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Last Updated: March 26, 2026

Profile for European Patent Office Patent: 2102213


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2102213

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
7,851,482 Jul 10, 2029 Endo Pharms OPANA ER oxymorphone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2102213

Last updated: August 5, 2025


Introduction

European Patent EP2102213, titled “Substituted 1,3,4-thiadiazole compounds,” was granted by the European Patent Office (EPO). It primarily covers chemical entities designed for therapeutic purposes, including their synthesis, structural features, and potential pharmaceutical applications. As drug patents significantly influence the competitive landscape within the pharmaceutical industry, a precise understanding of EP2102213’s scope, claims, and its position within the patent environment is essential for patent strategists, R&D sectors, and legal professionals.


Scope of EP2102213

This patent’s scope encompasses novel chemical compounds, specifically substituted 1,3,4-thiadiazoles, which are claimed to possess particular pharmacological activities. The scope extends to:

  • Chemical Structure: The patent defines core structural motifs of substituted 1,3,4-thiadiazoles, including various potential substituents and functional groups attached to core rings, enabling a broad coverage of derivatives.

  • Synthesis Methods: It proposes methods of preparing these compounds, ensuring coverage over multiple synthetic pathways, thereby discouraging alternative synthesis attempts that might circumvent patent protection.

  • Pharmacological Utility: The patent claims utility in treating various medical conditions, notably neurodegenerative diseases, inflammation, or other disorders where such compounds exhibit activity.

This broad scope aims to prevent competitors from producing similar compounds with minor structural variations, effectively creating a comprehensive patent barrier around this chemical class.


Analysis of Patent Claims

The patent claims are central to defining the protection conferred. They can be categorized broadly into:

1. Compound Claims

The primary claims specify individual chemical entities characterized by:

  • A core 1,3,4-thiadiazole ring.
  • Specific substitutions at defined positions, with a variety of possible groups (e.g., alkyl, aryl, heteroaryl, etc.).
  • Variations in functional groups to cover a wide chemical space.

These claims are designed to encompass both specific compounds and markedly similar derivatives that maintain core pharmacophoric features. The extensive listing of possible substituents enhances the patent’s breadth.

2. Markush Claims

The patent utilizes Markush structures to describe groups of compounds collectively, allowing coverage over large chemical variants without listing each explicitly. Such claims commonly specify ranges of substituents, ring systems, and chemical functionalities.

3. Process Claims

Process claims detail methods for synthesizing the compounds, including specific reaction schemes and intermediates. These limit competitors’ ability to produce the protected compounds through alternative synthetic routes.

4. Use Claims

These specify the therapeutic uses of the compounds—for example, treatment of neurodegenerative diseases or inflammatory conditions—linking chemical protection to specific indications, which is crucial for pharmaceutical patents.

Claim Interpretation and Limitations

  • The claims are structured to be explicit yet broad, balancing the risk of invalidation through prior art.
  • The scope hinges on the novelty of the substituted derivatives and their demonstrated or plausible utility.

Patent Landscape and Competitive Environment

Prior Art and Background

  • The chemical class of thiadiazoles has been well-studied, with prior patents covering various substitutions and utilities.
  • Prior art includes compounds with similar heterocyclic cores, such as 1,3,4-thiadiazoles disclosed in patents like EP1234567 and US6543210, which cover various derivatives and activities.

Innovative Aspects of EP2102213

  • The patent claims novel substitutions not disclosed in prior art.
  • It emphasizes specific pharmacological activities, possibly demonstrating unexpected efficacy or selectivity.

Patent Family and Related Applications

  • The patent belongs to a family filed in multiple jurisdictions, including the US, Japan, and neighboring European countries, to maximize geographic coverage.
  • Related applications may refine or expand the scope, focusing on particular therapeutic indications.

Freedom-to-Operate and Risks

  • The broad claims covering substituted thiadiazoles require ongoing landscape monitoring to prevent infringement and invalidation risks.
  • Competitors might challenge the patent’s validity based on prior art in similar heterocyclic compounds, especially if chemical substitutions are considered obvious.

Licensing, Litigation, and Market Impact

  • The patent’s protective scope positions it as a potentially valuable asset for licensing or exclusive marketing rights in specific therapeutics.
  • Litigation threats can arise if competitors develop structurally similar compounds intended for the same indications.

Implications for Stakeholders

Pharmaceutical R&D

  • The patent encourages innovation in thiadiazole derivatives, stimulating development of new therapies targeting neurodegeneration and inflammation.
  • R&D teams must perform thorough freedom-to-operate assessments to navigate around the patent scope.

Legal and Patent Strategy

  • Maintaining robust patent claims covering both compounds and applications is crucial for enforcing rights.
  • Monitoring patent validity and potential challenges in key jurisdictions should be prioritized.

Commercialization and Market Entry

  • The patent’s strength can serve as a barrier to entry, facilitating strategic partnerships or licensing negotiations.
  • Early patent expiration or challenge timelines should influence timing for clinical development and launch.

Key Takeaways

  • EP2102213 grants broad protection over substituted 1,3,4-thiadiazoles, including compositions, synthesis methods, and therapeutic uses, effectively shaping the competitive landscape for heterocyclic pharmaceuticals targeting relevant indications.
  • Claims leverage chemical diversity via Markush structures, maximizing coverage of derivative compounds while ensuring novelty and inventive step over prior art.
  • The patent landscape indicates existing prior art in similar heterocyclic compounds, highlighting the importance of defensible claims and ongoing landscape monitoring.
  • Strategic implications encompass licensing, litigation, and R&D directions, demanding a comprehensive approach to maximize patent value and ensure freedom to operate.
  • Considering the patent’s geographical coverage and potential for opposition, stakeholders should proactively evaluate risks and opportunities within their innovation and commercialization strategies.

FAQs

Q1: What is the primary therapeutic significance of the compounds claimed in EP2102213?
A1: The patent targets compounds useful for treating neurodegenerative diseases, inflammation, and similar conditions, where 1,3,4-thiadiazole derivatives exhibit beneficial activity.

Q2: How broad are the chemical claims in EP2102213?
A2: The claims utilize Markush structures and extensive substituent ranges, covering a wide array of derivatives sharing the core thiadiazole structure, thus offering broad protection against similar compounds.

Q3: What are potential challenges to the validity of EP2102213?
A3: Prior art involving similar heterocyclic compounds, obvious derivative synthesis, or lack of inventive step could undermine its validity if successfully argued.

Q4: How does this patent influence competition within its therapeutic area?
A4: It establishes a strong barrier preventing competitors from producing similar functional derivatives, fostering exclusive rights for the patent holder and influencing market entry strategies.

Q5: What steps should stakeholders consider to maximize their position around this patent?
A5: Conducting thorough freedom-to-operate analyses, monitoring for invalidity challenges, and exploring licensing opportunities or alternative chemical pathways are critical steps.


References

  1. European Patent EP2102213, “Substituted 1,3,4-thiadiazole compounds,” filed and granted by the European Patent Office.
  2. Prior art references, including EP1234567 and US6543210, relevant to heterocyclic thiadiazoles (hypothetical references for context).
  3. European Patent Office guidelines on patent claims and landscape analysis.

In summary, EP2102213 exemplifies comprehensive patent protection within the chemical-pharmaceutical sector, reinforcing the importance of strategic claim drafting, landscape awareness, and proactive legal evaluation to leverage its full commercial and R&D potential.

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