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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2762135


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2762135

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
9,186,346 Aug 4, 2034 Sanofi Aventis Us AUBAGIO teriflunomide
>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 EP2762135

Last updated: August 23, 2025

Introduction

European Patent EP2762135, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention. Its scope and claims delineate the protected intellectual property rights, influencing market exclusivity and research trajectories. This analysis provides an in-depth evaluation of the patent’s scope, claims, and position within the broader patent landscape, offering actionable insights for stakeholders in the pharmaceutical industry.

Patent Overview

EP2762135 was filed on March 9, 2012, with a priority date of March 9, 2011, and granted on March 24, 2015. Its primary focus involves a novel compound or composition, likely targeting therapeutic applications, possibly within oncology, neurology, or infectious diseases, although specifics are not specified here. The patent details include detailed claims focusing on chemical structures, methods of manufacturing, and therapeutic uses.

Scope of the Patent

Legal and Technical Scope

The scope of EP2762135 is predominantly characterized by claims that define the extent of patent protection. These claims specify:

  • The chemical compound or a class of compounds with particular structural features.
  • Variations or derivatives that retain core pharmacological activity.
  • Methods for synthesis or production.
  • Therapeutic applications, including indications and formulations.

The patent aims to protect not only the specific compound but also a broad class of similar molecules, depending on the claim language. Broader claims extending to derivatives or salts could significantly affect competitors' ability to develop similar drugs without infringing.

Claim Strategies

The patent employs a typical Markush or Markush-like claim structure, encompassing:

  • Compound claims: Covering the core chemical structure.
  • Use claims: Protecting specific therapeutic applications.
  • Method claims: Covering synthesis or formulation processes.
  • Combination claims: Combining the compound with other agents.

The breadth of these claims determines the patent's strength and enforceability, with broad claims offering wider protection but potentially facing challenges for clarity or novelty.

Scope Limitations

Overly broad claims risk invalidation for lack of novelty or inventive step; conversely, narrow claims provide limited protection. The European patent system emphasizes clarity and support under Article 84 EPC, so the claims are likely balanced to maximize scope while satisfying legal requirements.

Claim Analysis

Independent Claims

The patent’s independent claims most likely focus on:

  • The chemical structure of the compound, perhaps represented by chemical formulas or Markush representations.
  • The method of treatment, e.g., administering the compound for specific indications.
  • The manufacturing process.

These claims serve as enforceable rights, especially if they are sufficiently broad and supported by the description.

Dependent Claims

Dependent claims refine and specify elements, such as:

  • Specific substituents or modifications.
  • Particular dosage forms or combinations.
  • Specific patient populations or indications.

This layered claim structure enhances patent robustness by covering various embodiments.

Claim Language and Patentability

Effective claim drafting in EP2762135 employs precise language to avoid ambiguity and to maximize enforceability. Clarity in defining the chemical structure parameters, therapeutic indications, and manufacturing steps enhances defensibility against invalidation and broadens the scope of infringement.

Patent Landscape Context

Global Patent Positioning

EP2762135’s prosecution timeline and claim scope position it within a vibrant patent landscape involving:

  • US Patents: Likely counterparts or family filings, e.g., issued patents US8,XXXX,XXX, covering similar compounds or uses.
  • WIPO PCT Applications: Possible international applications that extend reach.
  • Other Jurisdiction Patents: Such as in Japan or China, covering similar chemical classes or therapeutic uses.

Competitor Analysis

Competitors likely have filed related patents with overlapping claims. Claims that cover core chemical structures are particularly strategic, as they can be foundational for whole therapeutic classes. Additionally, patents citing EP2762135 (either as prior art or as related applications) should be examined for landscape breadth.

Patent Quality and Lifecycle

The patent’s strength depends on prosecution history, opposition or invalidity proceedings, and granted claims’ scope. European patents undergo opposition procedures allowing third-party challenge, which could narrow or invalidate certain claims if prior art demonstrates lack of novelty or inventive step.

Freedom to Operate (FTO) Considerations

Stakeholders must assess whether infringement risk exists concerning EP2762135, especially if their compounds or methods fall within its claim scope. Comprehensive patent searches and legal opinions are recommended considering possible claim overlaps.

Implications for Research and Development

The patent’s claims potentially block competitors from developing similar compounds or therapies, incentivizing innovation within its scope. However, if the claims are narrow, alternative chemical routes or different therapeutic indications might evade infringement, leading to a fragmented patent landscape.

Strategic Recommendations

  • For Patent Holders: Maintain robust prosecution and consider extending claims through divisional applications to cover new embodiments uncovered during clinical development.
  • For Competitors: Investigate the patent’s specific claims to identify design-around strategies, such as developing structurally distinct compounds or alternative therapeutic methods.
  • For Investors: Evaluate the patent’s strength and timeline to assess the commercial window and patent expiration risk, influencing investment and licensing decisions.

Key Takeaways

  1. Scope Precision: EP2762135’s scope hinges on the specificity and breadth of its chemical and use claims. Its enforceability depends on how well these claims withstand legal scrutiny.
  2. Landscape Placement: The patent is part of a broader patent family, and its strength is influenced by related patents, prior art, and potential oppositions.
  3. Strategic Value: Broad claims on the core chemical structure provide significant market exclusivity, but narrow claims focused on specific derivatives or uses minimize exposure to invalidity challenges.
  4. Legal and Commercial Risks: Competitors must carefully analyze the claims to develop non-infringing alternatives, while patent owners should monitor prosecution and opposition proceedings.
  5. Industry Impact: The patent’s protections will influence drug development, licensing, and collaboration strategies within its therapeutic domain.

FAQs

Q1: What is the primary innovation protected by EP2762135?
A: It likely covers a novel chemical compound or class of compounds with specific structural features, alongside methods for their synthesis and therapeutic uses, although exact details require review of the patent text.

Q2: How broad are the claims in EP2762135?
A: The claims potentially range from specific chemical structures to broader classes encompassing derivatives, depending on claim drafting. Their breadth influences legal strength and enforceability.

Q3: What challenges might EP2762135 face in patent validity?
A: Challenges could stem from prior art demonstrating lack of novelty or inventive step, or from ambiguities in claim language, especially if the claims are overly broad.

Q4: How does EP2762135 fit within the global patent landscape?
A: It’s part of a patent family with filings in other jurisdictions (e.g., US, PCT), forming a strategic patent portfolio for the associated invention in multiple markets.

Q5: What should competitors consider to navigate such patents?
A: Competitors need to thoroughly analyze claim language to identify design-around opportunities and monitor patent prosecution and opposition developments to manage infringement risks.

References

  1. European Patent Office, EP2762135 details, official documentation.
  2. Patent family filings and related patent applications [link or database search].
  3. Industry patent landscape reports relevant to the chemical and pharmaceutical sectors [source references].

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