Genmab Improves Its 2022 Financial Guidance
November 03 2022 - 12:45PM
Company Announcement
- Genmab improves its
2022 financial
guidance
COPENHAGEN, Denmark;
November 3, 2022
– Genmab A/S
(Nasdaq:
GMAB) announced today
that it is improving
its 2022 financial guidance
published on August 8,
2022. The improved
guidance is driven primarily by the positive foreign exchange rate
impact on our royalty revenue, and the continued strong performance
of DARZALEX® net sales.
Genmab expects its 2022 revenue to be in the range of DKK 13,500
– 14,500 million, an increase to the previous guidance of DKK
12,000 – 13,000 million, driven primarily by the positive foreign
exchange rate impact on our royalty revenue, and the continued
strong performance of DARZALEX net sales. The upper end of the
revenue guidance range now assumes a significant milestone
associated with the potential acceptance by the U.S. Food and Drug
Administration to review the Biologics License Application
submission for epcoritamab. Genmab’s projected revenue for 2022
primarily consists of DARZALEX royalties. Such royalties are based
on Genmab’s revised estimate of DARZALEX 2022 net sales of USD 8.0
– 8.2 billion compared to Genmab’s previous estimate of USD 7.8 –
8.2 billion.
Genmab anticipates its 2022 operating expenses to be in the
range of DKK 8,000 – 8,400 million, an increase to the previous
guidance of DKK 7,600 – 8,200 million, primarily driven by the
negative impact of the strong U.S. Dollar. Operating expenses
continue to be driven by the advancement of Genmab’s clinical
programs, continued investment in research and development, as well
as building Genmab’s commercial organization and broader
organizational infrastructure.
Genmab now expects its 2022 operating profit to be in the range
of DKK 5,100 – 6,500 million, an increase to the previous guidance
of DKK 3,800 – 5,400 million, driven primarily by the items
described above.
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|
|
|
|
|
|
|
Revised |
|
Previous |
|
(DKK million) |
|
Guidance |
|
Guidance |
|
Revenue |
|
13,500 - 14,500 |
|
12,000 - 13,000 |
|
Operating expenses |
|
(8,000) - (8,400) |
|
(7,600) - (8,200) |
|
Operating profit |
|
5,100 - 6,500 |
|
3,800 - 5,400 |
|
Genmab’s financial results for the first nine months of 2022
will be published on November 9, 2022.
The above expectations are based on assumptions including those
described on pages 5 and 6 of the Interim Report for the first half
of 2022 (Company Announcement No. 41/2022) as well as an updated
USD/DKK exchange rate of 7.2, compared to the previous exchange
rate of 6.8.
About Genmab Genmab is an international
biotechnology company with a core purpose to improve the lives of
people with cancer. For more than 20 years, Genmab’s vision to
transform cancer treatment has driven its passionate, innovative
and collaborative teams to invent next-generation antibody
technology platforms and leverage translational research and data
sciences, fueling multiple differentiated cancer treatments that
make an impact on people’s lives. To develop and deliver novel
therapies to patients, Genmab has formed 20+ strategic partnerships
with biotechnology and pharmaceutical companies. Genmab’s
proprietary pipeline includes bispecific T-cell engagers,
next-generation immune checkpoint modulators, effector function
enhanced antibodies and antibody-drug conjugates.
Genmab is headquartered in Copenhagen, Denmark with
locations in Utrecht, the Netherlands, Princeton, New Jersey, U.S.
and Tokyo, Japan. For more information, please visit Genmab.com and
follow us on Twitter.com/Genmab.
Contact: Marisol
Peron, Senior Vice President, Communications and 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 pre-clinical 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®; DuoBody in combination with the
DuoBody logo®; HexaBody®; HexaBody in combination with the HexaBody
logo®; DuoHexaBody® and HexElect®; DARZALEX® is a trademark of
Johnson & Johnson.
Company Announcement no. 54CVR no. 2102 3884LEI Code
529900MTJPDPE4MHJ122
Genmab A/SKalvebod Brygge 431560 Copenhagen VDenmark
- 031122_CA54_Guidance Update
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