MorphoSys AG Reports First Quarter 2024 Financial Results
MorphoSys AG reported its first-quarter 2024 financial results, including a proposed acquisition by Novartis, receipt of antitrust approvals, sale of tafasitamab rights to Incyte, and upcoming medical conference presentations. The company's financials showed an increase in group revenues, cost of sales, research and development expenses, and general and administrative expenses. The operating loss and consolidated net loss also increased significantly. Full-year 2024 financial guidance was revoked due to the sale of tafasitamab. MorphoSys expects R&D expenses of €170-185 million and SG&A expenses of €90-105 million for the year.
- None.
Operating loss and consolidated net loss significantly increased in the first quarter of 2024 compared to the previous year.
Full-year 2024 financial guidance was revoked due to the sale and transfer of tafasitamab to Incyte, impacting revenue projections for the year.
Insights
The proposed acquisition of MorphoSys AG by Novartis at a cash offer price of
From a financial standpoint, this transaction is poised to deliver substantial liquidity to MorphoSys’ shareholders. Given the size of the deal at
The acquisition also sheds light on Novartis' strategy to enhance its presence in the oncology space. MorphoSys’ oncology programs, such as pelabresib and tulmimetostat, could fill strategic gaps in Novartis’ pipeline or complement its existing assets. The regulatory approvals of these drugs could potentially generate significant revenue streams for Novartis in the future.
Investors may also reflect on the sale of all tafasitamab rights to Incyte, which resulted in a cash increase for MorphoSys, as indicated by their financial assets totaling
The company has outlined plans to submit a New Drug Application for pelabresib with the FDA and a Marketing Authorization Application with the European Medicines Agency following the anticipated acquisition. The execution and approval of these applications are important for potential drug commercialization. Investors should monitor these regulatory milestones closely, as they are pivotal for the future growth and revenue potential of the drug candidates within Novartis’ portfolio.
It is also noteworthy that MorphoSys has received all necessary antitrust clearances, removing a significant regulatory hurdle for the acquisition, thus easing investor concerns about potential legal impediments to the deal closure.
– Entered into Business Combination Agreement to be acquired by Novartis for
– Received all mandatory antitrust approvals for the proposed acquisition by Novartis
– Shareholder acceptance period for the Novartis offer has commenced and will end on May 13, 2024, at 24:00 hours CEST
– Sold all tafasitamab rights worldwide to Incyte
–
PLANEGG/
“The proposed acquisition by Novartis is advancing steadily, and we continue to anticipate its closure in the first half of 2024. The acceptance period for the acquisition is currently underway, and both our Management Board and Supervisory Board unanimously recommend that our shareholders accept the offer and tender their shares given the highly attractive and equitable offer price,” said Jean-Paul Kress, M.D., Chief Executive Officer of MorphoSys. “Utilizing its extensive resources, broad scientific experience and worldwide presence, Novartis will help maximize commercial and expedite development opportunities across our promising oncology programs.”
Novartis’ Public Takeover Offer Highlights:
On February 5, 2024, MorphoSys announced the intention of Novartis BidCo AG, a wholly owned indirect subsidiary of Novartis AG (hereinafter collectively referred to as “Novartis”), to submit a voluntary public takeover offer for all outstanding MorphoSys no-par value bearer shares at an offer price of
On March 13, 2024, MorphoSys confirmed the receipt of antitrust clearance in
On April 11, 2024, Novartis published its offer document. Following the publication of the offer document, the MorphoSys Management Board and Supervisory Board issued a joint reasoned statement, recommending that shareholders accept the offer and tender their MorphoSys shares. The acceptance period for shareholders commenced with the publication of the offer document on April 11, 2024, and will end on May 13, 2024, at 24:00 hours CEST and 18:00 hours EDT (also on May 13, 2024).
Medical Conferences Highlights:
On April 24, 2024, MorphoSys announced that new efficacy and safety data from the Phase 3 MANIFEST-2 trial of pelabresib, an investigational BET inhibitor, in combination with the JAK inhibitor ruxolitinib in JAK inhibitor-naïve patients with myelofibrosis will be highlighted during an oral presentation on Friday, May 31, at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting. Additionally, new data from the Phase 2 study of tulmimetostat, an investigational next-generation dual inhibitor of EZH2 and EZH1, in patients with advanced solid tumors or hematologic malignancies will be showcased in a poster presentation at ASCO 2024 on Saturday, June 1.
Financial Results for the First Quarter of 2024 (IFRS):
The financial results presented for the first quarter of 2024 relate to continuing business operations of MorphoSys. Due to the announcement on February 5, 2024, of the sale and transfer of all rights worldwide related to tafasitamab to Incyte Corporation ("Incyte"), the entire tafasitamab business has been classified as discontinued operations. Consequently, the figures reported for the first quarter of 2023 were adapted due to this change in presentation.
Group Revenues: Group revenues from continued operations amounted to
Cost of Sales: Cost of sales in the first quarter of 2024 amounted to
Research and Development (R&D) Expenses: In the first quarter 2024, R&D expenses were
Selling, General and Administrative (SG&A) Expenses: Selling expenses in the first quarter 2024 were
Operating Loss: Operating loss amounted to
Consolidated Net Loss: For the first quarter 2024, consolidated net loss was
Monjuvi/Minjuvi® Update (Discontinued Operations):
On February 5, 2024, MorphoSys entered into a purchase agreement with Incyte to sell and transfer all rights worldwide related to tafasitamab to Incyte.
Monjuvi (tafasitamab-cxix)
Minjuvi royalty revenue of
Since February 5, 2024, all research and development activities in connection with tafasitamab are in the responsibility of Incyte, and hence MorphoSys does no longer recognize research and development expenses from such activities.
Full Year 2024 Financial Guidance:
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 the gross margin or revenues from Monjuvi product sales, as no such revenues are expected to be realized this year.
For 2024, MorphoSys expects R&D expenses of
Operational Outlook:
The following activity is planned for 2024:
-
Following the anticipated close of the proposed acquisition by Novartis in the first half of 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 second half of 2024.
MorphoSys Group Key Figures (IFRS, end of the first quarter: March 31, 2024) |
|||||||||
in € million |
|
Q1 2024 |
|
Q1 2023 |
|
Δ |
|||
Revenues |
|
27.5 |
|
|
24.3 |
|
|
13 |
% |
Royalties |
|
27.0 |
|
|
20.9 |
|
|
29 |
% |
Licenses, Milestones and Other |
|
0.5 |
|
|
3.5 |
|
|
(86 |
)% |
Cost of Sales |
|
(2.8 |
) |
|
(1.0 |
) |
|
> |
|
Gross Profit |
|
24.7 |
|
|
23.3 |
|
|
6 |
% |
Total Operating Expenses |
|
(289.1 |
) |
|
(79.4 |
) |
|
> |
|
Research and Development |
|
(85.2 |
) |
|
(65.4 |
) |
|
30 |
% |
Selling |
|
(18.5 |
) |
|
(3.4 |
) |
|
> |
|
General and Administrative |
|
(185.5 |
) |
|
(10.6 |
) |
|
> |
|
Operating Profit / (Loss) |
|
(264.4 |
) |
|
(56.1 |
) |
|
> |
|
Other Income |
|
0.8 |
|
|
2.1 |
|
|
(62 |
)% |
Other Expenses |
|
(0.4 |
) |
|
(1.8 |
) |
|
(78 |
)% |
Finance Income |
|
9.6 |
|
|
50.8 |
|
|
(81 |
)% |
Finance Expenses |
|
(56.8 |
) |
|
(25.2 |
) |
|
> |
|
Income from Reversals of Impairment Losses / (Impairment Losses) on Financial Assets |
|
0.1 |
|
|
0.5 |
|
|
(80 |
)% |
Share of Loss of Associates accounted for using the Equity Method |
|
(1.5 |
) |
|
(2.5 |
) |
|
(40 |
)% |
Income Tax Benefit / (Expenses) |
|
1.6 |
|
|
0.0 |
|
|
n/a |
|
Consolidated Net Profit / (Loss) from Continued Operations |
|
(311.0 |
) |
|
(32.2 |
) |
|
> |
|
Consolidated Net Profit / (Loss) from Discontinued Operations |
|
(3.9 |
) |
|
(12.2 |
) |
|
(68 |
)% |
Earnings per Share, Basic and Diluted (in €) from continued operations |
|
(8.27 |
) |
|
(0.94 |
) |
|
> |
|
Cash and other financial assets (end of period) |
|
631.9 |
|
|
680.5 * |
|
(7 |
)% |
|
|
|
|
|
|
|
|
|||
* Value as of December 31, 2023 |
|||||||||
Conference call
Due to the pending acquisition of MorphoSys by Novartis, MorphoSys will not be hosting its quarterly conference call and does not expect to do so in future quarters. Earnings materials are publicly available on the Investor Relations page of our website at www.morphosys.com/en/investors. Please direct any questions to MorphoSys Investor Relations using the contact information provided below.
About MorphoSys
At MorphoSys, we are driven by our mission: More life for people with cancer. As a global biopharmaceutical company, we develop and deliver innovative medicines, aspiring to redefine how cancer is treated. MorphoSys is headquartered in Planegg,
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 been approved by any regulatory authorities. Its safety and efficacy have not been established.
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
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 Tulmimetostat
Tulmimetostat (CPI-0209) is an investigational compound designed to exert anti-tumor activity by inhibiting the function of enhancer of zeste homolog 1 and 2 (EZH1 and EZH2) proteins to reactivate tumor suppressor genes or silencing the oncogenic pathways. Tulmimetostat is being tested as a once-daily oral treatment in a Phase 1/2 trial (NCT04104776) in patients with advanced solid tumors or lymphomas, including ARID1A-mutated ovarian clear cell carcinoma and endometrial carcinoma, diffuse large B-cell lymphoma, peripheral T-cell lymphoma, BAP1-mutated mesothelioma and castration-resistant prostate cancer. The primary objectives of the trial include determining the maximum tolerated dose and/or recommended Phase 2 dose and evaluating antitumor activity of tulmimetostat monotherapy. The safety and efficacy of tulmimetostat have not been established.
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
In
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
XmAb® is a registered trademark of Xencor, Inc.
Additional Information and Where to Find It
This communication is neither an offer to purchase nor a solicitation of an offer to sell shares of MorphoSys AG (the “Company”). Following approval by the German Federal Financial Supervisory Authority (the “BaFin”), Novartis BidCo AG (formerly known as Novartis data42 AG) (the “Bidder”) has published an offer document containing the final terms and further provisions regarding the offer to purchase all outstanding Company no-par value bearer shares, including all no-par value bearer shares represented by American Depositary Shares, at an offer price of
In addition to the Takeover Offer Documents and the Recommendation Statements, 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
Acceptance of the Takeover Offer by stockholders residing outside
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 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; 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 filed by the Company and the Tender Offer Statement on Schedule TO and related Takeover Offer Documents 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/20240429848432/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 Contact:
Dr. Julia Neugebauer
Vice President, Global Investor Relations
Tel: +49 (0)89 / 899 27 179
julia.neugebauer@morphosys.com
Source: MorphoSys AG
