Full-year 2024 revenue of $332 million, an
increase of 51% compared to 2023 and above previously reported
guidance
Delivered 96,071 total test reports in 2024, an
increase of 36% compared to 2023
Year-end 2024 cash, cash equivalents and
marketable investment securities of $293 million, a $50 million
increase compared to 2023
Anticipate generating between $280-295 million
in total revenue in 2025
Conference call and webcast today at 4:30 p.m.
ET
Castle Biosciences, Inc. (Nasdaq: CSTL), a company improving
health through innovative tests that guide patient care, today
announced its financial results for the fourth quarter and year
ended December 31, 2024.
“Castle delivered an outstanding fourth quarter that rounded out
an exceptional 2024, including 51% revenue growth and 36% test
report volume growth compared to 2023,” said Derek Maetzold,
president and chief executive officer of Castle Biosciences. “I am
incredibly proud of our team's hard work in achieving these
results, including achieving our previously provided 2025 revenue
guidance range one year ahead of expectations.
“We are extremely pleased with the progress we made across our
initiatives in 2024 in the areas of our core growth drivers,
including a 17% increase in our dermatologic test reports
(DecisionDx®-Melanoma and DecisionDx®-SCC combined) and a 130%
increase in our TissueCypher® Barrett’s Esophagus test reports,
over 2023. We believe this was driven largely by the clinical value
of our tests, strong execution on our commercial strategy and
expansion of our clinical evidence base.
“Building on our momentum and successes, we expect to continue
to focus on delivering operational excellence. Further, sound
capital allocation remains a priority, including pursuing strategic
opportunities, aimed at driving stockholder value in 2025 and
beyond.”
Twelve Months Ended December 31, 2024, Financial and
Operational Highlights
- Revenues were $332.1 million, a 51% increase compared to $219.8
million in 2023.
- Adjusted Revenues, which exclude the effects of revenue
adjustments related to tests delivered in prior periods, were
$333.8 million, a 49% increase compared to $224.3 million in
2023.
- Delivered 96,071 total test reports in 2024, an increase of 36%
compared to 70,429 in 2023:
- DecisionDx-Melanoma test reports delivered in 2024 were 36,008,
compared to 33,330 in 2023.
- DecisionDx-SCC test reports delivered in 2024 were 16,348,
compared to 11,442 in 2023.
- MyPath® Melanoma test reports delivered in 2024 were 3,909,
compared to 3,962 MyPath Melanoma and DiffDx®-Melanoma aggregate
test reports in 2023.
- TissueCypher Barrett’s Esophagus test reports delivered in 2024
were 20,956, compared to 9,100 in 2023.
- IDgenetix® test reports delivered in 2024 were 17,151, compared
to 10,921 in 2023.
- DecisionDx®-UM test reports delivered in 2024 were 1,699,
compared to 1,674 in 2023.
- Gross margin for 2024 was 79%, and Adjusted Gross Margin was
82%, compared to 75% and 80% respectively for the same periods in
2023.
- Net cash provided by operations was $64.9 million, compared to
net cash used in operations of $5.6 million in 2023.
- Net income for 2024, which includes non-cash stock-based
compensation expense of $50.3 million, was $18.2 million, compared
to a net loss of $57.5 million in 2023.
- Adjusted EBITDA for 2024 was $75.0 million, compared to $(4.4)
million in 2023.
Cash, Cash Equivalents and Marketable Investment
Securities
As of December 31, 2024, the Company’s cash, cash equivalents
and marketable investment securities totaled $293.1 million.
Fourth Quarter Ended December 31, 2024, Financial and
Operational Highlights
- Revenues were $86.3 million, a 31% increase compared to $66.1
million during the same period in 2023.
- Adjusted Revenues, which exclude the effects of revenue
adjustments related to tests delivered in prior periods, were $85.8
million, a 22% increase compared to $70.2 million for the same
period in 2023.
- Delivered 24,071 total test reports, an increase of 19%
compared to 20,284 in the same period of 2023:
- DecisionDx-Melanoma test reports delivered in the quarter were
8,672, compared to 8,591 in the fourth quarter of 2023.
- DecisionDx-SCC test reports delivered in the quarter were
4,299, compared to 3,530 in the fourth quarter of 2023.
- MyPath Melanoma test reports delivered in the quarter were 879,
compared to 1,018 in the fourth quarter of 2023.
- TissueCypher Barrett’s Esophagus test reports delivered in the
quarter were 6,672, compared to 3,441 in the fourth quarter of
2023.
- IDgenetix test reports delivered in the quarter were 3,125,
compared to 3,299 in the fourth quarter of 2023. In late 2024, the
Company made modifications to its promotional investments for
IDgenetix, shifting resources to inside sales and non-personal
promotion.
- DecisionDx-UM test reports delivered in the quarter were 424,
compared to 405 in the fourth quarter of 2023.
- Gross margin was 76%, and Adjusted Gross Margin was 81%,
compared to 78% and 82% respectively for the same periods in
2023.
- Net cash provided by operations was $24.4 million, compared to
$18.6 million for the same period in 2023.
- Net income, which includes non-cash stock-based compensation
expense of $11.4 million, was $9.6 million, compared to a net loss
of $2.6 million for the same period in 2023.
- Adjusted EBITDA was $21.3 million, compared to $9.4 million for
the same period in 2023.
2025 Outlook
The Company anticipates generating between $280-295 million in
total revenue in 2025.
Fourth Quarter and Recent Accomplishments and
Highlights
Dermatology
- DecisionDx-Melanoma: Findings from a prospective, multicenter
study demonstrating the significant impact of the
DecisionDx-Melanoma test on sentinel lymph node biopsy (SLNB)
decision-making for patients with melanoma were recently published
in the World Journal of Surgical Oncology; further, no patient with
a DecisionDx-Melanoma-predicted risk of SLN positivity of less than
5% who decided to have an SLNB procedure had a positive node.
- DecisionDx-Melanoma: The Company announced the publication of a
new independent meta-analysis in Cancers assessing the efficacy of
its DecisionDx-Melanoma test in predicting melanoma patient
outcomes. The article, titled “The Prognostic Value of the 31-Gene
Expression Profile Test in Cutaneous Melanoma: A Systematic Review
and Meta-Analysis,” concluded that DecisionDx-Melanoma consistently
provides improved risk stratification over staging alone to inform
personalized management strategies for patients with cutaneous
melanoma (CM). This recently published meta-analysis encompassed 13
peer-reviewed publications involving thousands of patients and
affirmed the powerful risk stratification provided by
DecisionDx-Melanoma and its potential to significantly improve care
for patients with CM. See the Company’s news release from Dec. 12,
2024, for more information.
- DecisionDx-Melanoma: The Company announced the latest data from
a prospective, multicenter study exploring the impact of
integrating DecisionDx-Melanoma test results into SLNB
decision-making for patients recently diagnosed with melanoma. The
updated findings demonstrated the power of the test’s results to
accurately identify patients with a low risk of metastasis who can
safely forgo SLNB, thereby reducing unnecessary SLNB procedures and
the associated costs and risks of complications that accompany
them. The data was presented in a poster and oral presentation at
The European Congress on Dermato-Oncology (Dermato-Onco2024)
recently held in Vienna, Austria. See the Company’s news release
from Nov. 6, 2024, for more information.
- DecisionDx-SCC: The Company announced that its poster on
DecisionDx-SCC was selected as a “Late Breakers” top five finalist
for the Akamai Award, recognizing the best posters at Maui Derm
Hawaii 2025. Specifically, the poster shared new data from a study
involving Castle’s largest cohort of patients with cutaneous
squamous cell carcinoma (SCC) to date (n=1,408). This study
demonstrated improved risk stratification of patients with SCC
tumors located on the head or neck when the test’s results are
combined with Brigham and Women’s Hospital (BWH) staging. See the
Company’s news release from Jan. 17, 2025, for more
information.
Gastroenterology
- The Company announced that it received assay approval from the
New York State Department of Health (NYSDOH) for its TissueCypher
Barrett’s Esophagus (BE) test. With this approval, all of the tests
in Castle’s dermatology, gastroenterology and ophthalmology
portfolios, as well as its clinical laboratories in Phoenix and
Pittsburgh, are now approved by the state of New York. See the
Company’s news release from Jan. 6, 2025, for more
information.
Corporate
- The Company announced that it was named a Houston Top Workplace
for 2024 by the Houston Chronicle. This was the fourth consecutive
year the Company was ranked among the Houston metro area’s top
workplaces. Castle also earned three Culture Excellence awards in
the areas of Employee Appreciation, Employee Well-Being and
Professional Development. See the Company’s news release from Nov.
19, 2024, for more information.
Conference Call and Webcast Details
Castle Biosciences will hold a conference call on Thursday, Feb.
27, 2025, at 4:30 p.m. Eastern time to discuss its fourth quarter
and full-year 2024 results and provide a corporate update.
A live webcast of the conference call can be accessed here:
https://events.q4inc.com/attendee/686536610 or via the webcast link
on the Investor Relations page of the Company’s website,
https://ir.castlebiosciences.com/overview/default.aspx. Please
access the webcast at least 10 minutes before the conference call
start time. An archive of the webcast will be available on the
Company’s website until March 20, 2025.
To access the live conference call via phone, please dial 833
470 1428 from the United States, or +1 404 975 4839
internationally, at least 10 minutes prior to the start of the
call, using the conference ID 944585.
There will be a brief Question & Answer session following
management commentary.
Use of Non-GAAP Financial Measures (UNAUDITED)
In this release, we use the metrics of Adjusted Revenues,
Adjusted Gross Margin and Adjusted EBITDA, which are non-GAAP
financial measures and are not calculated in accordance with
generally accepted accounting principles in the United States
(GAAP). Adjusted Revenues and Adjusted Gross Margin reflect
adjustments to GAAP net revenues to exclude net positive and/or net
negative revenue adjustments recorded in the current period
associated with changes in estimated variable consideration related
to test reports delivered in previous periods. Adjusted Gross
Margin further excludes acquisition-related intangible asset
amortization. Adjusted EBITDA excludes from net loss: interest
income, interest expense, income tax expense (benefit),
depreciation and amortization expense, stock-based compensation
expense and change in fair value of trading securities.
We use Adjusted Revenues, Adjusted Gross Margin and Adjusted
EBITDA internally because we believe these metrics provide useful
supplemental information in assessing our revenue and operating
performance reported in accordance with GAAP, respectively. We
believe that Adjusted Revenues, when used in conjunction with our
test report volume information, facilitates investors’ analysis of
our current-period revenue performance and average selling price
performance by excluding the effects of revenue adjustments related
to test reports delivered in prior periods, since these adjustments
may not be indicative of the current or future performance of our
business. We believe that providing Adjusted Revenues may also help
facilitate comparisons to our historical periods. Adjusted Gross
Margin is calculated using Adjusted Revenues and therefore excludes
the impact of revenue adjustments related to test reports delivered
in prior periods, which we believe is useful to investors as
described above. We further exclude acquisition-related intangible
asset amortization in the calculation of Adjusted Gross Margin. We
believe that excluding acquisition-related intangible asset
amortization may facilitate gross margin comparisons to historical
periods and may be useful in assessing current-period performance
without regard to the historical accounting valuations of
intangible assets, which are applicable only to tests we acquired
rather than internally developed. We believe Adjusted EBITDA may
enhance an evaluation of our operating performance because it
excludes the impact of prior decisions made about capital
investment, financing, investing and certain expenses we believe
are not indicative of our ongoing performance. However, these
non-GAAP financial measures may be different from non-GAAP
financial measures used by other companies, even when the same or
similarly titled terms are used to identify such measures, limiting
their usefulness for comparative purposes.
These non-GAAP financial measures are not meant to be considered
in isolation or used as substitutes for net revenues, gross margin
or net loss reported in accordance with GAAP; should be considered
in conjunction with our financial information presented in
accordance with GAAP; have no standardized meaning prescribed by
GAAP; are unaudited; and are not prepared under any comprehensive
set of accounting rules or principles. In addition, from time to
time in the future, there may be other items that we may exclude
for purposes of these non-GAAP financial measures, and we may in
the future cease to exclude items that we have historically
excluded for purposes of these non-GAAP financial measures.
Likewise, we may determine to modify the nature of adjustments to
arrive at these non-GAAP financial measures. Because of the
non-standardized definitions of non-GAAP financial measures, the
non-GAAP financial measure as used by us in this press release and
the accompanying reconciliation tables have limits in their
usefulness to investors and may be calculated differently from, and
therefore may not be directly comparable to, similarly titled
measures used by other companies. Accordingly, investors should not
place undue reliance on non-GAAP financial measures.
Reconciliations of these non-GAAP financial measures to the most
directly comparable GAAP financial measures are presented in the
tables at the end of this release.
About Castle Biosciences
Castle Biosciences (Nasdaq: CSTL) is a leading diagnostics
company improving health through innovative tests that guide
patient care. The Company aims to transform disease management by
keeping people first: patients, clinicians, employees and
investors.
Castle’s current portfolio consists of tests for skin cancers,
Barrett’s esophagus, mental health conditions and uveal melanoma.
Additionally, the Company has active research and development
programs for tests in these and other diseases with high clinical
need, including its test in development to help guide systemic
therapy selection for patients with moderate-to-severe atopic
dermatitis seeking biologic treatment. To learn more, please visit
www.CastleBiosciences.com and connect with us on LinkedIn,
Facebook, X and Instagram.
DecisionDx-Melanoma, DecisionDx-CMSeq, i31-SLNB, i31-ROR,
DecisionDx-SCC, MyPath Melanoma, DiffDx-Melanoma, TissueCypher,
IDgenetix, DecisionDx-UM, DecisionDx-PRAME and DecisionDx-UMSeq are
trademarks of Castle Biosciences, Inc.
Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of Section 27A of the Securities Act of 1933, as
amended, and Section 21E of the Securities Exchange Act of 1934, as
amended, which are subject to the “safe harbor” created by those
sections. These forward-looking statements include, but are not
limited to, statements concerning our expectations regarding: our
2025 total revenue guidance of $280-295 million; the impact of
non-coverage by Medicare of our DecisionDx-SCC test; our business
strategy, including our capital allocation and pursuit of strategic
opportunities; the impact of modifications to promotional
investments for IDgenetix; the ability of DecisionDx-Melanoma to
(i) provide improved risk stratification over staging alone to
inform personalized management strategies and significantly improve
care for patients with CM and (ii) reduce unnecessary SLNB
procedures and the associated costs and risks of complications that
accompany them; the ability of DecisionDx-SCC to improve risk
stratification of patients with SCC tumors located on the head or
neck when the test’s results are combined with BWH staging; and the
growing recognition among clinicians of the value of TissueCypher.
The words “anticipate,” “can,” “could,” “expect,” “goal,” “may,”
“plan” and similar expressions are intended to identify
forward-looking statements, although not all forward-looking
statements contain these identifying words. We may not actually
achieve the plans, intentions, or expectations disclosed in our
forward-looking statements and you should not place undue reliance
on our forward-looking statements. Actual results or events could
differ materially from the plans, intentions and expectations
disclosed in the forward-looking statements that we make. These
forward-looking statements involve risks and uncertainties that
could cause our actual results to differ materially from those in
the forward-looking statements, including, without limitation: our
assumptions or expectations regarding continued reimbursement for
our products and subsequent coverage decisions; Novitas’ local
coverage determination signifying non-coverage by Medicare of our
DecisionDx-SCC test; our estimated total addressable markets for
our products and product candidates; the expenses, capital
requirements and potential needs for additional financing; the
anticipated cost, timing and success of our product candidates; our
plans to research, develop and commercialize new tests; our ability
to successfully integrate new businesses, assets, products or
technologies acquired through acquisitions; the effects of
macroeconomic events and conditions, including inflation and
monetary supply shifts, labor shortages, liquidity concerns at, and
failures of, banks and other financial institutions or other
disruptions in the banking system or financing markets, recession
risks, international tariffs, supply chain disruptions, outbreaks
of contagious diseases and geopolitical events (such as the ongoing
Israel-Hamas War and Ukraine-Russia conflict), among others, on our
business and our efforts to address its impact on our business; the
possibility that subsequent study or trial results and findings may
contradict earlier study or trial results and findings or may not
support the results discussed in this press release, including with
respect to the tests discussed in this press release; our planned
installation of additional equipment and supporting technology
infrastructures and implementation of certain process efficiencies
may not enable us to increase the future scalability of our
TissueCypher Test; the possibility that the actual application of
our tests may not provide the aforementioned benefits to patients;
the possibility that our newer gastroenterology and mental health
franchises may not contribute to the achievement of our long-term
financial targets as anticipated; and the risks set forth under the
heading “Risk Factors” in our Annual Report on Form 10-K for the
year ended December 31, 2024, each filed or to be filed with the
SEC, and in our other filings with the SEC. The forward-looking
statements are applicable only as of the date on which they are
made, and we do not assume any obligation to update any
forward-looking statements, except as may be required by law.
CASTLE BIOSCIENCES,
INC.
CONDENSED CONSOLIDATED
STATEMENTS OF OPERATIONS
(in thousands, except per
share data)
Three Months Ended
December 31,
Twelve Months Ended
December 31,
2024
2023
2024
2023
(unaudited)
(unaudited)
NET REVENUES
$
86,311
$
66,120
$
332,069
$
219,788
OPERATING EXPENSES AND OTHER OPERATING
INCOME
Cost of sales (exclusive of amortization
of acquired intangible assets)
16,183
12,423
60,205
44,982
Research and development
11,773
12,994
52,041
53,618
Selling, general and administrative
49,965
44,090
200,047
180,152
Amortization of acquired intangible
assets
4,340
2,271
11,106
9,013
Total operating expenses, net
82,261
71,778
323,399
287,765
Operating income (loss)
4,050
(5,658
)
8,670
(67,977
)
Interest income
3,372
3,119
12,916
10,623
Changes in fair value of trading
securities
555
—
555
—
Interest expense
(92
)
(2
)
(577
)
(11
)
Income (loss) before income
taxes
7,885
(2,541
)
21,564
(57,365
)
Income tax (benefit) expense
(1,705
)
39
3,319
101
Net income (loss)
$
9,590
$
(2,580
)
$
18,245
$
(57,466
)
Earnings (loss) per share:
Basic
$
0.34
$
(0.10
)
$
0.66
$
(2.14
)
Diluted
$
0.32
$
(0.10
)
$
0.62
$
(2.14
)
Weighted-average shares outstanding:
Basic
28,126
27,030
27,776
26,802
Diluted
30,200
27,030
29,255
26,802
Stock-Based Compensation Expense
Stock-based compensation expense is included in the condensed
consolidated statements of operations as follows (in
thousands):
Three Months Ended
December 31,
Twelve Months Ended
December 31,
2024
2023
2024
2023
(unaudited)
(unaudited)
Cost of sales (exclusive of amortization
of acquired intangible assets)
$
1,350
$
1,219
$
5,529
$
4,938
Research and development
1,987
2,364
9,598
10,119
Selling, general and administrative
8,102
8,219
35,193
36,162
Total stock-based compensation expense
$
11,439
$
11,802
$
50,320
$
51,219
CASTLE BIOSCIENCES,
INC.
CONDENSED CONSOLIDATED
STATEMENTS OF COMPREHENSIVE LOSS
(in thousands)
Three Months Ended
December 31,
Twelve Months Ended
December 31,
2024
2023
2024
2023
(unaudited)
(unaudited)
Net income (loss)
$
9,590
$
(2,580
)
$
18,245
$
(57,466
)
Other comprehensive (loss)
income:
Net unrealized (loss) gain on debt
securities held as available-for-sale
(243
)
207
94
517
Comprehensive income (loss)
$
9,347
$
(2,373
)
$
18,339
$
(56,949
)
CASTLE BIOSCIENCES,
INC.
CONDENSED CONSOLIDATED BALANCE
SHEETS
(in thousands)
December 31, 2024
December 31, 2023
ASSETS
Current Assets
Cash and cash equivalents
$
119,709
$
98,841
Marketable investment securities
173,421
144,258
Accounts receivable, net
51,218
38,302
Inventory
8,135
7,942
Prepaid expenses and other current
assets
7,671
6,292
Total current assets
360,154
295,635
Long-term accounts receivable, net
918
1,191
Property and equipment, net
51,122
25,433
Operating lease assets
11,584
12,306
Goodwill and other intangible assets,
net
106,229
117,335
Other assets – long-term
1,228
1,440
Total assets
$
531,235
$
453,340
LIABILITIES AND STOCKHOLDERS’
EQUITY
Current Liabilities
Accounts payable
$
6,901
$
10,268
Accrued compensation
32,555
28,945
Operating lease liabilities
1,665
1,137
Current portion of long-term debt
278
—
Other accrued and current liabilities
7,993
7,317
Total current liabilities
49,392
47,667
Long term debt
9,745
—
Noncurrent operating lease liabilities
14,345
14,173
Noncurrent finance lease liabilities
311
25
Deferred tax liability
1,607
206
Total liabilities
75,400
62,071
Stockholders’ Equity
Common stock
28
27
Additional paid-in capital
655,703
609,477
Accumulated deficit
(200,126
)
(218,371
)
Accumulated other comprehensive income
230
136
Total stockholders’ equity
455,835
391,269
Total liabilities and stockholders’
equity
$
531,235
$
453,340
CASTLE BIOSCIENCES,
INC.
CONDENSED CONSOLIDATED
STATEMENTS OF CASH FLOWS
(in thousands)
Twelve Months Ended
December 31,
2024
2023
OPERATING ACTIVITIES
Net income (loss)
$
18,245
$
(57,466
)
Adjustments to reconcile net income (loss)
to net cash provided by (used in) operating activities:
Depreciation and amortization
15,997
12,330
Stock-based compensation expense
50,320
51,219
Change in fair value of trading
securities
(555
)
—
Deferred income taxes
1,401
(223
)
Accretion of discounts on marketable
investment securities
(6,685
)
(5,491
)
Other
268
635
Change in operating assets and
liabilities:
Accounts receivable
(12,643
)
(14,930
)
Prepaid expenses and other current
assets
(1,142
)
(435
)
Inventory
(193
)
(3,962
)
Operating lease assets
1,322
(258
)
Other assets
262
(330
)
Accounts payable
(4,372
)
5,707
Operating lease liabilities
(1,289
)
852
Accrued compensation
3,610
4,587
Other accrued and current liabilities
320
2,139
Net cash provided by (used in) operating
activities
64,866
(5,626
)
INVESTING ACTIVITIES
Purchases of marketable investment
securities
(205,729
)
(189,075
)
Proceeds from maturities of marketable
investment securities
183,900
186,500
Purchases of property and equipment
(28,326
)
(13,621
)
Proceeds from sale of property and
equipment
18
13
Net cash used in investing activities
(50,137
)
(16,183
)
FINANCING ACTIVITIES
Proceeds from exercise of common stock
options
2,017
269
Payment of employees’ taxes on vested
restricted stock units
(8,762
)
(5,134
)
Proceeds from contributions to the
employee stock purchase plan
2,981
2,709
Repayment of principal portion of finance
lease liabilities
(97
)
(142
)
Proceeds from issuance of term debt
10,000
—
Net cash provided by (used in) financing
activities
6,139
(2,298
)
NET CHANGE IN CASH AND CASH
EQUIVALENTS
20,868
(24,107
)
Beginning of year
98,841
122,948
End of year
$
119,709
$
98,841
CASTLE BIOSCIENCES, INC.
Reconciliation of Non-GAAP Financial
Measures (UNAUDITED)
The table below presents the reconciliation of adjusted revenues
and adjusted gross margin, which are non-GAAP financial measures.
See "Use of Non-GAAP Financial Measures (UNAUDITED)" above for
further information regarding the Company's use of non-GAAP
financial measures.
Three Months Ended
December 31,
Twelve Months Ended
December 31,
2024
2023
2024
2023
(in thousands)
Adjusted
revenues
Net revenues (GAAP)
$
86,311
$
66,120
$
332,069
$
219,788
Revenue associated with test reports
delivered in prior periods
(491
)
4,086
1,751
4,476
Adjusted revenues (Non-GAAP)
$
85,820
$
70,206
$
333,820
$
224,264
Adjusted gross
margin
Gross margin (GAAP)1
$
65,788
$
51,426
$
260,758
$
165,793
Amortization of acquired intangible
assets
4,340
2,271
11,106
9,013
Revenue associated with test reports
delivered in prior periods
(491
)
4,086
1,751
4,476
Adjusted gross margin (Non-GAAP)
$
69,637
$
57,783
$
273,615
$
179,282
Gross margin percentage (GAAP)2
76.2
%
77.8
%
78.5
%
75.4
%
Adjusted gross margin percentage
(Non-GAAP)3
81.1
%
82.3
%
82.0
%
79.9
%
_______________________
- Calculated as net revenues (GAAP) less the sum of cost of sales
(exclusive of amortization of acquired intangible assets) and
amortization of acquired intangible assets.
- Calculated as gross margin (GAAP) divided by net revenues
(GAAP).
- Calculated as adjusted gross margin (Non-GAAP) divided by
adjusted revenues (Non-GAAP).
The table below presents the reconciliation of adjusted EBITDA,
which is a non-GAAP financial measure. See "Use of Non-GAAP
Financial Measures (UNAUDITED)" above for further information
regarding the Company's use of non-GAAP financial measures.
Three Months Ended
December 31,
Twelve Months Ended
December 31,
2024
2023
2024
2023
(in thousands)
Adjusted
EBITDA
Net income (loss)
$
9,590
$
(2,580
)
$
18,245
$
(57,466
)
Interest income
(3,372
)
(3,119
)
(12,916
)
(10,623
)
Interest expense
92
2
577
11
Income tax (benefit) expense
(1,705
)
39
3,319
101
Depreciation and amortization expense
5,768
3,224
15,997
12,330
Stock-based compensation expense
11,439
11,802
50,320
51,219
Changes in fair value of trading
securities
(555
)
—
(555
)
—
Adjusted EBITDA (Non-GAAP)
$
21,257
$
9,368
$
74,987
$
(4,428
)
View source
version on businesswire.com: https://www.businesswire.com/news/home/20250227523284/en/
Investor Relations Contact: Camilla Zuckero
czuckero@castlebiosciences.com 281-906-3868
Media Contact: Allison Marshall
amarshall@castlebiosciences.com
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