquisitions. The margin improvement is forecast to be incremental for the remainder of the year, as we plan to make further investments and resources to position the company for longer-term growth.

For a full year 2023, utilizing a 28% tax rate and a share count of 31 million, we expect non-GAAP loss of approximately $1.25 per share for our shareholders, excluding stock-based compensation and amortization of intangible assets, as well as any one-time charges. Last quarter when we acquired the pharma business, we said we would report on this business separately. Revenue from this business is not anticipated in our 2023 guidance, and we expect associated cash burn for this business to be approximately $15 to $17 million this year, which is included in our EPS guidance. Overall, we have strengthened our core business and bolstered our portfolio through strategic acquisitions, and we see very good momentum ahead. Thank you for joining the call today.

Operator, you can open it up for questions.

Operator: Certainly. [Operator Instructions] Our first question is coming from Dan Leonard from Credit Suisse. Your line is now live.

Operator: Thank you. Your next question is coming from David Westenberg from Piper Sandler. Your line is now live.

Operator: Thank you. Next question today is coming from Andrew Cooper from Raymond James. Your line is now live.

Operator: Thank you. We reached the end of our question-and-answer session. I’d like to turn the floor back over for any further or closing comments.

Ming Hsieh: Yes. Thank you very much for everyone who joined our call today. And we are looking forward to provide you the update in the coming quarters. Thank you.

Operator: Thank you. That does conclude today’s teleconference webcast, and we disconnect your line at this time, and have a wonderful day. We thank you for your participation today.