HilleVax, Inc. (Nasdaq: HLVX), a clinical-stage biopharmaceutical
company focused on developing and commercializing novel vaccines,
and Chengdu Kanghua Biological Products Co., Ltd. (Kangh) (SHE:
300841), a biopharmaceutical company engaged in the research,
development, production, and sale of bioproducts, today announced
the entry into an exclusive license agreement for rights to Kangh’s
hexavalent virus-like particle (VLP) vaccine candidate for
norovirus, referred to by HilleVax as HIL-216, outside of Greater
China.
HIL-216 includes VLPs for six of the most common norovirus
genotypes, including GI.1, GII.2, GII.3, GII.4, GII.6, and GII.17.
The Investigational New Drug (IND) application for HIL-216 was
cleared by the U.S. FDA in September 2023. As part of the exclusive
license agreement, Kangh will supply HIL-216 for use in HilleVax’s
near-term clinical trials, including a Phase 1 trial that HilleVax
expects to initiate in 2024.
“We are extremely pleased to enter this collaboration with Kangh
as we seek to build out a long-term norovirus vaccine leadership
position,” said Rob Hershberg, MD, PhD, Chairman and Chief
Executive Officer at Hillevax. “Our bivalent norovirus VLP vaccine
candidate, HIL-214, remains the most advanced norovirus vaccine
candidate in clinical development, and we are on-track to report
topline safety and efficacy data in mid-2024 from our ongoing Phase
2b NEST-IN1 trial. We believe that HIL-214 will be the first
norovirus vaccine submitted for registration and, if approved,
would address the significant unmet medical need in infants and
other at-risk populations. We further believe that HIL-216 is an
exciting addition to the HilleVax portfolio as a next generation,
higher valency VLP-based vaccine and is an ideal fit with the
expertise, capabilities and long-term aspirations of HilleVax.”
“We are delighted to partner with HilleVax, a company with
world-class expertise in norovirus vaccine development and a deep
commitment to making an impact on the considerable morbidity,
mortality, and economic burden associated with norovirus,” said Mr.
Wang Zhentao, Chairman of Kangh. “This agreement represents a
significant milestone for Kangh in our aim to bring our novel
pipeline of vaccine products to global markets and is
representative of our significant vaccine discovery, development,
and manufacturing capabilities.”
HilleVax will pay Kangh an upfront payment of $15 million with
the potential for additional payments of up to $255.5 million upon
achieving certain development and sales milestones. Kangh is also
eligible to receive a single-digit tiered royalty on net sales
outside of Greater China.
BFC Group, Ltd. acted as advisors to HilleVax.
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.
About Kangh
Chengdu Kanghua Biological Products Co., Ltd. (SHE: 300841) is a
biopharmaceutical company engaged in the research, development,
production, and sale of bioproducts. Established in 2004, Kangh is
equipped with an animal testing center and high-tech GMP production
workshops for bacterial and viral vaccines. The current product
portfolio includes “ACYW135 Meningococcal Polysaccharide Vaccine”
(trade name: Micin®) and “Freeze-dried Human Rabies Vaccine (Human
Diploid Cells)” (trade name: HDCV®). Since its establishment,
Kanghua Biological has been honored with titles such as
“Postdoctoral Innovation Practice Base” and “Innovative Enterprise
Cultivation in Sichuan Province” by the Ministry of Personnel and
the Ministry of Science and Technology, and recognized as an
“Outstanding and Honest Demonstration Unit in Sichuan Province.”
The company has also obtained GMP certification from the National
Medical Products Administration. In recent years, Kanghua
Biological has undertaken several scientific and technological
projects and applied for over a hundred patents. For more
information about Kangh, please visit the website at
www.kangh.com.
HilleVax 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-216 and HIL-214, the planned initiation of a Phase 1 clinical
trial of HIL-216 and the timing thereof, the expected timing of a
data readout from the NEST-IN1 clinical trial, the advancement of
HIL-214 to registration as the first norovirus vaccine, and
longer-term market leadership plans. 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,
HIL-216 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 military conflicts or other
geopolitical developments outside our control; our reliance on
intellectual property rights under our license agreements with
Takeda Vaccines, Inc. and Kangh; 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.
Kangh Forward-Looking Statements
Kangh 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. 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: the vaccine product has characteristics such as a long
research and development cycle, high technical difficulty, and high
research and development risks. Additionally, considering the
changes in external environmental factors, there is a certain level
of uncertainty regarding the clinical trial progress, results, and
the successful achievement of large-scale production and sales of
the product. Furthermore, the milestone payments stipulated in the
agreement are subject to specific conditions, and the final
milestone payment amount remains uncertain. Investors are advised
to make decisions cautiously, taking note of and guarding against
investment risks. Kangh will closely monitor the subsequent
developments of the authorized licensing matters and promptly
fulfill the obligation of information disclosure.
HilleVax Contact:
Shane Maltbie
IR@hillevax.com
+1-617-213-5054
Kangh Contact:
Wennian Wu
khbso@kangh.com
+86-28-84882755
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