Valneva Submits Label Extension Applications for its Chikungunya Vaccine, IXCHIQ®, to EMA and Health Canada
September 18 2024 - 1:00AM
UK Regulatory
Valneva Submits Label Extension Applications for its Chikungunya
Vaccine, IXCHIQ®, to EMA and Health Canada
To potentially include
adolescents and antibody persistence up to two years
Saint Herblain (France), September 18,
2024 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a
specialty vaccine company, today announced that it has submitted
label extension applications to the European Medicines Agency (EMA)
and Health Canada to potentially expand the use of its chikungunya
vaccine, IXCHIQ®, to adolescents aged 12 to 17 years in
Europe and Canada. The Canadian label extension application also
includes two-year antibody persistence data, which is a key
differentiator for IXCHIQ® that was already included in
the initial EMA filing. Valneva expects to submit data to the U.S.
Food and Drug Administration (FDA) this year to also support
potential label extensions in the U.S.
IXCHIQ® is the world’s first and only
licensed chikungunya vaccine available to address this significant
unmet medical need. The vaccine is currently approved in the
U.S.1, Europe2, and Canada3 for
the prevention of disease caused by the chikungunya virus in
individuals 18 years of age and older. The U.S. launch is underway
while first sales in Canada and Europe are anticipated in the
fourth quarter of 2024.
In addition to ramping up sales, Valneva is
focused on expanding the vaccine’s label and access. The Company
expects a marketing authorization in Brazil in the second half of
2024 and recently expanded its partnership with The Coalition for
Epidemic Preparedness Innovations (CEPI)4 to support
broader access to the vaccine in Low Middle-Income Countries
(LMICs), post-marketing trials and potential label extensions in
children, adolescents and pregnant women. CEPI will provide Valneva
up to $41.3 million of additional funding over the next five years,
with support from the European Union’s (EU) Horizon Europe
program.
Juan Carlos Jaramillo, M.D., Chief
Medical Officer of Valneva, commented, “Given the
substantial risk that chikungunya presents to individuals residing
in or traveling to endemic regions, it's imperative to ensure the
vaccine is available to all age groups. This broader accessibility
would certainly help provide protection and mitigate the burden of
this debilitating illness which is currently spreading in areas
that were previously unaffected. The durability of the immune
response is also extremely important, especially for endemic
countries where access to immunization can be difficult."
EMA and Health Canada’s label extension
applications are based on positive six-month adolescent Phase 3
data which the Company reported in May 20245. These data
showed that a single-dose vaccination with IXCHIQ®
induces a high and sustained immune response in 99.1% of
adolescents, and that the vaccine was generally well tolerated.
The Lancet Infectious Diseases, a world leading infectious
diseases journal, also recently published an article showing that
the vaccine was well tolerated in adolescents aged 12 to 17 years
28 days after a single injection, regardless of previous CHIKV
infection.
In addition to the adolescent data, Health
Canada’s label extension application included IXCHIQ®‘s
antibody persistence data which showed that the vaccine’s immune
response was sustained for 24 months by 97% of participants and was
equally durable in younger and older adults6. The
Company expects to publish 36 months persistence data later this
year.
About Chikungunya
Chikungunya virus (CHIKV) is a mosquito-borne viral disease spread
by the bites of infected Aedes mosquitoes which causes
fever, severe joint and muscle pain, headache, nausea, fatigue and
rash. Joint pain is often debilitating and can persist for weeks to
years.7
In 2004, the disease began to spread quickly, causing large-scale
outbreaks around the world. Since the re-emergence of the virus,
CHIKV has now been identified in over 110 countries in Asia,
Africa, Europe and the Americas.8 Between 2013 and 2023,
more than 3.7 million cases were reported in the
Americas9 and the economic impact is considered to be
significant. The medical and economic burden is expected to grow
with climate change as the mosquito vectors that transmit the
disease continue to spread geographically. As such, the World
Health Organization (WHO) has highlighted chikungunya as a major
public health problem.10
About Valneva SE
We are a specialty vaccine company that develops, manufactures, and
commercializes prophylactic vaccines for infectious diseases
addressing unmet medical needs. We take a highly specialized and
targeted approach, applying our deep expertise across multiple
vaccine modalities, focused on providing either first-, best- or
only-in-class vaccine solutions.
We have a strong track record, having advanced multiple vaccines
from early R&D to approvals, and currently market three
proprietary travel vaccines, including the world’s first and only
chikungunya vaccine, as well as certain third-party vaccines.
Revenues from our growing commercial business help fuel the
continued advancement of our vaccine pipeline. This includes the
only Lyme disease vaccine candidate in advanced clinical
development, which is partnered with Pfizer, the world’s most
clinically advanced Shigella vaccine candidate, as well as vaccine
candidates against the Zika virus and other global public health
threats. More information is available at www.valneva.com.
Valneva Investor and Media Contacts
Laetitia Bachelot-Fontaine
VP Global Communications & European Investor Relations
M +33 (0)6 4516 7099
laetitia.bachelot-fontaine@valneva.com |
Joshua Drumm, Ph.D.
VP Global Investor Relations
M +001 917 815 4520
joshua.drumm@valneva.com |
Forward-Looking Statements
This press release contains certain
forward-looking statements relating to the business of Valneva,
including with respect to the progress, timing, results and
completion of research, development and clinical trials for product
candidates, to regulatory approval of product candidates and review
of existing products. In addition, even if the actual results or
development of Valneva are consistent with the forward-looking
statements contained in this press release, those results or
developments of Valneva may not be sustained in the future. In some
cases, you can identify forward-looking statements by words such as
“could,” “should,” “may,” “expects,” “anticipates,” “believes,”
“intends,” “estimates,” “aims,” “targets,” or similar words. These
forward-looking statements are based largely on the current
expectations of Valneva as of the date of this press release and
are subject to a number of known and unknown risks and
uncertainties and other factors that may cause actual results,
performance or achievements to be materially different from any
future results, performance or achievement expressed or implied by
these forward-looking statements. In particular, the expectations
of Valneva could be affected by, among other things, uncertainties
and delays involved in the development and manufacture of vaccines,
unexpected clinical trial results, unexpected regulatory actions or
delays, competition in general, currency fluctuations, the impact
of the global and European credit crisis, and the ability to obtain
or maintain patent or other proprietary intellectual property
protection. Success in preclinical studies or earlier clinical
trials may not be indicative of results in future clinical trials.
In light of these risks and uncertainties, there can be no
assurance that the forward-looking statements made in this press
release will in fact be realized. Valneva is providing this
information as of the date of this press release and disclaims any
intention or obligation to publicly update or revise any
forward-looking statements, whether as a result of new information,
future events, or otherwise.
1 Valneva Announces U.S. FDA Approval of World’s
First Chikungunya Vaccine, IXCHIQ® - Valneva
2 Valneva Receives Marketing Authorization in Europe
for the World’s First Chikungunya Vaccine, IXCHIQ® -
Valneva
3 Valneva Announces Health Canada Approval of the
World’s First Chikungunya Vaccine, IXCHIQ® - Valneva
4 CEPI Expands Partnership with Valneva with a $41.3
Million Grant to Support Broader Access to the World’s First
Chikungunya Vaccine - Valneva
5 Valneva Reports Further Positive Pivotal Phase 3
Data in Adolescents for its Single-Shot Chikungunya Vaccine -
Valneva
6 Valneva Reports Positive 24-Month Antibody
Persistence Data for its Single-Shot Chikungunya Vaccine IXCHIQ® -
Valneva
7
https://jvi.asm.org/content/jvi/88/20/11644.full.pdf
8 https://cmr.asm.org/content/31/1/e00104-16
9 PAHO/WHO data: Number of reported cases of chikungunya fever
in the Americas (Cumulative Cases 2018-2023 and Cases per year
2013-2017).
https://www.paho.org/data/index.php/en/mnu-topics/chikv-en/550-chikv-weekly-en.html.
Last accessed 01 Aug 2023.
10 Geographical expansion of cases of dengue and
chikungunya beyond the historical areas of transmission in the
Region of the Americas (who.int)
- 2024_09_18_IXCHIQ_Label_Extension_Application_PR_EN_Final
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