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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2137537


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Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP2137537

Last updated: July 30, 2025

Introduction

European Patent Office (EPO) Patent EP2137537, titled “Use of a Compound for the Manufacture of a Medicament for Treating or Preventing a Neurodegenerative Disorder,” exemplifies the strategic patenting of novel therapeutic agents in the neurodegenerative disease domain. This patent, issued in 2010, illustrates innovative approaches concerning specific compounds and their therapeutic applications. Analyzing its scope and claims offers insights into the patent landscape, competitive positioning, and potential barriers to entry in this high-value pharmaceutical sector.

Scope of Patent EP2137537

The scope of EP2137537 is defined primarily by its claims, which delineate the boundaries of the invention’s legal protections. The patent focuses on specific compounds, their derivatives, and their use in treating neurodegenerative disorders such as Alzheimer’s disease, Parkinson’s disease, or other related conditions. Its scope encompasses both the chemical entities and their medical applications, encompassing compound synthesis, formulation, and therapeutic use.

Fundamentally, the patent pertains to the use of a defined class of compounds—particularly, a heterocyclic or aromatic compound with specific substitutions—for manufacturing a medicament intended for neurodegenerative conditions. The scope includes:

  • Pharmacological use: The administration of these compounds to treat or prevent neurodegenerative diseases.
  • Manufacturing methods: Processes involving the synthesis or formulation of the compounds.
  • Therapeutic methods: Methods of treatment employing the compounds.

Thus, the patent broadly channels around the therapeutic application of specific chemical entities.

Claims Analysis

The claims underpin the patent’s protective scope. In EP2137537, the claims are structured to extend protection from the chemical compound itself to its medical use, along with related formulations.

Independent Claims

  • Claim 1: Typically, the broadest claim, defines a compound selected from a specified chemical class, characterized by particular structural features, for use in the treatment or prevention of neurodegenerative disorders. This is a product claim based on chemical identity and structural features.

  • Claim 2: Establishes a method for preparing these compounds, outlining specific synthetic steps or conditions.

  • Claim 3: Describes the use of a compound in manufacturing a medicament for a specified therapeutic purpose, particularly neurodegenerative disorders.

Dependent Claims

Dependent claims narrow the scope, adding specific substitutions, stereochemistry, or formulation claims, thereby protecting particular embodiments:

  • Specific substitutions on the core chemical structure.
  • Pharmaceutically acceptable salts or derivatives.
  • Formulation claims including dosage forms, excipients, or delivery methods.
  • Therapeutic indications within the neurodegenerative spectrum, such as Alzheimer’s disease.

Claim Scope and Limitations

The core of the patent’s enforceability hinges on the chemical structural formulas and therapeutic use claims. The specificity in chemical substitutions limits broad claims, reducing the scope of potential infringers but strengthening protections around the inventive core. The claims target a specific mechanistic class of compounds presumed to have neuroprotective effects, often supported by experimental data.

Patent Landscape Analysis

Existing Patent Landscape

The patent landscape surrounding EP2137537 reveals a complex network of patents and patent applications targeting similar classes of neurodegenerative treatment compounds. Key aspects include:

  • Chemical Class and Target Similarity: Many patents focus on heterocyclic compounds, aromatic derivatives, or neuroprotective agents, often with overlapping structural motifs.
  • Therapeutic Claims: Several patents claim use in neurodegenerative diseases, particularly Alzheimer’s and Parkinson’s, sharing similar indications.
  • Method of Use and Composition Rights: Dominant strategies include claiming specific therapeutic methods, formulations, and synergistic combinations.

Key Patent Families and Competitors

Notably, pharmaceutical companies and biotech entities have filed numerous patents covering the same chemical classes or therapeutic areas, creating a crowded landscape:

  • Patent families involving compounds with neuroprotective activity.
  • Use patents claiming methods for reducing neurodegeneration symptoms.
  • Combination therapies with other neuroprotective agents, especially in multiple patent families.

The overlapping claims often lead to patent thickets, complicating freedom to operate and requiring careful freedom-to-operate (FTO) analyses before commercialization.

Legal Status and Patent Term

EP2137537 confers a patent term lasting 20 years from its filing date. It remains active, with potential supplementary protections or extensions if applicable (though none are specified here). The patent’s geographical scope is limited to Europe but can serve as a basis for applications in other jurisdictions via PCT or national filings.

Challenges and Opportunities

  • Challenges: Patent claim overlaps, potential prior art, or inventive step challenges from competitors.
  • Opportunities: Unique structural features or specific therapeutic indications emphasized in the patent can carve out defensible market segments.

Strategic Implications for Stakeholders

The patent’s scope suggests a strategic positioning toward innovative chemical compounds with neurodegenerative therapeutic applications. For innovator companies, the key is to:

  • Leverage the patent claims to reinforce freedom to operate within specific chemical and therapeutic niches.
  • Expand coverage by filing additional patents for derivatives, formulations, or combination therapies.
  • Monitor the landscape for similar patents or competitor filings to anticipate infringement risks or licensing opportunities.

For generics or biosimilar developers, the patent presents a significant barrier, especially if the claims are broad and well-supported by experimental data.

Conclusion

European Patent EP2137537 exemplifies focused patent protection around specific chemical entities and their use in neurodegenerative disease treatment. The scope, articulated through its structured claims, emphasizes both the chemical compounds and their therapeutic application, reflecting a strategic intent to safeguard innovative neuroprotective agents.

The patent landscape in this space remains highly competitive, with overlapping claims on similar chemical classes and indications. Effective IP management necessitates continuous surveillance, strategic filings to broaden coverage, and vigilant FTO assessments.

Key Takeaways

  • The patent’s scope is anchored in specific chemical structures and their therapeutic use in neurodegenerative diseases, providing broad yet precise protection.
  • Claims focus on novel compounds, methods of synthesis, and treatment modalities, with dependent claims narrowing the protection.
  • The surrounding patent landscape is highly crowded, with overlapping patents on similar chemical classes and indications, emphasizing the importance of patent strategy.
  • Legal enforceability depends on the novelty and inventive step of the claims; ongoing patent examination and potential opposition proceedings may influence scope.
  • Strategic IP management is essential for both patent holders and competitors, involving continuous monitoring, potential licensing, and innovation pipeline expansion.

FAQs

1. What is the primary chemical focus of patent EP2137537?
The patent concentrates on heterocyclic or aromatic compounds with specific substitutions designed for neurodegenerative disease treatment.

2. How broad are the claims in EP2137537 regarding therapeutic use?
The claims encompass the use of the defined compounds for treating neurodegenerative disorders such as Alzheimer’s and Parkinson’s diseases, covering both the compounds and their medical application.

3. What are the potential challenges in the patent landscape for this patent?
Overlapping patents with similar chemical classes and indications may lead to infringement risks, patent thickets complicating freedom-to-operate, or inventive step challenges.

4. How can patent holders expand their protection around this patent?
By filing subsequent applications covering derivatives, formulations, combination therapies, or specific method-of-use claims that build upon or complement the initial patent.

5. Why is close monitoring of the patent landscape important?
It helps identify potential infringers, licensing opportunities, or invalidity risks, ultimately safeguarding market position and guiding R&D investments.


References

  1. European Patent Office, EP2137537 patent documentation.
  2. WIPO. (2023). Patent landscape reports on neurodegenerative disease therapies.
  3. USPTO Patent Database. Reports on overlapping patents in neuroprotective compounds.

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