Bavarian Nordic Announces First Half 2024 Results
22 August 2024 - 7:44AM
UK Regulatory
Bavarian Nordic Announces First Half 2024 Results
COPENHAGEN, Denmark, August 22,
2024 – Bavarian Nordic A/S (OMX: BAVA) announced today its
interim financial results and business progress for the first half
of 2024 and released its financial calendar for 2025.
- Revenue for the first half was DKK 2,259 million, and the
operating profit (EBITDA) was DKK 441 million.
- Revenue from travel health increased by 15% to DKK 1,119
million and revenue from public preparedness was DKK 1,024 million,
which is in line with the Company’s expectations. Other revenue was
DKK 116 million.
- Revenues from Rabipur/RabAvert and Encepur have reached levels
exceeding the original expectations at the time of acquisition,
thus triggering a sales milestone of DKK 186 million to GSK,
payable in the third quarter of 2024.
- Bavarian Nordic confirms its new guidance for the full year at
the upper end of the range, with aggregated revenue of
approximately DKK 5,300 million and EBITDA of approximately DKK
1,350 million. The public preparedness revenue included in the new
guidance is now largely all secured by contracts.
DKK million |
Q2 2024 |
Q2 2023 |
H1 2024 |
H1 2023 |
2024 Guidance |
Revenue |
1,427 |
1,987 |
2,259 |
3,239 |
~5,300 |
EBITDA |
420 |
690 |
441 |
1,171 |
~1,350 |
Paul Chaplin, President & Chief Executive
Officer of Bavarian Nordic said: “We are pleased to report strong
developments for Bavarian Nordic during the first half of 2024.
Unfortunately, mpox is again making global headlines as a result of
the record number of cases reported in Africa. The situation has
urged the African CDC and the WHO to declare public health
emergencies and Bavarian Nordic is working closely with all
stakeholders to ensure the equitable access to our mpox vaccine.
Importantly, we have built a strong partnership with the Africa
Centers of Disease Control (CDC), both on exploring supply, but
also expanding our manufacturing network to include Africa. We are
also working with the WHO on a regulatory path to ensure access to
all countries, while in parallel seeking approval for use in
adolescents and also conducting clinical studies in Africa to
further expand the use to children. A recent order for MVA-BN was
secured by an undisclosed European country, and this was
anticipated as part of the 2024 guidance and as such, has no impact
on the remaining vaccine capacity. Indeed, in response to recent
events the company plans to ramp-up vaccine manufacturing to ensure
the continued equitable access to our mpox vaccine. Consequently,
we have the capacity to manufacture 10 million doses by the end of
2025, in addition to our current orders, and could already supply
up to 2 million doses this year. Bavarian Nordic is prepared to
work with the international community to play our role in
protecting and saving lives around the World and to contain the
latest outbreak.”
Highlights from the period
- In April, Bavarian Nordic launched its mpox vaccine in the
U.S., thereby expanding access to JYNNEOS® for at-risk
populations.
- In April, Bavarian Nordic initiated a rolling BLA submission
for its chikungunya vaccine candidate to the U.S. Food and Drug
Administration (FDA). The submission was completed in June, and in
August, the FDA accepted the BLA with priority review.
- In April, Bavarian Nordic was awarded a contract valued at EUR
65 million for the supply of smallpox vaccines to the rescEU
stockpile in 2025.
- In May, Bavarian Nordic announced the departure of EVP and
Chief Medical Officer Laurence de Moerlooze. A search process to
identify the next Chief Medical Officer has been initiated.
- In May, Bavarian Nordic received funding from CEPI to advance a
clinical trial of the mpox vaccine in an African population,
potentially supporting expansion of the current regulatory
approvals to include children 2 years of age and older, as well as
potentially supporting approval of the vaccine in Africa.
- In May, Bavarian Nordic submitted a supplemental BLA seeking
FDA approval of a freeze-dried formulation of the MVA-BN smallpox
and mpox vaccine.
- In June, Bavarian Nordic submitted a Marketing Authorization
Application (MAA) for its chikungunya vaccine candidate to the
European Medicines Agency (EMA). The MAA was accepted in July,
marking the start of the centralized review procedure under
accelerated assessment.
- In June, Bavarian Nordic announced a donation of mpox vaccines
to support the public health response in Africa led by a consortium
of global partners, including Gavi, WHO and UNICEF.
Events after the reporting
date
- In July, Bavarian Nordic announced the conversion of its
existing undrawn DKK 1 billion revolving credit facility into a
sustainability-linked loan (SLL).
- In July, Bavarian Nordic received positive opinion from EMA’s
Committee for Medicinal Products for Human Use (CHMP), recommending
approval of a type II variation for IMVANEX® (MVA-BN)
smallpox and mpox vaccine, including real-world effectiveness data
from the use of the vaccine during the global 2022 mpox outbreak in
the marketing authorization.
- In August, Bavarian Nordic received a new order from the U.S.
government valued at USD 156.8 million, primarily for the
manufacture of additional bulk product for JYNNEOS®
smallpox/mpox vaccine. The bulk product will be manufactured and
invoiced in 2024.
- In August, Bavarian Nordic received a new order for 175,420
doses of the Company’s mpox vaccine from the European Health
Emergency Preparedness and Response Authority (HERA) for donation
to the Africa CDC. Bavarian Nordic will also donate 40,000 doses to
this initiative.
- In August, Bavarian Nordic submitted clinical data to the EMA
to support an extension of the IMVANEX® (MVA-BN®)
smallpox and mpox vaccine indication to include adolescents 12 to
17 years of age. Pending review, approval of the extension could
occur during fourth quarter of 2024.
- In August, Bavarian Nordic received a new order to supply
440,000 doses of smallpox and mpox vaccines to a non-disclosed
European country. The order was anticipated as part of the 2024
guidance and has no impact on the remaining 2024/25 capacity for
our smallpox and mpox vaccine.
Financial calendar 2025
2024 Annual Report
March 5, 2025
Annual General
Meeting
April 9, 2025
Three-month report
(Q1)
May 9, 2025
Half-year report
(Q2)
August 22, 2025
Nine-month report
(Q3)
November 14, 2025
Conference call and webcast
The management of Bavarian Nordic will host an investor/analyst
call today at 2 pm CEST (8 am EDT) 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/bavaQ22024. To join the Q&A session, please
register in advance via https://bit.ly/bavaQ22024reg.
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. 25 / 2024
About Bavarian Nordic
Bavarian Nordic is a fully integrated vaccine company with a
mission to protect and save lives through innovative vaccines. We
are a global leader in smallpox and mpox vaccines, supplied to
governments to enhance public health preparedness and have a strong
portfolio of vaccines for travelers and endemic diseases. 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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