Core royalty platform continued strong
performance, receiving GSK royalties of $67.2 million
Innoviva Specialty Therapeutics’ (IST) marketed
portfolio grew 38% year-over-year, achieving net product sales of
$21.7 million
Important treatment guidelines and guidance
updates recognized our key products: XACDURO® by 2024
Infectious Diseases Society of America (IDSA); XERAVA® by 2024
Surgical Infection Society
XACDURO® approved in China
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 second quarter ended June 30, 2024, and
highlighted select corporate achievements.
“Our robust second quarter continues to demonstrate the
successful transformation of Innoviva. We have strong performance
across multiple fronts, driven by our core GSK royalties portfolio
and accelerating growth from our commercial products, GIAPREZA®,
XACDURO® and XERAVA®,” said Pavel Raifeld, Chief Executive Officer
of Innoviva. “We remain committed to enhancing shareholder value
through thoughtful capital allocation and operational excellence.
We also are excited about our portfolio of strategic healthcare
assets, where we continue to see potential for significant value
creation.”
Mr. Raifeld added, “In addition to driving strong operational
delivery from our critical care and infectious disease platform
IST, we continue to expand its global footprint and enhance
recognition. Our partner in China, Zai Lab, successfully obtained
regulatory approval for XACDURO®, bringing us closer to making
XACDURO® available to all patients globally. In the U.S, important
treatment guidelines and guidance updates recognized our key
products, underscoring their life-saving potential. XACDURO® was
named the preferred agent for treatment of Carbapenem-resistant
Acinetobacter baumannii infections in the 2024 Infectious Diseases
Society of America (IDSA) treatment guidance. XERAVA® is
recommended by the 2024 Surgical Infection Society (SIS) treatment
guidelines for empiric therapy in the management of complicated
intra-abdominal infection.”
Financial Highlights
- Royalty revenue: Second quarter 2024 gross royalty
revenue from Glaxo Group Limited (“GSK”) was $67.2 million,
compared to $65.7 million for the second quarter 2023.
- Net Product Sales: Second quarter 2024 net product sales
were $21.7 million, which included $13.1 million from GIAPREZA®,
$6.2 million from XERAVA®, and $2.4 million from XACDURO®, a 38%
increase compared to $15.7 million for the second quarter
2023.
- License Revenue: Second quarter 2024 license revenue of
$14.5 million included an $8 million milestone payment from our
partner for the regulatory approval of XACDURO® in China and $6.5
million in non-recurring cost-sharing reimbursements from our
partner for product development.
- Equity and long-term investments: Second quarter 2024
net unfavorable change in fair values of equity and long-term
investments of $90.7 million was primarily attributable to lower
share price of Armata Pharmaceuticals (“Armata”), despite continued
operational progress.
- Net income: The change in fair values of our investments
negatively impacted second quarter 2024 earnings, resulting in a
net loss of $34.7 million, or ($0.55) basic per share, compared to
a net income of $1.3 million, or $0.02 basic per share, for the
second quarter of 2023.
- Share repurchases: During the second quarter 2024,
Innoviva completed its $100 million share repurchase program by
repurchasing 0.4 million shares, for a total amount of
approximately $5.3 million.
- Cash and cash equivalents: Totaled $217.0 million.
Royalty and net product sales receivables totaled $94.0 million as
of June 30, 2024.
Key Business and R&D Highlights
- XACDURO® (sulbactam for injection; durlobactam for
injection), co-packaged for intravenous use: targeted antibacterial
for the treatment of patients with hospital-acquired bacterial
pneumonia and ventilator-associated bacterial pneumonia (HABP/VABP)
caused by susceptible isolates of Acinetobacter baumannii
calcoaceticus complex.
- In May 2024, XACDURO® was approved in China by the National
Medical Products Administration (NMPA) for use in Chinese patients
18 years of age and older.
- In July 2024, XACDURO® was named as the preferred agent for the
treatment of Carbapenem-resistant Acinetobacter baumannii
infections, in combination with a carbapenem, in the updated 2024
IDSA treatment guidance.
- The World Health Organization considers Acinetobacter a
top-priority pathogen worldwide that needs novel antibiotics1.
- XERAVA® (eravacycline), for injection is indicated for
the treatment of complicated intra-abdominal infections (cIAI)
caused by susceptible microorganisms in patients 18 years or older.
- In July 2024, XERAVA® was named as a recommended agent for
empiric therapy in the updated 2024 SIS treatment guidelines for
the management of complicated intra-abdominal infections. SIS also
recommended XERAVA® be reserved for high-risk patients.
- Zoliflodacin: a potential first-in-class, single dose,
oral antibiotic in development for the treatment of patients with
uncomplicated gonorrhea is currently being developed in partnership
with The Global Antibiotic Research & Development Partnership
(GARDP).
- Zoliflodacin has successfully completed Phase 3 clinical trials
and the results were reported at ESCMID Global 2024. The Company
expects to submit an NDA to the U.S. FDA in early 2025.
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.
ANORO®, RELVAR® and BREO® are trademarks of the GSK group of
companies.
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® and XACDURO® 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.
References
(1) Tala, B., Jad, A., Claude, A., Jihad, I., Chantal, L.,
Rakan, N.,& Eid, A. (2017). Risk Factors, Clinical
Presentation, and Outcome of Acinetobacter baumannii Bacteremia.
Front. Cell. Infect. Microbiol., 04 May 2017, Sec. Molecular
Bacterial Pathogenesis Volume 7 – 2017:
https://doi.org/10.3389/fcimb.2017.00156
INNOVIVA, INC. Condensed Consolidated Statements of Income and
Comprehensive Income (in thousands, except per share data)
(unaudited) Three Months Ended Six Months Ended June 30,
June 30,
2024
2023
2024
2023
Revenue: Royalty revenue, net (1)
$
63,742
$
62,265
$
122,157
$
119,123
Net product sales
21,651
15,727
40,735
27,241
License revenue
14,505
3,000
14,505
11,000
Total revenue
99,898
80,992
177,397
157,364
Expenses: Cost of products sold (inclusive of amortization of
inventory fair value adjustments)
8,472
8,979
19,443
17,728
Cost of license revenue
-
-
-
1,600
Selling, general and administrative
27,740
23,542
58,145
43,277
Research and development
2,560
14,989
6,438
27,577
Amortization of acquired intangible assets
6,440
4,958
12,880
8,763
Changes in fair values of equity method investments, net
60,108
19,911
24,766
4,094
Changes in fair values of equity and long-term investments, net
30,556
83
43,891
2,247
Interest and dividend income
(3,474
)
(3,553
)
(7,873
)
(6,918
)
Interest expense
5,802
4,382
11,653
8,809
Other expense, net
973
1,896
2,209
3,242
Total expenses, net
139,177
75,187
171,552
110,419
Income (loss) before income taxes
(39,279
)
5,805
5,845
46,945
Income tax expense (benefit), net
(4,594
)
4,525
3,998
10,800
Net income (loss) and comprehensive income (loss)
$
(34,685
)
$
1,280
$
1,847
$
36,145
Net income (loss) per share Basic
$
(0.55
)
$
0.02
$
0.03
$
0.54
Diluted
$
(0.55
)
$
0.02
$
0.03
$
0.46
Shares used to compute net income (loss) per share Basic
62,526
65,341
62,856
66,557
Diluted
62,526
65,489
63,064
88,175
(1) Total net revenue is comprised of the following (in thousands):
Three Months Ended Six Months Ended June 30, June 30,
2024
2023
2024
2023
(unaudited) (unaudited) Royalties
$
67,198
$
65,721
$
129,069
$
126,035
Amortization of capitalized fees
(3,456
)
(3,456
)
(6,912
)
(6,912
)
Royalty revenue, net
$
63,742
$
62,265
$
122,157
$
119,123
INNOVIVA, INC. Condensed Consolidated Balance Sheets (in
thousands) (unaudited) June 30, December 31,
2024
2023
Assets Cash and cash equivalents
$
217,003
$
193,513
Royalty and product sale receivables
93,980
84,075
Inventory
36,664
40,737
Prepaid expense and other current assets
10,630
25,894
Property and equipment, net
427
483
Equity and long-term investments
536,435
560,978
Capitalized fees paid, net
76,872
83,784
Right-of-use assets
3,118
2,536
Goodwill
17,905
17,905
Intangible assets
217,455
230,335
Deferred tax asset, net
11,446
-
Other assets
2,982
3,267
Total assets
$
1,224,917
$
1,243,507
Liabilities and stockholders’ equity Other current
liabilities
$
23,929
$
33,435
Accrued interest payable
3,422
3,422
Deferred revenue
855
1,277
Convertible senior notes, due 2025, net
191,659
191,295
Convertible senior notes, due 2028, net
255,623
254,939
Other long-term liabilities
72,065
71,870
Deferred tax liabilities, net
-
563
Income tax payable, long-term
11,849
11,751
Innoviva stockholders’ equity
665,515
674,955
Total liabilities and stockholders’ equity
$
1,224,917
$
1,243,507
INNOVIVA, INC. Cash Flows Summary (in thousands) (unaudited)
Six Months Ended June 30,
2024
2023
Net cash provided by operating activities
$
80,765
$
63,866
Net cash used in investing activities
(43,038
)
(35,722
)
Net cash used in financing activities
(14,237
)
(146,168
)
Net change
$
23,490
$
(118,024
)
Cash and cash equivalents at beginning of period
193,513
291,049
Cash and cash equivalents at end of period
$
217,003
$
173,025
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240731216589/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
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