Arcturus Therapeutics Receives Clearance of an Investigational New Drug Application to U.S. Food and Drug Administration for ARCT-032, an Investigational Inhaled mRNA Therapeutic to Treat Cystic Fibrosis
03 Septiembre 2024 - 7:30AM
Business Wire
Arcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”,
Nasdaq: ARCT), a global messenger RNA medicines company focused on
the development of infectious disease vaccines and addressing unmet
medical needs within liver and respiratory rare diseases, today
announced that the U.S. Food and Drug Administration (FDA) has
issued a “Study May Proceed” notification for the Company’s
Investigational New Drug (IND) application, ARCT-032, to treat
cystic fibrosis (CF). FDA clearance of the ARCT-032 IND application
enables the Company to initiate a Phase 2 multiple ascending dose
study to evaluate the safety, tolerability and efficacy of ARCT-032
in people with Cystic Fibrosis.
“The Phase 2 Study May Proceed notification allows us to
investigate ARCT-032 as a potential treatment for CF patients and
provides the opportunity to further validate our LUNAR® technology
to deliver mRNA via inhalation,” said Dr. Juergen Froehlich, Chief
Medical Officer of Arcturus Therapeutics. “The study is designed to
evaluate the safety and effectiveness of ARCT-032 administered for
several weeks at multiple dose levels in people with CF who do not
qualify for, or benefit from, CFTR modulator therapy.”
About Cystic Fibrosis
Cystic fibrosis is a life-shortening disease with a worldwide
prevalence. Mutations in the cystic fibrosis transmembrane
conductance regulator (CFTR) gene result in a reduction or absence
of CFTR protein and/or function in the airways, causing
insufficient chloride transport to maintain airway surface
homeostasis. CF mucus is more difficult to clear, thus clogging the
airways and leading to infection, inflammation, respiratory
failure, or other life-threatening complications. Standard of care
for many CF individuals include CFTR modulators. Nearly 40,000
people in the U.S. and more than 105,000 people worldwide are
living with CF. Approximately 15% of individuals with CF do not
benefit from CFTR modulator medicines due to dysfunctional or
absent CFTR protein and/or drug intolerance.
About ARCT-032
ARCT-032 is an inhaled investigational mRNA therapeutic designed
to express normal functional CFTR in the lungs of individuals with
CF. ARCT-032 has received Orphan Medicinal Product Designation from
the European Medicines Agency (EMA) and Orphan Drug Designation
along with Rare Pediatric Disease Designation from the U.S. Food
and Drug Administration (FDA) to treat cystic fibrosis. ARCT-032
utilizes Arcturus' LUNAR® lipid-mediated aerosolized platform to
deliver CFTR messenger RNA to the lungs. Lung disease is the
leading cause of morbidity and mortality in people with CF.
Expression of a functional copy of the CFTR mRNA in the lungs of
people with CF has the potential to restore CFTR activity and
mitigate the downstream effects that cause progressive lung
disease. The ARCT-032 program is supported by preclinical data in
rodents, ferrets and primates, as well as demonstrating restoration
of CFTR expression and function in human bronchial epithelial
cells.
About Arcturus Therapeutics
Founded in 2013 and based in San Diego, California, Arcturus
Therapeutics Holdings Inc. (Nasdaq: ARCT) is a global mRNA
medicines and vaccines company with enabling technologies: (i)
LUNAR® lipid-mediated delivery, (ii) STARR® mRNA Technology
(sa-mRNA) and (iii) mRNA drug substance along with drug product
manufacturing expertise. Arcturus developed KOSTAIVE®, the first
self-amplifying messenger RNA (sa-mRNA) COVID vaccine in the world
to be approved. Arcturus has an ongoing global collaboration for
innovative mRNA vaccines with CSL Seqirus, and a joint venture in
Japan, ARCALIS, focused on the manufacture of mRNA vaccines and
therapeutics. Arcturus’ pipeline includes RNA therapeutic
candidates to potentially treat ornithine transcarbamylase (OTC)
deficiency and cystic fibrosis (CF), along with its partnered mRNA
vaccine programs for SARS-CoV-2 (COVID-19) and influenza. Arcturus’
versatile RNA therapeutics platforms can be applied toward multiple
types of nucleic acid medicines including messenger RNA, small
interfering RNA, circular RNA, antisense RNA, self-amplifying RNA,
DNA, and gene editing therapeutics. Arcturus’ technologies are
covered by its extensive patent portfolio (over 400 patents and
patent applications in the U.S., Europe, Japan, China, and other
countries). For more information, visit www.ArcturusRx.com. In
addition, please connect with us on Twitter and LinkedIn.
Forward-Looking Statements
This press release contains forward-looking statements that
involve substantial risks and uncertainties for purposes of the
safe harbor provided by the Private Securities Litigation Reform
Act of 1995. Any statements, other than statements of historical
fact included in this press release, are forward-looking
statements, including those regarding strategy, future operations,
the likelihood of success and continued advancement of the
Company’s pipeline and partnered programs, and the potential
initiation of a Phase 2 study of ARCT-032 and the timing thereof.
Arcturus may not actually achieve the plans, carry out the
intentions or meet the expectations or projections disclosed in any
forward-looking statements such as the foregoing and you should not
place undue reliance on such forward-looking statements. These
statements are only current predictions or expectations, and are
subject to known and unknown risks, uncertainties, and other
factors that may cause our or our industry’s actual results, levels
of activity, performance or achievements to be materially different
from those anticipated by the forward-looking statements, including
those discussed under the heading "Risk Factors" in Arcturus’ most
recent Annual Report on Form 10-K, and in subsequent filings with,
or submissions to, the SEC, which are available on the SEC’s
website at www.sec.gov. Except as otherwise required by law,
Arcturus disclaims any intention or obligation to update or revise
any forward-looking statements, which speak only as of the date
they were made, whether as a result of new information, future
events or circumstances or otherwise.
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IR and Media Contacts Arcturus Therapeutics Neda
Safarzadeh VP, Head of IR/PR/Marketing (858) 900-2682
IR@ArcturusRx.com
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