Moderna Reports Fourth Quarter and Fiscal Year 2023 Financial Results and Provides Business Updates
- Strong fourth-quarter revenues of $2.8 billion with net income of $217 million and diluted EPS of $0.55.
- Full-year revenues of $6.8 billion but a net loss of $(4.7) billion and diluted EPS of $(12.33).
- Reaffirmed 2024 expected product sales of $4 billion.
- Anticipates regulatory approvals for its investigational RSV vaccine in the first half of 2024.
- Moderna achieved 48% cumulative market share in the U.S. retail segment during the fall 2023 COVID season.
- Continued focus on public health efforts to increase vaccination coverage rates globally for the 2024/2025 season.
- Expectations for regulatory approvals of the RSV vaccine mRNA-1345 starting in the first half of 2024.
- Financial framework for 2024 includes revenue of approximately $4 billion, with expected research and development expenses of $4.5 billion.
- Upcoming late-stage pipeline milestones across vaccines and therapeutics portfolio.
- Key 2024 investor and analyst event dates announced.
- Significant decrease in total revenue for 2023 compared to 2022.
- Net product sales for 2023 decreased by 64% from 2022.
- Substantial net loss of $(4.7) billion for the full year 2023.
- Diluted loss per share of $(12.33) for the full year 2023.
- Cost of sales for 2023 was $4.7 billion, representing 70% of net product sales.
- Income tax provision for the full year 2023 was $772 million.
- Cash position decreased in 2023 to $13.3 billion compared to $18.2 billion in 2022.
Insights
The reported financials of a company like Moderna, which is a key player in the biotechnology industry, provide critical information for stakeholders and market participants. The significant decline in year-over-year quarterly revenue from $5.1 billion to $2.8 billion and the stark contrast between the previous year's net income of $8.4 billion and the current net loss of $(4.7) billion, are indicative of a major shift in the company's financial health. This shift is primarily attributed to the reduction in COVID-19 vaccine sales as the world transitions to an endemic phase of the virus. The reported net loss includes non-cash charges related to resizing and a tax valuation allowance, which are essential factors for investors to consider when assessing the company's operational efficiency and future profitability.
Moderna's reaffirmation of its 2024 expected product sales of approximately $4 billion suggests confidence in its pipeline, particularly its investigational RSV vaccine. The market's response to this projection will hinge on the vaccine's regulatory approval and market acceptance. Furthermore, the company's cash position, which has decreased from $18.2 billion to $13.3 billion, could raise concerns about liquidity and capital allocation strategies, particularly in light of the forecasted capital expenditures of approximately $0.9 billion for 2024. The anticipated negligible tax expense for the full year is another factor that could influence net earnings projections.
Moderna's strategic pivot to adapt to a seasonal endemic market is a significant move that could redefine its commercial strategy and market positioning. The company's increased market share in the U.S. retail segment for COVID-19 vaccines from 37% to 48% demonstrates its ability to capture demand despite challenging market conditions. The transition includes operational changes such as resizing manufacturing footprints and flattening commercial structures, which are intended to streamline operations and improve cash flow. These actions, while necessary for long-term sustainability, have resulted in short-term financial impacts, including inventory write-downs and charges related to the wind-down of contract manufacturing operations.
Moreover, Moderna's focus on public health efforts to increase vaccination coverage rates globally for future seasons and its participation in EU tendering procedures for mRNA COVID-19 vaccines underscore its commitment to maintaining a significant presence in the vaccine market. The company's anticipation of regulatory approvals for its RSV vaccine and the launch in key markets such as Australia and Germany could open new revenue streams and potentially offset declines in COVID-19 vaccine sales.
The clinical progress of Moderna's pipeline, particularly the investigational RSV vaccine, is a crucial aspect of the company's potential growth. The positive data from the pivotal ConquerRSV study, which demonstrated high vaccine efficacy against RSV-associated lower respiratory tract disease, positions mRNA-1345 as a strong contender in the vaccine market. The pre-filled syringe (PFS) formulation of the vaccine is an innovative approach that offers practical advantages in administration and could be a differentiating factor in market adoption.
The anticipation of regulatory approvals and the inclusion of mRNA-1345 in the upcoming CDC ACIP meeting agenda are key milestones that investors should monitor closely. Additionally, the robust pipeline with nine late-stage programs, including vaccines for seasonal flu, COVID-19 and CMV, as well as oncology therapeutics such as the Individualized Neoantigen Therapy (INT), provide a diverse portfolio that could mitigate risks associated with reliance on a single product. The continued development and potential commercial scale-up of these programs are pivotal for Moderna's future revenue streams and market relevance.
Posts fourth quarter revenues of
Reports full-year revenues of
Reaffirms 2024 expected product sales of approximately
Expects regulatory approvals for its investigational RSV vaccine for older adults beginning in first half of 2024, and anticipates additional key milestones from its late-stage pipeline this year
CAMBRIDGE, MA / ACCESSWIRE / February 22, 2024 / Moderna, Inc. (NASDAQ:MRNA) today reported financial results and provided business updates for the fourth quarter and fiscal year 2023.
"2023 was a year of transition for Moderna as we adapted to the endemic market. At the same time, our development team made significant pipeline advancements across infectious diseases, oncology and rare diseases, while our commercial team increased our COVID-19 market share in the U.S.," said Stéphane Bancel, Chief Executive Officer of Moderna. "We look forward to the anticipated approvals of our RSV vaccine beginning in the first half of the year. With multiple upcoming Phase 3 data readouts in 2024, we remain focused on commercial execution and continued investment in our pipeline with financial discipline."
Recent progress includes:
Commercial Updates
COVID-19: The Company reported
Moderna achieved
The Company is reaffirming its 2024 product sales outlook as it enters the second year of the U.S. commercial endemic COVID market with increased clarity of market size and dynamics. Moderna continues to focus on public health efforts to increase vaccination coverage rates globally for the 2024/2025 season to reduce the substantial burden of COVID-19. The Company is also prioritizing key international markets for greater commercial focus and is participating in the EU Health Emergency and Response Authority's tendering procedure for up to 36 million doses of mRNA COVID-19 vaccines per year for up to four years.
RSV: The Company continues to expect initial regulatory approvals of its RSV vaccine (mRNA-1345) starting in the first half of 2024.
Moderna is well-prepared for the launch of its second respiratory vaccine, which will build upon the success of its commercial efforts in the fall COVID-19 market. The Company is encouraged by early indications of widespread consumer awareness and established demand in the RSV market, which Moderna will enter with a strong competitive profile with robust efficacy data, a well-established safety and tolerability profile, and as the only pre-filled syringe (PFS) product available at the time of launch. The PFS ready-to-use formulation will save pharmacists and clinicians time as well as potentially help reduce administration errors.
The PDUFA (Prescription Drug User Fee Act) action date for mRNA-1345 is May 12, 2024, by which time the Company expects the U.S. FDA's response to its Biologics License Application (BLA). If the outcome is positive, the Company anticipates that the U.S. CDC Advisory Committee on Immunization Practices (ACIP) will include mRNA-1345 on the agenda of its June 26-28 meeting. Assuming that corresponding marketing authorizations would be granted as expected, the Company also plans to launch its RSV vaccine in Australia and Germany in 2024 and other markets in 2025 due to regulatory and tender timing.
Fourth Quarter 2023 Financial Results
Revenue: Total revenue for the fourth quarter of 2023 was
Cost of Sales: Cost of sales for the fourth quarter of 2023 totaled
Research and Development Expenses: Research and development expenses for the fourth quarter of 2023 increased by
Selling, General and Administrative Expenses: Selling, general and administrative expenses for the fourth quarter of 2023 increased by
Income Taxes: Income tax benefit for the fourth quarter of 2023 was
Net Income: Net income was
Earnings Per Share: Diluted earnings per share was
Full Year 2023 Financial Results
Revenue: Total revenue was
Cost of Sales: Cost of sales for the full year 2023 was
Research and Development Expenses: Research and development expenses increased by
Selling, General and Administrative Expenses: Selling, general and administrative expenses increased by
Income Taxes: Income tax provision for the full year 2023 was
Net Income (Loss): Net loss for the full year 2023 was
Earnings (Loss) Per Share: Diluted loss per share for the full year 2023 was
Cash Position: Cash, cash equivalents and investments as of December 31, 2023, and December 31, 2022, were
2024 Financial Framework
Revenue: The Company expects revenue of approximately
Cost of Sales: The Company expects cost of sales for 2024 to be approximately
Research and Development Expenses: The Company expects full-year 2024 research and development expenses of approximately
Selling, General and Administrative Expenses: The Company expects full-year 2024 selling, general and administrative expenses of approximately
Income Taxes: The Company anticipates its full-year tax expense to be negligible.
Capital Expenditures: The Company expects capital expenditures for 2024 of approximately
Cash and Investments: The Company expects 2024 year-end cash and investments of approximately
Recent Progress and Upcoming Late-Stage Pipeline Milestones
With nine late-stage programs, Moderna continues to advance its pipeline and expects numerous product milestones in 2024 across its vaccines and therapeutics portfolio.
Respiratory vaccines:
- RRespiratory syncytial virus (RSV) vaccine: Moderna has filed for regulatory approvals for its vaccine for the prevention of RSV-associated lower respiratory tract disease (RSV-LRTD) and acute respiratory disease (ARD) in adults ages 60 years or older (mRNA-1345). The regulatory applications are based on positive data from the pivotal ConquerRSV study, a randomized, double-blind, placebo-controlled study of approximately 37,000 adults, 60 years or older. The trial met both its primary efficacy endpoints, with a vaccine efficacy (VE) of
83.7% (95.88% CI:66.1% ,92.2% ; p<0.0001) against RSV-LRTD as defined by two or more symptoms, and a VE of82.4% (96.36% CI:34.8% ,95.3% ; p=0.0078) against RSV-LRTD defined by three or more symptoms. Most solicited adverse reactions were mild to moderate, and no cases of Guillain-Barre Syndrome (GBS) have been reported with mRNA-1345 in the Phase 3 RSV trial. These data were published in the New England Journal of Medicine in December 2023. Follow-up data from a Phase 3 RSV study with a median follow-up duration of 8.6 months, with a range of 15 days to 530 days, and including subjects from the Northern and Southern Hemispheres was recently presented at the RSVVW'24 conference. In this supplemental analysis, mRNA-1345 maintained durable efficacy, with sustained VE of63.3% (95.88% CI:48.7% ,73.7% ) against RSV-LRTD including two or more symptoms. VE was74.6% (95% CI, 50.7-86.9) against RSV-LRTD with ≥2 symptoms, including shortness of breath and63.0% (95% CI, 37.3-78.2) against RSV-LRTD including three of more symptoms. The stringent statistical criterion of the study, a lower bound on the95% CI of >20% , continued to be met for both endpoints. As mentioned above, the Company expects regulatory approvals beginning in the first half of 2024.
- Seasonal flu vaccine: Moderna's seasonal flu vaccine (mRNA-1010) demonstrated consistently acceptable safety and tolerability across three Phase 3 trials. In the most recent Phase 3 trial (P303), mRNA-1010 met all immunogenicity endpoints, demonstrating higher titers compared to a currently licensed standard-dose flu vaccine. mRNA-1010 has also shown higher or comparable titers compared to a currently licensed enhanced flu vaccine (Fluzone HD®) in a separate Phase 1/2 study. The Company is in ongoing discussions with regulators and intends to file in 2024.
- Next-generation COVID-19 vaccine: Moderna's Phase 3 study of its next-generation COVID-19 vaccine (mRNA-1283), which is designed to be refrigerator-stable, is fully enrolled. The Company anticipates data from the study in the first half of 2024.
- Seasonal flu + COVID vaccine: Moderna's Phase 3 trial of its combination vaccine against seasonal flu and COVID-19 (mRNA-1083) is fully enrolled. The Company anticipates data from the study in 2024.
Latent and other vaccines:
- CMV vaccine: The pivotal Phase 3 study of Moderna's CMV vaccine candidate (mRNA-1647) is fully enrolled and accruing cases, evaluating its efficacy, safety and immunogenicity in the prevention of primary infection in women of childbearing age. The Company anticipates potential efficacy data from the study in 2024.
Oncology therapeutics:
- Individualized Neoantigen Therapy (INT): Moderna continues to demonstrate the potential clinical benefit of its INT program (mRNA-4157). In partnership with Merck, Phase 3 trials continue to enroll in resected high-risk (stage III/IV) melanoma and completely resected stage II, IIIA or IIIB non-small cell lung cancer. Moderna and Merck plan to initiate clinical studies in additional tumor types in 2024. In December 2023, the Company announced results of a three-year analysis of its Phase 2b study evaluating INT in combination with KEYTRUDA®, Merck's anti-PD-1 therapy, in patients with resected high-risk melanoma. Compared to KEYTRUDA alone, this combination continued to show an improvement in recurrence-free survival, reducing the risk of recurrence or death by
49% , as well as in distant metastasis-free survival, reducing the risk of developing distant metastasis or death by62% . Additionally, the results of the primary analysis at two-year follow-up of its Phase 2 study were published in The Lancet. The Company has purchased and started build-out of a manufacturing site in Marlborough, MA, to enable commercial scale of its INT program.
Rare disease therapeutics:
- Propionic acidemia (PA) & methylmalonic acidemia (MMA): The Company expects to advance its PA (mRNA-3927) and MMA (mRNA-3705) programs into registrational studies in 2024.
Moderna Corporate Updates
- Highlighted the Company's digital and AI strategy and progress at its second Digital Investor Event on November 8, 2023.
- Reviewed the Company's progress and ambitions during its second Environmental, Social and Governance (ESG) Investor Event on December 7, 2023.
- Published Moderna CEO Stéphane Bancel's annual letter to shareholders on January 2, 2024.
- Provided business and pipeline updates at the 42nd Annual J.P. Morgan Healthcare Conference on January 8, 2024.
- Scheduled the Moderna Annual Meeting of Shareholders to be held on Monday, May 6, 2024, at 8:00 a.m. ET.
Company accolades:
- Moderna topped BioSpace's Best Places to Work in Biopharma ranking for the third consecutive year.
- Moderna was named to Fortune's list of World's Most Admired Companies for the first time.
- Stéphane Bancel, Chief Executive Officer of Moderna, was elected to the National Academy of Engineering.
Key 2024 Investor and Analyst Event Dates
- Vaccines Day: March 27 at 9 a.m. ET
- R&D Day: September 12
Investor Call and Webcast Information
Moderna will host a live conference call and webcast at 8:00 a.m. ET on February 22, 2024. To access the live conference call via telephone, please register at the link below. Once registered, dial-in numbers and a unique pin number will be provided. A live webcast of the call will also be available under "Events and Presentations" in the Investors section of the Moderna website.
- Telephone: https://register.vevent.com/register/BI0c7f1372a78b427d9f354a2630418034
- Webcast: https://investors.modernatx.com
The archived webcast will be available on Moderna's website approximately two hours after the conference call and will be available for one year following the call.
About Moderna
Moderna is a leader in the creation of the field of mRNA medicine. Through the advancement of mRNA technology, Moderna is reimagining how medicines are made and transforming how we treat and prevent disease for everyone. By working at the intersection of science, technology and health for more than a decade, the company has developed medicines at unprecedented speed and efficiency, including one of the earliest and most effective COVID-19 vaccines.
Moderna's mRNA platform has enabled the development of therapeutics and vaccines for infectious diseases, immuno-oncology, rare diseases and autoimmune diseases. With a unique culture and a global team driven by the Moderna values and mindsets to responsibly change the future of human health, Moderna strives to deliver the greatest possible impact to people through mRNA medicines. For more information about Moderna, please visit modernatx.com and connect with us on X (formerly Twitter), Facebook, Instagram, YouTube and LinkedIn.
MODERNA, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Unaudited, in millions, except per share data)
Three Months Ended December 31, | Years Ended December 31, | |||||||||||||||
2023 | 2022 | 2023 | 2022 | |||||||||||||
Revenue: | ||||||||||||||||
Net product sales | $ | 2,793 | $ | 4,859 | $ | 6,671 | $ | 18,435 | ||||||||
Other revenue1 | 18 | 225 | 177 | 828 | ||||||||||||
Total revenue | 2,811 | 5,084 | 6,848 | 19,263 | ||||||||||||
Operating expenses: | ||||||||||||||||
Cost of sales | 929 | 1,918 | 4,693 | 5,416 | ||||||||||||
Research and development | 1,406 | 1,211 | 4,845 | 3,295 | ||||||||||||
Selling, general and administrative | 470 | 375 | 1,549 | 1,132 | ||||||||||||
Total operating expenses | 2,805 | 3,504 | 11,087 | 9,843 | ||||||||||||
Income (loss) from operations | 6 | 1,580 | (4,239 | ) | 9,420 | |||||||||||
Interest income | 103 | 87 | 421 | 200 | ||||||||||||
Other expense, net | (39 | ) | (12 | ) | (124 | ) | (45 | ) | ||||||||
Income (loss) before income taxes | 70 | 1,655 | (3,942 | ) | 9,575 | |||||||||||
(Benefit from) provision for income taxes | (147 | ) | 190 | 772 | 1,213 | |||||||||||
Net income (loss) | $ | 217 | $ | 1,465 | $ | (4,714 | ) | $ | 8,362 | |||||||
Earnings (loss) per share: | ||||||||||||||||
Basic | $ | 0.57 | $ | 3.81 | $ | (12.33 | ) | $ | 21.26 | |||||||
Diluted | $ | 0.55 | $ | 3.61 | $ | (12.33 | ) | $ | 20.12 | |||||||
Weighted average common shares used in calculation of earnings (loss) per share: | ||||||||||||||||
Basic | 381 | 385 | 382 | 394 | ||||||||||||
Diluted | 395 | 405 | 382 | 416 |
1Includes grant revenue and collaboration revenue
MODERNA, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Unaudited, in millions)
December 31, | December 31, | |||||||
2023 | 2022 | |||||||
Assets | ||||||||
Current assets: | ||||||||
Cash and cash equivalents | $ | 2,907 | $ | 3,205 | ||||
Investments | 5,697 | 6,697 | ||||||
Accounts receivable, net | 892 | 1,385 | ||||||
Inventory | 202 | 949 | ||||||
Prepaid expenses and other current assets | 627 | 1,195 | ||||||
Total current assets | 10,325 | 13,431 | ||||||
Investments, non-current | 4,677 | 8,318 | ||||||
Property, plant and equipment, net | 1,945 | 2,018 | ||||||
Right-of-use assets, operating leases | 713 | 121 | ||||||
Deferred tax assets | 81 | 982 | ||||||
Other non-current assets | 685 | 988 | ||||||
Total assets | $ | 18,426 | $ | 25,858 | ||||
Liabilities and Stockholders' Equity | ||||||||
Current liabilities: | ||||||||
Accounts payable | $ | 520 | $ | 487 | ||||
Accrued liabilities | 1,798 | 2,101 | ||||||
Deferred revenue | 568 | 2,038 | ||||||
Income taxes payable | 63 | 48 | ||||||
Other current liabilities | 66 | 249 | ||||||
Total current liabilities | 3,015 | 4,923 | ||||||
Deferred revenue, non-current | 83 | 673 | ||||||
Operating lease liabilities, non-current | 643 | 92 | ||||||
Financing lease liabilities, non-current | 575 | 912 | ||||||
Other non-current liabilities | 256 | 135 | ||||||
Total liabilities | 4,572 | 6,735 | ||||||
Stockholders' equity: | ||||||||
Additional paid-in capital | 371 | 1,173 | ||||||
Accumulated other comprehensive loss | (123 | ) | (370 | ) | ||||
Retained earnings | 13,606 | 18,320 | ||||||
Total stockholders' equity | 13,854 | 19,123 | ||||||
Total liabilities and stockholders' equity | $ | 18,426 | $ | 25,858 |
MODERNA, INC.
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS
(Unaudited, in millions)
Years Ended December 31, | ||||||||
2023 | 2022 | |||||||
Operating activities | ||||||||
Net (loss) income | $ | (4,714 | ) | $ | 8,362 | |||
Adjustments to reconcile net (loss) income to net cash (used in) provided by operating activities: | ||||||||
Stock-based compensation | 305 | 226 | ||||||
Depreciation and amortization | 621 | 348 | ||||||
Amortization/accretion of investments | (61 | ) | 31 | |||||
Loss on equity investments, net | 35 | - | ||||||
Deferred income taxes | 828 | (559 | ) | |||||
Other non-cash items | 7 | 28 | ||||||
Changes in assets and liabilities, net of acquisition of business: | ||||||||
Accounts receivable, net | 493 | 1,790 | ||||||
Prepaid expenses and other assets | 974 | (1,699 | ) | |||||
Inventory | 747 | 492 | ||||||
Right-of-use assets, operating leases | (605 | ) | 21 | |||||
Accounts payable | 13 | 240 | ||||||
Accrued liabilities | (340 | ) | 612 | |||||
Deferred revenue | (2,060 | ) | (4,157 | ) | ||||
Income taxes payable | 15 | (828 | ) | |||||
Operating lease liabilities | 551 | (14 | ) | |||||
Other liabilities | 73 | 88 | ||||||
Net cash (used in) provided by operating activities | (3,118 | ) | 4,981 | |||||
Investing activities | ||||||||
Purchases of marketable securities | (3,760 | ) | (11,435 | ) | ||||
Proceeds from maturities of marketable securities | 5,575 | 3,151 | ||||||
Proceeds from sales of marketable securities | 3,206 | 3,548 | ||||||
Purchases of property, plant and equipment | (707 | ) | (400 | ) | ||||
Acquisition of business, net of cash acquired | (85 | ) | - | |||||
Investment in convertible notes and equity securities | (23 | ) | (40 | ) | ||||
Net cash provided by (used in) investing activities | 4,206 | (5,176 | ) | |||||
Financing activities | ||||||||
Proceeds from issuance of common stock through equity plans | 46 | 65 | ||||||
Repurchase of common stock, including excise tax | (1,153 | ) | (3,329 | ) | ||||
Changes in financing lease liabilities | (270 | ) | (184 | ) | ||||
Net cash used in financing activities | (1,377 | ) | (3,448 | ) | ||||
Net decrease in cash, cash equivalents and restricted cash | (289 | ) | (3,643 | ) | ||||
Cash, cash equivalents and restricted cash, beginning of year | 3,217 | 6,860 | ||||||
Cash, cash equivalents and restricted cash, end of period | $ | 2,928 | $ | 3,217 |
Spikevax® is a registered trademark of Moderna.
Fluzone® is a registered trademark of Sanofi Pasteur.
KEYTRUDA® is a registered trademark of Merck Sharp & Dohme Corp.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including statements regarding: Moderna's anticipated approval and launch of its RSV vaccine in 2024 and 2025, market dynamics, and its competitive profile; Moderna's 2024 financial framework and anticipated performance, including expected revenues; the potential for Moderna to launch up to 15 products in the next five years; anticipated milestones for Moderna's pipeline programs in 2024; and the future profitability of Moderna's COVID-19 vaccine franchise. In some cases, forward-looking statements can be identified by terminology such as "will," "may," "should," "could," "expects," "intends," "plans," "aims," "anticipates," "believes," "estimates," "predicts," "potential," "continue," or the negative of these terms or other comparable terminology, although not all forward-looking statements contain these words. The forward-looking statements in this press release are neither promises nor guarantees, and you should not place undue reliance on these forward-looking statements because they involve known and unknown risks, uncertainties, and other factors, many of which are beyond Moderna's control and which could cause actual results to differ materially from those expressed or implied by these forward-looking statements. These risks, uncertainties, and other factors include, among others, those risks and uncertainties described under the heading "Risk Factors" in Moderna's Annual Report on Form 10-K for the fiscal year ended December 31, 2022, filed with the U.S. Securities and Exchange Commission (SEC), and in subsequent filings made by Moderna with the SEC, which are available on the SEC's website at www.sec.gov. Except as required by law, Moderna disclaims any intention or responsibility for updating or revising any forward-looking statements contained in this press release in the event of new information, future developments or otherwise. These forward-looking statements are based on Moderna's current expectations and speak only as of the date of this press release.
1 Based on information licensed from IQVIA: IQVIA RAPID Weekly Audit for September-December 2023, reflecting estimates of real-world activity. All rights reserved.
###
Moderna Contacts
Media:
Chris Ridley
Head, Global Media Relations
+1 617-800-3651
Chris.Ridley@modernatx.com
Investors:
Lavina Talukdar
Senior Vice President & Head of Investor Relations
+1 617-209-5834
Lavina.Talukdar@modernatx.com
SOURCE: Moderna, Inc.
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