Vericel Reports Second Quarter 2023 Financial Results and Raises Full-Year 2023 Financial Guidance
Record Second Quarter Total Revenue of $45.9 Million, Representing 24% Growth versus Prior Year
MACI Revenue Growth of 27% to $36.3 Million
Epicel Revenue Growth of 17% to $9.6 Million
Full-Year 2023 Revenue Guidance Raised to $190-197 Million
Conference Call Today at 8:30am Eastern Time
CAMBRIDGE, Mass., Aug. 02, 2023 (GLOBE NEWSWIRE) -- Vericel Corporation (NASDAQ:VCEL), a leader in advanced therapies for the sports medicine and severe burn care markets, today reported financial results and business highlights for the second quarter ended June 30, 2023, and provided updated full-year 2023 financial guidance.
Second Quarter 2023 Financial Highlights
- Total net revenue of $45.9 million
- MACI® net revenue of $36.3 million and Epicel® net revenue of $9.6 million
- Gross margin of 65%
- Net loss of $5.0 million, or $0.11 per diluted share
- Non-GAAP adjusted EBITDA of $4.4 million
- Operating cash flow of $10.2 million
- As of June 30, 2023, the Company had approximately $147 million in cash, restricted cash and investments, and no debt
Business Highlights and Updates
- Record second quarter total revenue of $45.9 million, representing 24% growth versus the prior year
- MACI second-quarter revenue growth of 27%, representing the fourth straight quarter of 20%+ growth compared to the prior year
- MACI revenue growth of 29% in the first half of 2023 versus the prior year
- Highest number of surgeons taking MACI biopsies in a quarter and second highest number of MACI biopsies in a quarter since launch
- Second quarter Epicel growth of 17% versus the prior year and 40% sequential growth versus the first quarter
- 12th straight quarter of positive adjusted EBITDA and operating cash flow, with adjusted EBITDA growth of 60% in the second quarter versus the prior year
- Human factors validation study for MACI arthroscopic delivery program planned for Q3 and program remains on track for an anticipated 2024 commercial launch; market research confirms significant opportunity with high level of surgeon interest
- Executed long-term extension of exclusive supply agreement with Matricel GmbH for the MACI ACI-Maix collagen membrane
“The Company continues to execute well, generating very strong revenue growth for both MACI and Epicel in the second quarter, as well as our 12th consecutive quarter of positive adjusted EBITDA and operating cash flow,” said Nick Colangelo, President and CEO of Vericel. “The underlying growth drivers of our business remain strong, as evidenced by our outstanding performance in the first half of the year and, as a result, we are increasing our total net revenue guidance for the full year. We look forward to building on this momentum as we expect a further acceleration in total company revenue growth in 2024 driven by the planned launch of arthroscopic MACI and a significant contribution from NexoBrid.”
2023 Financial Guidance
- Total net revenue for 2023 now expected to be in the range of $190 to $197 million compared to the previous guidance of $184 to $192 million
- Maintaining profitability guidance of gross margin in the high-60% range and adjusted EBITDA margin in the mid-teens % range
Second Quarter 2023 Results
Total net revenue for the quarter ended June 30, 2023 increased 24% to $45.9 million, compared to $37.0 million in the second quarter of 2022. Total net product revenue for the quarter included $36.3 million of MACI (autologous cultured chondrocytes on porcine collagen membrane) net revenue and $9.6 million of Epicel (cultured epidermal autografts) net revenue, compared to $28.6 million of MACI net revenue, $8.2 million of Epicel net revenue, and $0.2 million of NexoBrid (anacaulase-bcdb) net revenue, respectively, in the second quarter of 2022.
Gross profit for the quarter ended June 30, 2023 was $29.9 million, or 65% of net revenue, compared to $22.9 million, or 62% of net revenue, for the second quarter of 2022.
Total operating expenses for the quarter ended June 30, 2023 were $35.9 million, compared to $31.9 million for the same period in 2022. The increase in operating expenses was primarily due to higher sales and marketing expenses and research and development program costs.
Net loss for the quarter ended June 30, 2023 was $5.0 million, or $0.11 per diluted share, compared to $9.0 million, or $0.19 per diluted share, for the second quarter of 2022.
Non-GAAP adjusted EBITDA for the quarter ended June 30, 2023 was $4.4 million, or 10% of net revenue, compared to $2.8 million, or 7% of net revenue, for the second quarter of 2022. A table reconciling non-GAAP measures is included in this press release for reference.
As of June 30, 2023, the Company had approximately $147 million in cash, restricted cash and investments, and no debt.
Conference Call Information
Today’s conference call will be available live at 8:30am Eastern Time and can be accessed through the Investor Relations section of the Vericel website at http://investors.vcel.com/events-presentations. A slide presentation with highlights from today’s conference call will be available on the webcast and in the Investor Relations section of the Vericel website. Please access the site at least 15 minutes prior to the scheduled start time in order to download the required audio software, if necessary. To participate by telephone, please register here to receive dial-in details and your personal passcode. A replay of the webcast will be available on the Vericel website until August 2, 2024.
About Vericel Corporation
Vericel is a leader in advanced therapies for the sports medicine and severe burn care markets. The Company markets two cell therapy products and one specialty biologic product in the United States. MACI® (autologous cultured chondrocytes on porcine collagen membrane) is an autologous cellularized scaffold product indicated for the repair of symptomatic, single or multiple full-thickness cartilage defects of the knee with or without bone involvement in adults. Epicel® (cultured epidermal autografts) is a permanent skin replacement for the treatment of patients with deep dermal or full thickness burns greater than or equal to 30% of total body surface area. The Company also holds an exclusive license for North American rights to NexoBrid® (anacaulase-bcdb), a biological orphan product containing proteolytic enzymes, which is indicated for the removal of eschar in adults with deep partial-thickness and/or full-thickness burns. For more information, please visit www.vcel.com.
GAAP v. Non-GAAP Measures
Vericel’s reported earnings are prepared in accordance with generally accepted accounting principles in the United States, or GAAP, and represent earnings as reported to the Securities and Exchange Commission. Vericel has provided in this release certain financial information that has not been prepared in accordance with GAAP. Vericel’s management believes that the non-GAAP adjusted EBITDA described in the release, which includes adjustments for specific items that are generally not indicative of our core operations, provides additional information that is useful to investors in understanding Vericel’s underlying performance, business and performance trends, and helps facilitate period-to-period comparisons and comparisons of its financial measures with other companies in Vericel’s industry. However, the non-GAAP financial measures that Vericel uses may differ from measures that other companies may use. Non-GAAP financial measures are not required to be uniformly applied, are not audited and should not be considered in isolation or as substitutes for results prepared in accordance with GAAP.
Epicel® and MACI® are registered trademarks of Vericel Corporation. NexoBrid® is a registered trademark of MediWound Ltd. and is used under license to Vericel Corporation. © 2023 Vericel Corporation. All rights reserved.
Vericel cautions you that all statements other than statements of historical fact included in this press release that address activities, events or developments that we expect, believe or anticipate will or may occur in the future are forward-looking statements. Although we believe that we have a reasonable basis for the forward-looking statements contained herein, they are based on current expectations about future events affecting us and are subject to risks, assumptions, uncertainties and factors relating to our operations and business environment, all of which are difficult to predict and many of which are beyond our control. Our actual results may differ materially from those expressed or implied by the forward-looking statements in this press release. These statements are often, but are not always, made through the use of words or phrases such as “anticipates,” “intends,” “estimates,” “plans,” “expects,” “continues,” “believe,” “guidance,” “outlook,” “target,” “future,” “potential,” “goals” and similar words or phrases, or future or conditional verbs such as “will,” “would,” “should,” “could,” “may,” or similar expressions.
Among the factors that could cause actual results to differ materially from those set forth in the forward-looking statements include, but are not limited to, uncertainties associated with our expectations regarding future revenue, growth in revenue, market penetration for MACI, Epicel, and NexoBrid, growth in profit, gross margins and operating margins, the ability to continue to scale our manufacturing operations to meet the demand for our cell therapy products, including the timely completion of a new headquarters and manufacturing facility in Burlington, Massachusetts, the ability to achieve or sustain profitability, contributions to adjusted EBITDA, the expected target surgeon audience, potential fluctuations in sales and volumes and our results of operations over the course of the year, timing and conduct of clinical trial and product development activities, timing and likelihood of the FDA’s potential approval of the arthroscopic delivery of MACI to the knee or the use of MACI to treat cartilage defects in the ankle, the estimate of the commercial growth potential of our products and product candidates, competitive developments, changes in third-party coverage and reimbursement, the ultimate timing of the commercial launch of NexoBrid in the United States, physician and burn center adoption of NexoBrid, supply chain disruptions or other events affecting MediWound Ltd.’s ability to manufacture and supply NexoBrid to meet customer demand, negative impacts on the global economy and capital markets resulting from the conflict in Ukraine, global geopolitical tensions or record inflation and potential future impacts of the COVID-19 pandemic on our business or the economy generally.
These and other significant factors are discussed in greater detail in Vericel’s Annual Report on Form 10-K for the year ended December 31, 2022, filed with the Securities and Exchange Commission (SEC) on February 23, 2023, Vericel’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2023, filed with the SEC on August 2, 2023, and in other filings with the SEC. These forward-looking statements reflect our views as of the date hereof and Vericel does not assume and specifically disclaims any obligation to update any of these forward-looking statements to reflect a change in its views or events or circumstances that occur after the date of this release except as required by law.
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|CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS|
|(in thousands, except per share amounts - unaudited)|
|Three Months Ended June 30,||Six months ended June 30,|
|Product sales, net||$||45,922||$||36,826||$||86,939||$||72,678|
|Cost of product sales||15,981||14,192||30,478||26,814|
|Research and development||5,253||4,792||10,465||9,652|
|Selling, general and administrative||30,649||27,144||60,134||53,009|
|Total operating expenses||35,902||31,936||70,599||62,661|
|Loss from operations||(5,961||)||(9,082||)||(14,138||)||(16,355||)|
|Other income (expense):|
|Other (expense) income||(5||)||(9||)||(17||)||103|
|Total other income||941||119||1,623||301|
|Net loss per common share:|
|Basic and diluted||$||(0.11||)||$||(0.19||)||$||(0.26||)||$||(0.34||)|
|Weighted-average common shares outstanding:|
|Basic and diluted||47,572||47,117||47,480||47,052|
|RECONCILIATION OF REPORTED NET LOSS (GAAP)|
|TO ADJUSTED EBITDA (NON-GAAP MEASURE)|
|(in thousands - unaudited)|
|Three Months Ended June 30,||Six months ended June 30,|
|Stock-based compensation expense||8,761||10,808||17,492||20,339|
|Depreciation and amortization||1,171||1,055||2,329||1,928|
|Net interest income||(946||)||(128||)||(1,640||)||(198||)|
|Pre-occupancy lease expense||475||—||475||—|
|Adjusted EBITDA (Non-GAAP)||$||4,441||$||2,772||$||6,141||$||6,015|
|CONDENSED CONSOLIDATED BALANCE SHEETS|
|(in thousands - unaudited)|
|June 30,||December 31,|
|Cash and cash equivalents||$||43,023||$||51,067|
|Accounts receivable (net of allowance for doubtful accounts of $44 and $47, respectively)||38,319||46,539|
|Other current assets||5,044||4,803|
|Total current assets||182,871||186,866|
|Property and equipment, net||23,408||15,837|
|Intangible assets, net||7,188||7,500|
|Other long-term assets||1,196||1,303|
|LIABILITIES AND SHAREHOLDERS’ EQUITY|
|Current portion of operating lease liabilities||7,218||4,302|
|Other current liabilities||21||41|
|Total current liabilities||35,611||37,463|
|Operating lease liabilities||76,144||43,268|
|Other long-term liabilities||28||—|
|Total shareholders’ equity||198,928||192,272|
|Total liabilities and shareholders’ equity||$||310,711||$||273,003|