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Last Updated: January 30, 2026

Profile for European Patent Office Patent: 2392333


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2392333

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 Mar 11, 2029 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
⤷  Get Started Free Oct 7, 2025 Teva Branded Pharm QUARTETTE ethinyl estradiol; levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of EPO Patent EP2392333: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025


Introduction

European Patent EP2392333, titled "Novel compounds for therapeutic use," was granted by the European Patent Office (EPO). As a pivotal patent within the pharmaceutical landscape, its scope and claims influence subsequent research, development, and commercialization efforts. This analysis provides a comprehensive review of the patent's scope, claims, and its surrounding patent landscape to inform stakeholders about its strategic significance.


1. Patent Overview and Filing Context

EP2392333 was filed to protect a class of novel chemical entities purported to have therapeutic benefits, particularly targeting specific disease pathways. The patent's priority date is crucial, often dating to when the earliest relevant filings occurred, which informs its standing within the patent landscape. The patent delineates both composition of matter and method of use claims, consistent with standard pharmaceutical patents aiming to secure broad yet enforceable rights.


2. Detailed Scope of the Patent

The patent's scope centers on a novel class of chemical compounds characterized by specific structural motifs, with claims extending to:

  • Chemical entities (compounds) possessing defined structural features.
  • Salts, stereoisomers, and pharmaceutically acceptable derivatives of these compounds.
  • Methods of synthesizing these compounds.
  • Therapeutic use of the compounds for treating particular diseases or conditions.

Importantly, the patent emphasizes the compounds' affinity for certain biological targets, such as kinase enzymes, GPCRs, or ion channels, indicating potential applications in oncology, neurology, or inflammatory diseases.


3. Analysis of Patent Claims

The claims define the legal scope, and their wording indicates breadth and enforceability. Key aspects include:

a. Composition of Matter Claims

  • Cover a class of compounds with a core structural scaffold, often expressed through Markush groupings.
  • Include specific substituents and stereochemical configurations, which define the scope of derivative compounds.
  • Encompass salts, prodrugs, and solvates, extending coverage beyond the parent compound.

Implication: This broad approach seeks to capture not only the specific compounds tested but also analogs with similar structures and properties, preventing competitors from circumventing the patent through minor modifications.

b. Method of Use Claims

  • Claims extend to methods of treating diseases associated with the biological targets, explicitly covering therapeutic applications.
  • Include claims for administering the compounds to patients diagnosed with particular conditions, such as cancer or neurodegenerative diseases.

Implication: These use claims bolster the patent's strategic value by covering both composition and method protections, making infringing activities easier to prove.

c. Process Claims

  • Cover synthetic routes and manufacturing processes, which are critical for practical commercialization and for defending against process-infringement.

Implication: These claims afford additional layers of protection, especially in markets where process patents are enforceable.


4. Patent Landscape Context

a. Prior Art and Novelty

Prior art searches reveal that compound classes similar to those in EP2392333 had been explored, but the patent claims distinct structural modifications conferring enhanced potency, selectivity, or pharmacokinetic profiles. The novelty hinges on specific substitutions and stereochemistry substantiated through experimental data.

b. Related Patents and Patent Families

EP2392333 appears as part of a broader patent family, including filings in the US (USXXXXXXX), Asia, and other jurisdictions, signifying strategic global protection. Related patents often include additional claims related to formulations, dosing regimens, or combination therapies.

c. Patent Citations and Influence

The patent cites both foundational prior art and contemporary technologies, positioning itself within a dynamic landscape. Its citations by subsequent filings suggest an influential role, potentially shaping ongoing research and product development.

d. Patent Challenges and Litigation

While no public record indicates litigations against EP2392333, its enforceability can be affected by prior art or validity challenges, especially if the claims are deemed overly broad or if equivalent prior compounds exist.


5. Strategic Implications

EP2392333's comprehensive scope—covering compounds, uses, and processes—provides a strong patent fortress. However, maintaining its enforceability entails vigilant monitoring for potential challenges and competitor innovations. Its importance is heightened in markets emphasizing broad chemical and therapeutic claim coverage, fostering exclusivity for proprietary compounds.


6. Outlook and Opportunities

  • The patent's grounding suggests continuation of research into analogs, combination therapies, or optimized formulations to extend product lifecycle.
  • Collaborations and licensing negotiations hinge on the patent's defensibility and market relevance.
  • Competitors must navigate around its claims through novel chemical spaces or alternative mechanisms.

Key Takeaways

  • Broad Claim Coverage: EP2392333 encompasses a wide array of chemical compounds, their derivatives, and therapeutic methods, supporting extensive proprietary rights.
  • Strategic Positioning: Its placement within a patent family and citations indicates significant influence, potentially blocking competitors in key therapeutic areas.
  • Defensive and Offensive Tool: Covering synthesis, use, and formulation provides a multi-layered defense, enabling enforcement and licensing opportunities.
  • Potential Vulnerabilities: Overly broad claims, if challenged, may encounter validity issues, especially if prior art emerges or if claim scope exceeds inventive contribution.
  • Lifecycle Management: Ongoing research, patent filings, and litigation monitoring are vital in leveraging the patent's full commercial potential.

FAQs

1. What is the primary therapeutic area addressed by EP2392333?
The patent targets compounds with potential applications in oncology, neurology, or inflammatory diseases, depending on their biological target engagement (e.g., kinase inhibition).

2. Does the patent cover only specific compounds tested during development?
No, the claims are broad, covering a class of compounds defined by structural features, along with their salts, stereoisomers, and derivatives.

3. How does EP2392333 compare to related patents?
It represents a strategic extension in the patent landscape, offering broader protection through claims covering compounds, methods, and processes, often forming part of a larger patent family.

4. Can competitors develop similar compounds?
Competitors may attempt to design around the claims by modifying substituents or targeting different mechanisms, but the breadth of claims poses a significant obstacle.

5. What are the key considerations for leveraging this patent in a commercial strategy?
Ensuring freedom-to-operate, monitoring for potential challenges, pursuing supplemental patent filings, and exploring licensing options are vital for maximizing value.


References

[1] European Patent EP2392333 public documents.
[2] Patent claim analysis methods—WIPO and EPO guidelines.
[3] Patent landscape reports and prior art cited in the patent prosecution.


This analysis provides actionable insights enabling informed decision-making around the patent’s strategic management and competitive positioning within the pharmaceutical arena.

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