MorphoSys AG
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About the company
MorphoSys AG is a biopharmaceutical firm with therapies already on the market, specializing in the discovery, advancement, and commercialization of antibody-based treatments for individuals battling cancer and autoimmune diseases. Among its key offerings is Tafasitamab, an antibody therapy approved for treating specific B-cell malignancies, including diffuse large B-cell lymphoma, follicular lymphoma, and marginal zone lymphoma. The company also boasts a robust pipeline, with several promising candidates under development.
- CEO
- Arkadius Pichota
- IPO
- 2010
- Employees
- 524
- HQ
- Planegg, DE
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- Market Cap
- $2.76B
- P/E
- -11.74
- Fwd P/E
- 20.81
- PEG
- -0.08
- P/S
- 10.26
- P/B
- 45.41
- EV/EBITDA
- -29.90
- Div Yield
- 0.00%
- Gross Margin
- 75.51%
- Op Margin
- -105.96%
- Net Margin
- -79.63%
- ROE
- -183.80%
- ROIC
- -14.13%
Latest fiscal year · YoY change
- Revenue
- $238.28M-14.4%
- Gross Profit
- $179.92M-21.7%
- Op Income
- $-252,475,802
- Net Income
- $-189,734,199-25.6%
- EPS
- $-5.53-25.1%
- OCF Growth
- +19.3%
- FCF Growth
- +21.8%
- 52W High
- $73.27
- 52W Low
- $25.56
- 50D MA
- $73.27
- 200D MA
- $72.22
- Beta
- 0.66
- RSI (14)
- 75
- Avg Volume
- 0
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
MorphoSys said 2023 was a pivotal year, highlighted by positive Phase 3 pelabresib data, a stronger cash position, and a proposed Novartis acquisition that management expects to close in the first half of 2024.· March 14, 2024
- Pelabresib + ruxolitinib met the Phase 3 primary endpoint in myelofibrosis and improved key disease hallmarks at 24 weeks.
- The Novartis deal offers EUR 68 per share in cash, implying a total equity value of EUR 2.7 billion and premiums of 94% and 142% versus prior VWAP periods.
- Full-year 2023 revenue was EUR 238.3 million, while net loss was EUR 189.7 million; Monjuvi U.S. sales reached $92 million.
- 2024 guidance was revoked after the tafasitamab sale, and new expense guidance was provided for the remaining company.
- Management expects pelabresib regulatory filings in the U.S. and Europe in the middle of 2024 and says the acquisition is progressing steadily.
Full-year 2023 total revenues were EUR 238.3 million versus EUR 278.3 million in 2022. Consolidated net loss was EUR 189.7 million versus a net loss of EUR 151.1 million in 2022. Net U.S. sales for Monjuvi grew to $92 million for the full year 2023. R&D expenses were EUR 283.6 million versus EUR 297.8 million in 2022; selling expenses were EUR 81.4 million versus EUR 92.4 million; G&A expenses were EUR 65.8 million versus EUR 60.1 million; and total cost of sales were EUR 58.4 million versus EUR 48.6 million. The company ended 2023 with cash and investments of EUR 680.5 million, including proceeds from EUR 102.7 million in gross funding. For 2024, MorphoSys now expects R&D expenses of EUR 170 million to EUR 185 million and SG&A expenses of EUR 90 million to EUR 105 million. Management said the prior 2024 guidance could not be maintained after the tafasitamab sale and was revoked.
Jean-Paul Kress framed 2023 as a “critical and exciting” year in which MorphoSys over-delivered on priorities, advanced its oncology pipeline, and strengthened its finances enough to enter into the Novartis business combination agreement. He emphasized that pelabresib remains the top priority, both for first-line myelofibrosis approval and for possible expansion into other myeloid diseases. His tone was confident on the deal and on the pipeline, repeatedly stressing that the acquisition process is progressing steadily and that the company expects no issues in closing.
Lucinda Crabtree focused on the year-over-year financial movements and the post-tafasitamab transition. She said Monjuvi U.S. sales reached $92 million, full-year revenue was EUR 238.3 million, and 2023 costs reflected higher write-downs in cost of sales, lower R&D and selling spend, and higher G&A due to share-based payment expense tied to the stock price. She also noted cash and investments of EUR 680.5 million, a cash runway into early 2026 including convertible debt repayment, and new 2024 expense guidance of EUR 170 million to EUR 185 million for R&D and EUR 90 million to EUR 105 million for SG&A.
Analysts asked about the timing of the Novartis closing, antitrust approvals, and who would submit the pelabresib NDA. Management reiterated that it expects the deal to close in H1 2024, said Germany and Austria have cleared the transaction and no other jurisdictions are expected to be needed, and stated the NDA would be submitted by MorphoSys unless the deal closes first. On the regulatory side, management said a pre-NDA meeting is not something they publicly discuss in detail, but described it as a typical formality after positive Phase 3 data and said the program remains on track for mid-2024 filings.
The call reinforced that pelabresib has meaningful clinical momentum: it met the primary endpoint, improved other myelofibrosis measures, and showed safety in line with prior studies. Management also highlighted a strong balance sheet, a cash runway into early 2026, and a premium all-cash Novartis bid that could crystallize value for shareholders.
Revenue fell year over year and the company posted a larger net loss in 2023, with inventory write-downs and share-based compensation affecting results. Near-term commercial uncertainty also increased because tafasitamab was sold, the 2024 guidance was revoked, and MorphoSys terminated customer-facing field sales employees as part of the transition.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 0.0%
- Shares Outstanding
- 37.66M
- Float Shares
- 0
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