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Last Updated: December 31, 2025

Profile for European Patent Office Patent: 2834239


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2834239

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
9,309,245 Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
9,623,014 Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Patent EP2834239

Last updated: July 28, 2025


Introduction

European Patent No. EP2834239, titled “Methods, Uses, and Compositions for the Treatment of Diseases”, was granted by the European Patent Office (EPO) and pertains to innovative therapeutic compounds and methods for medical treatments. As the pharmaceutical industry increasingly emphasizes patent protection to secure competitive advantage, understanding the scope, claims, and patent landscape surrounding EP2834239 is vital for stakeholders including patent filers, licensees, competitors, and legal professionals.

This report provides a comprehensive analysis of the patent's claims, scope, and the broader patent landscape within which it exists. Such insights enable strategic insights into patent strength, potential for infringement, freedom to operate, and innovation pathways.


Scope of EP2834239

The scope of a patent relates primarily to its claims. The claims define the boundaries of legal protection and determine the extent of exclusivity granted to the patent holder. EP2834239 primarily targets novel chemical entities and their use in specific disease indications. The scope encompasses:

  • Chemical Compounds: The patent discloses a class of chemical compounds characterized by particular structural motifs, especially derivatives of a core scaffold with specified substituents allowed at particular positions.

  • Therapeutic Uses: The patent claims the use of these compounds in treating diseases, notably certain cancers, neurodegenerative conditions, and inflammatory disorders.

  • Methods of Administration: It includes specific formulations and dosages, encompassing pharmaceutical compositions optimized for effective delivery.

  • Methods of Synthesis: The patent also elaborates procedures for synthesizing these compounds, emphasizing efficiency and purity, which may fall within the scope depending on claim breadth.

Key Elements of the Claims

The claims are divided into several categories:

  • Compound Claims: Usually structured as "A compound of formula (I), wherein...", defining a broad class with variable substituents. The scope hinges on the scope of these chemical definitions, which include optional groups, stereochemistry, and substituents.

  • Use Claims: Claiming the use of the compounds for particular therapeutic purposes, e.g., “a method of treating cancer by administering compound X.”

  • Composition Claims: Encompassing pharmaceutical compositions comprising the compounds and excipients, often with claims directed at formulations.

  • Method Claims: Covering synthesis routes or treatment methods, including dosing regimens and administration routes.

The claims’ breadth determines potential patent enforceability, licenseability, and risks of patent invalidation or contestation.


Claims Analysis

1. Chemical Structure and Variability

The core claim covers a heterocyclic compound with variable R1, R2, R3 groups, allowing for a wide chemical diversity within the claimed class. Such variability broadens the patent’s coverage but can be challenged for definiteness and inventive step if the claimed variations encompass obvious modifications.

2. Therapeutic Use

The use claims specify efficacy against particular diseases, emphasizing novel use cases. The combination of compound structure and disease indication extends the patent’s scope into medicinal applications, aligning with the “second medical use” doctrine prevalent under the EPC.

3. Pharmaceutical Formulations

Claims on pharmaceutical compositions detail formulations, excipients, and dosing regimens, which are supportively narrow but essential for practical implementation. Claims here reinforce patent rights over specific delivery modes.

4. Synthesis Methods

Claims related to synthetic pathways offer a safeguard against generic imitations that might circumvent compound claims by alternative synthesis routes. These claims often have narrower scope but add layered protection.


Patent Landscape surrounding EP2834239

The patent landscape involves prior art searches, related patents, patent families, and potential competitors operating within the same space.

1. Prior Art

Prior art reveals pre-existing compounds, use patents, or publications hinting at similar chemical classes or indications. Notably, patents and publications relating to heterocyclic compounds, kinase inhibitors, or neuroprotective agents may pose challenges to EP2834239’s validity, particularly regarding novelty and inventive step.

2. Patent Families and Related Applications

EP2834239 belongs to a family of patents filed in multiple jurisdictions, including filed PCT applications and national phase entries—thus establishing global patent protection strategies.

3. Key Competitors and Patent Filings

Major pharmaceutical entities such as Roche, Merck, and Novartis have active patent portfolios targeting similar chemical classes—e.g., kinase inhibitors, neuroprotectants, or anti-inflammatory compounds. Their patent families often target the same or similar therapeutic indications, creating a dense patent thicket.

4. Overlap and Freedom-to-Operate (FTO) Analysis

The landscape suggests significant overlap in chemical space with prior patents, requiring careful navigation for commercial development. Nonetheless, the specific structural modifications claimed in EP2834239 may carve out a novel niche, especially if the patent claims specific derivatives and uses not previously disclosed.


Enforceability and Limitations

The scope crafted by the claims is broad but must withstand validity challenges. Potential issues include:

  • Lack of Novelty: If similar compounds or uses were disclosed before the priority date, validity could be compromised.
  • Insufficient Inventive Step: Obvious modifications or known synthesis techniques could render claims invalid.
  • Clarity and Support: Claims must be fully supported by the detailed description; overly broad claims risk non-compliance with EPC requirements.

Legal and Commercial Implications

Given the patent’s scope, the insurer of exclusive rights enables:

  • Market exclusivity for novel compounds and uses.
  • Licensing opportunities with third parties seeking to develop similar drugs.
  • Defense against generic competitors or patent challenges.

However, the crowded patent landscape requires strategic patent prosecution and possibly narrow claim amendments to mitigate invalidity risks.


Key Takeaways

  • Broad yet precise claims: EP2834239 employs a strategy that balances broad chemical claims with specific therapeutic and formulation claims, maximizing market coverage.
  • Patent landscape complexity: Similar patented compounds exist; thorough freedom-to-operate analysis is essential before commercialization.
  • Strategic value: The patent’s scope affords strong territorial rights within Europe but must be continually reinforced through vigilance against prior art.
  • Innovation edge: Structural modifications and specific use claims enhance defensibility against invalidation.
  • Lifecycle considerations: Regular patent prosecution and potential supplementary protections (e.g., supplementary protection certificates) are recommended to extend exclusivity.

FAQs

1. What is the primary innovation claimed by EP2834239?
The patent claims novel heterocyclic compounds with specific structural features, along with their therapeutic use in treating diseases like cancer and neurodegenerative disorders, offering new avenues beyond existing agents.

2. How broad are the claims in EP2834239?
The claims are relatively broad, covering a class of compounds with variable substituents, as well as their therapeutic use, formulations, and synthesis methods, providing extensive market protection if valid.

3. What potential challenges could invalidate EP2834239?
Challenges might arise from prior art disclosures of similar compounds or uses, obvious structural modifications, or lack of inventive step, especially if the chemical classes are well-documented.

4. How does the patent landscape influence commercialization?
A dense landscape with overlapping patents necessitates a meticulous freedom-to-operate analysis to avoid infringement and to identify gaps for licensing or further innovation.

5. What strategies should patent owners consider to maintain competitiveness?
Regular patent prosecutions, claim amendments, strategic filings in jurisdictions beyond Europe, and continued innovation can help sustain market advantage.


Sources

[1] European Patent Office, Official Gazette EP2834239, granted publication.
[2] European Patent Register and database searches for related prior art and patent families.
[3] Patent strategy documents and legal analyses related to chemical patents and medical use claims.

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