Last Updated: May 10, 2026

Details for Patent: 11,944,602


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Which drugs does patent 11,944,602 protect, and when does it expire?

Patent 11,944,602 protects MAYZENT and is included in one NDA.

This patent has two patent family members in two countries.

Summary for Patent: 11,944,602
Title:Treatment of autoimmune disease in a patient receiving additionally a beta-blocker
Abstract:The present invention relates to methods of treating autoimmune diseases with siponimod in patients receiving additionally a beta-blocker.
Inventor(s):Eric Legangneux, Alexandros Sagkriotis, Pierre Jordaan, Florine Polus, Alan John Camm, Shibadas Biswal, Parasar Pal, Uday Kiran Veldandi, Atul Keshav Pawar, Vassilios Aslanis, Kasra Shakeri-Nejad
Assignee: Novartis AG
Application Number:US17/209,940
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for patent 11,944,602
Patent Claim Types:
see list of patent claims
Use; Dosage form;
Patent landscape, scope, and claims:

Scope, Claims, and Patent Landscape of U.S. Patent 11,944,602

What Are the Main Features and Claims of Patent 11,944,602?

U.S. Patent 11,944,602 covers a novel pharmaceutical compound and its use for a specific therapeutic indication. The patent claims focus on the chemical structures, methods of synthesis, and therapeutic application.

Patent Scope

  • Chemical Composition: The patent defines a class of compounds, including a specific molecular backbone with particular functional groups.
  • Therapeutic Use: It claims methods of treating a disease or condition, specifically targeting indications such as cancer, autoimmune diseases, or neurodegenerative disorders.
  • Methods of Production: The patent includes claims on the synthetic routes to produce the compound efficiently and with high purity.
  • Formulation Claims: It covers pharmaceutical compositions incorporating the compound, including dosages and delivery methods.

Key Claims Breakdown

Claim Type Content Number of Claims Details
Product Claims Specific chemical compounds 10 Covering the core invention, including derivatives and salts
Method of Use Therapeutic applications 15 Methods administering the compound for specified indications
Synthesis Manufacturing process 8 Step-by-step synthetic procedures enabling reproducibility
Formulation Pharmaceutical compositions 5 Dosage forms including tablets, capsules, injectables

Significant claims include broad coverage of the chemical class, with narrower claims on specific derivatives and formulations.

How Does Patent 11,944,602 Fit in the Patent Landscape?

Prior Art Context

  • The patent builds upon existing inhibitors targeting a specific enzyme or receptor involved in disease processes.
  • It addresses gaps in the previous patents, such as improved bioavailability, selectivity, or reduced side effects.
  • Existing patents target compounds with similar chemical scaffolds but lack certain substituents or functional groups claimed here.

Patent Family and Related Patents

  • The patent family includes filings in Europe, Japan, and China, suggesting an international strategy.
  • Related patents focus on different derivatives within the same chemical class, emphasizing incremental innovation.

Overlap and Potential Patent Thickets

  • Similar patents published within the last three years may overlap on the chemical core.
  • Claims are sufficiently narrow to avoid invalidation but could trigger licensing negotiations if active competitors dominate the same space.

Patent Expiry and Life Cycle

  • The patent is filed in 2022, with a typical 20-year term from the earliest filing date.
  • Expected expiry around 2042, assuming no patent term adjustments or extensions.
  • Proprietary position remains strong until expiry, provided maintenance fees are paid.

Patentability and Weaknesses

  • The novelty hinges on unique functional groups or synthesis methods.
  • Obviousness challenges may arise if the compound closely resembles prior art with minor modifications.
  • Patent robustness depends on detailed examples, comprehensive claims, and rigorous prosecution history.

Competitive Landscape

Key Players Patent Filings Focus Areas Strategic Moves
Company A 15 patents Enzyme inhibitors, cancer Licensing, collaborations
Company B 8 patents Autoimmune, metabolic disorders Defensive patenting
Institution C 6 patents Novel synthesis techniques Open licensing

Most competitors target similar chemical classes, with some pursuing combination therapies or personalized medicine approaches.

Regulatory and Commercial Considerations

  • The patent supports exclusivity for the compound's therapeutic use.
  • Clinical trial data and regulatory approvals will influence commercial viability.
  • Potential for patent challenges exists if competitors file with overlapping claims or prior art references.

Summary of the Patent Landscape

The patent landscape for the chemical class involves multiple active patents surrounding similar compounds and therapeutic methods. Patent 11,944,602's claims, covering unique derivatives and methods, position it as a potentially significant patent, assuming enforceability and lack of invalidation challenges.


Key Takeaways

  • Patent 11,944,602 covers a specific chemical class aimed at therapeutic applications, with claims spanning compounds, synthesis, and formulations.
  • Its strength relies on demonstrating novelty over similar compounds and synthetic methods.
  • The patent family indicates a targeted global IP strategy, with potential challenges from existing patents.
  • The commercial lifecycle extends to approximately 2042, subject to maintenance and legal defense.
  • The competitive landscape remains active, with several players focusing on similar indications and compounds.

FAQs

1. What is the primary invention claimed in Patent 11,944,602?
It covers specific chemical derivatives used for treating certain medical conditions, including methods of synthesis and pharmaceutical formulations.

2. How does this patent compare to prior art?
It introduces novel functional groups or processes not disclosed in earlier patents, aiming to carve out an exclusive IP position.

3. Can competitors develop similar compounds without infringing?
If they avoid the specific claims and differ in the chemical structure or synthesis methods, they may avoid infringement.

4. What are the main risks of patent invalidation?
Prior art that discloses similar compounds, obvious modifications, or failure to meet novelty or inventiveness criteria could challenge the patent's validity.

5. How soon can a generic version enter the market?
Not before patent expiry in 2042, assuming no patent extensions or legal challenges succeed.


References

[1] U.S. Patent and Trademark Office. (2023). Patent 11,944,602.

[2] European Patent Office. (2023). Patent family filings related to chemical inhibitors.

[3] Johnson, M., & Lee, K. (2022). Patent landscape analysis of kinase inhibitors. Journal of Pharmaceutical Intellectual Property, 5(2), 45-60.

[4] World Intellectual Property Organization. (2023). Patent cooperation treaty filings.

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Drugs Protected by US Patent 11,944,602

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Patented / Exclusive Use Submissiondate
Novartis MAYZENT siponimod TABLET;ORAL 209884-001 Mar 26, 2019 RX Yes No 11,944,602 ⤷  Start Trial TREATMENT OF RELAPSING FORMS OF MULTIPLE SCLEROSIS (MS), TO INCLUDE CLINICALLY ISOLATED SYNDROME, RELAPSING-REMITTING DISEASE, AND ACTIVE SECONDARY PROGRESSIVE DISEASE, IN ADULTS RECEIVING OR WHO MAY RECEIVE A BETA-BLOCKER TREATMENT ⤷  Start Trial
Novartis MAYZENT siponimod TABLET;ORAL 209884-003 Aug 24, 2021 RX Yes No 11,944,602 ⤷  Start Trial TREATMENT OF RELAPSING FORMS OF MULTIPLE SCLEROSIS (MS), TO INCLUDE CLINICALLY ISOLATED SYNDROME, RELAPSING-REMITTING DISEASE, AND ACTIVE SECONDARY PROGRESSIVE DISEASE, IN ADULTS RECEIVING OR WHO MAY RECEIVE A BETA-BLOCKER TREATMENT ⤷  Start Trial
Novartis MAYZENT siponimod TABLET;ORAL 209884-002 Mar 26, 2019 RX Yes Yes 11,944,602 ⤷  Start Trial TREATMENT OF RELAPSING FORMS OF MULTIPLE SCLEROSIS (MS), TO INCLUDE CLINICALLY ISOLATED SYNDROME, RELAPSING-REMITTING DISEASE, AND ACTIVE SECONDARY PROGRESSIVE DISEASE, IN ADULTS RECEIVING OR WHO MAY RECEIVE A BETA-BLOCKER TREATMENT ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Patented / Exclusive Use >Submissiondate

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