Bavarian Nordic Announces Interim Results for the First Nine Months of 2024
15 November 2024 - 7:38AM
UK Regulatory
Bavarian Nordic Announces Interim Results for the First Nine Months
of 2024
COPENHAGEN, Denmark, November 15,
2024 – Bavarian Nordic A/S (OMX: BAVA) announced today its
interim financial results for the first nine months of 2024 and
business progress for the third quarter of 2024.
- Revenue for the first nine months was DKK 3,622 million, and
the operating profit (EBITDA) was DKK 692 million.
- Revenue from Travel Health increased by 18% to DKK 1,892
million compared to the first nine months of 2023 and revenue from
Public Preparedness was DKK 1,549 million, which is in line with
the Company’s expectations. Other revenue was DKK 181 million.
- The financial guidance for the full year, which was upgraded on
September 26 as a result of additional mpox vaccine orders and
improved performance in the Travel Health business, is maintained
at a revenue between DKK 5,400 million and DKK 5,800 million and
EBITDA between DKK 1,450 million and DKK 1,700 million. The
intervals represent uncertainty related to logistics and supply
timing of deliveries of mpox vaccines dictated by among others the
level of preparedness to receive and handle the vaccines in the
receiving countries.
- For 2025, the Company has so far secured revenue from
mpox/smallpox vaccine orders of approximately DKK 2,400 million,
including previously announced deferred revenue.
DKK million |
Q3 2024 |
Q3 2023 |
9m 2024 |
9m 2023 |
2024 Guidance |
Revenue |
1,363 |
1,376 |
3,622 |
4,615 |
5,400 - 5,800 |
EBITDA |
250 |
380 |
692 |
1,552 |
1,450 - 1,700 |
Paul Chaplin, President & Chief
Executive Officer of Bavarian Nordic said: “We have had a
busy, but highly purposeful and rewarding third quarter, where we
have worked intensively to support the efforts to curb the ongoing
mpox outbreak in Africa. Only a few weeks after the declaration of
mpox as a public health emergency, the first vaccines arrived early
September in the Democratic Republic of Congo, the epicenter of the
outbreak. With speed and flexibility, we have once again
demonstrated our ability to step up in support of a global health
crisis. We have acted with global stakeholders to ensure the
availability of nearly 3 million doses of our mpox vaccine to
Africa through donations and agreements. In parallel, we have
continued to work with nations globally to strengthen their
mpox/smallpox preparedness, helping to build resilience beyond the
current outbreak, and enabling countries to make donations from
their existing stockpiles. To ensure the continued equitable access
to our vaccine we are exploring options to expand our capacity for
increased demand, including transferring the process to a
manufacturer in Africa and we applaud the support provided by the
Africa CDC and other stakeholders in this endeavor. The committed
orders for next year, combined with improved performance in our
Travel Health business, and the launch of our chikungunya vaccine
in Europe and the U.S. have set us up for another exciting and
eventful year in 2025 in line with our vision to expand our reach
and impact through life-changing solutions.”
Highlights from the third
quarter
Public Preparedness
- In response to the public health emergency declarations by the
Africa CDC and WHO in August, Bavarian Nordic has intensified its
collaboration with global stakeholders in efforts to curb the
ongoing mpox outbreak in Africa. Importantly, the Company has been
working towards maximizing the manufacturing capacity for the
MVA-BN mpox vaccine to meet the short- to medium-term demand.
- The Company’s donation of vaccines, together with donations
from the European Commission and the U.S. government were the first
to arrive in the Democratic Republic of Congo (DRC) in September,
ahead of their vaccination campaign. Nearly 3 million doses of
MVA-BN have been pledged to Africa by governments and organizations
to-date.
- Several new orders, including multi-year orders, were announced
during the third quarter, and included among other orders from
UNICEF, the U.S. government, the European Health Emergency
Preparedness and Response Authority (HERA), as well as from several
undisclosed countries. Bavarian Nordic retains sufficient capacity
to fulfil the requirement as stated by Africa CDC for at least 10
million doses by the end of 2025 and could even further scale up
capacity for future demand if needed.
- Several regulatory approvals were obtained for MVA-BN during
the third quarter. Most importantly, the vaccine received
prequalification from the WHO, representing an important step in
making the vaccine available for African countries. Furthermore,
the vaccine received a full approval in Singapore and Mexico and a
provisional approval in New Zealand. In Europe, real-world
effectiveness data from the global 2022 mpox outbreak was included
in the marketing authorization, which also was extended to include
adolescents 12 to 17 years of age – a decision also adopted in the
WHO prequalification. Several clinical studies are now ongoing to
generate clinical data in a pediatric population (2-11 years),
aiming to further expand the approval for this group.
Travel Health
- The Travel Health business has continued its strong
performance, demonstrating an overall growth of 18% in the first
nine months compared to 2023, primarily driven by higher sales of
Rabipur/RabAvert and Encepur. The combined revenues from both
products have reached levels exceeding the original expectations at
the time of acquisition, thus triggering a sales milestone of DKK
186 million to GSK in the third quarter. The expected revenue from
the Travel Health business for the full year was recently upgraded
from DKK 2,100 million to DKK 2,200 million.
- The bulk manufacturing process for Rabipur/RabAvert was
approved by the regulators in October, thus completing the entire
technology transfer for the product to Bavarian Nordic, as the fill
and finish process had already been established and approved. The
technology transfer for Encepur is progressing as planned with
anticipated completion and approval in 2025.
- Preparations for launch of the chikungunya vaccine in 2025 are
being intensified with a regulatory review underway in both the
U.S. and Europe. Following grant of priority review for the BLA in
August, the FDA is targeting a decision in February 2025, and in
Europe, the MAA is being reviewed under accelerated assessment,
with anticipated decision in the first half of 2025.
- Commercial presence is currently being expanded into new
territories to support both the launch of the chikungunya vaccine
in 2025 and the ongoing relaunch of Vivotif and Vaxchora, as well
as the gradual take-back of Rabipur/RabAvert and Encepur sales and
marketing in markets currently managed by Valneva.
Conference call and webcast
The management of Bavarian Nordic will host an investor/analyst
call today at 2 pm CET (8 am EST) to present the interim results
followed by a Q&A session. A listen-only version of the call
and presentation slides can be accessed via
https://bit.ly/bavaQ32024. To join the Q&A session, please
register in advance via https://bit.ly/bavaQ32024reg.
Contacts
Europe: Rolf Sass Sørensen, Vice President Investor Relations,
rss@bavarian-nordic.com, Tel: +45 61 77 47 43
US: Graham Morrell, Paddock Circle Advisors,
graham@paddockcircle.com, Tel: +1 781 686 9600
Company Announcement no. 35 / 2024
About Bavarian Nordic
Bavarian Nordic is a global vaccine company with a mission to
improve health and save lives through innovative vaccines. We are a
preferred supplier of mpox and smallpox vaccines to governments to
enhance public health preparedness and have a leading portfolio of
travel vaccines. For more information, visit
www.bavarian-nordic.com.
Forward-looking statements
This announcement includes forward-looking statements that involve
risks, uncertainties and other factors, many of which are outside
of our control, that could cause actual results to differ
materially from the results discussed in the forward-looking
statements. Forward-looking statements include statements
concerning our plans, objectives, goals, future events, performance
and/or other information that is not historical information. All
such forward-looking statements are expressly qualified by these
cautionary statements and any other cautionary statements which may
accompany the forward-looking statements. We undertake no
obligation to publicly update or revise forward-looking statements
to reflect subsequent events or circumstances after the date made,
except as required by law.
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