– Entered into Business Combination Agreement
to be acquired by Novartis for € 68.00 per share in cash or € 2.7
billion equity value
– Sold all tafasitamab rights worldwide to
Incyte
– Presented comprehensive Phase 3 MANIFEST-2
study results at ASH 2023 Annual Meeting, demonstrating pelabresib
improves all four disease hallmarks of myelofibrosis
– Monjuvi® U.S. net product sales of US$ 24.1
million (€ 22.4 million) for the fourth quarter of 2023 and US$
92.0 million (€ 85.0 million) for the full year of 2023
– € 680.5 million in cash and other financial
assets as of December 31, 2023
– MorphoSys to host conference call and webcast
on Thursday, March 14, 2024, at 1:00 pm CET (12:00 pm GMT; 8:00 am
EDT)
MorphoSys AG (FSE: MOR; NASDAQ: MOR) reports results for the
fourth quarter and the full year 2023.
“In 2023, we demonstrated the potential for pelabresib to shift
the myelofibrosis treatment paradigm, as results from our Phase 3
MANIFEST-2 study showed that all four disease hallmarks were
improved with the pelabresib and ruxolitinib combination therapy
over standard of care,” said Jean-Paul Kress, M.D., Chief Executive
Officer of MorphoSys. “Now, in 2024, we are pleased that Novartis
is committing to the future of our promising pipeline. With its
ample resources, additional scientific expertise and global
footprint, Novartis can help accelerate pelabresib's potential
worldwide. The acquisition process is progressing steadily, and we
expect to close the proposed transaction in the first half of the
year.”
Novartis’ Public Takeover
Offer:
On February 5, 2024, MorphoSys announced the company entered
into a Business Combination Agreement with Novartis BidCo AG
(formerly known as Novartis data42 AG) and Novartis AG (hereinafter
collectively referred to as “Novartis”) based on Novartis’
intention to submit a voluntary public takeover offer for all
outstanding MorphoSys no-par value bearer shares at an offer price
of € 68.00 per share in cash. The offer price corresponds to a
premium of 94% and 142% on the volume-weighted average price during
the last month and three months, as of the unaffected January 25,
2024, close, respectively. As part of the Business Combination
Agreement with Novartis, Novartis seeks to obtain exclusive,
worldwide rights to develop and commercialize pelabresib, an
investigational BET inhibitor, and tulmimetostat, an
investigational next-generation dual inhibitor of EZH2 and EZH1,
across all indications.
The offer will contain customary closing conditions, in
particular a minimum acceptance threshold of 65% of MorphoSys’
share capital and antitrust clearances. MorphoSys and Novartis have
received antitrust clearance in Germany and Austria. The companies
have also made antitrust filings in the U.S. under the HSR Act and
continue to expect the closing to take place in the first half of
2024.
Pelabresib Highlights:
On December 10, 2023, comprehensive results from the Phase 3
MANIFEST-2 study at 24 weeks were presented during an oral
presentation at the 65th American Society of Hematology (ASH)
Annual Meeting and Exposition. In MANIFEST-2, the combination of
pelabresib and the JAK inhibitor ruxolitinib improved all four
disease hallmarks of myelofibrosis, including a significant
reduction in spleen size with a response rate nearly double that of
placebo plus ruxolitinib. The combination therapy showed a strong
positive trend in reducing symptom burden and improvements in
measures of anemia and bone marrow fibrosis, and demonstrated
safety results in line with assessments from prior clinical
trials.
Monjuvi/Minjuvi®
Highlights:
Monjuvi (tafasitamab-cxix) U.S. net product sales of US$ 24.1
million (€ 22.4 million) for the fourth quarter 2023 (Q4 2022: US$
25.3 million (€ 24.7 million)) and US$ 92.0 million (€ 85.0
million) for the full year of 2023 (2022: US$ 89.4 million (€ 84.9
million)). Minjuvi royalty revenue of € 1.3 million for sales
outside of the U.S. in the fourth quarter 2023 (Q4 2022: € 0.7
million) and € 5.4 million for the full year of 2023 (2022: € 3.0
million).
On February 5, 2024, MorphoSys also announced it entered into a
Purchase Agreement to sell and transfer all rights worldwide
related to tafasitamab to Incyte Corporation (“Incyte”). Under the
terms of MorphoSys’ Purchase Agreement with Incyte, Incyte will
obtain exclusive rights worldwide, assume full responsibility and
cover all costs going forward for the development and
commercialization of tafasitamab for a purchase price of US$ 25
million.
Corporate Developments:
On December 14, 2023, MorphoSys announced the completion of a
share capital increase from € 34,231,943 by € 3,423,194 to €
37,655,137 through a full utilization of its authorized capital
2023-II, resulting in gross proceeds of € 102.7 million.
Financial Results for the Fourth
Quarter of 2023 (IFRS):
Total revenues for the fourth quarter 2023 were € 59.0
million compared to € 81.6 million for the same period in 2022. The
decrease resulted first and foremost from prior year revenues
stemming from the execution of an out-licensing agreement with
Novartis.
in € million*
Q4 2023
Q3 2023
Q4 2022
Q-Q Δ
Y-Y Δ
Total revenues
59.0
63.8
81.6
(8)%
(28)%
Monjuvi product sales
22.4
21.5
24.7
4%
(9)%
Royalties
34.0
34.0
29.1
0%
17%
Licenses, milestones and other
2.6
8.3
27.9
(69)%
(91)%
* Differences due to rounding.
Cost of Sales: In the fourth quarter of 2023, cost of
sales was € 14.6 million compared to € 15.4 million for the
comparable period in 2022.
Research and Development (R&D) Expenses: In the
fourth quarter 2023, R&D expenses were € 80.3 million compared
to € 94.0 million for the same period in 2022. The decrease mainly
resulted from lower expenses for external services.
Selling, General and Administrative (SG&A) Expenses:
Selling expenses in the fourth quarter 2023 were € 22.6 million
compared to € 23.0 million for the same period in 2022. General and
administrative (G&A) expenses amounted to € 22.9 million
compared to € 17.5 million for the same period in 2022.
Operating Loss: Operating loss amounted to € 81.4 million
in the fourth quarter 2023 compared to € 68.4 million for the same
period in 2022.
Consolidated Net Loss: For the fourth quarter 2023,
consolidated net loss was € 48.3 million compared to € 329.4
million for the same period in 2022.
Financial Results for the Full Year
2023 (IFRS):
Total Revenues for the full year 2023 were € 238.3
million compared to € 278.3 million in 2022. The decrease resulted
first and foremost from prior year revenues stemming from the
execution of out-licensing agreements with HI-Bio and Novartis.
Royalties in 2023 include € 5.4 million from the sale of Minjuvi
outside of the U.S. by our partner Incyte and € 111.0 million from
Tremfya® sales which is fully passed on to Royalty Pharma.
in € million*
2023
2022
Y-Y Δ
Total revenues
238.3
278.3
(14)%
Monjuvi product sales
85.0
84.9
0%
Royalties
116.4
99.9
17%
Licenses, milestones and other
36.9
93.5
(61)%
* Differences due to rounding.
Cost of Sales: For the full year 2023, cost of sales were
€ 58.4 million compared to € 48.6 million in 2022. The increase
compared to the previous year is mainly due to one-off effects from
write-downs on inventories in the amount of € 11.9 million
recognized in 2023.
R&D Expenses: For the full year 2023, R&D
expenses were € 283.6 million compared to € 297.8 million in 2022.
The decrease of R&D expenses reflects our current clinical
study progress as well as prioritization activities relating to our
R&D portfolio.
SG&A Expenses: Selling expenses for the full year
2023 were € 81.4 million compared to € 92.4 million in 2022. The
decrease is mainly due to the ongoing measures to streamline and
focus sales efforts. G&A expenses amounted to € 65.8 million
for 2023 compared to € 60.1 million in 2022. The increase was
mainly driven by the increase in share-based payment expenses.
Operating Loss: Operating loss amounted to € 252.5
million for the full year 2023 compared to a loss of € 220.7
million in 2022.
Consolidated Net Loss: For the full year 2023,
consolidated net loss was € 189.7 million compared to a net loss of
€ 151.1 million in 2022.
Cash and Other Financial Assets: As of December 31, 2023,
the Company had cash and other financial assets of € 680.5 million
compared to € 907.2 million on December 31, 2022. The liquid funds
are predominantly required to advance the development of the
proprietary portfolio to key clinical and regulatory milestones.
The Management Board believes that the cash and other financial
assets, which also incorporates the additional cash impacts from
the sale of tafasitamab to Incyte as announced on February 5, 2024,
will be sufficient to fund the operating activities and other cash
requirements until early 2026 including the repayment of the
convertible bonds. Any potential cashflows resulting from the
Novartis Business Combination Agreement as announced on February 5,
2024, were not considered in the recent corporate planning.
Under the Business Combination Agreement, Novartis agreed to use
all such efforts which are from the perspective of a prudent
business person reasonable and appropriate to provide MorphoSys
with the financial resources required following completion of the
Novartis Takeover Offer to enable MorphoSys to pay any obligations
of MorphoSys arising from the implementation of the Novartis
Takeover Offer as and when due, for example, but not limited to the
obligation from the convertible bonds and the obligations arising
from the long-term incentive plans, each to the extent triggered by
the completion of the Novartis Takeover Offer.
For the unlikely case that the proposed transaction with
Novartis is not consummated, and MorphoSys consequently would
remain a stand-alone company, management would need to assess
different financing options to ensure the going-concern assumption
beyond the said timeframe according to regulatory requirements.
Management would then consider both anti-dilutive financing
options, such as out-licensing of (pre-) clinical assets or the
sale of potential future royalties, but also consider accessing the
capital markets by way of issuance of new shares or share
instruments (ADSs) and/ or issuance or refinancing of convertible
debt.
Number of Shares: The number of shares issued totaled
37,655,137 on December 31, 2023.
Financial Guidance 2024:
As a consequence of the sale and transfer of tafasitamab to
Incyte on February 5, 2024, MorphoSys' 2024 financial guidance
published on January 30, 2024, cannot be maintained and therefore
was revoked. For the time being, MorphoSys will no longer make a
forecast for revenues from product sales, as no such revenues will
be realized.
For 2024, the Group expects R&D expenses of € 170 million to
€ 185 million. R&D expenses mainly represent our investments in
the development of pelabresib and tulmimetostat. Selling,
administrative and general expenses are expected to be between € 90
million and € 105 million. Any effects from the implementation of
the Novartis takeover offer are not included in this forecast.
The overall forecast is subject to a number of uncertainties,
including inflation and foreign currency effects.
Operational Outlook:
The following activity is planned for 2024:
- Submit a New Drug Application for pelabresib in combination
with ruxolitinib in myelofibrosis to the U.S. Food and Drug
Administration (FDA) and a Marketing Authorization Application to
the European Medicines Agency in the middle of 2024.
MorphoSys Group Key Figures (IFRS, end
of financial year: December 31, 2023)
in € million
Q4 2023
Q4 2022
Δ
2023
2022
Δ
Revenues
59.0
81.6
(28)%
238.3
278.3
(14)%
Product Sales
22.4
24.7
(9)%
85.0
84.9
0%
Royalties
34.0
29.1
17%
116.4
99.9
17%
Licenses, Milestones and Other
2.6
27.9
(91)%
36.9
93.5
(61)%
Cost of Sales
(14.6)
(15.4)
(5)%
(58.4)
(48.6)
20%
Gross Profit
44.4
66.2
(33)%
179.9
229.6
(22)%
Total Operating Expenses
(125.8)
(134.6)
(7)%
(432.4)
(450.4)
(4)%
Research and Development
(80.3)
(94.0)
(15)%
(283.6)
(297.8)
(5)%
Selling
(22.6)
(23.0)
(2)%
(81.4)
(92.4)
(12)%
General and Administrative
(22.9)
(17.5)
31%
(65.8)
(60.1)
9%
Impairment of Goodwill
(1.6)
—
n/a
(1.6)
—
n/a
Operating Profit / (Loss)
(81.4)
(68.4)
19%
(252.5)
(220.7)
14%
Other Income
0.1
(7.8)
>(100)%
5.0
12.0
(58)%
Other Expenses
(3.9)
7.4
>(100)%
(7.1)
(15.6)
(54)%
Finance Income
174.3
325.0
(46)%
213.4
412.1
(48)%
Finance Expenses
(40.8)
249.5
>(100)%
(142.0)
(165.9)
(14)%
Income from Reversals of Impairment Losses
/ (Impairment Losses) on Financial Assets
(0.1)
0.4
>(100)%
0.5
—
n/a
Share of Loss of Associates accounted for
using the Equity Method
(1.6)
(4.0)
(60)%
(8.2)
(4.3)
91%
Income Tax Benefit / (Expenses)
1.6
(172.7)
>(100)%
1.2
(168.6)
>(100)%
Consolidated Net Profit / (Loss)
48.3
329.4
(85)%
(189.7)
(151.1)
26%
Earnings per Share, Basic and Diluted (in
€)
—
—
n/a
(5.53)
(4.42)
25%
Earnings per Share, Basic (in €)
1.28
9.64
(87)%
—
—
n/a
Earnings per Share, Diluted (in €)
1.22
8.93
(86)%
—
—
n/a
Cash and other financial assets (end of
period)
680.5
907.2
(25)%
680.5
907.2
(25)%
MorphoSys will hold its conference call and webcast tomorrow,
March 14, 2024, at 1:00 pm CET (12:00 pm GMT/8:00 am EDT) to
present the results for the fourth quarter and the full year
2023.
Participants for the call may pre-register and will receive
dedicated dial-in details to easily and quickly access the
call:
https://services.choruscall.it/DiamondPassRegistration/register?confirmationNumber=3038013&linkSecurityString=637b0c07e
Please dial in 10 minutes before the beginning of the
conference.
The live webcast (audio and presentation) can be directly
accessed via https://www.webcast-eqs.com/morphosys-2023-ye or via
the Investors section under "Events & Conferences" on the
MorphoSys website, www.morphosys.com; after the call, a
slide-synchronized audio replay of the conference call will be
available at the same location.
Consolidated Financial Statements 2023 (IFRS) are available for
download at:
https://www.morphosys.com/en/investors/financial-information
About MorphoSys
At MorphoSys, we are driven by our mission: More life for people
with cancer. As a global commercial-stage biopharmaceutical
company, we develop and deliver innovative medicines, aspiring to
redefine how cancer is treated. MorphoSys is headquartered in
Planegg, Germany, and has its U.S. operations anchored in Boston,
Massachusetts. To learn more, visit us at www.morphosys.com and
follow us on Twitter at X and LinkedIn.
About Pelabresib
Pelabresib (CPI-0610) is an investigational selective small
molecule designed to promote anti-tumor activity by inhibiting the
function of bromodomain and extra-terminal domain (BET) proteins to
decrease the expression of abnormally expressed genes in cancer.
Pelabresib is being investigated as a treatment for myelofibrosis
and has not yet been approved by any regulatory authorities. Its
safety and efficacy have also not been established in a pivotal
trial.
The development of pelabresib was funded in part by The Leukemia
and Lymphoma Society®.
About MANIFEST-2
MANIFEST-2 (NCT04603495) is a global, double-blind, Phase 3
clinical trial that randomized 430 JAK inhibitor-naïve adult
patients with myelofibrosis 1:1 to receive pelabresib in
combination with ruxolitinib or placebo plus ruxolitinib. The
primary endpoint of the study is a 35% or greater reduction in
spleen volume (SVR35) from baseline at 24 weeks. The key secondary
endpoints of the study are the absolute change in total symptom
score (TSS) from baseline at 24 weeks and the proportion of
patients achieving a 50% or greater improvement in total symptom
score (TSS50) from baseline at 24 weeks. TSS is measured using the
myelofibrosis self-assessment form (MFSAF) v4.0, which asks
patients to report the severity of seven common symptoms, rating
each of them on a scale from 0 (absent) to 10 (worst
imaginable).
The new key secondary endpoint, absolute change in TSS, was
added to directly measure change in the average TSS from baseline
to week 24 of treatment and is listed as the first key secondary
endpoint in the MANIFEST-2 hierarchical testing scheme. The
decision to update the MANIFEST-2 clinical trial protocol was made
following a Type C meeting with the U.S. Food and Drug
Administration (FDA) in September 2023.
Additional secondary endpoints include progression-free
survival, overall survival, duration of the splenic and total
symptom score response, hemoglobin response rate and improvement in
bone marrow fibrosis, among others.
Constellation Pharmaceuticals, Inc., a MorphoSys company, is the
MANIFEST-2 trial sponsor.
About Tafasitamab
Tafasitamab is a humanized Fc-modified CD19 targeting
immunotherapy. In 2010, MorphoSys licensed exclusive worldwide
rights to develop and commercialize tafasitamab from Xencor, Inc.
Tafasitamab incorporates an XmAb® engineered Fc domain, which
mediates B-cell lysis through apoptosis and immune effector
mechanism including Antibody-Dependent Cell-Mediated Cytotoxicity
(ADCC) and Antibody-Dependent Cellular Phagocytosis (ADCP).
In the United States, Monjuvi® (tafasitamab-cxix) is approved by
the U.S. Food and Drug Administration in combination with
lenalidomide for the treatment of adult patients with relapsed or
refractory DLBCL not otherwise specified, including DLBCL arising
from low grade lymphoma, and who are not eligible for autologous
stem cell transplant (ASCT). This indication is approved under
accelerated approval based on overall response rate. Continued
approval for this indication may be contingent upon verification
and description of clinical benefit in a confirmatory trial(s).
Please see the U.S. full Prescribing Information for Monjuvi for
important safety information.
In Europe, Minjuvi® (tafasitamab) received conditional marketing
authorization in combination with lenalidomide, followed by Minjuvi
monotherapy, for the treatment of adult patients with relapsed or
refractory diffuse large B-cell lymphoma (DLBCL) who are not
eligible for autologous stem cell transplant (ASCT).
Tafasitamab is being clinically investigated as a therapeutic
option in B-cell malignancies in several ongoing combination
trials. Its safety and efficacy for these investigational uses have
not been established in pivotal trials.
Monjuvi® and Minjuvi® are registered trademarks of Incyte.
Tafasitamab is marketed under the brand name Monjuvi® in the U.S.,
and Minjuvi® in Europe and Canada.
XmAb® is a registered trademark of Xencor, Inc.
Additional Information and Where to Find it
The takeover offer described in this communication (the
“Takeover Offer”) has not yet commenced. This communication is
neither an offer to purchase nor a solicitation of an offer to sell
shares of MorphoSys AG (the “Company”). The final terms and further
provisions regarding the Takeover Offer will be in the offer
document once the publication of the offer document by Novartis
BidCo AG (formerly known as Novartis data42 AG) (the “Bidder”) has
been approved by the German Federal Financial Supervisory Authority
(the “BaFin”), after which the offer document will be filed with
the U.S. Securities and Exchange Commission (the “SEC”). A
solicitation and an offer to buy shares of the Company will be made
only pursuant the offer document. In connection with the Takeover
Offer, the Bidder and Novartis AG will file a Tender Offer
Statement on Schedule TO with the SEC (together with the offer
document, an Offer to Purchase including the means to tender and
other related documents, the “Takeover Offer Documents”), the
Company’s management board and supervisory board will issue a joint
reasoned statement in accordance with sec. 27 of the German
Securities Acquisition and Takeover Act and the Company will file a
Solicitation/Recommendation Statement on Schedule 14D-9 with the
SEC (together with the joint reasoned statement, the
“Recommendation Statements”). THE COMPANY’S STOCKHOLDERS AND OTHER
INVESTORS ARE URGED TO READ THE TAKEOVER OFFER DOCUMENTS AND THE
RECOMMENDATION STATEMENTS BECAUSE THEY WILL CONTAIN IMPORTANT
INFORMATION WHICH SHOULD BE READ CAREFULLY BEFORE ANY DECISION IS
MADE WITH RESPECT TO THE TAKEOVER OFFER. The Takeover Offer
Documents and the Recommendation Statements will be distributed to
all stockholders of the Company in accordance with German and U.S.
securities laws. The Tender Offer Statement on Schedule TO and the
Solicitation/Recommendation Statement on Schedule 14D-9 will be
made available for free at the SEC’s website at www.sec.gov.
Additional copies may be obtained for free by contacting the Bidder
or the Company. Free copies of these materials and certain other
offering documents will be made available on the Company’s website
in English at morphosys.com/en/investors/Novartis-TakeoverOffer and
in German at morphosys.com/de/investoren/Novartis-TakeoverOffer, by
mail to MorphoSys AG, Semmelweisstrasse 7, 82152 Planegg, Germany
or by phone at +49 89 8992 7179.
In addition to the Offer to Purchase, including the means to
tender and certain other Takeover Offer Documents, as well as the
Solicitation/Recommendation Statement, the Company files other
information with the SEC. The Company’s filings with the SEC are
also available for free to the public from commercial
document-retrieval services and at the website maintained by the
SEC at www.sec.gov and are also available free of charge under the
“SEC Filings” section of the Company’s website at
www.morphosys.com/en/investors.
In order to reconcile certain areas where German law and U.S.
law conflict, Novartis AG and the Bidder expect to request
no-action and exemptive relief from the SEC to conduct the Takeover
Offer in the manner described in the offer document.
Acceptance of the Takeover Offer by stockholders residing
outside Germany and the United States of America may be subject to
further legal requirements. With respect to the acceptance of the
Takeover Offer outside Germany and the United States, no
responsibility is assumed for the compliance with such legal
requirements applicable in the respective jurisdiction.
Forward Looking Statements
This communication contains certain forward-looking statements
concerning the Company, the Bidder and the Takeover Offer that
involve substantial risks and uncertainties. Forward-looking
statements include any statements containing the words
“anticipate,” “believe,” “estimate,” “expect,” “intend,” “goal,”
“may,” “might,” “plan,” “predict,” “project,” “seek,” “target,”
“potential,” “will,” “would,” “could,” “should,” “continue” and
similar expressions. In this communication, the Company’s
forward-looking statements include statements about the parties’
ability to satisfy the conditions to the consummation of the
Takeover Offer; statements about the expected timetable for the
consummation of the Takeover Offer; the Company’s plans,
objectives, expectations and intentions; and the financial
condition, results of operations and business of the Company and
Novartis AG.
The forward-looking statements contained in this communication
represent the judgment of the Company as of the date of this
communication and involve known and unknown risks and
uncertainties, which might cause the actual results, financial
condition and liquidity, performance or achievements of the
Company, or industry results, to be materially different from any
historic or future results, financial conditions and liquidity,
performance or achievements expressed or implied by such
forward-looking statements. In addition, even if the Company's
results, performance, financial condition and liquidity, and the
development of the industry in which it operates are consistent
with such forward-looking statements, they may not be predictive of
results or developments in future periods. Those risks and
uncertainties that could cause the actual results to differ from
expectations contemplated by forward-looking statements include,
among other things: uncertainties as to the timing of the Takeover
Offer; uncertainties as to how many of the Company’s stockholders
will tender their stock in the Takeover Offer; the possibility that
competing offers will be made; the possibility that various
conditions for the Takeover Offer may not be satisfied or waived,
including that a governmental entity may prohibit, delay or refuse
to grant approval for the consummation of the Takeover Offer; the
effects of the Takeover Offer on relationships with employees,
other business partners or governmental entities; that the Bidder
and Novartis AG may not realize the potential benefits of the
Takeover Offer; transaction costs associated with the Takeover
Offer; that the Company’s expectations may be incorrect; the
inherent uncertainties associated with competitive developments,
clinical trial and product development activities and regulatory
approval requirements; the Company's reliance on collaborations
with third parties; estimating the commercial potential of the
Company’s development programs; and other risks indicated in the
risk factors included in the Company’s filings with the SEC,
including the Company’s Annual Report on Form 20-F, as well as the
Solicitation/Recommendation Statement on Schedule 14D-9 to be filed
by the Company and the Tender Offer Statement on Schedule TO and
related Takeover Offer Documents to be filed by the Bidder and
Novartis AG. Given these uncertainties, the reader is advised not
to place any undue reliance on such forward-looking statements.
These forward-looking statements speak only as of the date of
publication of this communication. The Company and the Bidder
expressly disclaim any obligation to update any such
forward-looking statements in this communication to reflect any
change in its expectations with regard thereto or any change in
events, conditions or circumstances on which any such statement is
based or that may affect the likelihood that actual results will
differ from those set forth in the forward-looking statements,
unless specifically required by law or regulation.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240313374964/en/
Media Contacts: Thomas Biegi Senior Vice President,
Corporate Affairs Tel.: +49 (0)89 / 899 27 26079
thomas.biegi@morphosys.com
Eamonn Nolan Senior Director, Corporate Communications &
Investor Relations Tel: +1 617-548-9271
eamonn.nolan@morphosys.com
Investor Contacts: Dr. Julia Neugebauer Vice President,
Global Investor Relations Tel: +49 (0)89 / 899 27 179
julia.neugebauer@morphosys.com
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