– Revenue of $1,021.8 Million Grows 0.9% --
-- Revenue Increases 1.0% on Constant Currency
Basis, In-Line with Guidance –
– GAAP and Non-GAAP EPS Expected to be Near
High End of Guidance Ranges –
Hologic, Inc. (Nasdaq: HOLX) announced today preliminary revenue
results for its first fiscal quarter ended December 28, 2024.
The Company expects to report total revenues of approximately
$1,021.8 million, an increase of 0.9% compared to the prior year
period, or 1.0% in constant currency.
“Our fiscal Q1 revenue finished in line with our guidance on a
constant currency basis, as the strengthening of the U.S. dollar
reduced revenue by approximately $9 million compared to when we
provided guidance in early November,” said Karleen Oberton, the
Company’s Chief Financial Officer. “Despite this headwind, we
expect GAAP and non-GAAP earnings per share to be near the high end
of our guidance ranges.”
Global revenues by division are expected to be:
$s in millions
Preliminary Q1’25
Q1’24
Reported Change
Constant Currency Change
Diagnostics
$470.6
$447.8
5.1%
5.2%
Organic excluding COVID-191
$422.9
$388.1
9.0%
9.1%
Breast Health
$369.1
$377.7
(2.3%)
(2.1%)
Organic excluding SSI and
Endomagnetics2
$354.6
$377.0
(5.9%)
(5.8%)
GYN Surgical
$166.3
$162.2
2.5%
2.5%
Skeletal Health
$15.8
$25.4
(37.8%)
(37.4%)
Total
$1,021.8
$1,013.1
0.9%
1.0%
Organic revenue
$1,003.2
$1,004.4
(0.1%)
(0.0%)
Organic revenue excluding COVID-191,2
$959.6
$952.7
0.7%
0.8%
1
Preliminary Q1’25 organic Diagnostics
excluding COVID-19 revenues exclude COVID-19 assay revenue of $16.9
million, COVID-19 related revenue of $26.7 million, and Blood
Screening revenue of $4.1 million.
2
Preliminary Q1’25 organic Breast Health
revenues exclude SSI revenues of $0.3 million and Endomagnetics
revenue of $14.2 million.
Hologic has not yet completed its financial close processes for
the first quarter of fiscal 2025, therefore GAAP financial results
for the quarter have not yet been finalized. However, the Company
expects GAAP and non-GAAP diluted earnings per share (EPS) to be
toward the high-end of the guidance ranges provided on November 4,
2024.
Hologic intends to provide its full financial results for the
first quarter on February 5, 2025. Until that time, the preliminary
revenue and expected GAAP and non-GAAP EPS results described in
this press release are estimates only, are subject to the
finalization of quarter-end financial and accounting procedures,
and may differ materially from the actual results when they are
finalized and publicly disclosed. When the Company reports its
first quarter results, it also expects to provide updated financial
guidance for the second quarter and full year of fiscal 2025,
following the completion of its quarterly forecasting process.
J.P. Morgan Healthcare
Conference
Hologic is providing these updates in advance of its
participation in the 43rd Annual J.P. Morgan Healthcare Conference,
which begins tomorrow. The Company will post its conference
presentation to the investors section of its website at
http://investors.hologic.com/. A live webcast of the Company’s
presentation and question and answer session, which begins at 4:30
p.m. Eastern Time on Tuesday, January 14, 2025, also may be
accessed there. The webcast will be available for 30 days.
Use of
Non-GAAP Financial Measures
The Company has presented the following non-GAAP financial
measures in this press release: constant currency revenues, organic
revenues, organic revenues excluding COVID-19, and non-GAAP EPS.
Constant currency percentage changes show current period revenue
results as if the foreign exchange rates were the same as those in
the prior year period. Organic revenue for the fiscal first quarter
of 2025 excludes the divested Blood Screening and SSI ultrasound
imaging businesses, and the acquired Endomagnetics business. Both
reported and organic revenue for the fiscal first quarter of 2025
exclude the acquired Gynesonics business, which closed in Hologic’s
fiscal second quarter of 2025. Revenue from acquired businesses is
generally included in organic revenue starting a year after the
acquisition. Organic revenue excluding COVID-19 revenues is organic
revenue less COVID-19 assay revenue, COVID-19 related sales of
instruments, COVID-19 related revenue from Diagenode and Mobidiag,
collection kits and ancillaries, as well as license revenue, and
revenues from discontinued products. The Company defines its
non-GAAP EPS and other non-GAAP financial measures to exclude, as
applicable: (i) the amortization of intangible assets; (ii) the
impairment of goodwill and intangible assets and equipment, and
charges for the purchase of intellectual property to be used in a
development project that has no future alternative use; (iii)
adjustments to record contingent consideration at fair value; (iv)
charges to write-off inventory for a product line discontinuance;
(v) restructuring charges, facility closure and consolidation
charges (including accelerated depreciation), and costs incurred to
integrate acquisitions (including retention, contract termination
costs, legal and professional consulting services); (vi)
transaction related expenses for acquisitions; (vii) the step-up to
fair value for acquired inventory sold; (viii) debt extinguishment
losses and related transaction costs; (ix) the unrealized (gains)
losses on the mark-to-market of foreign currency contracts to hedge
revenue and operating results for which the Company has not elected
hedge accounting; (x) litigation settlement charges (benefits) and
non-income tax related charges (benefits); (xi)
other-than-temporary impairment losses on investments and realized
gains and losses resulting from the sale of investments; (xii) the
one-time discrete impacts related to internal restructurings and
non-operational items; (xiii) other one-time, non-recurring,
unusual or infrequent charges, expenses or gains that may not be
indicative of the Company's core business results; and (xiv) income
taxes related to such adjustments.
The non-GAAP financial measures used in this press release
adjust for specified items that can be highly variable or difficult
to predict. The Company generally uses non-GAAP financial measures
to facilitate management's financial and operational
decision-making, including evaluation of Hologic's historical
operating results and comparison to competitors' operating results.
Non-GAAP financial measures reflect an additional way of viewing
aspects of the Company's operations that, when viewed with GAAP
results and the reconciliations to corresponding GAAP financial
measures, may provide a more complete understanding of factors and
trends affecting Hologic's business. These non-GAAP financial
measures should be considered supplemental to, and not a substitute
for, financial information prepared in accordance with GAAP. The
Company's definition of non-GAAP measures may differ from similarly
titled measures used by others. Because non-GAAP financial measures
exclude the effect of items that increase or decrease the company's
reported results of operations, management strongly encourages
investors to review, when they become available, the Company's
consolidated financial statements and publicly filed reports in
their entirety.
About Hologic, Inc.
Hologic, Inc. is an innovative medical technology company
primarily focused on improving women's health and well-being
through early detection and treatment. For more information on
Hologic, visit www.hologic.com.
Hologic and associated logos are trademarks and/or registered
trademarks of Hologic, Inc. and/or its subsidiaries in the United
States and/or other countries.
Forward-Looking
Statements
This news release contains forward-looking information that
involves risks and uncertainties, including statements about the
Company’s plans, objectives, expectations and intentions. Such
statements include, without limitation: financial or other
information based upon or otherwise incorporating judgments or
estimates relating to future performance, events or expectations;
the Company’s strategies, positioning, resources, capabilities, and
expectations for future performance; and the Company's outlook and
financial and other guidance. These forward-looking statements are
based upon assumptions made by the Company as of the date hereof
and are subject to known and unknown risks and uncertainties that
could cause actual results to differ materially from those
anticipated.
Risks and uncertainties that could adversely affect the
Company’s business and prospects, and otherwise cause actual
results to differ materially from those anticipated, include,
without limitation: the development of new or improved competitive
technologies and products and competition; the anticipated
development of markets the Company sells its products into and the
success of the Company’s products in these markets; the Company’s
ability to predict accurately the demand for its products, and
products under development and to develop strategies to address
markets successfully; the anticipated performance and benefits of
the Company’s products; the Company’s business strategies; the
effect of consolidation in the healthcare industry; the ability to
execute acquisitions and the impact and anticipated benefits of
completed acquisitions and acquisitions the Company may complete in
the future; the coverage and reimbursement decisions of third-party
payors; the uncertainty of the impact of cost containment efforts
and federal healthcare reform legislation on our business and
results of operations; the guidelines, recommendations, and studies
published by various organizations relating to the use of the
Company’s products; the Company’s ability to obtain and maintain
regulatory approvals and clearances for its products, including the
implementation of the European Union Medical Device and In Vitro
Diagnostic Regulation requirements, and maintain compliance with
complex and evolving regulations and quality standards, as well as
the uncertainty of costs required to obtain and maintain compliance
with such regulatory and quality matters; the possibility that
products may contain undetected errors or defects or otherwise not
perform as anticipated; the impact and costs and expenses of
investigative and legal proceedings and compliance risks the
Company may be subject to now or in the future; potential negative
impacts resulting from climate change or other environmental,
social, and governance and sustainability related matters; the
impact of future tax legislation; the ongoing and possible future
effects of global challenges, including macroeconomic
uncertainties, such as inflation, bank failures, rising interest
rates and availability of capital markets, wars, conflicts, other
economic disruptions and U.S. and global recession concerns, on the
Company’s customers and suppliers and on the Company’s business,
financial condition, results of operations and cash flows and the
Company’s ability to draw down its revolver; the effect of the
worldwide political and social uncertainty and divisions, including
the impact on trade regulations and tariffs, that may adversely
impact the cost and sale of the Company’s products in certain
countries, or increase the costs the Company may incur to purchase
materials, parts and equipment from its suppliers; conducting
business internationally; potential cybersecurity threats and
targeted computer crime; the ongoing and possible future effects of
supply chain constraints, including the availability of critical
raw materials and components, as well as cost inflation in
materials, packaging and transportation; the possibility of
interruptions or delays at the Company’s manufacturing facilities,
or the failure to secure alternative suppliers if any of the
Company’s sole source third-party manufacturers fail to supply the
Company; the ability to consolidate certain of the Company’s
manufacturing and other operations on a timely basis and within
budget, without disrupting the Company’s business and to achieve
anticipated cost synergies related to such actions; the Company’s
ability to meet production and delivery schedules for its products;
the effect of any future public health pandemic or other crises,
including the timing, scope and effect of U.S. and international
governmental, regulatory, fiscal, monetary and public health
responses to such crises; the ability to successfully manage
ongoing organizational and strategic changes, including the
Company’s ability to attract, motivate and retain key employees and
maintain engagement and efficiency in remote work environments; the
Company’s ability to protect its intellectual property rights;
anticipated trends relating to the Company’s financial condition or
results of operations, including the impact of interest rate and
foreign currency exchange fluctuations; estimated asset and
liability values; compliance with covenants contained in the
Company’s debt agreements; and the Company’s liquidity, capital
resources and the adequacy thereof.
The risks included above are not exhaustive. Other factors that
could adversely affect the Company's business and prospects are
described in the filings made by the Company with the SEC,
including its most recent Annual Report on Form 10-K and Quarterly
Report on Form 10-Q. The Company expressly disclaims any obligation
or undertaking to release publicly any updates or revisions to any
such statements presented herein to reflect any change in
expectations or any change in events, conditions or circumstances
on which any such statements are based.
SOURCE: Hologic, Inc.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20250112871764/en/
Mike Watts Corporate Vice President, Investor Relations
michael.watts@hologic.com (858) 410-8514
Pete Sattler Senior Manager, Investor Relations
peter.sattler@hologic.com (619) 871-1606
Hologic (NASDAQ:HOLX)
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