MorphoSys

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MorphoSys AG
TypePublic Company
IndustryBiotechnology
Founded1992 (1992)
Headquarters
Planegg, Germany
Key people
Dr. Jean-Paul Kress, Chief Executive Officer
Sung Lee, Chief Financial Officer
Dr. Malte Peters, Chief Research & Development Officer
Dr. Roland Wandeler, Chief Commercial Officer
Dr. Marc Cluzel, Chairman of Supervisory Board
ProductsImmunotherapy
Revenue€327.7 million (2020)[1]
€27.4 million (2020)[1]
€97.9 million (2020)[1]
Total assets€1,659.5 million (end 2020)[1]
Total equity€621.3 million (end 2020)[1]
Number of employees
615 (end 2020)[1]
Websitewww.morphosys.com

MorphoSys AG is a biopharmaceutical company founded in 1992. The company is headquartered near Munich, Germany and has a wholly owned subsidiary, MorphoSys US Inc., in Boston MA 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 for a variety of diseases.[1][2][3] 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 is listed on the Frankfurt Stock Exchange and on the US Nasdaq stock exchange.

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.[4] Following the publication of promising results in rheumatoid arthritis, MorphoSys signed a license agreement with GlaxoSmithKline for otilimab.[5] In 2019, GlaxoSmithKline initiated a phase 3 clinical development program with otilimab (now GSK3196165).[6]

In 2010, MorphoSys signed a license agreement with Xencor Inc. for MOR208 (now tafasitamab).[7]

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.[8][9]

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, also under the symbol "MOR."[10][11]

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

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.[12] The submission was accepted for filing in February 2020, and a decision on the filing is expected in August 2020.[13]

In January 2020, MorphoSys and Incyte Corporation signed a collaboration and license agreement for the global development and commercialization of tafasitamab.[14] On March 3, 2020, the agreement received antitrust clearance and thus became effective.[15]

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.[16]

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).[17][18]

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 are already approved and marketed. [1][3]

Tafasitamab (MOR208) is a humanized monoclonal antibody directed against CD19 in clinical development for the treatment of B-cell malignancies.[2][19] Tafasitamab is being evaluated in several clinical trials, alone and in combination with other anti-cancer drugs.[1][3][19]

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.[2] 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.[20] Felzartamab (MOR202/TJ202) is currently under investigation by I-Mab in three clinical trials.[21]

Otilimab (MOR103/GSK3196165) is a fully human monoclonal antibody directed against GM-CSF.[2] The program is outlicensed to GlaxoSmithKline.[4][5] Otilimab is currently under investigation in a Phase 3 trial in rheumatoid arthritis that started in July 2019.[6]

Technology[]

MorphoSys has discovered a number of antibody technologies that are use for drug development.

MorphoSys’ 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.[22]

Another technology recently developed is the OkapY bispecific antibody technology. MorphoSys’ OkapY technology is a new proprietary “2+1” bispecific antibody format with the hysicochemical properties to simplify the development and large-scale production of such molecules.[1][23]

References[]

  1. ^ Jump up to: a b c d e f g h i j k "Annual Report 2020". MorphoSys. Retrieved 29 April 2021.
  2. ^ Jump up to: a b c d "MorphoSys' therapeutic pipeline". MorphoSys.
  3. ^ Jump up to: a b c "Form 20-F". U.S. Securities and Exchange Commission.
  4. ^ Jump up to: a b "otilimab (MOR103/GSK3196165)". MorphoSys. 2014-10-27. Retrieved 2018-06-23.
  5. ^ Jump up to: a b "MorphoSys Signs Global License Agreement with GlaxoSmithKline for Anti-Inflammatory Program MOR103". MorphoSys. 2013-06-03. Retrieved 2020-04-29.
  6. ^ Jump up to: a b "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.
  7. ^ "MorphoSys and Xencor Sign License and Collaboration Agreement for Clinical Antibody Program". MorphoSys. 2010-06-27. Retrieved 2020-04-29.
  8. ^ "MorphoSys' licensee Janssen receives Japanese approval for Tremfya to treat moderate to severe forms of psoriasis & psoriatic arthritis". pharmabiz.com. Retrieved 2018-06-05.
  9. ^ Guselkumab BLA Approval Letter
  10. ^ "Nasdaq Welcomes MorphoSys AG (Nasdaq: MOR) to The Nasdaq Stock Market". Nasdaq. 2018-04-19. Retrieved 2020-04-29.
  11. ^ "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.
  12. ^ "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.
  13. ^ "MorphoSys Initiates Expanded Access Program for Tafasitamab in the U.S." dgap.de. 2020-01-13. Retrieved 2020-04-29.
  14. ^ "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.
  15. ^ "MorphoSys and Incyte Announce Antitrust Clearance of Global Collaboration and License Agreement for Tafasitamab". dgap.de. 2020-03-03. Retrieved 2020-04-29.
  16. ^ "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.
  17. ^ "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.
  18. ^ "FDA grants accelerated approval to tafasitamab-cxix for diffuse large B-cell lymphoma". FDA.gov. 2020-08-03. Retrieved 2021-04-30.
  19. ^ Jump up to: a b "tafasitamab". MorphoSys.
  20. ^ "MorphoSys Signs Regional License Agreement for Antibody MOR202 with I-Mab". dgap.de. 2017-11-30. Retrieved 2020-04-29.
  21. ^ "I-Mab Biopharma's therapeutic pipeline". I-Man Biopharma.
  22. ^ "HuCaL". MorphoSys.
  23. ^ MorphoSys (January 13, 2021). Engineering theMedicinesofTomorrow (PDF) (Speech). J.P. Morgan HealthcareConference. Retrieved April 29, 2021.

External links[]

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