HilleVax Reports Second Quarter 2023 Financial Results and Highlights Recent Company Progress
14 Agosto 2023 - 1:00PM
HilleVax, Inc. (Nasdaq: HLVX), a clinical-stage biopharmaceutical
company focused on developing and commercializing novel vaccines,
today reported financial results for the quarter ended June 30,
2023, highlighted recent progress and outlined key upcoming
milestones for HIL-214, the company’s investigational virus-like
particle (VLP) based vaccine for the prevention of
moderate-to-severe norovirus-related acute gastroenteritis.
“HilleVax has continued to make excellent progress in our
HIL-214 program following completion of enrollment of our NEST-IN1
clinical trial in late April 2023. Due to issues relating solely to
the logistical complexity of processing diarrheal samples from
various geographies, we are adjusting our guidance to read out top
line clinical data on all subjects in our NEST-IN1 clinical trial
to mid-2024,” said Rob Hershberg, MD, PhD, Chairman and Chief
Executive Officer of HilleVax. “We remain committed to potentially
bringing the first vaccine to market to address the global unmet
need associated with norovirus infections.”
Recent Business Highlights
- In Q2 2023, HilleVax announced
completion of enrollment of the NEST-IN1 (Norovirus Efficacy and
Safety Trial for INfants) Phase 2b clinical trial with over 3,000
subjects enrolled in six countries.
- In Q2 2023, HilleVax announced the
appointment of Nanette Cocero, Ph.D., MBA, to its Board of
Directors.
Upcoming Expected Milestones
- Topline safety and
clinical efficacy data from NEST-IN1 in mid-2024.
Second Quarter 2023 Financial
Results
As of June 30, 2023, the company had cash, cash equivalents and
marketable securities totaling $244.1 million.
Research and development expenses for the second quarter 2023
were $23.0 million, compared to $8.8 million for the second quarter
2022. The increase was primarily due to increased activities for
the development of HIL-214 and the growth in the number of R&D
employees.
General and administrative expenses for the second quarter 2023
were $7.2 million, compared to $4.0 million for the second quarter
2022. The increase was primarily due to the growth in the number of
G&A employees.
Other income for the second quarter 2023 was $2.3 million,
compared to $41.1 million of other expense for the second quarter
2022. The other income in the second quarter of 2023 was primarily
driven by interest income on the company’s cash, cash equivalents
and marketable securities, while the other expense in the second
quarter of 2022 was primarily driven by changes in the fair value
of convertible promissory notes and warrant liabilities.
Net loss for the second quarter 2023 was $27.9 million, compared
to $53.9 million for the second quarter 2022.
About HilleVax
HilleVax is a clinical-stage biopharmaceutical company focused
on developing and commercializing novel vaccines. Its initial
program, HIL-214, is a virus-like particle (VLP) based vaccine
candidate in development for the prevention of moderate-to-severe
acute gastroenteritis (AGE) caused by norovirus infection.
Globally, norovirus is estimated to result in over approximately
700 million cases of AGE and 200,000 deaths per year, resulting in
over $4 billion in direct health system costs and $60 billion in
societal costs per year. The burden of norovirus falls
disproportionately on young children and older adults. For more
information about HilleVax, visit the company’s website at
http://www.HilleVax.com.
Forward-Looking Statements
HilleVax cautions you that statements contained in this press
release regarding matters that are not historical facts are
forward-looking statements. The forward-looking statements are
based on our current beliefs and expectations and include, but are
not limited to, the potential opportunity for and benefits of
HIL-214 and the expected timing of a data readout from the NEST-IN1
clinical trial. Actual results may differ from those set forth in
this press release due to the risks and uncertainties inherent in
our business, including, without limitation: we currently depend
entirely on the success of HIL-214, and we have not yet completed
any clinical trials of HIL-214; potential delays in the
commencement, enrollment, data readouts and completion of clinical
trials and preclinical studies; our dependence on third parties in
connection with manufacturing, research and clinical and
preclinical testing; unexpected adverse side effects or inadequate
immunogenicity or efficacy of HIL-214 or any future vaccine
candidates that may limit their development, regulatory approval,
and/or commercialization; unfavorable results from clinical trials;
results from prior clinical trials and studies not necessarily
being predictive of future results; and unstable market and
economic conditions may adversely affect our business and financial
condition and the broader economy and biotechnology industry;
regulatory developments in the United States and foreign countries;
any future impacts to our business resulting from the conflict
between Russia and Ukraine or other geopolitical developments
outside our control; our reliance on intellectual property rights
under our license agreement with Takeda Vaccines, Inc.; our ability
to obtain, maintain and enforce intellectual property protection
for our vaccine candidates; we may use our capital resources sooner
than we expect; and other risks described in our prior press
releases and our filings with the Securities and Exchange
Commission (SEC), including under the heading “Risk Factors” in our
annual report on Form 10-K and any subsequent filings with the SEC.
You are cautioned not to place undue reliance on these
forward-looking statements, which speak only as of the date hereof,
and we undertake no obligation to update such statements to reflect
events that occur or circumstances that exist after the date
hereof. All forward-looking statements are qualified in their
entirety by this cautionary statement, which is made under the safe
harbor provisions of the Private Securities Litigation Reform Act
of 1995.
Contact:
Shane MaltbieIR@hillevax.com+1-617-213-5054
HilleVax, Inc.Condensed
Consolidated Statement of Operations Data(in
thousands, except share and per share
data)(unaudited)
|
|
Three Months Ended |
|
|
Six Months Ended |
|
|
|
June 30, |
|
|
June 30, |
|
|
|
2023 |
|
|
2022 |
|
|
2023 |
|
|
2022 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
Research and development |
|
$ |
22,953 |
|
|
$ |
8,826 |
|
|
$ |
46,117 |
|
|
$ |
15,037 |
|
In-process research and development |
|
|
— |
|
|
|
— |
|
|
|
— |
|
|
|
2,500 |
|
General and administrative |
|
|
7,231 |
|
|
|
3,982 |
|
|
|
13,026 |
|
|
|
6,585 |
|
Total operating expenses |
|
|
30,184 |
|
|
|
12,808 |
|
|
|
59,143 |
|
|
|
24,122 |
|
Loss from operations |
|
|
(30,184 |
) |
|
|
(12,808 |
) |
|
|
(59,143 |
) |
|
|
(24,122 |
) |
Total other income (expense) |
|
|
2,282 |
|
|
|
(41,121 |
) |
|
|
4,352 |
|
|
|
(97,694 |
) |
Net loss |
|
$ |
(27,902 |
) |
|
$ |
(53,929 |
) |
|
$ |
(54,791 |
) |
|
$ |
(121,816 |
) |
Net loss per share, basic and
diluted |
|
$ |
(0.74 |
) |
|
$ |
(2.03 |
) |
|
$ |
(1.45 |
) |
|
$ |
(7.30 |
) |
Weighted-average shares of common
stock outstanding, basic and diluted |
|
|
37,951,735 |
|
|
|
26,512,881 |
|
|
|
37,853,176 |
|
|
|
16,685,372 |
|
HilleVax, Inc. Condensed
Consolidated Balance Sheet Data(in
thousands)(unaudited)
|
|
June 30,2023 |
|
|
December 31,2022 |
|
Cash, cash equivalents and
marketable securities |
|
$ |
244,050 |
|
|
$ |
279,401 |
|
Total assets |
|
|
286,522 |
|
|
|
317,211 |
|
Total liabilities |
|
|
67,759 |
|
|
|
49,982 |
|
Total stockholders’ equity |
|
|
218,763 |
|
|
|
267,229 |
|
Total liabilities and
stockholders’ equity |
|
|
286,522 |
|
|
|
317,211 |
|
Grafico Azioni HilleVax (NASDAQ:HLVX)
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