Valneva Successfully Expands Access to Asia for its Chikungunya
Vaccine with Serum Institute of India
Saint-Herblain (France), Pune, (India),
December 19, 2024 – Valneva SE (“Valneva” or “the
Company”), a specialty vaccine company, and Serum Institute of
India (SII), the world’s largest manufacturer of vaccines by number
of doses, today announced an exclusive license agreement for
Valneva’s single-shot chikungunya vaccine that enables supply of
the vaccine in Asia. The collaboration to support broader access to
the vaccine in low-and-middle-income countries (LMICs) in the
region falls within the framework of the $41.3 million funding
agreement Valneva signed with the Coalition for Epidemic
Preparedness Innovations (CEPI) in July 2024 with co-funding from
the European Union1.
The companies will work urgently to bring the
vaccine to the Indian market, and certain other Asian countries,
subject to local regulatory approvals, as India is currently
enduring one of its worst chikungunya outbreaks. Nearly 370,000
cases were confirmed in India between January 2019 and July 2024, a
number rapidly increasing due to the current
outbreak2.
Under the agreement, the Companies will conduct
a technology transfer of the current drug product manufacturing
process. Valneva will supply its chikungunya vaccine drug substance
to SII, which will complete manufacturing and be responsible for
seeking and maintaining regulatory approval of the vaccine in India
and other countries in Asia. Future commercialization will be based
on a profit-sharing model along with single-digit million milestone
payments towards technology transfer and regulatory
approvals to Valneva.
Thomas Lingelbach, Chief Executive
Officer of Valneva, commented, “The current outbreak in
India underscores the fact that containing chikungunya is an
international public health priority. SII has extensive
manufacturing and commercialization infrastructure and broad market
reach in the Asian territory. We are very pleased to enter into
this collaboration to help address this urgent medical need by
accelerating further access to our highly differentiated
vaccine.”
Adar Poonawalla, CEO of Serum Institute
of India, said, “We are pleased to collaborate with
Valneva to bring this chikungunya vaccine to India and other parts
of Asia. This collaboration reflects our focus on providing
effective and accessible vaccines to address pressing public health
needs.”
SII, Valneva and CEPI are committed to enabling
equitable access to chikungunya vaccine doses manufactured and
licensed by SII for the region.
Under the terms of the agreement, SII has
committed to priority supply of the chikungunya vaccine at an
affordable price to public health markets in LMICs.
SII will also make available a stockpile of
100,000 doses of the drug product to CEPI as an ‘investigational
ready reserve’ that could be used in clinical trials in the region.
Such research could provide additional data on the performance of
the vaccine among local populations.
A safety stock of up to 100,000 doses of the
chikungunya vaccine will also be made available and directly
accessible to CEPI, at costs incurred by CEPI, for potential use
when responding to a future chikungunya outbreak in the region.
Dr Richard Hatchett, CEO of
CEPI, said: “Chikungunya continues to pose a troubling and
debilitating danger to the world, including in Asia, with climate
change threatening to worsen its spread. Today’s new collaboration
is a historic achievement which provides a crucial launchpad for
the manufacture of a chikungunya vaccine in Asia, for Asia, while
also enhancing regional health security and guaranteeing the
priority supply of affordable doses to local populations most in
need.”
Valneva’s chikungunya vaccine is the world’s
first and only licensed chikungunya vaccine, currently approved in
the U.S.3, Europe4, and Canada5
for the prevention of disease caused by the chikungunya virus in
individuals 18 years of age and older. Regulatory reviews to expand
the age range to individuals 12 years of age and older are
currently ongoing34
Supported by CEPI and the European Union (EU)’s
Horizon program, Valneva remains focused on expanding the vaccine’s
access in LMICs. Under an earlier funding agreement with
CEPI5, Valneva partnered with Brazil’s Instituto
Butantan (IB) to expand access to the vaccine in the Americas.
Review of the marketing authorization application by the Brazilian
Health Regulatory Agency (ANVISA) is ongoing.
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
years6.
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 Americas7. Between 2013 and 2023,
more than 3.7 million cases were reported in the
Americas8 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.9
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.
About Serum Institute of
India
Serum Institute of India Pvt. Ltd, is a global leader in vaccine
manufacturing, dedicated to providing affordable vaccines
worldwide. Present across 170+ countries, including the US, UK, and
Europe, SII holds the distinction of being the world's largest
vaccine manufacturer. SII's multifunctional production and
one-of-the-largest facility in Manjri, Pune, with an annual
capacity of 4 billion doses, has saved over 30 million lives over
the years.
Founded in 1966, SII's primary mission is to
produce life-saving immunobiological drugs, with a particular
emphasis on affordability and accessibility. Guided by a strong
commitment to improving global health, the company has played a
pivotal role in reducing the prices of essential vaccines, such as
Diphtheria, Tetanus, Pertussis, HIB, BCG, r-Hepatitis B, Measles,
Mumps, and Rubella. Notably, they are the manufacturers of
'Pneumosil,' the world's most affordable PCV, 'Cervavac' the first
indigenous qHPV vaccine in India, and R21/Matrix-M™, the second
malaria vaccine to be authorized for use in children in
malaria-endemic regions. Moreover, SII has been at the forefront of
the global fight against COVID-19, delivering over 2 billion doses
of the COVID-19 vaccine worldwide.
To further expand its global presence and ensure
widespread vaccine availability, SII has established Serum Life
Sciences Ltd, a subsidiary in the UK. Through relentless pursuit of
innovation, SII continues to champion the cause of affordable
vaccines, making a positive impact on the lives of millions
worldwide
www.seruminstitute.com
About CEPI
CEPI was launched in 2017 as an innovative
partnership between public, private, philanthropic and civil
organizations. Its mission is to accelerate the development of
vaccines and other biologic countermeasures against epidemic and
pandemic threats so they can be accessible to all people in need.
CEPI has supported the development of more than 50 vaccine
candidates or platform technologies against multiple known
high-risk pathogens or a future Disease X. Central to CEPI’s
pandemic-beating five-year plan for 2022-2026 is the ‘100 Days
Mission’ to compress the time taken to develop safe, effective,
globally accessible vaccines against new threats to just 100
days.
Learn more at CEPI.net. Follow us on X
(@CEPIvaccines), LinkedIn and Facebook.
About Horizon Europe
Horizon Europe — #HorizonEU — is the European Union's
flagship Research and Innovation programme, part of the
EU-long-term Multiannual Financial Framework (MFF) with a budget of
€95,5 billion to spend over a seven-year period
(2021-2027). Under Horizon Europe, health research will
be supported with the aim to find new ways to keep people healthy,
prevent diseases, develop better diagnostics and more effective
therapies, use personalised medicine approaches to improve
healthcare and wellbeing, and take up innovative health
technologies, such as digital ones.
Media and Investor Relations
Contacts
Valneva
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 |
CEPI
press@cepi.net
+44 7387 055214
Forward-Looking Statements
This press release contains certain
forward-looking statements relating to the business of Valneva,
including with respect to business partnerships and the progress,
timing, results and completion of technology transfer and
regulatory approvals in additional markets. 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 CEPI awards up to US$23.4 million
to Valneva for late-stage development of a single-dose chikungunya
vaccine
2
https://bluedot.global/vaccines-on-the-table-as-chikungunya-outbreak-intensifies-in-india/
3 Valneva Submits Label Extension Applications for its
Chikungunya Vaccine, IXCHIQ®, to EMA and Health Canada -
Valneva
4 Valneva Submits Label Extension Application for its
Chikungunya Vaccine, IXCHIQ®, to the U.S. FDA - Valneva
5 CEPI awards up to $23.4 million to Valneva for late-stage
development of a single-dose Chikungunya vaccine
6
https://jvi.asm.org/content/jvi/88/20/11644.full.pdf
7 https://cmr.asm.org/content/31/1/e00104-16
8 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.
9 Geographical expansion of cases of dengue and
chikungunya beyond the historical areas of transmission in the
Region of the Americas (who.int)
- 2024_12_19_VLA_SII_PR_EN_Final
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