Myriad Genetics Reports Strong Second Quarter 2024 Financial Results, including 15% Revenue Growth Year-Over-Year; Raises 2024 Financial Guidance and Long-Term Revenue Growth Target to 12%
Myriad Genetics (NASDAQ: MYGN) reported strong Q2 2024 results, with revenue growing 15% year-over-year to $212 million. Growth was driven by Prenatal (25%), Pharmacogenomics (22%), and Hereditary Cancer (19%). GAAP EPS improved to $(0.41) from $(1.42) in Q2 2023, while adjusted EPS rose to $0.05 from $(0.08). The company raised its 2024 financial guidance, projecting full-year revenue of $835-$845 million (11-12% growth) and adjusted EPS of $0.08-$0.12. Myriad also increased its long-term revenue growth target to 12%. Test volumes increased 9% year-over-year, with improvements in average revenue per test across the portfolio. The company reported positive cash flow from operations and continues to invest in innovation while growing profitably.
Myriad Genetics (NASDAQ: MYGN) ha riportato risultati solidi per il secondo trimestre del 2024, con un aumento dei ricavi del 15% rispetto all'anno precedente, raggiungendo $212 milioni. La crescita è stata trainata da Prenatale (25%), Farmacogenomica (22%) e Cancro Ereditario (19%). Il GAAP EPS è migliorato a $(0,41) rispetto a $(1,42)l'EPS rettificato è salito a $0,05 rispetto a $(0,08). L'azienda ha alzato le previsioni finanziarie per il 2024, prevedendo ricavi totali nell'intero anno tra $835-$845 milioni (crescita dell'11-12%) e un EPS rettificato di $0,08-$0,12. Myriad ha anche incrementato il suo obiettivo di crescita dei ricavi a lungo termine al 12%. I volumi dei test sono aumentati del 9% su base annua, con miglioramenti nel ricavo medio per test in tutta la gamma. L'azienda ha riportato un flusso di cassa positivo dalle operazioni e continua a investire in innovazione mentre cresce in modo redditizio.
Myriad Genetics (NASDAQ: MYGN) reportó sólidos resultados para el segundo trimestre de 2024, con un aumento del 15% en los ingresos interanuales, alcanzando los $212 millones. El crecimiento fue impulsado por Prenatal (25%), Farmacogenómica (22%) y Cáncer Hereditario (19%). El EPS GAAP mejoró a $(0.41) desde $(1.42) en el segundo trimestre de 2023, mientras que el EPS ajustado aumentó a $0.05 desde $(0.08). La compañía incrementó sus proyecciones financieras para 2024, pronosticando ingresos anuales totales de $835-$845 millones (crecimiento del 11-12%) y un EPS ajustado de $0.08-$0.12. Myriad también aumentó su objetivo de crecimiento de ingresos a largo plazo al 12%. Los volúmenes de pruebas crecieron un 9% interanual, con mejoras en el ingreso promedio por prueba en todo el portafolio. La empresa reportó un flujo de caja positivo de operaciones y continúa invirtiendo en innovación mientras crece de manera rentable.
Myriad Genetics (NASDAQ: MYGN)는 2024년 2분기 실적을 발표하며 매출이 전년 대비 15% 증가한 2억 1200만 달러를 기록했습니다. 성장은 산전(25%), 약물유전학(22%), 유전성 암(19%)에 의해 주도되었습니다. GAAP EPS는 2023년 2분기의 $(1.42)에서 $(0.41)로 개선되었습니다, 그리고 조정 EPS는 $(0.08)에서 $0.05로 상승했습니다. 회사는 2024년 재무 가이던스를 상향 조정했습니다, 올해 총 매출을 8억 3500만~8억 4500만 달러(11-12% 성장)와 조정 EPS를 $0.08~$0.12로 전망했습니다. Myriad는 또한 장기 매출 성장 목표를 12%로 상향했습니다. 테스트 볼륨은 전년 대비 9% 증가했으며 전체 포트폴리오에서 테스트당 평균 수익이 개선되었습니다. 이 회사는 운영에서 긍정적인 현금 흐름을 보고하고 있으며 수익성 있게 성장하면서 혁신에 계속 투자하고 있습니다.
Myriad Genetics (NASDAQ: MYGN) a annoncé des résultats solides pour le deuxième trimestre 2024, avec des revenus en hausse de 15 % par rapport à l’année précédente, atteignant 212 millions de dollars. La croissance a été soutenue par les tests prénatals (25 %), la pharmacogénomique (22 %) et le cancer héréditaire (19 %). Le BPA GAAP s'est amélioré à $(0,41) contre $(1,42) au deuxième trimestre 2023, tandis que le BPA ajusté est passé de $(0,08) à $0,05. L'entreprise a relevé ses prévisions financières pour 2024, prévoyant un chiffre d'affaires total de 835 à 845 millions de dollars pour l'année (croissance de 11-12 %) et un BPA ajusté de $0,08 à $0,12. Myriad a également augmenté son objectif de croissance des revenus à long terme à 12 %. Les volumes de tests ont augmenté de 9 % d'une année sur l'autre, avec des améliorations du revenu moyen par test dans l'ensemble du portefeuille. L'entreprise a rapporté un flux de trésorerie positif provenant de ses opérations et continue d'investir dans l'innovation tout en croissant de manière rentable.
Myriad Genetics (NASDAQ: MYGN) hat solide Ergebnisse für das zweite Quartal 2024 berichtet, mit einem Anstieg des Umsatzes um 15 % im Jahresvergleich auf 212 Millionen US-Dollar. Das Wachstum wurde durch Pränataltests (25 %), Pharmakogenomik (22 %) und erbliche Krebserkrankungen (19 %) vorangetrieben. Das GAAP EPS verbesserte sich von $(1,42) auf $(0,41) im zweiten Quartal 2023, während das angepasste EPS von $(0,08) auf $0,05 stieg. Das Unternehmen hat seine finanziellen Prognosen für 2024 angehoben und rechnet mit einem Umsatz von 835 bis 845 Millionen US-Dollar für das Gesamtjahr (Wachstum von 11-12 %) und einem angepassten EPS von $0,08 bis $0,12. Myriad hat auch sein langfristiges Umsatzziel auf 12 % angehoben. Die Testvolumina stiegen um 9 % im Jahresvergleich, mit Verbesserungen beim durchschnittlichen Umsatz pro Test im gesamten Portfolio. Das Unternehmen berichtete von einem positiven Cashflow aus der Betriebstätigkeit und investiert weiterhin in Innovation, während es profitabel wächst.
- Revenue grew 15% year-over-year to $212 million in Q2 2024
- Adjusted EPS improved to $0.05 from $(0.08) in Q2 2023
- Full-year 2024 revenue guidance raised to $835-$845 million (11-12% growth)
- Long-term revenue growth target increased to 12%
- Gross margin improved 110 basis points year-over-year to 69.6%
- Positive cash flow from operations of $2.6 million
- Hereditary cancer testing revenue in Women's Health grew 31% year-over-year
- Prenatal testing revenue grew 25% year-over-year
- Tumor profiling revenue decreased 9% year-over-year to $32.6 million
- GAAP EPS still negative at $(0.41), despite improvement from previous year
- Operating loss of $36.5 million in Q2 2024, although improved from previous year
Insights
This is a highly impactful earnings report for Myriad Genetics, showing strong financial performance and improved outlook. Key points:
- Q2 revenue grew
15% year-over-year to$212 million , driven by strong growth in Prenatal (25% ), Pharmacogenomics (22% ) and Hereditary Cancer (19% ) segments. - Adjusted EPS improved to
$0.05 from$(0.08) last year, showing profitability improvement. - Full-year 2024 guidance raised: revenue now
$835-845 million (11-12% growth) and adjusted EPS$0.08-0.12 . - Long-term revenue growth target increased to
12% , indicating confidence in sustained growth.
The improved profitability and cash flow generation while still investing in innovation is particularly encouraging for long-term prospects.
Myriad's strong performance reflects growing adoption of genetic testing in healthcare. Notable developments:
- Market share gains in prenatal testing, with
25% revenue growth and12% volume growth. - Expanded coverage and clinical validation studies supporting product adoption.
- New patent for circulating tumor DNA detection, advancing Molecular Residual Disease (MRD) testing capabilities.
- Collaboration with GSK to expand access to HRD testing for ovarian cancer patients globally.
- Launch of enhanced Universal Plus Panel for carrier screening, covering 272 genes.
These advancements position Myriad well in the rapidly evolving precision medicine landscape, particularly in oncology and women's health. The focus on EMR integration and lab modernization should further drive adoption and efficiency.
Myriad's Q2 results reveal significant market dynamics:
- Strong growth in prenatal and pharmacogenomics segments indicates increasing market acceptance of genetic testing in these areas.
- Hereditary cancer testing growth (
19% ) suggests continued market expansion, possibly driven by increased awareness and broader testing criteria. - Tumor profiling revenue decline (
-9% ) highlights challenges in the biopharma sector and international markets. - Expanded payer coverage, including Blue Shield of California for GeneSight, points to improving reimbursement landscape.
- Progress in biomarker legislation (15 states) could drive further adoption of pharmacogenomic testing.
The company's focus on revenue cycle management and average revenue per test improvement is paying off, contributing to both top-line growth and margin expansion. The raised guidance and long-term growth target suggest management's confidence in sustaining this momentum.
Highlights
- Second quarter revenue grew
15% year-over-year to$212 million , driven by Prenatal (25% ), Pharmacogenomics (22% ), and Hereditary Cancer (19% ). - Second quarter GAAP earnings per share improved to
$(0.41) from$(1.42) in the second quarter of 2023; adjusted earnings per share improved to$0.05 from$(0.08) in the second quarter of 2023. - Increasing 2024 financial guidance with full year revenue moving to a range of
$835 -$845 million , or an annual growth rate of between11% and12% , and increasing adjusted earnings per share (EPS) to a range of$0.08 -$0.12 .1
_________________________
1 The company does not forecast GAAP EPS because it cannot predict certain elements that are included in the reported GAAP results. Please see below under "Financial Guidance" for a full explanation.
SALT LAKE CITY, Aug. 06, 2024 (GLOBE NEWSWIRE) -- Myriad Genetics, Inc. (NASDAQ: MYGN), a leader in genetic testing and precision medicine, today announced financial results for its second quarter ended June 30, 2024 and raised its previously issued financial guidance on business performance for the full-year 2024.
“We are very proud to have delivered another quarter of strong double digit year-over-year revenue growth in the second quarter of 2024. Our year-to-date 2024 revenue growth of
Financial and Operational Highlights
- Test volumes of 389,000 in the second quarter of 2024 increased
9% year-over-year. - The following table summarizes year-over-year testing volume changes in the company's core product categories:
| Three months ended | Six months ended | ||||||||||||
| (in thousands) | June 30, 2024 | June 30, 2023 | % Change | June 30, 2024 | June 30, 2023 | % Change | |||||||
| Product volumes: | |||||||||||||
| Hereditary cancer | 73 | 71 | 3 | % | 144 | 136 | 6 | % | |||||
| Tumor profiling | 14 | 16 | (13 | )% | 28 | 32 | (13 | )% | |||||
| Prenatal | 173 | 154 | 12 | % | 345 | 312 | 11 | % | |||||
| Pharmacogenomics | 129 | 117 | 10 | % | 253 | 227 | 11 | % | |||||
| Total | 389 | 358 | 9 | % | 770 | 707 | 9 | % | |||||
- The following table summarizes year-over-year revenue changes in the company's core product categories:
| Three months ended | Six months ended | ||||||||||||||||
| (in millions) | June 30, 2024 | June 30, 2023 | % Change | June 30, 2024 | June 30, 2023 | % Change | |||||||||||
| Product revenues: | |||||||||||||||||
| Hereditary cancer | $ | 91.5 | $ | 76.7 | 19 | % | $ | 179.6 | $ | 152.4 | 18 | % | |||||
| Tumor profiling | 32.6 | 36.0 | (9 | )% | 63.5 | 73.3 | (13 | )% | |||||||||
| Prenatal | 44.4 | 35.6 | 25 | % | 88.7 | 71.8 | 24 | % | |||||||||
| Pharmacogenomics | 43.0 | 35.2 | 22 | % | 81.9 | 67.2 | 22 | % | |||||||||
| Total | $ | 211.5 | $ | 183.5 | 15 | % | $ | 413.7 | $ | 364.7 | 13 | % | |||||
- Gross margin of
69.6% in the second quarter of 2024 increased 110 basis points year-over-year, reflecting operating leverage and improved average revenue per test. Adjusted gross margin in the second quarter of 2024 was70.1% , an increase of 110 basis points year-over-year as the company's revenue cycle, Labs of the Future and supply chain initiatives begin to take hold. - Second quarter of 2024 operating expenses were
$183.6 million . Adjusted operating expenses were$140.8 million , increasing6% over the year ago period. This increase was driven by investments in technology, product development and R&D. Adjusted operating expenses accounted for67% of total revenue in the second quarter of 2024, down from73% of total revenue in the second quarter of 2023. - Operating loss in the second quarter of 2024 was
$36.5 million , improving$77.2 million year-over-year; adjusted operating income in the second quarter of 2024 was$7.4 million , improving$14.2 million year-over-year.
Business Performance and Highlights
Oncology
The Oncology business delivered revenue of
- Second quarter 2024 hereditary cancer testing revenue in Oncology grew
11% year-over-year, reflecting ongoing initiatives to improve average revenue per test through payer coverage expansion and revenue cycle process improvements that are reducing the company's no pay rate. - Second quarter 2024 tumor profiling revenue of
$32.6 million grew5% compared to first quarter 2024 but decreased10% year-over-year, reflecting the ongoing challenging biopharma environment, slow ramp of biopharma contracts executed in 2023, and challenges in the international business. - In July 2024, Myriad Genetics received a patent relating to detecting circulating tumor DNA in patient fluid samples, which is complementary to a patent granted earlier in the year for the company’s methods of preparing cell-free DNA. Both of these patents support advancing commercialization of the company's high sensitivity tumor informed Molecular Residual Disease (MRD) assay.
- In July 2024, Myriad Genetics entered into an agreement with Personalis, Inc. (Nasdaq: PSNL) to cross-license patent estates covering tumor-informed approaches to detect MRD. The agreement helps solidify each company’s freedom to operate in the MRD market and broadens patient access to the benefits of MRD testing.
- Announced a collaboration with GSK (NYSE: GSK) aimed at improving access to homologous recombination deficiency (HRD) diagnostic testing for high-grade serous ovarian cancer (HGSOC) patients, leveraging Myriad Genetics' MyChoice HRD Plus and MyChoice CDx Plus tests in nine countries outside the United States.
- Myriad Genetics and QIAGEN (NYSE: QGEN) agreed to develop a globally distributable kit-based test for analyzing HRD status to support research into personalized medicine in multiple solid tumor types, including ovarian cancer.
- In August 2024, Myriad Genetics announced that it further advanced its international reorganization efforts, including the closing of the sale of its EndoPredict business to Eurobio Scientific. The reorganization of its international operations better aligns company resources to its domestic opportunities while continuing to serve key biopharma partners and patients globally and builds on Myriad Genetics' efforts this year to accelerate profitable business growth across its portfolio.
Women’s Health
The Women’s Health business delivered revenue of
- Second quarter 2024 hereditary cancer testing revenue in Women's Health grew
31% year-over-year as more practitioners see the benefit of incorporating MyRisk with RiskScore as part of a comprehensive breast cancer risk assessment program. - Prenatal testing revenue in the second quarter of 2024 grew
25% year-over-year, reflecting market share gains, expanded coverage by payers, and ongoing initiatives to improve average revenue per test. - Myriad Genetics launched the Universal Plus Panel for Foresight® Carrier Screen, which includes 39 new conditions and screens up to 272 genes associated with serious inherited conditions.
- Ten abstracts, including four on FirstGene, have been accepted to be showcased at the National Society of Genetic Counselors' 43rd annual meeting, which begins on September 17, 2024, in New Orleans, LA.
Pharmacogenomics
In the pharmacogenomics category, GeneSight test revenue was
- Second quarter 2024 GeneSight testing revenue grew
22% year-over-year, reflecting ongoing initiatives to improve average revenue per test. - Currently, biomarker legislation for state-regulated plans has passed in 15 states. In many of these states, commercial and managed Medicaid payers have modified their coverage policies to include GeneSight and Prolaris. Additionally, there are a number of states that have legislation in process. Myriad Genetics continues to see an increasing number of payors incorporating, or planning to incorporate, GeneSight into their coverage. Notably, this includes Blue Shield of California, a major commercial and managed Medicaid plan, effective July 1, 2024.
Financial Guidance
Myriad Genetics does not provide forward-looking guidance on a GAAP basis for the measures on which it provides forward-looking non-GAAP guidance as the company is unable to provide a quantitative reconciliation of forward-looking non-GAAP measures to the most directly comparable forward-looking GAAP measure, without unreasonable effort, because of the inherent difficulty in accurately forecasting the occurrence and financial impact of the various adjusting items necessary for such reconciliations that have not yet occurred, are dependent on various factors, are out of the company's control, or cannot be reasonably predicted. Such adjustments include, but are not limited to, real estate optimization and transformation initiatives, certain litigation charges and loss contingencies, costs related to acquisitions/divestitures and the related amortization, impairment and related charges, and other adjustments. For example, stock-based compensation may fluctuate based on the timing of employee stock transactions and unpredictable fluctuations in the company's stock price. Any associated estimate of these items and its impact on GAAP performance could vary materially.
Below is a table summarizing Myriad Genetics' fiscal year 2024 financial guidance*:
| (in millions, except per share amounts) | PRIOR FY 2024 | CURRENT FY 2024 | Expected Year-Over-Year Change | ||
| Revenue | |||||
| Gross margin % | 100 - 150 bps | ||||
| Adjusted OPEX | |||||
| Adjusted EBITDA** | |||||
| Adjusted EPS*** | |||||
| * | Assumes currency rates as of August 6, 2024. | ||||
| ** | Adjusted EBITDA is defined as Net Income (loss) plus income tax expense (benefit), total other income (expense), non-cash operating expenses, such as amortization of intangible assets, depreciation, impairment of long-lived assets, and share-based compensation expense, and one-time expenses such as expenses from real estate optimization initiatives, transformation initiatives, legal settlements, and divestitures and acquisitions. | ||||
| *** | Full-year 2024 adjusted EPS is based on a 91 million share count. | ||||
These projections are forward-looking statements and are subject to the risks summarized in the safe harbor statement at the end of this press release.
Conference Call and Webcast
A conference call will be held today, Tuesday, August 6, 2024, at 4:30 p.m. EDT to discuss Myriad Genetics’ financial results and business developments for the second quarter 2024. A live webcast of the conference call can be accessed on Myriad Genetics' Investor Relations website at investor.myriad.com. To participate in the live conference call via telephone, please register at https://register.vevent.com/register/BI620080625d0e42be9b313c17391abf61. Upon registering, a dial-in number and unique PIN will be provided to join the conference call. Following the conference call, an archived webcast of the call will be available at investor.myriad.com.
About Myriad Genetics
Myriad Genetics is a leading genetic testing and precision medicine company dedicated to advancing health and well-being for all. Myriad Genetics provides insights that help people take control of their health and enable healthcare providers to better detect, treat, and prevent disease. Myriad Genetics develops and offers genetic tests that help assess the risk of developing disease or disease progression and guide treatment decisions across medical specialties where critical genetic insights can significantly improve patient care and lower healthcare costs. For more information, visit www.myriad.com.
Myriad, the Myriad logo, BRACAnalysis, BRACAnalysis CDx, Colaris, ColarisAP, MyRisk, Myriad MyRisk, MyRisk Hereditary Cancer, MyChoice, Tumor BRACAnalysis CDx, MyChoice CDx, Prequel, Prequel with Amplify, Amplify, Foresight, Foresight Universal Plus, Precise Tumor, Precise Oncology Solutions, Precise Liquid, Precise MRD, FirstGene, SneakPeek, SneakPeek Early Gender DNA Test, SneakPeek Snap, Urosuite, Mygenehistory, Health.Illuminated., RiskScore, Prolaris, GeneSight, and EndoPredict are registered trademarks or trademarks of Myriad Genetics, Inc. All third-party marks—® and ™—are the property of their respective owners. © 2024 Myriad Genetics, Inc. All rights reserved.
Revenue by Product (Unaudited)
| Three months ended June 30, | ||||||||||||||||||||
| (in millions) | 2024 | 2023 | ||||||||||||||||||
| WH | ONC | PGx | Total | WH | ONC | PGx | Total | % | ||||||||||||
| Hereditary Cancer | $ | 41.9 | $ | 49.6 | $ | — | $ | 91.5 | $ | 32.1 | $ | 44.6 | $ | — | $ | 76.7 | 19 | % | ||
| Tumor Profiling | — | 32.6 | — | 32.6 | — | 36.1 | — | 36.1 | (10 | )% | ||||||||||
| Prenatal | 44.4 | — | — | 44.4 | 35.5 | — | — | 35.5 | 25 | % | ||||||||||
| Pharmacogenomics | — | — | 43.0 | 43.0 | — | — | 35.2 | 35.2 | 22 | % | ||||||||||
| Total Revenue | $ | 86.3 | $ | 82.2 | $ | 43.0 | $ | 211.5 | $ | 67.6 | $ | 80.7 | $ | 35.2 | $ | 183.5 | 15 | % | ||
| Six months ended June 30, | ||||||||||||||||||||
| (in millions) | 2024 | 2023 | ||||||||||||||||||
| WH | ONC | PGx | Total | WH | ONC | PGx | Total | % | ||||||||||||
| Hereditary Cancer | $ | 81.5 | $ | 98.1 | $ | — | $ | 179.6 | $ | 67.4 | $ | 85.0 | $ | — | $ | 152.4 | 18 | % | ||
| Tumor Profiling | — | 63.5 | — | 63.5 | — | 73.4 | — | 73.4 | (13 | )% | ||||||||||
| Prenatal | 88.7 | — | — | 88.7 | 71.7 | — | — | 71.7 | 24 | % | ||||||||||
| Pharmacogenomics | — | — | 81.9 | 81.9 | — | — | 67.2 | 67.2 | 22 | % | ||||||||||
| Total Revenue | $ | 170.2 | $ | 161.6 | $ | 81.9 | $ | 413.7 | $ | 139.1 | $ | 158.4 | $ | 67.2 | $ | 364.7 | 13 | % | ||
Business Units:
WH = Women’s Health
ONC = Oncology
PGx = Pharmacogenomics
Product Categories:
Hereditary Cancer – MyRisk, BRACAnalysis, BRACAnalysis CDx
Tumor Profiling – MyChoice CDx, Prolaris, Precise Tumor, EndoPredict
Prenatal – Foresight, Prequel, SneakPeek
Pharmacogenomics – GeneSight
| MYRIAD GENETICS, INC. AND SUBSIDIARIES Condensed Consolidated Statements of Operations (unaudited) (in millions, except per share amounts) | |||||||||||||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Testing revenue | $ | 211.5 | $ | 183.5 | $ | 413.7 | $ | 364.7 | |||||||
| Costs and expenses: | |||||||||||||||
| Cost of testing revenue | 64.4 | 57.8 | 128.9 | 117.0 | |||||||||||
| Research and development expense | 27.1 | 21.2 | 52.7 | 43.7 | |||||||||||
| Selling, general, and administrative expense | 144.9 | 140.7 | 284.9 | 292.4 | |||||||||||
| Legal settlements | — | 77.5 | — | 77.5 | |||||||||||
| Goodwill and long-lived asset impairment charges | 11.6 | — | 11.6 | — | |||||||||||
| Total costs and expenses | 248.0 | 297.2 | 478.1 | 530.6 | |||||||||||
| Operating loss | (36.5 | ) | (113.7 | ) | (64.4 | ) | (165.9 | ) | |||||||
| Other income (expense): | |||||||||||||||
| Interest income | 0.4 | 0.5 | 1.0 | 1.2 | |||||||||||
| Interest expense | (0.8 | ) | (0.5 | ) | (1.3 | ) | (1.0 | ) | |||||||
| Other | (0.3 | ) | (2.4 | ) | 1.6 | (3.0 | ) | ||||||||
| Total other income (expense), net | (0.7 | ) | (2.4 | ) | 1.3 | (2.8 | ) | ||||||||
| Loss before income tax | (37.2 | ) | (116.1 | ) | (63.1 | ) | (168.7 | ) | |||||||
| Income tax (benefit) expense | (0.5 | ) | — | (0.4 | ) | 2.1 | |||||||||
| Net loss | $ | (36.7 | ) | $ | (116.1 | ) | $ | (62.7 | ) | $ | (170.8 | ) | |||
| Net loss per share: | |||||||||||||||
| Basic and diluted | $ | (0.41 | ) | $ | (1.42 | ) | $ | (0.69 | ) | $ | (2.10 | ) | |||
| Weighted average shares outstanding: | |||||||||||||||
| Basic and diluted | 90.6 | 81.7 | 90.3 | 81.5 | |||||||||||
| MYRIAD GENETICS, INC. AND SUBSIDIARIES Condensed Consolidated Balance Sheets (unaudited) (in millions, except share information) | |||||||
| June 30, 2024 | December 31, 2023 | ||||||
| ASSETS | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 92.4 | $ | 132.1 | |||
| Marketable investment securities | 4.9 | 8.8 | |||||
| Trade accounts receivable | 117.8 | 114.3 | |||||
| Inventory | 26.1 | 22.0 | |||||
| Prepaid taxes | 18.4 | 17.0 | |||||
| Prepaid expenses and other current assets | 21.6 | 19.4 | |||||
| Assets held for sale | 10.4 | — | |||||
| Total current assets | 291.6 | 313.6 | |||||
| Operating lease right-of-use assets | 56.5 | 61.6 | |||||
| Property, plant and equipment, net | 116.3 | 119.0 | |||||
| Intangibles, net | 319.5 | 349.5 | |||||
| Goodwill | 286.3 | 287.4 | |||||
| Other assets | 14.9 | 15.4 | |||||
| Total assets | $ | 1,085.1 | $ | 1,146.5 | |||
| LIABILITIES AND STOCKHOLDERS' EQUITY | |||||||
| Current liabilities: | |||||||
| Accounts payable | 33.3 | 25.8 | |||||
| Accrued liabilities | 98.3 | 113.9 | |||||
| Current maturities of operating lease liabilities | 13.3 | 16.2 | |||||
| Liabilities held for sale | 4.0 | — | |||||
| Total current liabilities | 148.9 | 155.9 | |||||
| Unrecognized tax benefits | 31.1 | 30.2 | |||||
| Long-term debt | 38.8 | 38.5 | |||||
| Noncurrent operating lease liabilities | 91.2 | 97.4 | |||||
| Other long-term liabilities | 34.6 | 41.3 | |||||
| Total liabilities | 344.6 | 363.3 | |||||
| Commitments and contingencies | |||||||
| Stockholders’ equity: | |||||||
| Common stock, 90.9 and 89.9 shares outstanding at June 30, 2024 and December 31, 2023, respectively | 0.9 | 0.9 | |||||
| Additional paid-in capital | 1,435.8 | 1,415.5 | |||||
| Accumulated other comprehensive loss | (4.0 | ) | (3.7 | ) | |||
| Accumulated deficit | (692.2 | ) | (629.5 | ) | |||
| Total stockholders' equity | 740.5 | 783.2 | |||||
| Total liabilities and stockholders’ equity | $ | 1,085.1 | $ | 1,146.5 | |||
| MYRIAD GENETICS, INC. AND SUBSIDIARIES Condensed Consolidated Statements of Cash Flows (unaudited) (in millions) | |||||||||||||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Net cash provided by (used in) operating activities | $ | 2.6 | $ | (0.9 | ) | $ | (16.0 | ) | $ | (34.1 | ) | ||||
| Net cash (used in) provided by investing activities | (6.4 | ) | 11.8 | (13.5 | ) | 46.4 | |||||||||
| Net cash provided by (used in) financing activities | 2.4 | 38.4 | (6.4 | ) | 33.5 | ||||||||||
| Effect of foreign exchange rates on cash, cash equivalents, and restricted cash | (0.7 | ) | 0.3 | (1.5 | ) | 0.5 | |||||||||
| Change in cash and cash equivalents classified as held for sale | (2.3 | ) | — | (2.3 | ) | — | |||||||||
| Net (decrease) increase in cash, cash equivalents, and restricted cash | (4.4 | ) | 49.6 | (39.7 | ) | 46.3 | |||||||||
| Cash, cash equivalents, and restricted cash at beginning of the period | 105.6 | 63.1 | 140.9 | 66.4 | |||||||||||
| Cash, cash equivalents, and restricted cash at end of the period | $ | 101.2 | $ | 112.7 | $ | 101.2 | $ | 112.7 | |||||||
Safe Harbor Statement
This press release contains “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including the company's updated fiscal year 2024 financial guidance, the expectations of trends in financial performance to continue through the year and into 2025, the company's long-term revenue growth target, the company's expectation of additional market share gains in prenatal testing, the company's plans to continue to publish additional clinical validation studies and launch new products, statements relating to the company improving access and ease of use for customers as the company accelerates EMR integrations for new customers and makes progress in its Labs of the Future initiative, and that the company is growing profitably, delivering improved financial results, and continuing to invest in the innovation required to achieve its mission and vision to reach more patients with life-saving precision medicine. These “forward-looking statements” are management’s present expectations of future events as of the date hereof and are subject to a number of known and unknown risks and uncertainties that could cause actual results, conditions, and events to differ materially and adversely from those anticipated.
These risks include, but are not limited to: the risk that sales and profit margins of the company’s existing tests may decline; the risk that the company may not be able to operate its business on a profitable basis; risks related to the company’s ability to achieve certain revenue growth targets and generate sufficient revenue from its existing product portfolio or in launching and commercializing new tests to be profitable; risks related to changes in governmental or private insurers’ coverage and reimbursement levels for the company’s tests or the company’s ability to obtain reimbursement for its new tests at comparable levels to its existing tests; risks related to increased competition and the development of new competing tests; the risk that the company may be unable to develop or achieve commercial success for additional tests in a timely manner, or at all; the risk that the company may not successfully develop new markets or channels for its tests; the risk that licenses to the technology underlying the company’s tests and any future tests are terminated or cannot be maintained on satisfactory terms; risks related to delays or other problems with operating the company’s laboratory testing facilities and the transition of such facilities to the company's new laboratory testing facilities; risks related to public concern over genetic testing in general or the company’s tests in particular; risks related to regulatory requirements or enforcement in the United States and foreign countries and changes in the structure of the healthcare system or healthcare payment systems; risks related to the company’s ability to obtain new corporate collaborations or licenses and acquire or develop new technologies or businesses on satisfactory terms, if at all; risks related to the company’s ability to successfully integrate and derive benefits from any technologies or businesses that it licenses, acquires or develops; the risk that the company is not able to secure additional financing to fund its business, if needed, in a timely manner or on favorable terms, if it all; risks related to the company’s projections or estimates about the potential market opportunity for the company’s current and future products; the risk that the company or its licensors may be unable to protect or that third parties will infringe the proprietary technologies underlying the company’s tests; the risk of patent-infringement claims or challenges to the validity of the company’s patents; risks related to changes in intellectual property laws covering the company’s tests, or patents or enforcement, in the United States and foreign countries; risks related to security breaches, loss of data and other disruptions, including from cyberattacks; risks of new, changing and competitive technologies in the United States and internationally and that the company may not be able to keep pace with the rapid technology changes in its industry, or properly leverage new technologies to achieve or sustain competitive advantages in its products; the risk that the company may be unable to comply with financial or operating covenants under the company’s credit or lending agreements; the risk that the company may not be able to maintain effective disclosure controls and procedures and internal control over financial reporting; risks related to current and future investigations, claims or lawsuits, including derivative claims, product or professional liability claims, and risks related to the amount of the company's insurance coverage limits and scope of insurance coverage with respect thereto; and other factors discussed under the heading “Risk Factors” contained in Item 1A of the company’s Annual Report on Form 10-K filed with the U.S. Securities and Exchange Commission (SEC) on February 28, 2024 as updated in the company's Quarterly Report on Form 10-Q filed with the SEC on May 8, 2024, as well as any further updates to those risk factors filed from time to time in the company’s Quarterly Reports on Form 10-Q or Current Reports on Form 8-K. Myriad Genetics is not under any obligation, and it expressly disclaims any obligation, to update or alter any forward-looking statements, whether as a result of new information, future events or otherwise except as required by law.
Statement regarding use of non-GAAP financial measures
In this press release, the company’s financial results and financial guidance are provided in accordance with accounting principles generally accepted in the United States (GAAP) and using certain non-GAAP financial measures. Management believes that presentation of operating results using non-GAAP financial measures provides useful supplemental information to investors and facilitates the analysis of the company’s core operating results and comparison of operating results across reporting periods. Management also uses non-GAAP financial measures to establish budgets and to manage the company’s business. A reconciliation of the GAAP financial results to non-GAAP financial results is included in the schedules below and a description of the adjustments made to the GAAP financial measures is included at the end of the schedules.
The company encourages investors to carefully consider its results under GAAP, as well as its supplemental non-GAAP information and the reconciliation between these presentations, to more fully understand its business. Non-GAAP financial results are reported in addition to, and not as a substitute for, or superior to, financial measures calculated in accordance with GAAP.
The company does not forecast GAAP operating expenses, net income (loss) or earnings per share because it cannot predict certain elements that are included in reported GAAP results. Please see above under “Financial Guidance” for a full explanation.
Reconciliation of GAAP to Non-GAAP Financial Measures
for the Three and Six Months Ended June 30, 2024 and 2023
(unaudited data in millions, except per share amounts)
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Adjusted Gross Margin | |||||||||||||||
| Gross Profit(1) | $ | 147.1 | $ | 125.7 | $ | 284.8 | $ | 247.7 | |||||||
| Acquisition - amortization of intangible assets | 0.3 | 0.3 | 0.6 | 0.6 | |||||||||||
| Equity compensation | 0.6 | 0.4 | 0.9 | 0.7 | |||||||||||
| Transformation initiatives | — | 0.2 | — | 0.2 | |||||||||||
| Other adjustments | 0.2 | — | 0.4 | — | |||||||||||
| Adjusted Gross Profit | $ | 148.2 | $ | 126.6 | $ | 286.7 | $ | 249.2 | |||||||
| Adjusted Gross Margin | 70.1 | % | 69.0 | % | 69.3 | % | 68.3 | % | |||||||
| (1) Consists of total revenues less cost of testing revenue from the Condensed Consolidated Statements of Operations. | |||||||||||||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Adjusted Operating Expenses | |||||||||||||||
| Operating Expenses(1) | $ | 183.6 | $ | 239.4 | $ | 349.2 | $ | 413.6 | |||||||
| Acquisition - amortization of intangible assets | (10.2 | ) | (10.3 | ) | (20.6 | ) | (20.6 | ) | |||||||
| Goodwill and long-lived asset impairment charges | (11.6 | ) | — | (11.6 | ) | — | |||||||||
| Equity compensation | (14.0 | ) | (10.8 | ) | (25.6 | ) | (17.9 | ) | |||||||
| Real estate optimization | (2.3 | ) | (3.5 | ) | (3.5 | ) | (11.0 | ) | |||||||
| Transformation initiatives | (2.0 | ) | (2.7 | ) | (4.0 | ) | (6.8 | ) | |||||||
| Legal charges, net of insurance reimbursement | (0.5 | ) | (77.9 | ) | (0.4 | ) | (78.2 | ) | |||||||
| Other adjustments | (2.2 | ) | (0.8 | ) | (3.6 | ) | (1.2 | ) | |||||||
| Adjusted Operating Expenses | $ | 140.8 | $ | 133.4 | $ | 279.9 | $ | 277.9 | |||||||
| (1) Consists of research and development expense and selling, general and administrative expense, goodwill and lived-asset impairment charges, and legal settlements from the Condensed Consolidated Statements of Operations. | |||||||||||||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Adjusted Operating Income (Loss) | |||||||||||||||
| Operating Loss | $ | (36.5 | ) | $ | (113.7 | ) | $ | (64.4 | ) | $ | (165.9 | ) | |||
| Acquisition - amortization of intangible assets | 10.4 | 10.7 | 21.1 | 21.3 | |||||||||||
| Goodwill and long-lived asset impairment charges | 11.6 | — | 11.6 | — | |||||||||||
| Equity compensation | 14.6 | 11.1 | 26.5 | 18.5 | |||||||||||
| Real estate optimization | 2.3 | 3.5 | 3.5 | 11.0 | |||||||||||
| Transformation initiatives | 2.1 | 2.9 | 4.0 | 7.0 | |||||||||||
| Legal charges, net of insurance reimbursement | 0.6 | 77.9 | 0.5 | 78.2 | |||||||||||
| Other adjustments | 2.3 | 0.8 | 4.0 | 1.2 | |||||||||||
| Adjusted Operating Income (Loss) | $ | 7.4 | $ | (6.8 | ) | $ | 6.8 | $ | (28.7 | ) | |||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Adjusted Net Income (Loss)(1) | |||||||||||||||
| Net Loss | $ | (36.7 | ) | $ | (116.1 | ) | $ | (62.7 | ) | $ | (170.8 | ) | |||
| Acquisition - amortization of intangible assets | 10.4 | 10.7 | 21.1 | 21.3 | |||||||||||
| Goodwill and long-lived asset impairment charges | 11.6 | — | 11.6 | — | |||||||||||
| Equity compensation | 14.6 | 11.1 | 26.5 | 18.5 | |||||||||||
| Real estate optimization | 2.3 | 3.5 | 3.5 | 11.0 | |||||||||||
| Transformation initiatives | 2.1 | 2.9 | 4.0 | 7.0 | |||||||||||
| Legal charges, net of insurance reimbursement | 0.6 | 77.9 | 0.5 | 78.2 | |||||||||||
| Other adjustments | 2.3 | 0.8 | 2.5 | 1.2 | |||||||||||
| Tax adjustments | (2.7 | ) | 2.8 | (3.0 | ) | 9.8 | |||||||||
| Adjusted Net Income (Loss) | $ | 4.5 | $ | (6.4 | ) | $ | 4.0 | $ | (23.8 | ) | |||||
| Weighted average shares outstanding: | |||||||||||||||
| Basic | 90.6 | 81.7 | 90.3 | 81.5 | |||||||||||
| Diluted | 91.5 | 81.7 | 91.5 | 81.5 | |||||||||||
| Adjusted Earnings (Loss) Per Share | |||||||||||||||
| Basic | $ | 0.05 | $ | (0.08 | ) | $ | 0.04 | $ | (0.29 | ) | |||||
| Diluted | $ | 0.05 | $ | (0.08 | ) | $ | 0.04 | $ | (0.29 | ) | |||||
| (1) To determine Adjusted Earnings (Loss) Per Share, or adjusted EPS. | |||||||||||||||
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Adjusted EBITDA | |||||||||||||||
| Net Loss | $ | (36.7 | ) | $ | (116.1 | ) | $ | (62.7 | ) | $ | (170.8 | ) | |||
| Acquisition - amortization of intangible assets | 10.4 | 10.7 | 21.1 | 21.3 | |||||||||||
| Depreciation expense | 4.3 | 2.7 | 8.8 | 5.6 | |||||||||||
| Goodwill and long-lived asset impairment charges | 11.6 | — | 11.6 | — | |||||||||||
| Equity compensation | 14.6 | 11.1 | 26.5 | 18.5 | |||||||||||
| Real estate optimization(1) | 2.3 | 3.5 | 3.5 | 11.0 | |||||||||||
| Transformation initiatives | 2.1 | 2.9 | 4.0 | 7.0 | |||||||||||
| Legal charges, net of insurance reimbursement | 0.6 | 77.9 | 0.5 | 78.2 | |||||||||||
| Interest expense, net of interest income(2) | 0.4 | — | 0.3 | (0.2 | ) | ||||||||||
| Other adjustments | 2.6 | 3.2 | 2.5 | 4.2 | |||||||||||
| Income tax (benefit) expense(3) | (0.5 | ) | — | (0.4 | ) | 2.1 | |||||||||
| Adjusted EBITDA | $ | 11.7 | $ | (4.1 | ) | $ | 15.7 | $ | (23.1 | ) | |||||
| (1) Real estate optimization includes | |||||||||||||||
| (2) Derived from interest expense and interest income from the Condensed Consolidated Statements of Operations. | |||||||||||||||
| (3) Derived from income tax (benefit) from the Condensed Consolidated Statement of Operations. | |||||||||||||||
Adjusted Free Cash Flow Reconciliation
for the Three Months Ended June 30, 2024 and 2023
(unaudited data in millions)
| Three months ended June 30, | Six months ended June 30, | ||||||||||||||
| 2024 | 2023 | 2024 | 2023 | ||||||||||||
| Cash flow from operations | $ | 2.6 | $ | (0.9 | ) | $ | (16.0 | ) | $ | (34.1 | ) | ||||
| Real estate optimization | 3.0 | 3.5 | 9.2 | 11.0 | |||||||||||
| Transformation initiatives | 2.1 | 2.9 | 4.0 | 1.3 | |||||||||||
| Legal charges, net of insurance reimbursement | 0.6 | 0.4 | 0.6 | 2.2 | |||||||||||
| Contingent consideration payment | 5.8 | — | 5.8 | — | |||||||||||
| Other adjustments | 2.3 | — | 3.5 | 0.4 | |||||||||||
| Adjusted operating cash flow | $ | 16.4 | $ | 5.9 | $ | 7.1 | $ | (19.2 | ) | ||||||
| Capital expenditures | (5.2 | ) | (18.8 | ) | (11.9 | ) | (42.3 | ) | |||||||
| Capitalization of internal-use software costs | (3.7 | ) | — | (5.6 | ) | — | |||||||||
| Adjusted free cash flow | $ | 7.5 | $ | (12.9 | ) | $ | (10.4 | ) | $ | (61.5 | ) | ||||
Following is a description of the adjustments made to GAAP financial measures:
- Acquisition – amortization of intangible assets – represents recurring amortization charges resulting from the acquisition of intangible assets.
- Equity compensation – non-cash equity-based compensation provided to Myriad Genetics employees and directors.
- Real estate optimization – costs related to real estate initiatives. Prior to the fourth quarter 2023 reporting period, these costs were included in the transformation initiatives category. With respect to the adjusted free cash flow reconciliation, the cash flow effect of real estate optimizations excludes non-cash items such as accelerated depreciation. These costs include the following:
- For the three months ended June 30, 2024, additional rent as a result of the build-out of our new laboratories in Salt Lake City, Utah, and South Francisco, California, while maintaining our current laboratories in those locations and testing and set-up costs for equipment in our new facilities.
- For the three months ended June 30, 2023, additional rent as a result of the build-out of our new laboratories in Salt Lake City, Utah, and South San Francisco, California, while maintaining our current laboratories in those locations.
- For the six months ended June 30, 2024, additional rent as a result of the build-out of our new laboratories in Salt Lake City, Utah, and South Francisco, California, while maintaining our current laboratories in those locations and testing and set-up costs for equipment in our new facilities, lease terminations gains, net of lease termination losses, impairment charges and other abandonment costs.
- For the six months ended June 30, 2023, additional rent as a result of the build-out of our new laboratories in Salt Lake City, Utah, and South San Francisco, California, while maintaining our current laboratories in those locations, and accelerated depreciation in connection with our decision to cease the use of our former corporate headquarters in Salt Lake City, Utah.
- Transformation initiatives – costs related to transformation initiatives including:
- For the three and six months ended June 30, 2024, consulting and professional fees.
- For the three and six months ended June 30, 2023, consulting and professional fees and severance costs related to restructuring.
- Legal charges, net of insurance reimbursement – one-time legal expenses, net of insurance reimbursement. With respect to the adjusted free cash flow reconciliation, the cash flow effect includes cash paid for settlements in the related period.
- Other adjustments – other one-time non-recurring expenses including:
- For the three months ended June 30, 2024, changes in the fair value of contingent consideration related to acquisitions from prior years, severance, and other consulting costs.
- For the three months ended June 30, 2023, primarily includes changes in the fair value of contingent consideration related to acquisitions from prior years.
- For the six months ended June 30, 2024, primarily includes a gain recognized on acquisition, changes in the fair value of contingent consideration related to acquisitions from prior years, the reclassifications of cumulative translation adjustments to income upon liquidation of an investment in a foreign entity, severance, and costs incurred in connection with executive personnel changes.
- For the six months ended June 30, 2023, consulting and professional fees related to prior year acquisitions and changes in the fair value of contingent consideration related to acquisitions from prior years.
- For purposes of adjusted EBITDA, other adjustments include the items listed above as well as amounts included in other income/expense in the financial statements.
- Depreciation expense - depreciation expense recognized on our fixed assets.
- Goodwill and long-lived asset impairment charges – for the three and six months ended June 30, 2024, primarily the impairment of assets held for sale related to the sale of the EndoPredict business to Eurobio Scientific.
- Contingent consideration payment – for the three months ended June 30, 2024, the payment of contingent consideration related to the previous acquisition of Sividon Diagnostics GmbH.
- Tax adjustments – tax expense/(benefit) due to non-GAAP adjustments, differences between stock compensation recorded for book purposes as compared to the allowable tax deductions, and valuation allowance recognized against federal and state deferred tax assets in the United States.
- As of June 30, 2024, a valuation allowance of
$63.3 million was not recognized for non-GAAP purposes given our historical and forecasted positive earnings performance. - As of June 30, 2023, a valuation allowance of
$37.2 million was not recognized for non-GAAP purposes given our historical and forecasted positive earnings performance. - For purposes of adjusted EBITDA, the income tax expense adjustment includes the income tax expense (benefit) recognized in the financial statements.
- As of June 30, 2024, a valuation allowance of
| Media Contact: | Megan Manzari (385) 318-3718 megan.manzari@myriad.com | Investor Contact: | Matt Scalo (801) 584-3532 matt.scalo@myriad.com |
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