Genedx Holdings Corp. · NASDAQ:WGS

Genedx — Q2 2024 Earnings Presentation

34 slides from Genedx's earnings presentation, Jul 30, 2024

  1. Slide 1: GeneDx 2Q 2024 Earnings Presentation

    One test. Big picture. Brighter futures. GeneDx (Nasdaq: WGS)​ 2Q 2024 Earnings Presentation July 30, 2024

  2. Slide 2: Disclaimer

    Disclaimer This presentation contains forward-looking statements under the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that do not relate to historical facts and events and such statements and opinions pertaining to the future that, for

  3. Slide 3: WGS Q2 2024 Results

    WGS Q2 2024 Results Second quarter 2024 revenue from continuing operations1 of $68.9M with 77% year-over- year revenue growth for exome and genome test revenue Expanded second quarter 2024 adjusted gross margin from continuing operations1,2 to 62% Second quarter 2024 total cash burn of $6M; ending J

  4. Slide 4: Revenue – strong growth driven by high value whole exome and genome

    Revenue – strong growth driven by high value whole exome and genome Revenue1 Q2 2024 Increase in 2Q24 exome/genome Revenue from continuing operations $68.9M 77% revenue year-over-year; Growth year-over-year 52% +15% sequentially Growth sequentially 12% Increase in 2Q24 exome/genome Exome and genome

  5. Slide 5: Gross profit – expansion driven by mix shift, cost per test reductions

    Gross profit – expansion driven by mix shift, cost per test reductions and improved reimbursement Exome/genome can be the best test for patients. They are also best for our business. Adjusted gross margins1 from 31% Exome/genome test result volume 62% continuing operations in 2Q24, up from 37% in 2Q

  6. Slide 6: Cash – balance sheet bolstered to execute growth strategy

    Cash – balance sheet bolstered to execute growth strategy 1 Cash, cash equivalents, marketable securities and $108M1 restricted cash on hand at June 30, 2024 $6M 89% 9 Net use of cash for the Improvement in total company net Consecutive quarters of total company in Q2 cash burn rate year-over-year;

  7. Slide 7: 2024 Guidance Update

    2024 Guidance Update Drive full year 2024 revenues between $255 to $265 million (previous guidance was between $235 to $245 million) Expand full year 2024 adjusted gross margin profile to at least 60% (no change) Use between $65 to $70 million of net cash for full year 2024 (previous guidance was be

  8. Slide 8: Appendix

    Appendix Genek

  9. Slide 9: GeneDx is a leader in improving health outcomes through genomic insights

    GeneDx is a leader in improving health outcomes through genomic insights.

  10. Slide 10: We address the costly and prolonged path to diagnosis

    We address the costly and prolonged path to diagnosis The diagnostic odyssey: Endless specialist visits, ongoing mismanagement of undiagnosed disease, and expensive, ineffective and often invasive diagnostic testing Outcomes Years of avoidable expenses and still no diagnosis 1. Pre-exome standard of

  11. Slide 11: Exome sequencing can break the cycle of misdiagnosis and uncertainty

    Exome sequencing can break the cycle of misdiagnosis and uncertainty Expedited Diagnoses Improved Outcomes Reduced Costs Starting with the most vulnerable patients $30,000 per case average savings1* Rapid results Patient retention ✓ ✓ Patient Tests ordered $6,800 savings Patients connected Healthier

  12. Slide 12: Exome sequencing is a cost-effective solution to avoid the diagnostic odyssey

    Exome sequencing is a cost-effective solution to avoid the diagnostic odyssey A look at the average diagnostic odyssey 3 misdiagnoses1 5 uninformative tests3 years to an in additional 6+ >$10k accurate diagnosis2 healthcare costs3 >70% have a change in management with a genetic diagnosis4 1. Genetic

  13. Slide 13: GeneDx offers leading exome and genome products

    GeneDx offers leading exome and genome products Translating complex genomic data into definitive diagnoses for patients • Genome sequencing – Analyzes the entirety of an individual’s DNA, which is known as the genome. The genome includes ~20,000 genes. • Exome sequencing – Analyzes the protein codin

  14. Slide 14: Changing the perception of exome and genome sequencing

    Changing the perception of exome and genome sequencing GeneDx has spent over a decade solving for limitations of the past and differentiating our products Then GeneDx Now “These tests take months to get results” “I can get results in days to weeks” Turnaround time “These tests are wildly expensive”

  15. Slide 15: Patients we serve today are difficult to diagnose and have complex needs

    Patients we serve today are difficult to diagnose and have complex needs Patients typically have 2+ of the indications below o Congenital abnormalities (birth defects) o Significant Intellectual disability o Global developmental delay o Seizures/epilepsy o Failure to thrive or other growth concerns

  16. Slide 16: Exome sequencing offers greater diagnostic yields vs. other technologies

    Exome sequencing offers greater diagnostic yields vs. other technologies 1. Savatt JM et al. Front Pediatr. 2021;9:526779. 2. Srivastava S et al. Genet Med. 2019;21(11):2413–2421. 3. Pekeles H et al. Pediatr Neurol. 2019;92:32-36. 4. Stefanski A et al. Epilepsia. 2021;62(1):143-151. 5. Mellone S et

  17. Slide 17: GeneDx is positioned to enable a data-informed future for healthcare

    GeneDx is positioned to enable a data-informed future for healthcare.

  18. Slide 18: New market expansion enables us to serve more patients

    New market expansion enables us to serve more patients GeneDx is starting with a focus on rare disease and pediatrics and then expanding into larger markets Rare Disease Newborn Adults: $16B & Pediatrics: $3B Screening: $10B Rapidly growing patient Currently participating in Expanding into adult mar

  19. Slide 19: We're focused on the Rare Disease & Pediatrics market today

    We're focused on the Rare Disease & Pediatrics market today Outpatient Inpatient Target Clinicians: o Geneticists Target Clinicians: o Pediatric Neurologists​ o Geneticists o Developmental Pediatricians o Neonatologists​ o Pediatricians (long-term) Products: Products: o Primarily rapid whole o Prima

  20. Slide 20: Payor coverage for exome and genome sequencing is expanding

    Payor coverage for exome and genome sequencing is expanding 〉 GeneDx is contracted with over 80% of covered lives, including all large national commercial payers 〉 Medicaid and commercial insurance coverage continues to grow for exome and genome o 28 states cover exome sequencing o 14 states cover r

  21. Slide 21: Medicaid programs across the country are expanding access

    Medicaid programs across the country are expanding access Current Medicaid Coverage Landscape Whole Exome Sequencing Rapid Genetic Testing Both No Coverage 21 Data through April 2024.

  22. Slide 22: Medical practice guidelines recommend exome and genome sequencing

    Medical practice guidelines recommend exome and genome sequencing for patients ACMG Practice Guideline1: “Strong recommendation based on the available evidence to support the use of ES/GS as either a first- (or second-) line test in patients …. ES/ GS demonstrates clinical utility for the patients a

  23. Slide 23: Pay-it-forward data strategy

    Additional Additional ore answ ers patients patients for patients tested providers tested Pay-it-forward mproved igher interpretation data strategy diagnostic yield platform fewer S For every patient that we test, our ore underlying interpretation platform answ ers for patients gets smarter, and we

  24. Slide 24: Data is at the center of our business

    Data is at the center of our business Our huge dataset and intelligent interpretation platform set us apart and fuel innovation Advanced interpretation platform Simplifies complex genomic data >600K sequenced exomes Significant clinical and Reduces variants of genomic data unknown significance Fuels

  25. Slide 25: Common diseases are in fact a constellation of genetic diagnoses

    Common diseases are in fact a constellation of genetic diagnoses One example is epilepsy. At least 768 different genes are related to seizures. Only 43% are tested on many commercial epilepsy panels 25 Butler L. et al. Exome-based testing for patients with seizures: Advantages over panel-based testi

  26. Slide 26: Common diseases are in fact a constellation of genetic diagnoses

    Common diseases are in fact a constellation of genetic diagnoses One example is epilepsy. At least 768 different genes are related to seizures. Only 43% are tested on many commercial epilepsy panels Exome sequencing checks all 768 genes 26 Butler L. et al. Exome-based testing for patients with seizu

  27. Slide 27: We are translating our leadership in exome and investing in a genome future

    We are translating our leadership in exome and investing in a genome future It’s the right time to lean in and improve solutions for our providers to deliver the best patient care Integrating with Epic Aura Improving WGS products Expanding access by integrating into existing Adding repeat expansions

  28. Slide 28: 1 in 3 babies in the NICU is likely to have a genetic condition

    1 in 3 babies in the NICU is likely to have a genetic condition that could be diagnosed with rapid whole genome sequencing (rWGS)1 Cost associated with NICU/PICU care for suspected or confirmed genetic disease is ~ $26B, or 50% of the US pediatric inpatient health spend2,3 Medicaid coverage has expa

  29. Slide 29: Today, we shorten the diagnostic journey. Tomorrow, we hope to prevent it.

    Today, we shorten the diagnostic journey. Tomorrow, we hope to prevent it.

  30. Slide 30: Building the future: The SeqFirst Study

    Building the future: The SeqFirst Study Shorter hospital stays. Less uncertainty. Better care. In phase one of the SeqFirst study, 125 infants were offered rapid WGS: 63% of infants had abnormal rapid WGS results, and 88% of these cases resulted in a change in management 90% of diagnoses made by WGS

  31. Slide 31: Building the future: Newborn screening

    Building the future: Newborn screening Fast diagnosis. Clear next steps. Reduced healthcare costs. Screened 5,000 healthy infants, toward goal of >100,000​ 4.3% positive rate​ Average age of diagnosis for these conditions is 7-11 years old​ 31

  32. Slide 32: Building the future: Partnerships

    Building the future: Partnerships Enriched data. Empowered drug discovery. mproved outcomes.​ GeneDx offers solutions across the pharma drug development pipeline​ Find Connect Understand 32

  33. Slide 33: One test. Big picture. Brighter futures.

    One test. Big picture. Brighter futures. 33

  34. Slide 34: Reconciliation of Non-GAAP Financial Measures

    Reconciliation of Non-GAAP Financial Measures Three months ended June 30, Three months ended March 31, 2024 2023 2024 Legacy Legacy Legacy GeneDx Total GeneDx Total GeneDx Total Sema4 Sema4 Sema4 Revenue $ 68,924 $ 1,590 $ 70,514 $ 45,226 $ 3,480 $ 48,706 $ 61,461 $ 961 $ 62,422 Cost of services 27,

GeneDx Holdings — Q2 2024 Earnings Presentation on 6ix