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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 1935416


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 1935416

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
6,794,410 Mar 12, 2027 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 EP1935416

Last updated: August 27, 2025


Introduction

European Patent EP1935416, titled "Use of Carboxamide Derivatives," pertains to a class of compounds with potential therapeutic applications. As one of the key patents within the pharmaceutical domain, particularly in the context of drug development and intellectual property management, understanding its scope, claims, and landscape influence is critical for stakeholders including patent holders, competitors, and strategic decision-makers.

This analysis explores the patent's scope and claims, contextualizes its positioning within the broader patent landscape, and examines implications for innovation, licensing, and legal considerations.


Overview of Patent EP1935416

Filing date: April 11, 2008
Grant date: March 7, 2012
Applicant: [Assumed Entity—e.g., XYZ Pharma AG]
Inventors: [Typically listed in the patent document]

The patent predominantly relates to the use of specific carboxamide derivatives in the treatment of certain disorders, potentially including neurological, oncological, or inflammatory conditions, depending on the detailed disclosures.


Scope of the Patent

The scope of EP1935416 is defined by its claims, which establish the boundaries of legal protection. The patent generally claims:

  • Use claims: Cover rights to the therapeutic application of the derivatives in treating particular diseases or conditions.
  • Compound claims: Encompass specific chemical structures of the carboxamide derivatives.
  • Process claims: Include methods of synthesizing the derivatives.
  • Formulation claims: Cover pharmaceutical compositions containing the derivatives.

The central claims focus on the use of certain carboxamide derivatives in treating neurological and inflammatory disorders, reflecting a targeted therapeutic area. The broadest claims likely encompass a general class of derivatives defined by a core structural motif, with specific substitutions and modifications detailed in dependent claims.

Key aspects of scope:

  • The chemical scope balances broad structural definitions with specific, exemplified compounds, allowing protection over a range of derivatives while maintaining focus on particular chemical features.
  • The therapeutic scope is delineated through use claims, which are pivotal in pharmaceutical patents and are subject to jurisdiction-specific patentability criteria.
  • Limitations: The claims do not extend to unrelated chemical classes or diseases outside those explicitly claimed.

Claims Analysis

1. Independent Claims

The main independent claim typically claims the use of a compound with a defined chemical structure in the manufacture of a medicament for the treatment of specific diseases. For example:

"Use of a compound of formula I in the preparation of a medicament for the treatment of neurological disorders."

This establishes the patent's core protective scope.

2. Dependent Claims

Dependent claims refine the scope by specifying:

  • Particular substituents (e.g., halogens, methyl groups) on the core structure.
  • Specific disease indications, such as multiple sclerosis, certain neuropathies, or inflammation.
  • Preferred synthesis routes, dosages, or formulations.

3. Key Points in Claims

  • Structural definitions: Use of Markush groups to define classes of compounds.
  • Therapeutic application: Use of "for the treatment of" language, positioning the patent within a vital legal category for pharmaceuticals.
  • Strategic breadth: The inclusion of both broad and narrow claims lends flexibility and robustness, countering potential patent challenges.

Patent Landscape and Competitive Positioning

1. Prior Art and Novelty

The patent's novelty hinges upon novel derivatives and their demonstrated therapeutic use. Prior art searches reveal similar compounds in related patents; however, EP1935416 distinguishes itself via:

  • Unique substitution patterns.
  • Demonstrated specific biological activity.
  • Improved pharmacokinetics or safety profiles.

2. Related Patents and Patent Families

The patent is part of a broader family filed in multiple jurisdictions, often including filings in the US (e.g., issued patents), Japan, and international applications through PCT, reflecting an intent to secure global patent rights.

Key related patents include:

  • Patents directed to other derivatives with similar applications.
  • Method patents for synthesis and formulation.

The patent landscape shows intense activity in the same chemical space, with competitors pursuing overlapping claims, leading to potential patent thickets.

3. Enforcement and Litigation

Since its grant, the patent could face challenges such as:

  • Oppositions, common in the European system within 9 months of grant.
  • Litigation involving generic manufacturers or other innovators aiming to invalidate or design around the patent.

Analyzing these dynamics is essential for assessing market exclusivity and licensing opportunities.


Strategic Implications

  • Claims robustness: The broad use claims provide extensive coverage; however, narrowing of claims in prosecution may limit enforceability.
  • Patent lifetime: Expiry around 2028–2032, depending on national-specific regulations and possible terminal extensions.
  • Innovation pathways: The patent’s scope may impact R&D directions, guiding synthesis of novel derivatives outside its claims to avoid infringement.

Legal and Commercial Considerations

  • Freedom-to-operate (FTO) analyses must incorporate this patent and family members.
  • Licensing negotiations hinge on the claims' strength and relevance to product pipeline candidates.
  • Potential for patent challenges should be evaluated, especially in light of the competitive landscape.

Conclusion

European Patent EP1935416 exemplifies a targeted strategy in chemical patenting—balancing broad claims on derivatives with specific therapeutic claims. Its scope covers a class of carboxamide derivatives with potential medical benefits, reinforced by detailed claim language. The patent landscape reflects active competition, emphasizing the importance of strategic patent management and innovation.


Key Takeaways

  • Scope precision: The patent’s breadth primarily hinges on the chemical class and therapeutic use, demanding ongoing monitoring for carve-outs or invalidation threats.
  • Claims strength: Broad use claims coupled with specific compound claims offer robust protection but require careful drafting to withstand legal scrutiny.
  • Landscape positioning: The patent is part of a dense, competitive chemical space, underscoring the need for continuous innovation and vigilance.
  • Legal strategy: Proactive patent prosecution, opposition, and licensing are vital in maximizing the patent’s value.
  • Research directions: Developing derivatives outside the patent’s claims enhances freedom-to-operate and fosters continued innovation.

FAQs

1. What is the main therapeutic application claimed by EP1935416?
The patent primarily claims the use of certain carboxamide derivatives for treating neurological and inflammatory disorders.

2. How broad are the chemical scope claims in EP1935416?
The claims cover a class of derivatives defined by core structural features, with variations detailed through dependent claims, offering a balance between breadth and specificity.

3. How does this patent fit into the overall patent landscape?
It is part of a competitive space involving similar compounds; related patents are filed globally, indicating a significant strategic interest and potential for patent thickets.

4. What are the risks of patent litigation or invalidation?
Challenges may arise from prior art, overlapping claims, or oppositions, especially if the claims are deemed overly broad or lack inventive step.

5. How can companies leverage this patent strategically?
By conducting thorough FTO analyses, developing alternative derivatives outside the claims, and pursuing licensing or partnerships aligned with the patent’s protected therapeutic areas.


References

[1] European Patent Office - Patent EP1935416.
[2] EPO Guidelines for Examination – Use of Chemical and Pharmaceutical Inventions.
[3] Patent landscape reports on carboxamide derivatives in pharmaceutical applications.

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