GeneDx Holdings Corp. Q1 2023 Earnings Call

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Good day, and thank you for standing by and welcome to the Gtx first quarter 'twenty to 'twenty three conference call. At this time all participants are in a listen only mode. After the speaker's presentation, there will be a question and answer session.

To ask a question during the session you will need to press star one on your telephone.

Then here an automated message advising you that your hand is raised to withdraw your question. Please press star. One again, please be advised that today's conference call is being recorded I would now like to hand, the conference over to your Speaker Trisha <unk> head of Investor Relations. Please go ahead.

Thank you and thank you to everyone who is joining us today on this call I'm Trisha <unk> head of Investor Relations at Ges.

On the call today, we have Catherine Stevens, President and Chief Executive Officer, Kevin Seeley, Chief Financial Officer, and Jennifer Brindel, Chief Commercial Officer earlier today <unk> released financial results for the first quarter of 2023 ended March 31 2020.

A copy of the press release, and our first quarter earnings slide deck are available on the company's website.

Before we begin I'd like to remind you that management will make forward looking statements within the meaning of federal Securities laws, which are made pursuant to the safe Harbor provisions of the private Securities Litigation Reform Act of $19 95.

Any statements contained in this call that relate to expectations or predictions of future events results or performance are forward looking statements.

Actual results may differ materially from those expressed or implied in the forward looking statements due to a variety of factors.

Additionally, these forward looking statements, particularly our 2020 financial guidance, our expectations for revenue growth gross margin and profitability over the next several years.

And our expected cost savings and reduction in cash burn involve a number of risks and <unk>.

Certainties and assumptions for a list and description of the risks and uncertainties associated with <unk> business. Please refer to the risk factors section of our latest Form 10-K filed with the Securities and Exchange Commission and the other documents filed by US from time to time with the SEC.

We urge you to consider these factors and you should be aware that these statements should be considered estimates only and are not a guarantee of future performance during.

During the call we may discuss certain non-GAAP financial measures for reconciliations of the non-GAAP measures to GAAP financial measures as well as other information regarding these measures. Please.

Refer to our earnings release and other materials in the Investor Relations section of our website.

This conference call contains time sensitive information and is accurate only as of the live broadcast today may nine 2023.

<unk> disclaims any intention or obligation, except as required by law to update or revise any financial projections or forward looking statements.

Whether because of new information future events or otherwise.

And with that I will turn the call over to Katherine.

Thank you Tricia I'm excited to share our progress so far in 2023, but to begin I would like to take a step back and remind you why we're here at <unk>.

Over the past decade, we've seen a massive conversion from single gene testing to multi gene panels.

<unk> played an instrumental role in assuring in this new era, while also pioneering an even more comprehensive set of services with whole exome and whole genome testing.

With more data supporting the clinical necessity of exome sequencing versus multi gene panels. <unk> is now poised to lead this conversion to deliver more comprehensive more definitive answers to more patients.

We're focused on rare disease testing in the pediatric setting where.

The current standard of care is generally a lack of testing unusually resulting in a multiyear diagnostic odyssey for children and for their parents in fact on average it takes eight years to diagnose a rare disease.

We know the exome and genome testing dramatically shorten that timeframe from years to weeks.

And we also know that these pediatric rare diseases are not at all rare when taken as a whole.

Think of how cancer is actually a constellation of hundreds of diseases.

Similarly, there are 7000 rare diseases that together are nearly as communist cancer.

Consider the one in eight women will be diagnosed with breast cancer.

Or one in 10 people have a rare disease half of whom are children.

In fact, we estimate that each year over 1 million infants and children in the U S alone would benefit from whole exome or genome testing. Unfortunately, we're not alone in our mission to expand care.

Medical societies, such as ACM G N S D C and the American Epilepsy Society are calling for exome and genome sequencing as a first line test and major national payers are moving to cover highly validated whole exome and our whole genome testing given the costly alternative.

450000, exome gene Dx's tested over the past decade, a quarter of them have been completed in just the past year momentum is building.

If we look to the future we expect the whole exome and genome tests will become increasingly standard of care for patients with broader diseases, such as cardiovascular and neuro degenerative disease.

Allowing us to expand into the adult population.

Today job number one is expanding utilization of our services primarily in pediatric testing with an emphasis on converting physicians use of exome as well as panel tests that serve a stepping stone to exome testing.

Let's dive into our 2023 progress I am pleased to say that we have generated over $40 million in revenue in the first quarter of 2023.

We saw increased volume across all of our testing coming in at nearly 53000 tests this quarter, giving us confidence that the market is growing.

And patients and physicians are turning to genetic testing ended gene Dx more and more.

The growth in all test lines from Q4 to Q1 gives us conviction that the strategy is working and these volume gains will materialize into revenue growth.

Furthermore, our focus on accelerating use of xoma's working our progress is reflected in a robust increase of volume and revenues of whole exome and genome tests, which delivered $22 $4 million of the $40 million in revenue, representing a 22% increase in whole exome revenues year over year in the first quarter.

We continue to see the momentum of growth in our <unk> volume and revenue in April and we expect to see margin expansion throughout the course of this year as these tests deliver a gross margin of approximately 60%.

Given the timeframe from ordering to revenue recognition and we expect to see revenue and gross margin shift in the second quarter results and build towards a significant amount of growth in the second half of this year.

There are five factors that will enable this acceleration first we're continuing to strengthen our commercial footprint and strategy. Our team is focused on converting physicians to test that are better for patients and better for our business.

This includes the increased volume of certain non exome test that are strategically important as physicians become comfortable with broader genetic testing, we see them stepping stones to exome.

We are educating clinicians that exome testing provides a higher diagnostic yield compared to tests like CMA FMR, one in multi gene panels, which leaves many patients behind.

We're also targeting non geneticists, who may be new to genetic diagnostics.

Encouraged by data that show that 30% of physicians, who ordered their first to XOMA gene Dx in Q1 were new customers to <unk> and orders among neurologists and pediatric specialists were significantly higher compared to last year.

We've taken the first part of the year to continue to invest in our commercial team. We expanded sales territories from 58 to 66 across the United States and also add a dedicated cross functional team mates for each sales rep to support growth.

<unk> Medical science liaisons client relationship managers and our managed care team. We've also built our incentive plans to drive conversion of orders from panel tests to exome sequencing.

Second in our acceleration is marketing our team is focused on meeting the clinician, where they are in and outside of the clinic, we're talking to them at conferences generating data through publications, increasing brand awareness efforts and launching a variety of initiatives in Q1 to eight and education engagement and <unk>.

<unk> build share and accelerate growth our cross channel activities drive awareness through advertising and E mail campaigns, and social media presence, bringing brand recognition <unk> has offerings and differentiation from others as we build and expand the market and in fact, we've doubled traffic to our websites since Q4 of 2022 when we.

To continue to build on that.

Third we're continuing to contribute to clinical research, which is also providing insightful data into the value of exome sequencing for patients. We recently presented new data at the <unk> annual meeting, which demonstrated the diagnostic advantages of exome sequencing over chromosomal microarray our CMA.

And the poster with compared reported copy number a number of areas our CNBC.

More than 8000 patients who had CMA in exome sequencing and showed the exome sequencing is a much higher diagnostic yield as it covers both sequence variants and cnbc's, whereas CMA is limited to detecting only CND.

PMA is a commonly as test that is a current standard of care driven by outdated guidelines and.

These critical data presented at <unk> are guiding our conversations to convince clinicians why they should order exome first.

During this research and driving adoption takes time.

Fourth is our focus on product improvement to improve our customer experience and operating efficiency.

We've been working to automate and shorten our turnaround time to facilitate quicker results for patients with the same high quality.

Automation is also key to decreasing our Cogs and expanded gross margins.

We will also introduce buccal swab collection for genome sequencing include.

Including a rapid testing option, which enables easier collection of parental or relative samples for trio testing, which has been shown to increase the diagnosis the diagnosis rate by nearly double.

The fifth factor goes beyond our own efforts. Our work is amplified by medical societies and in particular, Payors, who are taking notice of the favorable clinical and health economic benefits of exome and genome sequencing.

United Healthcare and Cigna have adopted favorable coverage of genome sequencing recently and.

And we are working with physicians to be sure. They are aware of these policy changes.

Recently state coverage groups are continuing to make meaningful progress.

North Carolina, Medicaid published updated clinical coverage policy to add coverage for exome sequencing in the outpatient setting becoming the 28.

State to do so.

One of the many key barriers to the adoption of testing is what to do with the results for so many getting an answer as a relief and we're committed to going a step further by working with a broader ecosystem of biopharma payers and advocacy groups to help connect patients to the best possible treatment for them our.

Our opportunity to partner with Biopharma is significant we're seeing deal flow generated across various therapeutic areas based on the clinical and genomic data assets, which are part of our centrella platform in the first quarter, we signed data agreements with five companies.

On rare diseases or neurological disorders, including farming group.

We also launched a new centrella product called data explorer, which helps our internal teams more efficiently gather data and deliver these opportunities.

We believe these agreements are highly scalable and have high gross margins with high value to our partners and patients as well.

With strong performance year to date, we're on our way to reach profitability in 2025.

We're clearly in an exciting moment in health care to accelerate the delivery of personalized and actual health insights to inform diagnosis direct treatment and improve drug discovery and development.

And with that I'd like to pass the call to Kevin. Thank you Katherine with another quarter past since our 2022 restructuring, we're seeing a meaningful financial improvements across all aspects of our business I would like to first take you through revenues and gross margins from continuing operations and then address spend and cash burn on a total company basis.

Wrap up with 2023 guidance, which we are reaffirming.

During the first quarter of 2023 pro forma revenue from continuing operations was $40 7 million compared to $38 million in the first quarter of 2022, the increase was driven by 22% growth in whole exome sequencing revenue totaled.

Total test volumes are up 8% sequentially and 29% year over year.

The first quarter revenues are reflective of a few transitory effects to be aware of.

First the <unk>.

Neural reset of insurance deductibles and co pays.

The first quarter typically brings the reset of patient insurance plans and that creates a seasonal decline in average room <unk> rates that then ramp up as the year progresses.

Second we adjusted some direct billing rates for certain long standing clients, we made that change to match current pricing in line with our plan and in order to accelerate growth, while also maintaining a favorable gross margin profile.

Third test mix, our sales team intentionally built up volumes on certain non exon tests that are often the precursors to our client ordering whole exome sequencing.

These carry lower average reimbursement rates and lower gross margins compared to exome sequencing tests, but as Katherine mentioned, we think of them as stepping stone store higher value exome.

Pro forma adjusted gross margin from continuing operations in the quarter was 34%.

Adjusted gross margin for whole exome sequencing was approximately 60% and whole exome sequencing represents 17% of total volume in the first quarter.

Has the March and April volume mix that Catherine highlighted makes its way through production and as a result, we expect accretion in our blended gross margins.

Beyond mix shifts and seasonal effects, which will naturally expand gross margins through the year. Our teams are working to implement a number of projects aimed at further improving both turnaround times and Cogs throughout our lab operations.

These include but are not limited to the introduction of next generation of Illumina equipment consolidation of our library preparation processes <unk> Biosciences.

And the implementation of further automation and AI across a number of in production report, writing and genetic counseling steps.

Additionally, there are promising initiatives underway across revenue cycle management to optimize the strong and improving coverage policy environment for whole exome in order to ensure we're properly reimbursed.

You should also expect us to continue to monitor the clinical and economic performance of our tests and simplify the test menu, where we see the ability to improve both patient care and expand gross margins at the same time.

We have a best in class operations and product and technology team that is hard at work lowering costs and optimizing the customer experience.

Total company adjusted net loss in the first quarter of 2023 inclusive of all activity, including the now discontinued legacy similar for diagnostic operation was $48 8 million compared to an adjusted net loss of $59 7 million in the same period of 2022.

First quarter is an improvement of 34% compared to an adjusted net loss of $72 5 million for the fourth quarter of 2022.

Our ongoing cost mitigation efforts are delivering and we have improved our cash burn by 31% year over year to approximately $59 million in the first quarter of which a substantial portion as it related to discontinued operations, we expect the quarterly burn rate to reduce through each sequential quarter of this year.

Operating expenses have come down in line with expectations and we arent done.

Expenses and in particular G&A expense will continue to reduce as we completed the separation from discontinued operations in the first quarter will finalize some remaining integration activities between <unk> and our legacy business in the second quarter.

Our sharp focus on gaining efficiencies across all aspects of our business.

Cash and cash equivalents and restricted cash was $214 1 million as of March 31 2023.

In April 2023, we received the final tranche of $7 million from the registered direct offering that was part of the $150 million capital raise in January 2023.

Okay.

Turning to guidance, we reaffirm our previously issued 2023 guidance of $205 million to $220 million in revenue and we expect to expand the gross margins in 'twenty three and beyond we believe we are fully funded to profitability in 2025, and we expect to use 95 to 100.

$10 million of cash in 2023 for continuing operations.

<unk> of servicing obligations of the exited business activities, we expect to use $130 million to $145 million in 2023.

Finally last week, we affected a reverse stock split.

At a 1% to 33 ratio accordingly, all common stock shares per share amounts in additional paid in capital amounts for all periods presented today and filed in our 10-Q have been retroactively adjusted where applicable to reflect the reverse stock split.

As of March 31, 2023, we had $24 million or 193436 shares of common stock outstanding.

It is important to note that in April 2023, we issued an additional 1 million 378328 shares as milestone payments previously disclosed as part of the <unk> acquisition and the closing of the registered direct offering and with that I will turn the call over to the operator for Q&A.

Thank you at this time, we will conduct a question and answer session. As a reminder to ask a question you will need to press star one on your telephone and wait for your name to be announced to withdraw your question. Please press star one again.

Stand by while we compile those.

Sure.

Okay.

Our first question comes from the line of.

Brandon Your line is now open.

Hey, Thanks, good afternoon.

Katherine or Kevin I think you spoke to some of this in your prepared remarks, but if we just look at the single.

In multi gene test in the quarter, just help us reconcile the volumes being up with the revenues down.

The ASP trend behind that do you expect that realized ASP to improve or normalize as we move through the year and strategically.

I guess the rationale of using of the sales team as you described it.

Driving those monarch, some test as a stepping stone.

That seems to be I guess newer aspects of the commercial strategy.

Absolutely so.

The overall volume.

Was up across the board, but.

Indeed, the sales team.

Is.

Is incentivized to be able to really sell exome.

And one of the key strategies to get and clinicians. There does include moving from CMA FMR, one and offer them testing so.

As we're spending a lot of time educating them on some of the data that came out last fall.

Ed.

Assay to see at AAN on why Exome is a superior test and why CMA and guidelines, calling for CMA maybe outdated.

We are continuing to see that momentum is building in April and expect that the exome growth.

The momentum will continue beyond April into Q2, and the rest of the year.

I think as we look at the percentage of revenue the exome drives it.

A huge aspect of our strategy here, but we're also ensuring that we can really meet clinicians where theyre at give them. The data is one of the reasons why the MSL team that we've invested in.

To really spend time educating them on.

Relatively new data as it pertains to exome.

They should be taking.

The step forward to get there sooner and we also see that clinicians start with exome and they want to see that it's working and they want to see that the message that we're delivering that four out of five pesos has zero out of pocket for exome with us and want to say that thats.

The case, so we expect this momentum to build in the second half of the year and that Asps will include on the trajectory.

Debt that we have set out to be able to achieve.

Okay. That's helpful and then Kevin anymore color you'd be willing to share with us in terms of the pace and magnitude of gross margins as we move through the year and what.

What should we think about it.

The top one or two drivers of that whether it's mix better reimbursement lab efficiencies how would you expect renters.

Yes so.

Consistent with our.

Reiteration of the full year guidance, we'd expect the full year to average out above where we ended 2022.

In the fourth quarter at 41% adjusted gross margin.

The way, we see that playing out.

Sequential growth from through each quarter of the year.

Towards.

Something.

Towards the mid mid forties.

The main drivers of that really is.

Continuation of Cogs improvement efforts that we have underway I gave a few examples of those in my prepared remarks, we do expect to see seasonal.

Sequential improvements in Asps as the year progresses, and then the overall effects of mix shift towards higher margin tests. So it really takes does take the combination of all of those.

But see us getting back.

Towards fourth quarter gross margin profile in the second quarter, and then beyond that to be able to reaffirm our guide the full year will be above where we exited 2022.

Okay and then.

How much of a cash burn in the first quarter was tied to restructuring, yes, I'd expect those outlays be fully behind you at the end of Q2.

A substantial amount was included in the first quarter, we still have some remaining payments to go.

Although there are shutdown activities of the some of our diagnostic business are now complete.

There's some further paydowns of accounts payable.

And some facility leases that will remain with us into the future, but I think the way we look at the burn was.

Very much pleased with where we ended the first quarter. It was in line.

With our plans overall operating expense improved substantially if you look at the bottom line on an adjusted basis really just taking out noncash items of depreciation and stock based compensation.

33% sequential improvement on the bottom line versus the fourth quarter.

More impactful items to further reduce our burn include finishing up some integration activities that were left over.

Following the acquisition of Gtx and getting them off of.

Previous ownership in it systems and merged with <unk> four we.

We will see those activities really.

Wind down in the second quarter and then.

Continued focus on taking down G&A, but overall pleased with the leverage we are driving in Opex and expect to.

See sequential improvements with the fourth quarter coming in the neighborhood of $20 million of burn for the fourth quarter of 2023.

Hey, guys. Thank you.

Thank you very much.

To turn the call back to Catherine Catherine stool for closing remarks.

Want to just thank the customers and patients too.

Trust US wanted to say, thank you to our teammates who we rely on to serve our customers and most definitely to the shareholders.

Who are putting their trust in our ability to continue to.

Grow this business it plays a meaningful role in the lives of so many patients. So thank you very much and we look forward to talking with you all soon.

Okay.

Thank you for your participation in today's conference. This does conclude the program you may now disconnect.

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GeneDx Holdings Corp. Q1 2023 Earnings Call

Demo

GeneDx Holdings

Earnings

GeneDx Holdings Corp. Q1 2023 Earnings Call

WGS

Tuesday, May 9th, 2023 at 8:30 PM

Transcript

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