Genmab Updates 2024 Financial Guidance
08 Agosto 2024 - 12:00PM
Company Announcement
- Genmab updates its 2024 financial
guidance
- Increase in revenue driven by higher royalties and
reimbursement revenue
- Increase in operating profit excluding acquisition and
integration charges, driven by higher revenue and focused
investments
COPENHAGEN, Denmark; August 8, 2024 –
Genmab A/S (Nasdaq: GMAB) announced today
that it is updating its 2024 financial guidance last published on
May 2, 2024, following the acquisition of ProfoundBio, Inc.
(ProfoundBio). The revised guidance reflects an updated revenue
outlook, incremental R&D investment to support the advancement
of ProfoundBio’s clinical programs, primarily rinatabart sesutecan
(Rina-S), as well as acquisition and integration related
charges.
Genmab expects its 2024 revenue to be in the range of DKK 20.5 –
21.7 billion, an increase to the previous guidance of DKK 18.7–
20.5 billion, driven by higher royalties and reimbursement revenue.
This increase in Genmab’s revenue reflects the continued strong
growth of DARZALEX® and Kesimpta® net sales.
As previously disclosed in Company Announcement Nos. 26.2024 and
28.2024, following the closing of the ProfoundBio acquisition,
Genmab’s operating expenses not including expenses incurred in
connection with acquisition and integration charges, were expected
to be at or moderately above the upper end of the previously
disclosed guidance range of DKK 12.4 – 13.4 billion. Genmab has
updated its operating expense range excluding acquisition and
integration charges to DKK 13.7 – 14.3 billion. The increase
primarily relates to the incremental R&D investment to support
the advancement of ProfoundBio’s clinical programs, primarily
Rina-S as well as a revenue and expense classification change for
programs that remain in Genmab’s collaboration with BioNTech SE
(BioNTech). This classification change has resulted in Genmab
increasing both cost reimbursement revenue and operating expense by
approximately DKK 600 million, resulting in no impact on operating
profit. Excluding the DKK 600 million related to the classification
change and the acquisition and integration charges, the underlying
operating expense range remains within the directional financial
guidance provided at the time we announced the ProfoundBio
acquisition. Including acquisition and integration related charges,
Genmab expects operating expenses for 2024 to be in the range of
DKK 14.1 – 14.7 billion.
Genmab now expects its 2024 operating profit excluding
acquisition and integration related charges to be in the range of
DKK 5.3 – 7.1 billion, compared to the previous guidance of DKK 4.6
– 7.1 billion, primarily driven by the items described above.
Including acquisition and integration related charges, Genmab
expects operating profit for 2024 to be in the range of DKK 4.9 –
6.7 billion.
|
Revised |
|
Revised |
|
|
|
Guidance |
|
Guidance |
|
|
(DKK million) |
ex. Acquisition and Integration related
charges |
|
incl. Acquisition and Integration related
charges |
|
Previous Guidance |
Revenue |
20,500 - 21,700 |
|
20,500 - 21,700 |
|
18,700 - 20,500 |
Royalties |
16,600 - 17,400 |
|
16,600 - 17,400 |
|
15,600 - 16,700 |
Net product
sales/Collaboration revenue* |
2,000 - 2,200 |
|
2,000 - 2,200 |
|
1,700 - 2,200 |
Milestones/Reimbursement revenue |
1,900 - 2,100 |
|
1,900 - 2,100 |
|
1,400 - 1,600 |
Gross
profit** |
19,600 - 20,800 |
|
19,600 - 20,800 |
|
18,000 - 19,500 |
Operating
expenses** |
(13,700) - (14,300) |
|
(14,100) - (14,700) |
|
(12,400) - (13,400) |
Operating
profit |
5,300 - 7,100 |
|
4,900 - 6,700 |
|
4,600 - 7,100 |
*Net Product Sales and Collaboration Revenue consists of EPKINLY
Net Product Sales in the U.S. and Japan and Tivdak (Genmab’s share
of net profits) in the U.S.**Operating Expenses Range excludes Cost
of Product Sales Range, which is included in Gross Profit Range
Genmab’s financial results for the first six months of 2024 will
be published immediately following the publication of this Company
Announcement, on August 8, 2024.
The above expectations are based on assumptions including those
described on pages 5 and 6 of the Interim Report for the first
quarter of 2024 (Company Announcement No. 33/2024).
About Genmab Genmab is an international
biotechnology company with a core purpose of guiding its
unstoppable team to strive toward improving the lives of patients
with innovative and differentiated antibody therapeutics. For 25
years, its passionate, innovative and collaborative team has
invented next-generation antibody technology platforms and
leveraged translational, quantitative and data sciences, resulting
in a proprietary pipeline including bispecific T-cell engagers,
antibody-drug conjugates, next-generation immune checkpoint
modulators and effector function-enhanced antibodies. By 2030,
Genmab’s vision is to transform the lives of people with cancer and
other serious diseases with knock-your-socks-off (KYSO®) antibody
medicines.
Established in 1999, Genmab is headquartered in Copenhagen,
Denmark, with international presence across North America, Europe
and Asia Pacific. For more information, please visit Genmab.com and
follow us on LinkedIn and
X.Contact: Marisol
Peron, Senior Vice President, Global Communications & Corporate
AffairsT: +1 609 524 0065; E: mmp@genmab.com
Andrew Carlsen, Vice President, Head of Investor RelationsT: +45
3377 9558; E: acn@genmab.com This Company Announcement contains
forward looking statements. The words “believe,” “expect,”
“anticipate,” “intend” and “plan” and similar expressions identify
forward looking statements. Actual results or performance may
differ materially from any future results or performance expressed
or implied by such statements. The important factors that could
cause our actual results or performance to differ materially
include, among others, risks associated with preclinical and
clinical development of products, uncertainties related to the
outcome and conduct of clinical trials including unforeseen safety
issues, uncertainties related to product manufacturing, the lack of
market acceptance of our products, our inability to manage growth,
the competitive environment in relation to our business area and
markets, our inability to attract and retain suitably qualified
personnel, the unenforceability or lack of protection of our
patents and proprietary rights, our relationships with affiliated
entities, changes and developments in technology which may render
our products or technologies obsolete, and other factors. For a
further discussion of these risks, please refer to the risk
management sections in Genmab’s most recent financial reports,
which are available on www.genmab.com and the risk factors included
in Genmab’s most recent Annual Report on Form 20-F and other
filings with the U.S. Securities and Exchange Commission (SEC),
which are available at www.sec.gov. Genmab does not undertake any
obligation to update or revise forward looking statements in this
Company Announcement nor to confirm such statements to reflect
subsequent events or circumstances after the date made or in
relation to actual results, unless required by law. Genmab A/S
and/or its subsidiaries own the following trademarks: Genmab®; the
Y-shaped Genmab logo®; Genmab in combination with the Y-shaped
Genmab logo®; HuMax®; DuoBody®; HexaBody®; DuoHexaBody®, HexElect®
and KYSO®; Tivdak® is a trademark of Seagen Inc.; EPKINLY® and its
design are trademarks of AbbVie Biotechnology Ltd.; Kesimpta® is a
trademark of Novartis AG or its affiliates; DARZALEX® is a
trademark of Johnson & Johnson.
Company Announcement no. 52 CVR no. 2102 3884 LEI Code
529900MTJPDPE4MHJ122
Genmab A/SCarl Jacobsens Vej 302500 Valby Denmark
- 080824_CA52_Guidance Update
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