Core royalty platform continues to deliver with
GSK royalties of $66.0 million for the fourth quarter and $255.6
million for the full year
Innoviva Specialty Therapeutics achieved U.S.
net product sales of $24.9 million for the fourth quarter and $80.9
million for the full year, reflecting 47% year-over-year growth
Therapeutics platform strengthened with
acquisition of exclusive U.S. commercialization and distribution
rights to ZEVTERA® (ceftobiprole), launching mid-2025
Innoviva, Inc. (NASDAQ: INVA) (“Innoviva” or the “Company”), a
diversified holding company with a core royalties portfolio, a
leading critical care and infectious disease platform known as
Innoviva Specialty Therapeutics (“IST”), and a portfolio of
strategic investments in healthcare assets, today reported
financial results for the fourth quarter and full year ended
December 31, 2024, and highlighted select corporate progress and
achievements.
Pavel Raifeld, Chief Executive Officer of Innoviva, said: “2024
was an exceptional year for Innoviva. Our core royalty portfolio
and therapeutics business both delivered strong year-over-year
revenue growth. The excellent performance of IST in 2024 –
including revenue growth, new product acquisition through
partnership, and significant pipeline progress – is a clear
validation of our strategy to build a leading commercial business
in critical care and infectious disease.”
Mr. Raifeld continued, “In 2024, IST’s revenue growth was driven
by the successful launch of XACDURO® and a renewed commercial
strategy unlocking new opportunities for GIAPREZA®. Additionally,
both XACDURO® and XERAVA® received favorable guidelines placement,
which has helped increase access to patients. We also added a
fourth approved product to our leverageable commercial
infrastructure by licensing ZEVTERA® in the U.S., showcasing both
our potential to be a preferred commercial partner and the value
creation opportunities enabled by the strength of our operating
platform.”
“Looking ahead, we anticipate another strong year in 2025
highlighted by an NDA submission for zoliflodacin, the launch of
ZEVTERA® in mid-2025, and continued growth for our marketed
products, with U.S. net product sales forecasted to exceed $100
million. Backed by nearly $400 million cash and receivables,
Innoviva is a well-capitalized company focused on continued value
creation through disciplined capital deployment and operational
excellence,” concluded Mr. Raifeld.
Financial Highlights
- Royalty revenue: Fourth quarter 2024 gross royalty
revenue from Glaxo Group Limited (“GSK”) was $66.0 million and full
year was $255.6 million, compared to $69.6 million for the fourth
quarter of 2023 and $252.7 million for the full year 2023.
- Net Product Sales: Fourth quarter 2024 net product sales
were $28.9 million, which included U.S. net product sales of $24.9
million, compared to $19.7 million for the fourth quarter of 2023,
and ex-U.S. net product sales of $4.0 million. U.S. net product
sales consisted of $15.9 million from GIAPREZA®, $3.1 million from
XERAVA®, and $5.9 million from XACDURO®. Full year 2024 net product
sales were $97.5 million, which included U.S. net product sales of
$80.9 million, compared to $55.1 million for full year 2023, and
ex-U.S. net product sales of $16.6 million. U.S. net product sales
consisted of $53.4 million from GIAPREZA®, $12.8 million from
XERAVA®, $14.7 million from XACDURO®.
- License revenue: Fourth quarter 2024 license revenue of
$0.4 million included product development cost-sharing
reimbursements from our partner. Full year 2024 license revenue of
$19.5 million consisted of an $8.0 million milestone payment and
$11.5 million cost-sharing reimbursements, compared to $11.0
million milestone payments in full year 2023.
- Equity and long-term investments: Fourth quarter and
full year 2024 changes in fair values of equity and long-term
investments of $19.6 million and $123.4 million, respectively, were
primarily attributable to share price depreciation of Armata
Pharmaceuticals and other equity investments.
- Net income: Fourth quarter 2024 net income of $20.3
million ($0.32 basic earnings per share) and full year 2024
net income of $23.4 million ($0.37 basic earnings per share) were
driven primarily by higher revenue, offset by the negative impact
of changes in the fair values of equity investments.
- Cash and cash equivalents: Totaled $305.0 million.
Royalty and net product sales receivables totaled $86.4 million as
of December 31, 2024.
Key Business and R&D Highlights
- ZEVTERA® (ceftibiprole): an advanced-generation
cephalosporin antibiotic that is approved in the U.S. for three
specific treatment indications. ZEVTERA® is the only FDA-approved
methicillin-resistant Staphylococcus aureus (MRSA) cephalosporin
antibiotic for treating adult patients with Staphylococcus aureus
bloodstream infections (bacteremia) (SAB) and endocarditis.
ZEVTERA® is indicated for the treatment of adult patients with SAB,
including right-sided infective endocarditis, adult patients with
acute bacterial skin and skin structure infections (ABSSSI) and for
adult and pediatric patients (3 months to less than 18 years old)
with community-acquired bacterial pneumonia (CABP).
- In the fourth quarter of 2024, Innoviva licensed U.S.
commercialization and distribution rights to ZEVTERA® from Basilea
Pharmaceutica Ltd, Allschwil (SIX: BSLN).
- The Company anticipates launching ZEVTERA® in the U.S. in
mid-2025.
- Zoliflodacin: a potential first-in-class, single dose,
oral antibiotic is currently being developed in partnership with
The Global Antibiotic Research & Development Partnership
("GARDP") for the treatment of patients with uncomplicated
gonorrhea.
- In 2024, the Company reported positive Phase 3 data for
zoliflodacin, in which a single dose of oral zoliflodacin achieved
a statistically non-inferior microbiological cure rate compared to
the current global standard of care. Oral zoliflodacin was
generally well tolerated and emergent adverse events were
comparable between treatment arms. No deaths or other serious
adverse events were reported.
- The Company remains on track to submit the zoliflodacin NDA to
the U.S. FDA in early 2025.
- XACDURO® (sulbactam for injection; durlobactam for
injection), co-packaged for intravenous use: a targeted
antibacterial treatment for patients with hospital-acquired
bacterial pneumonia and ventilator-associated bacterial pneumonia
(HABP/VABP) caused by susceptible isolates of Acinetobacter
baumannii calcoaceticus complex.
- XACDURO® was approved in China by the National Medical Products
Administration for use in Chinese patients 18 years of age and
older in May 2024.
- In July, XACDURO® was named as the preferred agent for the
treatment of Carbapenem-resistant Acinetobacter baumannaii
infections, in combination with a carbapenem, in the updated 2024
IDSA treatment guidance.
- In August, XACDURO® was nominated for the prestigious Prix
Galien USA award for Best Biotechnology Product.
Update on Strategic Healthcare Assets
- Our portfolio of strategic assets under the Company’s various
subsidiaries was valued at $501.5 million as of December 31, 2024.
In the fourth quarter 2024, we continued to support product
developments and invested $10.9 million in Gate Neurosciences,
Inc., a leader in developing precision medicines targeting synaptic
health.
About Innoviva
Innoviva is a diversified holding company with a core royalties
portfolio, a leading critical care and infectious disease platform
known as Innoviva Specialty Therapeutics (“IST”), and a portfolio
of strategic investments in healthcare assets. Innoviva’s royalty
portfolio includes respiratory assets partnered with Glaxo Group
Limited (“GSK”). Innoviva is entitled to receive royalties from GSK
on sales of RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®. Innoviva’s
other innovative healthcare assets include infectious disease and
critical care assets stemming from acquisitions of Entasis
Therapeutics, including XACDURO® (sulbactam for injection;
durlobactam for injection), co-packaged for intravenous use
approved for the treatment of adults with hospital-acquired
bacterial pneumonia and ventilator-associated bacterial pneumonia
caused by susceptible strains of Acinetobacter
baumannii-calcoaceticus complex and the investigational
zoliflodacin currently being developed for the treatment of
uncomplicated gonorrhea, and La Jolla Pharmaceutical Company,
including GIAPREZA® (angiotensin II), approved to increase blood
pressure in adults with septic or other distributive shock and
XERAVA® (eravacycline) for the treatment of complicated
intra-abdominal infections in adults. On December 14, 2024,
Innoviva entered into an exclusive distribution and license
agreement with Basilea Pharmaceutica Ltd, Allschwil for the
commercialization of ZEVTERA® (ceftobiprole), an
advanced-generation cephalosporin antibiotic, in the U.S.
ANORO®, RELVAR® and BREO® are trademarks of the GSK group of
companies. ZEVTERA® is a trademark of Basilea Pharmaceutica Ltd,
Allschwil.
Forward Looking Statements
This press release contains certain “forward-looking” statements
as that term is defined in the Private Securities Litigation Reform
Act of 1995 regarding, among other things, statements relating to
goals, plans, objectives, and future events. Innoviva intends such
forward-looking statements to be covered by the safe harbor
provisions for forward-looking statements contained in Section 21E
of the Securities Exchange Act of 1934 and the Private Securities
Litigation Reform Act of 1995. The words “anticipate”, “expect”,
“goal”, “intend”, “objective”, “opportunity”, “plan”, “potential”,
“target” and similar expressions are intended to identify such
forward-looking statements. Such forward-looking statements involve
substantial risks, uncertainties, and assumptions. These statements
are based on the current estimates and assumptions of the
management of Innoviva as of the date of this press release and are
subject to known and unknown risks, uncertainties, changes in
circumstances, assumptions and other factors that may cause the
actual results of Innoviva to be materially different from those
reflected in the forward-looking statements. Important factors that
could cause actual results to differ materially from those
indicated by such forward-looking statements include, among others,
risks related to: expected cost savings; lower than expected future
royalty revenue from respiratory products partnered with GSK; the
commercialization of RELVAR®/BREO® ELLIPTA®, ANORO® ELLIPTA®,
GIAPREZA®, XERAVA®, XACDURO® and ZEVTERA® in the jurisdictions in
which these products have been approved; the strategies, plans and
objectives of Innoviva (including Innoviva’s growth strategy and
corporate development initiatives); the timing, manner, and amount
of potential capital returns to shareholders; the status and timing
of clinical studies, data analysis and communication of results;
the potential benefits and mechanisms of action of product
candidates; expectations for product candidates through development
and commercialization; the timing of regulatory approval of product
candidates; and projections of revenue, expenses and other
financial items; the impact of the novel coronavirus (“COVID-19”);
the timing, manner and amount of capital deployment, including
potential capital returns to stockholders; and risks related to the
Company’s growth strategy. Other risks affecting Innoviva are
described under the headings “Risk Factors” and “Management’s
Discussion and Analysis of Financial Condition and Results of
Operations” contained in Innoviva’s Annual Report on Form 10-K for
the year ended December 31, 2023 and Quarterly Reports on Form
10-Q, which are on file with the Securities and Exchange Commission
(“SEC”) and available on the SEC’s website at www.sec.gov. Past
performance is not necessarily indicative of future results. No
forward-looking statements can be guaranteed, and actual results
may differ materially from such statements. Given these
uncertainties, you should not place undue reliance on these
forward-looking statements. The information in this press release
is provided only as of the date hereof, and Innoviva assumes no
obligation to update its forward-looking statements on account of
new information, future events or otherwise, except as required by
law.
INNOVIVA, INC. Condensed Consolidated Statements of Income (in
thousands, except per share data) (Unaudited) Three Months
Ended Year Ended December 31, December 31,
2024
2023
2024
2023
Revenue: Royalty revenue, net (1)
$
62,520
$
66,165
$
241,733
$
238,846
Net product sales
28,935
19,675
97,492
60,617
License Revenue
351
-
19,486
11,000
Total revenue
91,806
85,840
358,711
310,463
Expenses: Cost of products sold (inclusive of amortization of
inventory fair value adjustments)
7,165
13,130
36,598
41,040
Cost of license revenue
-
-
-
1,600
Selling, general and administrative
31,326
26,319
115,690
98,232
Research and development
3,665
2,356
13,654
33,922
Amortization of acquired intangible assets
6,511
6,510
25,902
21,784
Changes in fair values of equity method investments, net
21,256
(9,506
)
64,253
(77,392
)
Changes in fair values of equity and long-term investments, net
(1,666
)
(16,016
)
59,161
(11,129
)
Interest and dividend income
(5,768
)
(4,786
)
(19,141
)
(15,818
)
Interest expense
4,749
5,952
22,209
19,157
Other expense (income), net
(126
)
680
2,997
4,969
Total expenses
67,112
24,639
321,323
116,365
Income before income taxes
24,694
61,201
37,388
194,098
Income tax expense
4,362
(330
)
13,996
14,376
Net income
20,332
61,531
23,392
179,722
Net income per share Basic net income per share attributable
to Innoviva stockholders
$
0,32
$
0,97
$
0,37
$
2,75
Diluted net income per share attributable to Innoviva stockholders
$
0,26
$
0,76
$
0,36
$
2,20
Shares used to compute basic net income per share
62,626
63,710
62,726
65,435
Shares used to compute diluted net income per share
84,200
84,995
74,187
86,876
(1) Total net revenue is comprised of the following (in thousands):
Three Months Ended Year Ended December 31, December 31,
2024
2023
2024
2023
(unaudited) (unaudited) Royalties
$
65,975
$
69,620
$
255,556
$
252,669
Amortization of capitalized fees
(3,455
)
(3,455
)
(13,823
)
(13,823
)
Royalty revenue, net
$
62,520
$
66,165
$
241,733
$
238,846
INNOVIVA, INC. Condensed Consolidated Balance Sheets (in thousands)
(unaudited) December 31, December 31,
2024
2023
Assets Cash and cash equivalents
$
304,964
$
193,513
Royalty and product sale receivables
86,366
84,075
Inventory, net
33,725
40,737
Prepaid expense and other current assets
21,719
25,894
Current portion of ISP Fund investments
107,532
-
Property and equipment, net
514
483
Equity and long-term investments
393,957
560,978
Capitalized fees
69,961
83,784
Right-of-use assets
2,453
2,536
Goodwill
17,905
17,905
Intangible assets
208,433
230,335
Deferred tax assets
12,054
-
Other assets
41,477
3,267
Total assets
$
1,301,060
$
1,243,507
Liabilities and stockholders’ equity Other current
liabilities
$
39,507
$
33,435
Accrued interest payable
3,422
3,422
Deferred revenues
1,126
1,277
Convertible senior notes, due 2025, net
192,028
191,295
Convertible senior notes, due 2028, net
256,316
254,939
Other long term liabilities
64,275
71,870
Deferred tax liabilities
-
563
Income tax payable - long term
53,227
11,751
Innoviva stockholders’ equity
691,159
674,955
Total liabilities and stockholders’ equity
$
1,301,060
$
1,243,507
INNOVIVA, INC. Cash Flows Summary (in thousands) (unaudited)
Year Ended December 31,
2024
2023
Net cash provided by operating activities
$
188,690
$
141,064
Net cash used in investing activities
(63,786
)
(66,761
)
Net cash used in financing activities
(13,453
)
(171,839
)
Net change
$
111,451
$
(97,536
)
Cash and cash equivalents at beginning of period
193,513
291,049
Cash and cash equivalents at end of period
$
304,964
$
193,513
View source
version on businesswire.com: https://www.businesswire.com/news/home/20250226009848/en/
Innoviva, Inc. David Patti Corporate Communications (908)
421-5971 david.patti@inva.com
Investors and Media: Argot Partners (212) 600-1902
innoviva@argotpartners.com
Innoviva (NASDAQ:INVA)
Historical Stock Chart
From Feb 2025 to Mar 2025
Innoviva (NASDAQ:INVA)
Historical Stock Chart
From Mar 2024 to Mar 2025