MorphoSys

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MorphoSys AG
Company type
Public
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Headquarters
Planegg, Upper Bavaria
,
Germany
Key people
Dr. Jean-Paul Kress (CEO)
Sung Lee (CFO)
Dr. Malte Peters (Chief Research & Development Officer)
Dr. Roland Wandeler (CCO)
Dr. Marc Cluzel (chairman of Supervisory Board)
ProductsImmunotherapy
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Total equity€621.3 million (end 2020)[1]
Number of employees
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ParentNovartis
Websitemorphosys.com

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MorphoSys AG is a German biopharmaceutical company founded in 1992. The company is headquartered near Munich, Germany, and has a wholly owned subsidiary, MorphoSys US Inc.,[2] in Boston, Massachusetts, in the US. The company has various antibody, protein and peptide technologies that it uses to discover and develop both proprietary and partnered drug candidates. The company has more than 100 drugs in its wider pipeline that are being investigated as treatments for a variety of diseases.[1][3][4] While many of these are being developed in partnership with pharma and biotech companies, MorphoSys also has a proprietary pipeline with a focus on cancer and autoimmune diseases.

MorphoSys AG was listed on the Frankfurt Stock Exchange and on the US Nasdaq stock exchange. Novartis agreed to acquire the company in February 2024.[5]

History

The company was founded in 1992. In 1999, MorphoSys listed on the Frankfurt Stock Exchange under the ticker symbol "MOR".

In 2004, MorphoSys and Novartis entered into a strategic partnership for the research and development of biopharmaceuticals, which was expanded in 2007.[1] Additional discovery partnerships included: Bayer (1999), Roche (2000), Centocor (now Janssen Biotech, 2000), Schering AG (2001) and Pfizer (2003).

In 2008, the company's first proprietary antibody, MOR103 (now otilimab), entered clinical development.[6] Following the publication of promising results in rheumatoid arthritis, MorphoSys signed a license agreement with GlaxoSmithKline for otilimab.[7] In 2019, GlaxoSmithKline initiated a phase 3 clinical development program with otilimab (now GSK3196165).[8]

In 2010, MorphoSys signed a license agreement with Xencor Inc. for MOR208 (now tafasitamab).[9]

In July 2017, the first of MorphoSys’ platform drugs received US marketing approval. Guselkumab (brand name Tremfya), which was developed and is being commercialized by Janssen Biotech, a subsidiary of Johnson & Johnson, was first approved for the treatment of moderate-to-severe plaque psoriasis in the United States, the European Union and Canada.[10][11]

In April 2018, following a US initial public offering in which the company raised $239 million, American depositary shares of MorphoSys began trading on the Nasdaq stock exchange under the symbol "MOR."[12][13]

In 2018, the company established a wholly owned US subsidiary, MorphoSys US Inc.[2]

In December 2019, based on positive clinical trial results, the company submitted a Biologics License Application (BLA) to the FDA for tafasitamab in combination with lenalidomide for the treatment of relapsed/refractory diffuse large B-cell lymphoma.[14] The submission was accepted for filing in February 2020, and a decision on the filing is expected in August 2020.[15]

In January 2020, MorphoSys and Incyte Corporation signed a collaboration and license agreement for the global development and commercialization of tafasitamab.[16] On March 3, 2020, the agreement received antitrust clearance and thus became effective.[17]

In March 2020, MorphoSys announced that the FDA had accepted the Biologics License Application (BLA) for filing and granted priority review for tafasitamab, setting a Prescription Drug User Fee Act (PDUFA) goal date of August 30, 2020.[18]

On July 31, 2020, Monjuvi (tafasitamab-cxix) was approved by the U.S. FDA in combination with lenalidomide for the medical treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) not otherwise specified, including DLBCL arising from low grade lymphoma, and who are not eligible for autologous stem cell transplant (ASCT).[19][20]

In June 2021, MorphoSys announced its acquisition of clinical stage biotechnology company Constellation Pharma for US$1.7 billion.[21]

In February 2024, Novartis agreed to acquire MorphoSys for €2.7 billion.[5] In June 2024, MorphoSys announced its intention to delist from the Frankfurt Stock Exchange and merge into Novartis. The merger was approved in August 2024.[5][22][23]

Pipeline

As of December 2020, MorphoSys had 116 drug candidates which are developed by MorphoSys and other pharmaceutical companies, 28 of which were in clinical development. Two antibodies developed by MorphoSys have already been approved and are currently being marketed.[1][4]

Tafasitamab (MOR208) is a humanized monoclonal antibody directed against CD19 in clinical development for the treatment of B-cell malignancies.[3][24] Tafasitamab is being evaluated in several clinical trials, alone and in combination with other anti-cancer drugs.[1][4][24]

Felzartamab (MOR202) is a humanized monoclonal antibody directed against CD38 for the treatment of anti-PLA2R-positive membranous nephropathy, an autoimmune disease affecting the kidneys.[3] In 2017, MorphoSys entered into a regional licensing agreement with I-Mab Biopharma to develop and commercialize Felzartamab (called TJ202 by I-Mab) in Greater China.[25] Felzartamab is currently under investigation by I-Mab in three clinical trials.[26]

Otilimab (MOR103/GSK3196165) is a fully human monoclonal antibody directed against GM-CSF.[3] The program is outlicensed to GlaxoSmithKline.[6][7] Otilimab is currently under investigation in a Phase 3 trial in rheumatoid arthritis that started in July 2019.[8]

On March 2, 2023, MorphoSys announced that the company would end its preclinical research programs and cease all related activities. It stated that challenges in the pharmaceutical market forced it to optimize its cost structure and to focus all resources on oncology products in the mid to late stage of development.[27]

Technology

MorphoSys has discovered a number of antibody technologies that are used for drug development. Its main technology is HuCAL (Human Combinatorial Antibody Library), which is a collection of more than ten billion fully human antibodies in the form of a phage display bank and a system for their optimization.[28]

Another technology recently developed is the OkapY bispecific antibody technology, which is a proprietary “2+1” bispecific antibody format with the physicochemical properties to simplify the development and large-scale production of such molecules.[<span title="Script error: No such module "decodeEncode".">clarification needed][1][29]

References

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  1. ^ a b c d e f g h i j k Page Module:Citation/CS1/styles.css has no content."Annual Report 2020". MorphoSys. Retrieved 29 April 2021.
  2. ^ a b Page Module:Citation/CS1/styles.css has no content."MorphoSys US, Inc". Archived from the original on June 15, 2021.
  3. ^ a b c d Page Module:Citation/CS1/styles.css has no content."MorphoSys' therapeutic pipeline". MorphoSys.
  4. ^ a b c Page Module:Citation/CS1/styles.css has no content."Form 20-F". U.S. Securities and Exchange Commission.
  5. ^ a b c Page Module:Citation/CS1/styles.css has no content."Novartis to acquire cancer-centric MorphoSys for $2.9 bln". Reuters. 2024-02-05.
  6. ^ a b Page Module:Citation/CS1/styles.css has no content."otilimab (MOR103/GSK3196165)". MorphoSys. 2014-10-27. Retrieved 2018-06-23.
  7. ^ a b Page Module:Citation/CS1/styles.css has no content."MorphoSys Signs Global License Agreement with GlaxoSmithKline for Anti-Inflammatory Program MOR103". MorphoSys. 2013-06-03. Retrieved 2020-04-29.
  8. ^ a b Page Module:Citation/CS1/styles.css has no content."MorphoSys's Licensing Partner GSK Initiates Phase 3 Clinical Program With Otilimab (MOR103/GSK3196165) in Rheumatoid Arthritis". dgap.de. 2019-07-03. Retrieved 2020-04-29.
  9. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys and Xencor Sign License and Collaboration Agreement for Clinical Antibody Program". MorphoSys. 2010-06-27. Retrieved 2020-04-29.
  10. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys' licensee Janssen receives Japanese approval for Tremfya to treat moderate to severe forms of psoriasis & psoriatic arthritis". pharmabiz.com. Retrieved 2018-06-05.
  11. ^ Guselkumab BLA Approval Letter
  12. ^ Page Module:Citation/CS1/styles.css has no content."Nasdaq Welcomes MorphoSys AG (Nasdaq: MOR) to The Nasdaq Stock Market". Nasdaq. 2018-04-19. Retrieved 2020-04-29.
  13. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys Announces Closing of Nasdaq IPO through an ADS Offering and Exercise of the Underwriters' Option to Purchase Additional ADSs, Leading to Total Gross Proceeds of USD 239 million". dgap.de. 2018-04-24. Retrieved 2020-04-29.
  14. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys Announces Submission of Biologics License Application for Tafasitamab in r/r DLBCL to the FDA". dgap.de. 2019-12-30. Retrieved 2020-04-29.
  15. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys Initiates Expanded Access Program for Tafasitamab in the U.S." dgap.de. 2020-01-13. Retrieved 2020-04-29.
  16. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys and Incyte Sign Global Collaboration and License Agreement, including U.S. Co-Commercialization and Ex-U.S. Commercialization Rights, for Tafasitamab". dgap.de. 2020-01-13. Retrieved 2020-04-29.
  17. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys and Incyte Announce Antitrust Clearance of Global Collaboration and License Agreement for Tafasitamab". dgap.de. 2020-03-03. Retrieved 2020-04-29.
  18. ^ Page Module:Citation/CS1/styles.css has no content."FDA Accepts MorphoSys' Biologics License Application (BLA) and Grants Priority Review for Tafasitamab and Lenalidomide for the Treatment of Relapsed/Refractory DLBCL". dgap.de. 2020-03-02. Retrieved 2020-04-29.
  19. ^ Page Module:Citation/CS1/styles.css has no content."FDA Approves Monjuvi(R) (tafasitamab-cxix) in Combination with Lenalidomide for the Treatment of Adult Patients with Relapsed or Refractory Diffuse Large B-cell Lymphoma (DLBCL)". dgap.de. 2020-08-01. Retrieved 2021-04-30.
  20. ^ Page Module:Citation/CS1/styles.css has no content."FDA grants accelerated approval to tafasitamab-cxix for diffuse large B-cell lymphoma". FDA.gov. 2020-08-03. Archived from the original on August 8, 2020. Retrieved 2021-04-30.
  21. ^ Page Module:Citation/CS1/styles.css has no content.Nathan-Kazis, Josh (2021-06-02). "MorphoSys Buys Constellation Pharma in $1.7B Deal. Is Biotech M&A Back?". Barron's.
  22. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys and Novartis Sign Delisting Agreement and Intend to Implement a Merger Squeeze-out of MorphoSys' Minority Shareholders – Company Announcement - FT.com". markets.ft.com. Retrieved 2024-06-21.
  23. ^ Page Module:Citation/CS1/styles.css has no content."Merger Squeeze-Out of MorphoSys Minority Shareholders Approved at 2024 Annual General Meeting". Morphosys de. Retrieved 2024-08-28.
  24. ^ a b Page Module:Citation/CS1/styles.css has no content."tafasitamab". MorphoSys.
  25. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys Signs Regional License Agreement for Antibody MOR202 with I-Mab". dgap.de. 2017-11-30. Retrieved 2020-04-29.
  26. ^ Page Module:Citation/CS1/styles.css has no content."I-Mab Biopharma's therapeutic pipeline". I-Man Biopharma.
  27. ^ Page Module:Citation/CS1/styles.css has no content."MorphoSys Stops Work and Operations on Pre-Clinical Research Programs". Retrieved 2023-03-02.
  28. ^ Page Module:Citation/CS1/styles.css has no content."HuCaL". MorphoSys.
  29. ^ Page Module:Citation/CS1/styles.css has no content.MorphoSys (January 13, 2021). Engineering the Medicines of Tomorrow (PDF) (Speech). J.P. Morgan Healthcare Conference. Archived from the original (PDF) on April 29, 2021. Retrieved April 29, 2021.

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