HilleVax Reports Second Quarter 2024 Financial Results and Highlights Recent Company Progress
August 08 2024 - 6:20PM
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,
2024 and highlighted recent progress.
Recent Business Highlights
- In Q3 2024, HilleVax announced that the
NEST-IN1 clinical study did not meet its primary or secondary
efficacy endpoints and that the company would discontinue further
development of HIL-214 in infants.
- In Q3 2024, HilleVax announced a
workforce reduction of approximately 40% of its workforce to reduce
operating expenses while maintaining core capabilities as the
company explores the potential for continued development of its
HIL-214 and HIL-216 norovirus candidates as well as business
development-related activities for these vaccine candidates.
Second Quarter 2024 Financial
Results
As of June 30, 2024 and December 31, 2023, the company
had cash, cash equivalents and marketable securities totaling
$245.0 million and $303.5 million, respectively.
Research and development expenses for the second quarter 2024
were $26.6 million, compared to $23.0 for the second quarter 2023.
The increase was primarily due to the growth in the number of
R&D employees.
General and administrative expenses for the second quarter 2024
were $8.1 million, compared to $7.2 million for the second quarter
2023. The increase was primarily due to the growth in the number of
G&A employees.
Other income for the second quarter 2024 and second quarter 2023
was $2.3 million.
Net loss for the second quarter 2024 was $40.7 million, compared
to $27.9 million for the second quarter 2023.
About HilleVax
HilleVax is a clinical-stage biopharmaceutical company focused
on developing and commercializing novel vaccines. Its initial
programs, HIL-214 and HIL-216, are virus-like particle (VLP) based
vaccine candidates 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
The company 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 the company’s current beliefs and expectations and
include, but are not limited to, the company’s plans to explore
continued development efforts on, and advance the development of,
HIL-214 and HIL-216 in adults and the potential opportunity for and
benefits of HIL-214 and HIL-216, and intended objectives and
benefits of the workforce reduction. Actual results may differ from
those set forth in this press release due to the risks and
uncertainties inherent in the company’s business, including,
without limitation: to-date the company has depended primarily on
the success of HIL-214, and the company may be unable to identify a
viable development path forward for HIL-214 or HIL-216; if the
company does identify a development path forward for its vaccine
candidates, the company may require additional capital and other
resources, including business development partnerships or other
strategic collaborations, and the company may be unable to secure
partnerships, other strategic collaborations or other resources on
acceptable terms or at all; topline results are based on
preliminary analysis of key efficacy and safety data, and such data
may change following a more comprehensive review of the data
related to the NEST-IN1 study and such topline data may not
accurately reflect the complete results of a clinical trial; to the
extent the company pursues future studies, the company may
experience potential delays in the commencement, enrollment, data
readouts and completion of clinical trials and preclinical studies;
the company depends 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, HIL-216 or any future vaccine candidates that
may limit their development, regulatory approval, commercialization
and/or business development potential; further unfavorable results
from clinical trials; results from prior clinical trials and
studies are not necessarily predictive of future results; the
company relies on intellectual property rights under its license
agreements with Takeda Vaccines, Inc. and Kanghua Biological
Products Co., Ltd.; the company may be unable to obtain, maintain
and enforce intellectual property protection for its vaccine
candidates; the company may use its capital resources sooner than
it expects; and other risks described in the company’s prior press
releases and the company’s filings with the Securities and Exchange
Commission (SEC), including under the heading “Risk Factors” in the
company’s 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 the company undertakes 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, |
|
|
|
2024 |
|
|
2023 |
|
|
2024 |
|
|
2023 |
|
Operating expenses: |
|
|
|
|
|
|
|
|
|
|
|
|
Research and development |
|
$ |
26,601 |
|
|
$ |
22,953 |
|
|
$ |
52,579 |
|
|
$ |
46,117 |
|
In-process research and development |
|
|
— |
|
|
|
— |
|
|
|
15,325 |
|
|
|
— |
|
General and administrative |
|
|
8,127 |
|
|
|
7,231 |
|
|
|
16,621 |
|
|
|
13,026 |
|
Impairment charges |
|
|
8,235 |
|
|
|
— |
|
|
|
8,235 |
|
|
|
— |
|
Total operating expenses |
|
|
42,963 |
|
|
|
30,184 |
|
|
|
92,760 |
|
|
|
59,143 |
|
Loss from operations |
|
|
(42,963 |
) |
|
|
(30,184 |
) |
|
|
(92,760 |
) |
|
|
(59,143 |
) |
Total other income |
|
|
2,295 |
|
|
|
2,282 |
|
|
|
5,263 |
|
|
|
4,352 |
|
Net loss |
|
$ |
(40,668 |
) |
|
$ |
(27,902 |
) |
|
$ |
(87,497 |
) |
|
$ |
(54,791 |
) |
Net loss per share, basic and
diluted |
|
$ |
(0.83 |
) |
|
$ |
(0.74 |
) |
|
$ |
(1.79 |
) |
|
$ |
(1.45 |
) |
Weighted-average shares of
common stock outstanding, basic and diluted |
|
|
49,179,109 |
|
|
|
37,951,735 |
|
|
|
48,819,729 |
|
|
|
37,853,176 |
|
HilleVax, Inc. |
Condensed Consolidated Balance Sheet Data |
(in thousands) |
(unaudited) |
|
|
|
June 30,2024 |
|
|
December 31,2023 |
|
Cash, cash equivalents and marketable securities |
|
$ |
245,040 |
|
|
$ |
303,483 |
|
Total assets |
|
|
276,931 |
|
|
|
344,434 |
|
Total liabilities |
|
|
72,001 |
|
|
|
78,909 |
|
Total stockholders’
equity |
|
|
204,930 |
|
|
|
265,525 |
|
Total liabilities and
stockholders’ equity |
|
|
276,931 |
|
|
|
344,434 |
|
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