01.08.2018
MorphoSys AG DE0006632003
DGAP-News: MorphoSys AG Reports Second Quarter 2018 Financial Results
DGAP-News: MorphoSys AG / Key word(s): Half Year Results
MorphoSys AG Reports Second Quarter 2018 Financial Results (news with
additional features)
01.08.2018 / 22:01
The issuer is solely responsible for the content of this announcement.
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Planegg/Munich, Germany, August 1, 2018
MorphoSys AG Reports Second Quarter 2018 Financial Results
The Company has further advanced its pipeline, including proprietary and
partnered programs, and established a U.S. footprint to prepare for
commercialization in the U.S.
Conference call and webcast (in English) to be held on August 2, 2018, at
2:00 pm CEST (1:00 pm BST / 8:00 am EDT)
- Ongoing discussions with U.S. FDA regarding path to market for MOR208 as
potential therapy for aggressive lymphoma (DLBCL) under the existing
breakthrough therapy designation
- First clinical data from ongoing phase 2 trial of MOR208 plus idelalisib
in CLL presented at European Hematology Association (EHA) Annual Meeting
- Jennifer Herron to head newly founded MorphoSys US Inc. and build
commercial capabilities for MOR208
- MorphoSys and Galapagos entered into a global license agreement with
Novartis for MOR106. MorphoSys and Galapagos to jointly receive up-front
payment of EUR 95 million as well as significant potential future milestone
payments plus double-digit royalties
- Partner Janssen initiated pivotal phase 2/3 program of Tremfya(R) in
Crohn's disease
- First patient dosed in phase 3 trial conducted by Roche with gantenerumab
as a potential therapy for early Alzheimer's disease
- U.S. Nasdaq listing and successful capital increase with gross proceeds of
USD 239 million completed in April 2018
- Cash position increased to EUR 450.5 million as of June 30, 2018
- Following the signature of a deal with Novartis for MOR106 in July 2018
and subject to U.S. antitrust clearance, MorphoSys is increasing its
financial guidance for 2018, expecting revenues of between EUR 67 and 72
million, EBIT of EUR -55 to -65 million, and expenses for proprietary
development and technology development of EUR 87 to 97 million
MorphoSys AG (FSE: MOR; Prime Standard Segment, TecDAX; NASDAQ: MOR) today
reported financial results for the second quarter of 2018.
"MorphoSys has made excellent progress on a number of fronts during the
quarter. We continued our constructive discussions with the FDA regarding a
path to market for MOR208 in aggressive lymphoma (DLBCL) and presented
positive data from our ongoing phase 2 trial of MOR208 in chronic
lymphocytic lymphoma (CLL)," commented Dr. Simon Moroney, CEO of MorphoSys
AG. "With the establishment of our new U.S. subsidiary MorphoSys US Inc. and
the appointment of Jennifer Herron as the head of this organization, we have
laid the foundation for a strong commercial presence in preparation for the
potential future commercialization of MOR208, subject of course to FDA
approval of this investigational drug."
"We are also very pleased with the advances made by our partners, notably
the continued successful marketing of Tremfya(R) in psoriasis by Janssen as
well as the start of additional pivotal programs with Tremfya(R) in Crohn's
disease by Janssen and with gantenerumab in Alzheimer's disease by Roche,"
Dr. Moroney continued.
"This has been an exciting quarter at MorphoSys and we are encouraged by the
recent corporate developments. We successfully listed at Nasdaq in April
and, shortly after the quarter, signed an exclusive licensing deal with
Novartis for MOR106," said Jens Holstein, CFO of MorphoSys AG. "Our strong
financial position provides us with the flexibility to allocate the
necessary resources to our lead program MOR208, continue the advancement of
our other pipeline programs and build out our U.S. commercial operations."
Financial Review for the second quarter of 2018 (IFRS; all figures rounded)
In Q2 2018 MorphoSys continued to focus on the research and development of
drug candidates both for its own account as well as with its partners. Group
revenues amounted to EUR 8.1 million in Q2 2018 (Q2 2017: EUR 11.7 million).
The expected decline compared to the previous year's second quarter resulted
mainly from the completion of a partnership with Novartis in 2017. As the
contractual royalty reporting from Janssen for Q2 2018 has not yet been
received due to the reporting schedules of Janssen and MorphoSys, Tremfya(R)
royalties booked for Q2 2018 were estimated based on public announcements
made by Janssen/J&J on Tremfya(R) sales in Q2 2018.
In the Proprietary Development segment, MorphoSys focuses on research into,
and clinical development of, its own drug candidates in the fields of cancer
and inflammation. In Q2 2018, this segment recorded revenues of EUR 0.1
million (Q2 2017: EUR 0.3 million). In the Partnered Discovery segment,
MorphoSys applies its proprietary technology to discover new antibodies for
pharmaceutical companies, benefiting from its partners' development
advancements through R&D funding, licensing fees, success-based milestone
payments and royalties. In Q2 2018, revenues in this segment amounted to EUR
8.1 million (Q2 2017: EUR 11.5 million).
Total operating expenses reached EUR 32.7 million in the second quarter of
2018 (Q2 2017: EUR 27.5 million). Proprietary development expenses and
technology development expenses amounted to EUR 24.7 million (Q2 2017: EUR
18.6 million). The increase over the previous year's quarter is mainly due
to costs to advance the development of MOR208.
Earnings before interest and taxes (EBIT) in Q2 2018 amounted to EUR -24.1
million (Q2 2017: EUR -15.4 million). The Proprietary Development segment
reported an EBIT of EUR -24.6 million (Q2 2017: EUR -18.3 million). EBIT in
the Partnered Discovery segment was EUR 5.5 million (Q2 2017: EUR 6.8
million). In Q2 2018, the consolidated net result amounted to EUR -23.5
million (Q2 2017: EUR -16.1 million). The earnings per share for Q2 2018
reached EUR -0.76 (Q2 2017: EUR -0.56).
At the end of Q2 2018, the Company had a cash position of EUR 450.5 million,
compared to EUR 312.2 million on December 31, 2017. On the balance sheet,
this cash position is reported under the following items: cash and cash
equivalents; financial assets at fair value through profit or loss; and
current and non-current other financial assets at amortized cost. The
increase in funds resulted mainly from the capital increase together with
the successful Nasdaq listing completed in April with gross proceeds of USD
239 million. This was partially offset by the use of cash for operating
activities in the second quarter of 2018. This cash position does not
include the upfront payment to be made by Novartis in connection with the
license agreement for MOR106, subject to U.S. antitrust clearance, that was
signed after the end of the reporting period.
The number of shares issued totaled 31,808,035 at the end of Q2 2018
(year-end 2017: 29,420,785). The main reason for the increase in the number
of shares was the capital increase in connection with the Nasdaq listing in
April 2018.
Results for the first six months 2018
During the first six months of 2018, group revenues amounted to EUR 10.9
million (Q1-Q2 2017: EUR 23.6 million). Expenditure for proprietary
development and technology development amounted to EUR 39.2 million in the
first six months of 2018 (Q1-Q2 2017: EUR 37.3 million). Consequently the
EBIT in the first six months of 2018 amounted to EUR -43.2 million, compared
to EUR -30.3 million in the first half of 2017.
Financial Guidance and Operational Outlook for 2018
Following the recent signature of a deal with Novartis on MOR106 and pending
U.S. antitrust clearance, MorphoSys is increasing its financial guidance for
2018. Subject to U.S. antitrust clearance, MorphoSys expects Group revenues
in the range of EUR 67 to 72 million and earnings before interest and taxes
(EBIT) of EUR -55 to -65 million. Expenses for proprietary development and
technology development are expected to be in a corridor of EUR 87 to 97
million. This guidance does not include any additional revenue from
potential new collaborations and/or licensing partnerships nor effects from
potential in-licensing or co-development deals for new development
candidates.
MorphoSys expects the following events and activities in the Proprietary
Development segment for 2018:
MOR208
- L-MIND: Continue analysis of maturing data of all 81 patients with
relapsed/refractory diffuse large B cell lymphoma (r/r DLBCL) enrolled in
the trial and present updated clinical data at an appropriate medical
conference.
- B-MIND: Continue the pivotal phase 3 study evaluating MOR208 plus
bendamustine versus rituximab plus bendamustine in r/r DLBCL.
- COSMOS: Continue the phase 2 trial of MOR208 plus idelalisib or venetoclax
in CLL/SLL and present data from cohort B (MOR208 plus venetoclax) at an
appropriate medical conference.
- Commercial activities: Continue establishment of commercial capabilities
for MOR208 in the U.S. under the roof of the newly established MorphoSys US
Inc., in preparation for a potential launch currently anticipated in 2020
pending FDA approval.
MOR202
- Multiple myeloma (MM): MorphoSys has decided not to continue development
of MOR202 in MM beyond completion of the currently ongoing phase 1/2a trial;
final data are expected to be presented at an upcoming medical conference.
MorphoSys will continue to support its partner I-Mab's development of MOR202
for the greater Chinese market as planned.
- Lung cancer (NSCLC): Following the discontinuation of a clinical study by
Janssen of the CD38 antibody daratumumab in combination with a checkpoint
inhibitor, MorphoSys has decided not to continue activities in NSCLC for the
time being
- Other indications: MorphoSys continues to evaluate the development of
MOR202 in other indications.
MOR106: Continue the ongoing development together with partner Galapagos
under the new global licensing agreement with Novartis.
- Continue the ongoing phase 2 IGUANA trial in atopic dermatitis.
- Initiate phase 1 study to evaluate a subcutaneous formulation of MOR106.
- All future costs related to MOR106 development to be borne by Novartis.
- Agreement between MorphoSys, Galapagos, and Novartis is subject to
clearance by the U.S. antitrust authorities.
MOR107: Continue preclinical investigations of MOR107 with a focus on
oncology indications to inform a decision regarding potential further
clinical testing.
MOR103/GSK3196165: Following GSK's recent announcement that positive phase
2b results in rheumatoid arthritis are to be presented at a future
scientific congress and that the osteoarthritis indication has been
terminated, the publication of clinical data by GSK is expected.
In its Partnered Discovery segment, MorphoSys expects the following events
in 2018:
Tremfya(R) (guselkumab): Several phase 3 trials in psoriasis are scheduled
for primary completion in 2018 according to clinicaltrials.gov, including a
head-to-head trial comparing Tremfya(R) to Cosentyx(R) (secukinumab) in
plaque psoriasis.
Other partnered programs: Clinical data and potential regulatory milestones
from a number of other partnered programs to be potentially published during
the year.
MorphoSys will continue to support its proprietary development activities by
evaluating potential in-licensing, co-development, and/or acquisition
opportunities or the potential initiation of new proprietary development
programs with the goal of maintaining and expanding the Company's position
in its current therapeutic and technological fields of activities.
MorphoSys Group Key Figures (IFRS, end of reporting period: June 30)
in EUR million Q2/201- Q2/201- ∆ Q1-Q2 Q1-Q2 ∆
8 7 2018 2017
Revenues 8.1 11.7 (31%) 10.9 23.6 (54%)
Total operating expenses 32.7 27.5 +19% 54.6 54.3 +0.6%
R&D expenses 25.8 22.5 +15% 43.0 45.4 (5%)
thereof expenses for 23.7 18.3 +30% 39.2 37.3 +5%
proprietary development
and technology development
Selling expenses 1.5 0.8 +88% 2.3 1.3 +77%
G&A expenses 5.5 4.2 +31% 9.3 7.6 +22%
Other income/expense 0.5 0.3 +67% 0.5 0.4 +25%
EBIT (24.1) (15.4) (56%) (43.2) (30.3) (43%)
Net loss (23.5) (16.1) (46%) (43.0) (31.1) (38%)
Net loss per share (in (0.76) (0.56) (36%) (1.38) (1.08) (28%)
EUR)
Cash position (end of 450.5 334.8 +35% 450.5 334.8 +35%
period)
Equity ratio (end of 91.1 87.0 +4.1 91.1 87.0 +4.1
period) (in %) PP* PP*
No. of R&D programs (end 115 114 +1% 115 114 +1%
of period)
No. of clinical programs 29 29 - 29 29 -
(end of period)**
No. of proprietary 5 6 (17%) 5 6 (17%)
clinical programs (end of
period)***
* Percentage points
** Including MOR107, which concluded a phase 1 study in 2017 and is
currently in preclinical investigation with a focus on oncology indications.
Tremfya(R) is still considered as a clinical program due to ongoing studies
in various indications.
*** Including MOR103/GSK3196165 which is fully out-licensed to GSK.
MorphoSys will hold its conference call and webcast on August 2, 2018 to
present the second quarter 2018 financial results and the further outlook
for 2018.
Dial-in number for the analyst conference call (in English) at 2:00 pm CEST;
1:00 pm BST; 8:00 am EDT (listen-only):
Germany: +49 (0) 69 201 744 210
For UK residents: +44 (0) 203 009 2470
For US residents: +1 (0) 877 423 0830
Participant PIN: 63419794#
Participants are asked to dial in 10 minutes before the beginning of the
conference. A live webcast and slides will be made available at
https://www.morphosys.com. After the conference call, a slide-synchronized
audio replay of the conference and a transcript will be available at
https://www.morphosys.com.
The interim statement for the second quarter of 2018 (IFRS) is available
online:
http://www.morphosys.com/FinancialReports
About MorphoSys:
MorphoSys is a late-stage, biopharmaceutical company devoted to the
development of innovative and differentiated therapies for patients
suffering from serious diseases. Based on its technological leadership in
generating antibodies, MorphoSys, together with its partners, has developed
and contributed to the development of more than 100 product candidates, of
which 29 are currently in clinical development. This broad pipeline spans
MorphoSys's two business segments: Proprietary Development, in which
MorphoSys invests in product candidates for its own account, and Partnered
Discovery, in which product candidates are developed exclusively for a
variety of Pharma and Biotech partners. In 2017, Tremfya(R) (guselkumab),
marketed by Janssen, became the first therapeutic antibody based on
MorphoSys's proprietary technology to receive marketing approval for the
treatment of moderate to severe plaque psoriasis in the United States, the
European Union and Canada. MorphoSys is listed on the Frankfurt Stock
Exchange and on the U.S. stock exchange Nasdaq, under the symbol MOR. For
regular updates about MorphoSys, visit https://www.morphosys.com.
HuCAL(R), HuCAL GOLD(R), HuCAL PLATINUM(R), CysDisplay(R), RapMAT(R),
arYla(R),
Ylanthia(R), 100 billion high potentials(R), Slonomics(R), Lanthio Pharma(R)
and LanthioPep(R) are registered trademarks of the MorphoSys Group.
Tremfya(R)
is a trademark of Janssen Biotech, Inc. Cosentyx(R) is a trademark of
Novartis AG.
This communication contains certain forward-looking statements concerning
the MorphoSys group of companies, including its financial guidance for 2018,
the commencement, timing and results of clinical trials and release of
clinical data both in respect of its proprietary product candidates and of
product candidates of its collaborators, the development of commercial
capabilities, in particular with respect to MOR208, and the transition of
MorphoSys to a fully integrated biopharmaceutical company, the expected time
of launch of MOR208, interaction with regulators, including the potential
approval of MorphoSys's current or future drug candidates, including
discussions with the U.S. FDA regarding the potential approval to market
MOR208, and expected royalty and milestone payments in connection with
MorphoSys's collaborations. The forward-looking statements contained herein
represent the judgment of MorphoSys as of the date of this release and
involve known and unknown risks and uncertainties, which might cause the
actual results, financial condition and liquidity, performance or
achievements of MorphoSys, 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 MorphoSys' 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. Among the
factors that may result in differences are that MorphoSys' expectations
regarding its 2018 results of operations may be incorrect, MorphoSys'
expectations regarding its development programs may be incorrect, the
inherent uncertainties associated with competitive developments, clinical
trial and product development activities and regulatory approval
requirements (including that MorphoSys may fail to obtain regulatory
approval for MOR208 and that data from MorphoSys' ongoing clinical research
programs may not support registration or further development of its product
candidates due to safety, efficacy or other reasons), MorphoSys' reliance on
collaborations with third parties, estimating the commercial potential of
its development programs and other risks indicated in the risk factors
included in MorphoSys's Registration Statement on Form F-1 and other filings
with the US Securities and Exchange Commission. 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 document. MorphoSys expressly disclaims
any obligation to update any such forward-looking statements in this
document 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.
For more information, please contact:
MorphoSys AG
Alexandra Goller
Associate Director Corporate Communications & IR
Jochen Orlowski
Associate Director Corporate Communications & IR
Dr. Claudia Gutjahr-Löser
Investor Relations Officer
Tel: +49 (0) 89 / 899 27-404
[email protected]
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Additional features:
Document: http://n.eqs.com/c/fncls.ssp?u=KCINRBWBUH
Document title: Q2 Media Release
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01.08.2018 Dissemination of a Corporate News, transmitted by DGAP - a
service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.
The DGAP Distribution Services include Regulatory Announcements,
Financial/Corporate News and Press Releases.
Archive at www.dgap.de
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Language: English
Company: MorphoSys AG
Semmelweisstr. 7
82152 Planegg
Germany
Phone: +49 (0)89 899 27-0
Fax: +49 (0)89 899 27-222
E-mail: [email protected]
Internet: www.morphosys.com
ISIN: DE0006632003
WKN: 663200
Indices: TecDAX
Listed: Regulated Market in Frankfurt (Prime Standard); Regulated
Unofficial Market in Berlin, Dusseldorf, Hamburg, Hanover,
Munich, Stuttgart, Tradegate Exchange
End of News DGAP News Service
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