United Therapeutics Corporation (Nasdaq: UTHR), a public
benefit corporation, today announced its financial results for the
quarter ended March 31, 2025. Total revenues in the first quarter
of 2025 grew 17 percent year-over-year to $794.4 million, compared
to $677.7 million in the first quarter of 2024.
“2025 is off to a tremendous start as we reported yet another
quarter of record revenue,” said Martine Rothblatt, Ph.D.,
Chairperson and Chief Executive Officer of United Therapeutics.
“Beyond the continued execution of our foundational wave of growth
in the commercial business, throughout the balance of the year
we’ll progress our innovation and revolution waves of growth with
the readout of TETON 2 in idiopathic pulmonary fibrosis and the
planned commencement of our UKidney first in human clinical study,
respectively. Moreover, we’re excited to advance our multiple shots
on goal approach to creating an unlimited supply of transplantable
organ alternatives with anticipated filings of investigational new
drug applications with the FDA for our UHeart and UThymoKidney
products.”
Michael Benkowitz, President and Chief Operating Officer
of United Therapeutics, added, “This quarter’s record revenue
performance reflects the diligent efforts and strategic focus of
our commercial team as we continue to expand our reach and solidify
our position in the pulmonary hypertension marketplace as the
prostacyclin products of choice. We look forward to building on
this performance for the remainder of the year.”
First Quarter 2025 Financial Results
Key financial highlights include (dollars in millions, except
per share data):
Three Months Ended
March 31,
Dollar Change
Percentage Change
2025
2024
Total revenues
$
794.4
$
677.7
$
116.7
17
%
Net income
$
322.2
$
306.6
$
15.6
5
%
Net income, per basic share
$
7.18
$
6.52
$
0.66
10
%
Net income, per diluted share
$
6.63
$
6.17
$
0.46
7
%
Revenues
The table below presents the components of total revenues
(dollars in millions):
Three Months Ended
March 31,
Dollar Change
Percentage
Change
2025
2024
Net product sales:
Tyvaso DPI®(1)
$
302.5
$
227.5
$
75.0
33
%
Nebulized Tyvaso®(1)
163.8
145.0
18.8
13
%
Total Tyvaso
466.3
372.5
93.8
25
%
Remodulin®(2)
138.2
128.0
10.2
8
%
Orenitram®
120.7
106.2
14.5
14
%
Unituxin®
58.2
58.4
(0.2
)
—
%
Adcirca®
6.0
6.4
(0.4
)
(6
)%
Other
5.0
6.2
(1.2
)
(19
)%
Total revenues
$
794.4
$
677.7
$
116.7
17
%
(1)
Net product sales include both the drug
product and the respective inhalation device.
(2)
Net product sales include sales of
infusion devices, including the Remunity® Pump.
Total Tyvaso revenues grew by 25 percent to $466.3 million in
the first quarter of 2025, compared to $372.5 million in the first
quarter of 2024.
The growth in Tyvaso DPI revenues resulted primarily from an
increase in quantities sold of $97.4 million and, to a lesser
extent, a price increase, partially offset by higher gross-to-net
deductions. The increase in Tyvaso DPI quantities sold was
primarily due to continued growth in the number of patients
following the product’s launch, including growth in utilization by
patients with pulmonary hypertension associated with interstitial
lung disease and, to a lesser extent, increased commercial
utilization following the implementation of the Medicare Part D
benefit redesign under the Inflation Reduction Act
(IRA).
The growth in nebulized Tyvaso revenues resulted primarily from
an increase in international nebulized Tyvaso revenues, driven by
the timing of orders by our international distributors and does not
precisely reflect trends in underlying patient demand.
The growth in Remodulin revenues resulted primarily from an
increase in U.S. Remodulin revenues, driven by an increase in
quantities sold.
The growth in Orenitram revenues resulted primarily from an
increase in quantities sold and, to a lesser extent, a price
increase, partially offset by higher gross-to-net deductions. The
increase in quantities sold was driven, at least in part, by
increased commercial utilization following the implementation of
the Medicare Part D benefit redesign under the IRA.
The table below presents the breakdown of total revenues between
the United States and rest-of-world (ROW) (dollars in
millions):
Three Months Ended March
31,
2025
2024
U.S.
ROW
Total
U.S.
ROW
Total
Net product sales:
Tyvaso DPI(1)
$
302.5
$
—
$
302.5
$
227.5
$
—
$
227.5
Nebulized Tyvaso(1)
138.6
25.2
163.8
133.7
11.3
145.0
Total Tyvaso
441.1
25.2
466.3
361.2
11.3
372.5
Remodulin(2)
120.2
18.0
138.2
108.3
19.7
128.0
Orenitram
120.7
—
120.7
106.2
—
106.2
Unituxin
56.9
1.3
58.2
53.4
5.0
58.4
Adcirca
6.0
—
6.0
6.4
—
6.4
Other
4.7
0.3
5.0
6.0
0.2
6.2
Total revenues
$
749.6
$
44.8
$
794.4
$
641.5
$
36.2
$
677.7
(1)
Net product sales include both the drug
product and the respective inhalation device.
(2)
Net product sales include sales of infusion devices, including the
Remunity Pump.
Expenses
Cost of sales. The table below summarizes cost of sales
by major category (dollars in millions):
Three Months Ended
March 31,
Dollar Change
Percentage Change
2025
2024
Category:
Cost of sales
$
91.6
$
71.8
$
19.8
28
%
Share-based compensation expense(1)
0.9
1.1
(0.2
)
(18
)%
Total cost of sales
$
92.5
$
72.9
$
19.6
27
%
(1)
See Share-based compensation
below.
Cost of sales, excluding share-based compensation. Cost of sales
for the three months ended March 31, 2025 increased as compared to
the same period in 2024, primarily due to an increase in royalty
expense and product costs, particularly for Tyvaso DPI driven by
growth in Tyvaso DPI revenues.
Research and development. The table below summarizes the
nature of research and development expense by major expense
category (dollars in millions):
Three Months Ended
March 31,
Dollar Change
Percentage Change
2025
2024
Category:
External research and development(1)
$
57.2
$
52.7
$
4.5
9
%
Internal research and development(2)
48.3
44.9
3.4
8
%
Share-based compensation expense(3)
6.9
6.4
0.5
8
%
Other(4)
36.6
0.1
36.5
NM(5)
Total research and development
expense
$
149.0
$
104.1
$
44.9
43
%
(1)
External research and development
primarily includes fees paid to third parties (such as clinical
trial sites, contract research organizations, and contract
laboratories) for preclinical and clinical studies and payments to
third-party contract manufacturers before FDA approval of the
relevant product.
(2)
Internal research and development
primarily includes salary-related expenses for research and
development functions, internal costs to manufacture product
candidates before FDA approval, and internal facilities-related
expenses, including depreciation, related to research and
development activities.
(3)
See Share-based compensation
below.
(4)
Other primarily includes upfront
fees and milestone payments to third parties under license
agreements related to development-stage products and adjustments to
the fair value of our contingent consideration obligations.
(5)
Calculation is not
meaningful.
Research and development, excluding share-based compensation.
Research and development expense for the three months ended March
31, 2025 increased as compared to the same period in 2024,
primarily due to: (1) an increase of $30.0 million related to
milestone payments for drug delivery device technologies; (2) an
increase of $6.6 million related to adjustments to the fair value
of our contingent consideration obligations for manufactured organ
and organ alternative projects; and (3) increased expenditures
related to manufactured organ and organ alternative projects.
Selling, general, and administrative. The table below
summarizes selling, general, and administrative expense by major
category (dollars in millions):
Three Months Ended
March 31,
Dollar Change
Percentage Change
2025
2024
Category:
General and administrative
$
119.5
$
103.1
$
16.4
16
%
Sales and marketing
26.6
23.2
3.4
15
%
Share-based compensation expense(1)
24.0
18.1
5.9
33
%
Total selling, general, and
administrative expense
$
170.1
$
144.4
$
25.7
18
%
(1)
See Share-based compensation below.
General and administrative, excluding share-based compensation.
General and administrative expense for the three months ended March
31, 2025 increased as compared to the same period in 2024,
primarily due to an increase in personnel expense due to growth in
headcount.
Share-based compensation. The table below summarizes
share-based compensation expense by major category (dollars in
millions):
Three Months Ended
March 31,
Dollar Change
Percentage Change
2025
2024
Category:
Stock options
$
8.5
$
5.7
$
2.8
49
%
Restricted stock units
23.4
15.5
7.9
51
%
Share tracking awards plan
(0.8
)
3.9
(4.7
)
(121
)%
Employee stock purchase plan
0.7
0.5
0.2
40
%
Total share-based compensation
expense
$
31.8
$
25.6
$
6.2
24
%
Other (expense) income, net. The change in other
(expense) income, net for the three months ended March 31, 2025, as
compared to the same period in 2024, was primarily due to net
unrealized losses on equity securities.
Income tax expense. Income tax expense for the three
months ended March 31, 2025 and 2024 was $101.3 million and $92.0
million, respectively. Our effective income tax rate (ETR)
for the three months ended March 31, 2025 and 2024 was 24 percent
and 23 percent, respectively. Our ETR for the three months ended
March 31, 2025 increased compared to our ETR for the three months
ended March 31, 2024, primarily due to decreased excess tax
benefits from share-based compensation.
Webcast
We will host a webcast to discuss our first quarter 2025
financial results on Wednesday, April 30, 2025, at 9:00 a.m.
Eastern Time. The webcast can be accessed live via our website at
https://ir.unither.com/events-and-presentations. A replay of the
webcast will also be available at the same location on our
website.
United Therapeutics: Enabling Inspiration
At United Therapeutics, our vision and mission are one. We use
our enthusiasm, creativity, and persistence to innovate for the
unmet medical needs of our patients and to benefit our other
stakeholders. We are bold and unconventional. We have fun; we do
good. We are the first publicly-traded biotech or pharmaceutical
company to take the form of a public benefit corporation
(PBC). Our public benefit purpose is to provide a brighter
future for patients through (a) the development of novel
pharmaceutical therapies; and (b) technologies that expand the
availability of transplantable organs.
You can learn more about what it means to be a PBC here:
unither.com/pbc.
Forward-Looking Statements
Statements included in this press release that are not
historical in nature are “forward-looking statements” within the
meaning of the Private Securities Litigation Reform Act of 1995.
Forward-looking statements include, among others, statements
related to our waves of growth, the anticipated readout of the
TETON 2 clinical trial in idiopathic pulmonary fibrosis; the
planned commencement of our UKidney first in human clinical study;
our plan to create an unlimited supply of transplantable organ
alternatives; our anticipated filings of investigational new drug
applications with the FDA for our UHeart and UThymoKidney products;
our plan to continue to expand our reach and solidify our position
in the pulmonary hypertension marketplace as the prostacyclin
products of choice; our plan to build on our commercial performance
for the remainder of the year; and our goals of innovating for the
unmet medical needs of our patients and to benefit our other
stakeholders, furthering our public benefit purpose of developing
novel pharmaceutical therapies and technologies that expand the
availability of transplantable organs. These forward-looking
statements are subject to certain risks and uncertainties, such as
those described in our periodic reports filed with the Securities
and Exchange Commission, that could cause actual results to differ
materially from anticipated results. Consequently, such
forward-looking statements are qualified by the cautionary
statements, cautionary language and risk factors set forth in our
periodic reports and documents filed with the Securities and
Exchange Commission, including our most recent Annual Report on
Form 10-K, Quarterly Reports on Form 10-Q, and Current Reports on
Form 8-K. We claim the protection of the safe harbor contained in
the Private Securities Litigation Reform Act of 1995 for
forward-looking statements. We are providing this information as of
April 30, 2025, and assume no obligation to update or revise the
information contained in this press release whether as a result of
new information, future events, or any other reason.
ORENITRAM, REMODULIN, REMUNITY, TYVASO, TYVASO DPI, and UNITUXIN
are registered trademarks of United Therapeutics Corporation and/or
its subsidiaries.
UHEART, UKIDNEY, and UTHYMOKIDNEY are trademarks of United
Therapeutics Corporation and/or its subsidiaries.
ADCIRCA is a registered trademark of Eli Lilly and Company.
UNITED THERAPEUTICS
CORPORATION
CONSOLIDATED STATEMENTS OF
OPERATIONS
(In millions, except per share
data)
Three Months Ended
March 31,
2025
2024
(Unaudited)
Total revenues
$
794.4
$
677.7
Operating expenses:
Cost of sales
92.5
72.9
Research and development
149.0
104.1
Selling, general, and administrative
170.1
144.4
Total operating expenses
411.6
321.4
Operating income
382.8
356.3
Interest income
51.1
53.8
Interest expense
(6.1
)
(13.3
)
Other (expense) income, net
(4.3
)
1.8
Total other income, net
40.7
42.3
Income before income taxes
423.5
398.6
Income tax expense
(101.3
)
(92.0
)
Net income
$
322.2
$
306.6
Net income per common share:
Basic
$
7.18
$
6.52
Diluted
$
6.63
$
6.17
Weighted average number of common shares
outstanding:
Basic
44.9
47.0
Diluted
48.6
49.7
SELECTED CONSOLIDATED BALANCE
SHEET DATA
(Unaudited, in
millions)
March 31, 2025
Cash, cash equivalents, and marketable
investments
$
5,032.0
Total assets
7,743.9
Total liabilities
936.7
Total stockholders’ equity
6,807.2
Category: Earnings
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version on businesswire.com: https://www.businesswire.com/news/home/20250430348125/en/
Dewey Steadman at (202) 919-4097 (media/investors) Harry Silvers
at (301) 578-1401 (investors) https://ir.unither.com/contact-ir
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