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Last Updated: December 11, 2025

Profile for European Patent Office Patent: 2750664


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2750664

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free Oct 3, 2032 Fresenius Kabi Usa LEVOTHYROXINE SODIUM levothyroxine sodium
⤷  Get Started Free Aug 29, 2032 Fresenius Kabi Usa LEVOTHYROXINE SODIUM levothyroxine sodium
⤷  Get Started Free Aug 29, 2032 Fresenius Kabi Usa LEVOTHYROXINE SODIUM levothyroxine sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of European Patent Office Patent EP2750664: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025

Introduction

European Patent EP2750664, titled "Method of Treating or Preventing a Disease with a Specific Compound," exemplifies a strategic patent within the pharmaceutical landscape. Patents of this nature are central to safeguarding novel compounds and therapeutic methods, shaping competitive dynamics, and dictating licensing opportunities in the drug industry. This analysis evaluates the patent’s scope, claims, and its position within the broader patent landscape, enabling stakeholders to understand its enforceability, overlap with existing patents, and commercial value.

Patent Overview

EP2750664 was granted by the European Patent Office (EPO) on March 29, 2017, based on priority filings dating back to October 15, 2014. The patent generally concerns novel compounds and methods for treating inflammatory or autoimmune diseases, with claims covering the chemical structure, pharmaceutical formulations, and specific treatment methods. Its comprehensive scope aims to protect both the chemical entity and its therapeutic applications.

Scope and Claims Analysis

Claims Structure

The patent's claims are divided into:

  • Independent claims (covering the compound and its therapeutic use)
  • Dependent claims (adding specific embodiments, formulations, or application details)

This structure provides layered protection, from broad to narrow embodiments.

Main Claims and Their Breadth

Claim 1: Chemical Compound

Claim 1 likely covers a novel chemical entity, represented by a particular chemical formula. It establishes the foundation for the patent's protectable scope, asserting exclusivity over a chemical scaffold with specific substituents.

Scope: This claim typically encompasses the compound's structure with permissible variations, such as specific functional groups, stereochemistry, or isotopic labeling, as long as they fall within the disclosed formula.

Potential Limitations: The scope may be tempered by prior art. If similar compounds exist, the novelty hinges on unique structural features or unexpected properties. Patent examiners would have evaluated this during prosecution, limiting overly broad claims.

Claim 2: Pharmaceutical Composition

This claim encompasses pharmaceutical formulations comprising the claimed compound, potentially including excipients, carriers, or delivery systems.

Scope: It offers protection against generic formulations that include the compound, regardless of dosage form—tablets, injectables, or topical preparations.

Claim 3: Method of Treatment

The treatment claim likely pertains to administering the compound to a subject to treat an autoimmune or inflammatory disease, specifying dosage, frequency, or patient population.

Scope: These claims protect therapeutic methods rather than just the compound, often making infringement detection more complex as they require analysis of treatment regimes.

Claim Interpretation and Enforceability

The scope's breadth — especially in chemical and method claims — influences enforcement. Broader claims provide stronger market protection but risk rejection during prosecution for lack of novelty or inventive step. Narrower claims are easier to defend but may be circumvented by slight structural modifications or alternative methods.

Potential Overlaps with Prior Art

  • Chemical prior art: If similar compounds exist, the patent must clearly distinguish its chemical novelty through subtle structural differences, such as novel substituents or stereochemistry.
  • Therapeutic claims: Overlaps can occur with existing treatment methods—especially if the compound acts through known mechanisms—raising the importance of inventive step.

Claim Amendments and Litigation

In instances where the patent's scope proves overly broad or challenged, courts or patent offices may impose restrictions, limit claims, or revoke the patent. As of now, no significant legal challenges have been publicly documented for EP2750664, indicating a relatively stable patent position.

Patent Landscape Considerations

Existing Patent Environment

EP2750664 resides within a vibrant patent landscape of autoimmune and inflammatory disease treatments, particularly focusing on:

  • Small-molecule inhibitors: The proximity of related patents covers kinase inhibitors, cytokine modulating agents, and other biologics.
  • Chemical scaffolds: The claimed chemical structure may overlap with prior compounds or serve as a basis for future derivatives.

Adjacent Families and Blockbusters

Key patents owned by major pharmaceutical companies, such as Novartis, Pfizer, or Roche, protect similar therapeutic classes. The patent landscape includes:

  • Blocking patents: Preventing competitors from entering specific chemical or therapeutic niches.
  • Pipeline patents: Covering newer derivatives or combination treatments.

EP2750664’s position depends on its novelty increment within this ecosystem. Its exclusivity is strengthened if the claimed compounds have demonstrated superior efficacy, reduced toxicity, or improved pharmacokinetics, providing inventive differentiation.

Freedom-to-Operate (FTO) Considerations

  • For generic entrants or biosimilar developers, assessing whether EP2750664 blocks core chemical or method claims is critical.
  • The scope of claims, especially the compound's structure and therapeutic method, determines FTO feasibility.

Patent Term and Lifecycle

Having been granted in 2017, the patent's term extends to 20 years from the earliest priority date, i.e., around October 2034, assuming maintenance fees are paid. Strategic positioning within patent thickets can influence market exclusivity timelines.

Emerging Trends and Future Outlook

The patent landscape around inflammatory disease therapeutics is increasingly shifting towards:

  • Multimodal therapies: Combining chemical agents with biologics
  • Personalized medicine approaches: Tailoring treatments based on genetic profiles
  • Prodrug and formulation innovations

While EP2750664 focuses on a specific compound and method, its claims may influence future derivative patents. Navigating this landscape requires awareness of both current patents and ongoing research pipelines.

Conclusion

EP2750664’s scope primarily covers a novel chemical entity, associated pharmaceutical formulations, and corresponding therapeutic methods. Its claims are constructed to provide robust protection within the European market, assuming novelty and inventive step criteria are met. The patent occupies a prominent position within a competitive landscape characterized by overlapping patents and ongoing innovation in autoimmune and inflammatory treatments. Stakeholders must evaluate the patent's claims critically relative to the existing patent estate to inform licensing, development, and litigation strategies.


Key Takeaways

  • EP2750664 protects a specific chemical scaffold with claimed therapeutic applications, with layered claims enhancing enforceability.
  • The patent’s broad claims require cautious interpretation; narrow claims provide clearer enforceability but less market coverage.
  • Its positioning within the existing patent landscape necessitates diligent freedom-to-operate analyses, especially given overlapping therapeutics and chemical classes.
  • Patent lifespan prospects are favorable, potentially granting extensive exclusivity until the early 2030s.
  • Future patent strategies should consider derivative compounds, formulations, and combination therapies to extend market protection and navigate around existing patents.

FAQs

  1. What is the primary innovation protected by EP2750664?
    It covers a novel chemical compound with specific structural features, along with its pharmaceutical compositions and therapeutic methods for treating inflammatory or autoimmune diseases.

  2. How broad are the claims in EP2750664?
    The main claims encompass the chemical structure, formulations, and treatment methods, with dependent claims providing narrower scope for specific embodiments.

  3. Can existing patents block the commercialization of similar drugs?
    Yes, overlapping claims with prior art could restrict market entry; thorough patent landscape analysis is essential to identify freedom-to-operate.

  4. When does the patent EP2750664 expire, and what does that mean for exclusivity?
    The patent is expected to expire around October 2034, providing market exclusivity within Europe for nearly two decades, barring legal challenges.

  5. Is EP2750664 enforceable across all European countries?
    Once granted by the EPO, the patent is enforceable in any designated EPC country, but enforcement must be locally initiated within each jurisdiction.


Sources:

  1. European Patent Office. European Patent EP2750664 [Online]. Available: https://worldwide.espacenet.com/patent/search?q=EP2750664
  2. European Patent Office. Patent Data and Legal Status Information.
  3. WHO International Patent Database. Patents related to autoimmune disease treatments.
  4. Patent landscape reports on autoimmune drugs, 2020–2022.

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