OPKO Health Reports Third Quarter 2024 Business Highlights and Financial Results
November 07 2024 - 4:05PM
OPKO Health, Inc. (NASDAQ: OPK) reports business
highlights and financial results for the three and nine months
ended September 30, 2024.
Highlights from the third quarter of 2024 and
recent weeks include the following:
- Completed sale of select
assets of BioReference Health to Labcorp for $237.5
million. OPKO completed the sale of BioReference Health’s
laboratory testing businesses focused on clinical diagnostics and
women’s health, excluding operations in New York and New Jersey,
for $237.5 million. BioReference Health will continue to offer
oncology and urology diagnostic services nationwide, as well as
maintain its full operations in New York and New Jersey. This
transaction streamlines BioReference Health’s laboratory services
business while retaining its core operations to better position the
division for sustained growth and profitability. Net sales from
operations continuing at BioReference Health exceeded $400 million
in 2023.
- Entered into a $250 million
note purchase agreement with HealthCare Royalty secured by profit
share payments related to NGENLA. Under the terms of the
note purchase agreement, in the near term OPKO retains a
significant portion of the profit share payments from Pfizer
received pursuant to its license agreement relating to NGENLA with
upside over the long term, as well as the full $100 million of
remaining potential milestone payments.
- OPKO’s Board of Directors
authorized a $100 million share repurchase program. Under
the program, OPKO may repurchase shares of its common stock from
time to time through open-market purchases, block trades, privately
negotiated transactions, accelerated share repurchase transactions
and/or pursuant to Rule 10b5-1 plans, in compliance with applicable
securities laws and other legal requirements. The Company
repurchased and retired 14.9 million shares for approximately $23.8
million during the three months ended September 30, 2024, and
thereafter, through November 6, 2024 repurchased and retired an
additional 8.7 million shares for approximately $13.0 million. In
addition, the Company repurchased approximately $3.5 million in
principal of its Convertible Notes.
- Enrollment and dosing
underway in the MDX2001 Phase 1 trial for the treatment of solid
tumor cancers. MDX2001, a tetraspecific
antibody, is designed to optimize T-cell function while preventing
tumor antigen escape. This Phase 1 open-label trial is expected to
enroll up to 45 patients at four clinical trial sites. The Phase 1a
portion is primarily designed to evaluate the safety and
immunogenicity of ascending doses of MDX2001 in patients with
various solid tumors.
- Awarded $51 million of
additional funding under an existing BARDA contract to develop
COVID multispecific antibodies and to initiate an influenza
program. ModeX Therapeutics was awarded $26.9 million of
additional funding under an existing contract with the Biomedical
Advanced Research and Development Authority (BARDA). This funding
will support the development of a second novel multispecific
antibody to SARS-CoV-2 from preclinical through Phase 1 trials, as
well as preclinical work on gene-based expression of multispecific
antibodies to SARS-CoV-2 including mRNA and/or DNA vectors. In
addition, BARDA activated an option for the second phase of funding
totaling $24.1 million for ModeX to begin development of influenza
multispecifics with gene and/or protein delivery modalities.
Together, these funds bring the total support awarded to ModeX to
$110 million, with up to $205 million in total, if all options are
executed.
- Announced promising results
of an orally delivered oxyntomodulin analog. OPKO is
continuing to progress development of its long-acting oxyntomodulin
analog in both its subcutaneous and oral formulations. The
polyethylene glycol (PEG) linked peptide was studied and progressed
to Phase 2 clinical trials before it was suspended due to dose
limiting its formulation. The same key peptide as an acylated
compound, OPK-88006, has been confirmed in in vitro assays and
animal disease models to be a strong candidate for once-weekly
subcutaneous administration. Entera and OPKO recently announced
results from their ongoing collaborative research combining
OPK-88006 and Entera’s proprietary N-Tab™ technology. The program
is focused on developing the first oral dual-agonist GLP-1/glucagon
peptide as a potential once-daily treatment for patients with
obesity and metabolic disorders. In vivo studies in rodent and pig
models showed single dose administration, delivered orally,
resulted in a desirable PK profile and bioavailability.
Third Quarter Financial
Results
- Consolidated:
Consolidated total revenues for the third quarter of 2024 were
$173.6 million compared with $178.6 million for the comparable
period of 2023. Operating income for the third quarter of 2024 was
$14.2 million compared with operating loss of $64.4 million for the
2023 quarter. The third quarter of 2024 included a gain of $121.5
million from the sale of certain BioReference assets and a gain of
$10.5 million from the sale of shares of GeneDx, as well as
non-cash other income of $35.4 million compared with non-cash other
expense of $8.3 million in the year-ago quarter related to the
change in the fair value of the GeneDx Holdings investment. As a
result, net income for the third quarter of 2024 was $24.9 million,
or $0.03 per diluted share, compared with net loss of $84.5
million, or $0.11 per share, for the 2023 quarter.
- Pharmaceuticals:
Revenue from products in the third quarter of 2024 was $39.1
million compared with $40.7 million in the third quarter of 2023,
reflecting lower Rayaldee sales and foreign currency exchange
fluctuations. Revenue from sales of Rayaldee was $5.8 million
compared with $7.3 million in the same period in 2023. Revenue from
the transfer of intellectual property and other was $13.2 million
in the third quarter of 2024 compared with $6.2 million in the 2023
period, primarily attributable to $5.5 million related to the BARDA
contract. Gross profit share and royalty payments for NGENLA and
Pfizer's Genotropin was $7.0 million in the 2024 quarter compared
with $4.9 million in the same period for 2023. Total costs and
expenses increased to $84.6 million in the third quarter of 2024
from $72.3 million in the prior-year period primarily due to higher
research and development expenses related to increased activity
within the ModeX development programs. Operating loss was $32.2
million in the third quarter of 2024, which included $18.0 million
of depreciation and amortization expense, compared with $25.4
million in the third quarter of 2023, which included $17.8 million
of depreciation and amortization expense.
- Diagnostics:
Revenue from services in the third quarter of 2024 was $121.3
million compared with $131.7 million in the prior-year period, with
the decrease primarily due to lower clinical test volume,
principally as a result of the Labcorp transaction and a reduction
in reimbursement rates. Total costs and expenses, net of the gain
on the sale of assets, were $62.7 million in the third quarter of
2024 compared with $160.8 million in the third quarter of 2023. The
decrease in costs and expenses were primarily attributable to a
$121.5 million gain on the Labcorp transaction, partially offset by
severance expense of $26.3 million and costs related to the closure
of an office building, which reflect the continued progress with
cost-reduction initiatives. The third quarter of 2024 included
revenue from services of approximately $19.9 million and total
costs and expenses of approximately $31.7 million related to assets
acquired by Labcorp. Operating income was $58.5 million in the
third quarter of 2024 compared with a loss of $29.1 million in the
2023 period and included $6.1 million and $8.4 million of
depreciation and amortization expense, respectively.
- Cash, cash equivalents,
marketable securities and restricted cash: Cash and cash
equivalents were $400.1 million, marketable securities,
principally shares of GeneDx were $92.2 million and restricted cash
and escrow was $43.7 million (including $6.3 million of current
restricted cash) as of September 30, 2024. In the third quarter,
OPKO entered into a $250 million note purchase agreement secured by
OPKO’s profit share payments to be received from Pfizer relating to
NGENLA. In addition, OPKO received $237.5 million upon closing of
the Labcorp transaction, of which $23.7 million was deposited in an
escrow account and will be released upon the one-year anniversary
of the transaction close less any outstanding adjustments or
claims.
Conference Call and Webcast
Information
OPKO’s senior management will provide a business
update, discuss third quarter financial results, provide financial
guidance and answer questions during a conference call and live
audio webcast today beginning at 4:30 p.m. Eastern time.
Participants are encouraged to pre-register for the conference call
here. Callers who pre-register will receive a unique PIN to gain
immediate access to the call and bypass the live operator.
Participants may register at any time, including up to and after
the call start time. Those unable to pre-register may participate
by dialing 833-630-0584 (U.S.) or 412-317-1815 (International). A
webcast of the call can also be accessed at OPKO’s Investor
Relations page and here.
A telephone replay will be available until
November 14, 2024, by dialing 877-344-7529 (U.S.) or 412-317-0088
(International) and providing the passcode 6323665. A webcast
replay will be available beginning approximately one hour after the
completion of the live conference call here.
About OPKO Health
OPKO is a multinational biopharmaceutical and
diagnostics company that seeks to establish industry-leading
positions in large, rapidly growing markets by leveraging its
discovery, development, and commercialization expertise and novel
and proprietary technologies. For more information, visit
www.opko.com.
Cautionary Statement Regarding Forward
Looking Statements
This press release contains "forward-looking
statements," as that term is defined under the Private Securities
Litigation Reform Act of 1995 (PSLRA), which statements may be
identified by words such as "expects," "plans," "projects," "will,"
"may," "anticipates," "believes," "should," "intends," "estimates,"
and other words of similar meaning, including statements regarding
expected financial performance and expectations regarding the
market for and sales of our products, whether our product
development efforts will be successful and whether the expected
benefits of our products will be realized, including whether
enrollment in a Phase 1 clinical trial for MDX2001 will be
successful and whether the data will be positive, whether efforts
to develop a daily oral dual-agonist GLP-1/glucagon peptide will
succeed, whether and how many of our shares we will repurchase
under a buyback program, whether NGENLA profits will be sufficient
to provide long term upside after satisfying our obligations under
the note purchase agreement, whether we can successfully progress
the development of oxyntomodulin in both subcutaneous and oral
formulations, whether the relationship with our commercial and
strategic partners will be successful, whether our commercial and
strategic partners will be able to commercialize our products and
successfully utilize our technologies, our ability to market and
sell any of our products in development, whether we will continue
to successfully advance products in our pipeline and whether they
can be commercialized, whether BioReference will be able to
streamline its laboratory services business and better position the
division for sustained growth and profitability, whether
BioReference’s attempts at returning its core business to
profitability will be successful, as well as other non-historical
statements about our expectations, beliefs or intentions regarding
our business, technologies and products, financial condition,
strategies or prospects. Many factors could cause our actual
activities or results to differ materially from the activities and
results anticipated in forward-looking statements. These factors
include those described in our Annual Reports on Form 10-K filed
and to be filed with the Securities and Exchange Commission and
under the heading “Risk Factors” in our other filings with the
Securities and Exchange Commission, as well as the continuation and
success of our relationship with our commercial partners, liquidity
issues and the risks inherent in funding, developing and obtaining
regulatory approvals of new, commercially-viable and competitive
products and treatments. In addition, forward-looking statements
may also be adversely affected by general market factors,
competitive product development, product availability, federal and
state regulations and legislation, the regulatory process for new
products and indications, manufacturing issues that may arise,
patent positions and litigation, among other factors. The
forward-looking statements contained in this press release speak
only as of the date the statements were made, and we do not
undertake any obligation to update forward-looking statements. We
intend that all forward-looking statements be subject to the
safe-harbor provisions of the PSLRA.
Contacts:Alliance
Advisors IRYvonne Briggs,
310-691-7100ybriggs@allianceadvisors.com orBruce Voss, 310-691-7100
bvoss@allianceadvisors.com
—Tables to Follow—
OPKO Health, Inc. and Subsidiaries |
Condensed Consolidated Balance Sheets |
(in millions) |
Unaudited |
|
As of |
|
September 30, 2024 |
|
December 31, 2023 |
Assets: |
|
|
|
|
|
|
|
Cash, cash equivalents, and current restricted cash |
$ |
406.4 |
|
|
$ |
95.9 |
|
Accounts receivable, net |
|
106.6 |
|
|
|
123.4 |
|
Other current assets |
|
116.6 |
|
|
|
90.2 |
|
Total current assets |
|
629.6 |
|
|
|
309.5 |
|
In-process research and
development and goodwill |
|
730.9 |
|
|
|
793.3 |
|
Other assets |
|
895.6 |
|
|
|
908.9 |
|
Total Assets |
$ |
2,256.1 |
|
|
$ |
2,011.7 |
|
|
|
|
|
|
|
|
|
Liabilities and Equity: |
|
|
|
|
|
|
|
Accounts payable |
$ |
62.7 |
|
|
$ |
69.7 |
|
Accrued expenses |
|
122.8 |
|
|
|
90.1 |
|
Current portion of convertible notes |
|
0.2 |
|
|
|
0.0 |
|
Other current liabilities |
|
25.9 |
|
|
|
40.3 |
|
Total current liabilities |
|
211.6 |
|
|
|
200.1 |
|
Long-term portion of convertible notes |
|
178.7 |
|
|
|
214.3 |
|
Senior secured notes |
|
245.4 |
|
|
|
0.0 |
|
Deferred tax liabilities, net |
|
128.4 |
|
|
|
126.8 |
|
Other long-term liabilities, principally leases, and lines of
credit |
|
88.6 |
|
|
|
81.3 |
|
Total Liabilities |
|
852.7 |
|
|
|
622.5 |
|
Equity |
|
1,403.4 |
|
|
|
1,389.2 |
|
Total Liabilities and Equity |
$ |
2,256.1 |
|
|
$ |
2,011.7 |
|
|
|
|
|
|
|
|
|
OPKO Health, Inc. and Subsidiaries |
Condensed Consolidated Statements of Operations |
(in millions, except share and per share data) |
Unaudited |
|
|
For the three months endedSeptember 30, |
|
For the nine months endedSeptember 30, |
|
2024 |
|
2023 |
|
2024 |
|
2023 |
Revenues |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Revenue from services |
$ |
121.3 |
|
|
$ |
131.7 |
|
|
$ |
377.5 |
|
|
$ |
391.1 |
|
Revenue from products |
|
39.1 |
|
|
|
40.7 |
|
|
|
117.7 |
|
|
|
124.6 |
|
Revenue from transfer of intellectual property and other |
|
13.2 |
|
|
|
6.2 |
|
|
|
34.3 |
|
|
|
165.9 |
|
Total revenues |
|
173.6 |
|
|
|
178.6 |
|
|
|
529.5 |
|
|
|
681.6 |
|
Costs and expenses |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost of service revenues |
|
108.8 |
|
|
|
106.4 |
|
|
|
325.8 |
|
|
|
333.5 |
|
Cost of product revenues |
|
24.7 |
|
|
|
24.5 |
|
|
|
69.8 |
|
|
|
74.7 |
|
Selling, general and administrative |
|
98.2 |
|
|
|
72.3 |
|
|
|
237.2 |
|
|
|
227.7 |
|
Research and development |
|
28.8 |
|
|
|
19.4 |
|
|
|
74.8 |
|
|
|
70.2 |
|
Contingent consideration |
|
0.0 |
|
|
|
(1.1 |
) |
|
|
0.0 |
|
|
|
(1.0 |
) |
Amortization of intangible assets |
|
20.4 |
|
|
|
21.5 |
|
|
|
62.3 |
|
|
|
64.5 |
|
Gain on sale of assets |
|
(121.5 |
) |
|
|
0.0 |
|
|
|
(121.5 |
) |
|
|
0.0 |
|
Total costs and expenses |
|
159.4 |
|
|
|
243.0 |
|
|
|
648.4 |
|
|
|
769.6 |
|
Operating income (loss) |
|
14.2 |
|
|
|
(64.4 |
) |
|
|
(118.9 |
) |
|
|
(88.0 |
) |
Other income (expense),
net |
|
34.2 |
|
|
|
(14.0 |
) |
|
|
73.6 |
|
|
|
(23.8 |
) |
Income (loss) before income
taxes and investment losses |
|
48.4 |
|
|
|
(78.4 |
) |
|
|
(45.3 |
) |
|
|
(111.8 |
) |
Income tax provision |
|
(23.5 |
) |
|
|
(6.1 |
) |
|
|
(21.9 |
) |
|
|
(10.5 |
) |
Loss before investment
losses |
|
24.9 |
|
|
|
(84.5 |
) |
|
|
(67.2 |
) |
|
|
(122.3 |
) |
Loss from investments in
investees |
|
(0.0 |
) |
|
|
(0.0 |
) |
|
|
(0.0 |
) |
|
|
(0.1 |
) |
Net income (loss) |
$ |
24.9 |
|
|
$ |
(84.5 |
) |
|
$ |
(67.2 |
) |
|
$ |
(122.4 |
) |
Income (loss) per share,
basic |
$ |
0.04 |
|
|
$ |
(0.11 |
) |
|
$ |
(0.10 |
) |
|
$ |
(0.16 |
) |
Income (loss) per share,
diluted |
$ |
0.03 |
|
|
$ |
(0.11 |
) |
|
$ |
(0.10 |
) |
|
$ |
(0.16 |
) |
Weighted average common shares
outstanding, basic |
|
694,622,466 |
|
|
|
751,525,007 |
|
|
|
699,675,944 |
|
|
|
751,716,692 |
|
Weighted average common shares
outstanding, diluted |
|
998,363,636 |
|
|
|
751,525,007 |
|
|
|
699,675,944 |
|
|
|
751,716,692 |
|
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