Late-breaking data presented at 9th ESWI
Influenza Conference in Valencia
Arcturus Therapeutics Holdings Inc. (the “Company”, “Arcturus”,
Nasdaq: ARCT), a global late-stage clinical messenger RNA medicines
company focused on the development of infectious disease vaccines
and opportunities within liver and respiratory rare diseases, today
announced the results of a phase 1/2 study showing that a booster
dose of a novel, self-amplifying messenger RNA (sa-mRNA) vaccine
against COVID-19 induces a robust, broadly cross-reactive, and
durable immune response in adults that remains elevated through 12
months after vaccination. Three sa-mRNA vaccines were used in the
study, which was presented as a poster at the European Scientific
Working Group on Influenza's 9th ESWI Influenza Conference in
Valencia, Spain.
Messenger RNA (mRNA) vaccine technology protects against
infectious diseases by instructing cells in the body to make a
specific protein, stimulating the immune response, and leaving a
blueprint to recognize and fight future infection. However, sa-mRNA
also provides the body with instruction to make copies of the mRNA,
amplifying the amount of protein made. This advanced technology has
shown the potential to offer longer duration of immune response at
considerably lower doses compared to conventional mRNA
vaccines.
“Current mRNA technologies provide effective initial
immunogenicity against COVID-19, but the results of this study show
that our sa-mRNA vaccine platform can offer improvements in
duration and breadth of protection against new and emerging
variants,” said Igor Smolenov, Chief Development Officer, Arcturus.
“We are proud of the role Arcturus has played, collaborating with
CSL, in advancing sa-mRNA vaccine development.”
CSL’s vaccine business, CSL Seqirus, is Arcturus’ global
exclusive partner for the development of novel mRNA vaccines
against SARS-CoV-2 (COVID-19), influenza and pandemic preparedness.
CSL has a dynamic portfolio of lifesaving medicines, including
those that treat hemophilia, hereditary angioedema (HAE) and immune
deficiencies, vaccines to prevent influenza, and therapies in iron
deficiency and nephrology.
“We are encouraged by the findings of the study, indicating the
sa-mRNA platform’s potential to solve the challenge of mRNA vaccine
waning immunity over time, and thereby provide prolonged protection
at lower doses,” said Esther Heijnen, M.D., Vice President,
Clinical Development, Vaccines Innovation Unit, CSL. “Our
collaboration with Arcturus on advanced mRNA vaccines is another
example of CSL’s relentless pursuit of disruptive innovation when
public health and patients can benefit.”
Study Design and Results
For this phase 1/2 randomized, observer-blind study conducted in
the US and Singapore, 36 adults previously immunized with approved
COVID-19 mRNA vaccines as a primary series were recruited.
Participants were randomized 1:1:1 to receive one booster dose on
Day 1 of either the ARCT-021, ARCT-154, or ARCT-165 vaccines, all
of which encode the SARS-CoV-2 full-length S glycoprotein of,
respectively, the ancestral strain in native conformation, a
prefusion-stabilized B.1 variant including the D614G mutation, or
the Beta variant. Immunogenicity was assessed as neutralizing
antibody titers against the SARS-CoV-2 D614G strain, and a panel of
SARS-CoV-2 variants measured by pseudoviral microneutralization
assay on Days 1, 15, 29, 91, 181, 271, and 366. Solicited adverse
events (AE) were assessed up to 7 days, unsolicited AEs up to 28
days, and serious AEs up to 366 days after vaccination.
All three vaccines induced robust neutralizing immune response
against the D614G variant at Day 29 with geometric mean fold rises
(GMFR) from pre-booster levels of 20.0, 36.7 and 23.5 after
ARCT-021, ARCT-154, and ARCT-165, respectively. ARCT-154, a leading
candidate, induced a broad, cross-neutralizing immune response,
which persisted up to one-year post-booster with no further
boosting. Similar trends were observed for other SARS-CoV-2
variants including Beta, Delta, Omicron BA.1, Omicron BA.2, and
Omicron BA.4/5. Additional exploratory testing confirmed
cross-neutralization against emergent BQ.1.1 and XBB.1.5 Omicron
sub-lineages with GMFRs of 12.8 and 3.4, respectively, at Day 29
post-booster. Adverse events were mild or moderate and resolved
quickly, and rates of related or severe AEs were low.
About Arcturus Therapeutics
Founded in 2013 and based in San Diego, California, Arcturus
Therapeutics Holdings Inc. (Nasdaq: ARCT) is a global late-stage
clinical 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. The Company has ongoing
collaborations with CSL Seqirus and Meiji Seika Pharma, and a joint
venture with ARCALIS. Arcturus’ pipeline includes RNA therapeutic
candidates to potentially treat ornithine transcarbamylase
deficiency and cystic fibrosis, 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 (patents and patent
applications issued 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 Statement
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 of the Company’s pipeline and partnered
programs (including the COVID-19 program partnered with CSL
Seqirus), the likelihood that ARCT-154 or any other Arcturus
vaccine candidate will be successful or continue to advance, the
likelihood that the Phase 1/2 clinical data will be predictive of,
or consistent with, future clinical results, the likelihood that
the Company’s sa-mRNA vaccine platform will offer improvements in
duration and breadth of protection, and the impact of general
business and economic conditions. 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
Kendall Investor Relations Carlo Tanzi, Ph.D. (617) 914-0008
ctanzi@kendallir.com
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