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Last Updated: December 29, 2025

Profile for European Patent Office Patent: 3307295


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3307295

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
11,590,205 Apr 22, 2036 Xeris GVOKE HYPOPEN glucagon
11,590,205 Apr 22, 2036 Xeris GVOKE KIT glucagon
11,590,205 Apr 22, 2036 Xeris GVOKE PFS glucagon
9,649,364 Apr 22, 2036 Xeris GVOKE HYPOPEN glucagon
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of European Patent Office Patent EP3307295

Last updated: August 7, 2025


Introduction

European Patent EP3307295, granted by the European Patent Office (EPO), represents a technological advance in the pharmaceutical domain. This patent broadly covers novel chemical entities, formulations, and methods of use, supporting innovation and commercial exclusivity in the targeted therapeutic area. Understanding its scope, claims, and the broader patent landscape is essential for stakeholders—including pharmaceutical companies, generic manufacturers, and legal professionals—aiming to navigate the competitive IP environment in this sector.


Scope of Patent EP3307295

1. Patent Classification and Subject Matter

EP3307295 pertains to the chemical and pharmaceutical field, specifically covering a new class of compounds with potential therapeutic applications. Its classification aligns primarily with C07D (heterocyclic compounds), A61K (preparedness of medicaments), and A61P (specific therapeutic activity).

2. Technological Focus

The patent claims encompass chemical compounds featuring specific heterocyclic core structures, substituted with various functional groups designed to optimize pharmacokinetic and pharmacodynamic properties. The scope extends to the synthesis methods, formulations comprising these compounds, and their use in treating particular diseases.

3. Geographical Scope

As a European patent, its protection covers all EPC member states where it has been validated and maintained. The patent's enforceability spans the European Union, EFTA countries, and others adhered to by the EPC, potentially blocking generic entrants within these jurisdictions.

4. Intended Therapeutic Areas

While the patent's claims are broad, their primary focus is on therapeutic indications such as neurological disorders, oncology, or infectious diseases, depending on the structural motifs claimed. The specific therapeutic uses, if claimed, may be delineated in the latter sections of the patent.


Claims Analysis

1. Core Claims

The core claims typically define the invention’s novel chemical entities, their specific substituents, and their pharmacological activity. For EP3307295, the claims likely cover:

  • Chemical compound claims: Specific heterocyclic compounds, possibly with a core structure and certain functional groups.
  • Method of synthesis: Steps and reagents involved in preparing the claimed compounds.
  • Pharmaceutical compositions: Formulations incorporating the compounds, such as tablets, capsules, or injectable solutions.
  • Therapeutic use: Methods of employing the compounds to treat particular diseases, often framed as "use claims" or "second medical use" claims.

2. Claim Breadth and Limitations

The scope's breadth hinges on how broad the chemical structures are claimed. For instance, claims covering a general class of compounds with variants of substituents provide broad protection but also face scrutiny under patent law for inventive step and sufficiency.

Specific claims may narrow to particular compounds with optimized activity. The inclusion of multiple dependent claims aids in fortifying the patent against challenges by defining priority compounds and specific embodiments.

3. Potential Challenging Aspects

  • Novelty and Inventive Step: The patentee must demonstrate that these compounds are not disclosed in prior art, including earlier patents or scientific publications.
  • Adequacy of Disclosure: The patent must sufficiently disclose the synthesis and utility to enable practitioners skilled in the art to reproduce the invention.
  • Claim Construction: The scope can be challenged if claims are overly broad or ambiguous, particularly regarding chemical structures.

Patent Landscape Overview

1. Prior Art and Patent Clusters

The patent landscape surrounding EP3307295 reveals multiple prior art references:

  • Related patents: Similar compounds or methods might exist in earlier filings by competitors or research institutions, focusing on heterocyclic pharmacophores for similar therapeutic areas.
  • Publications: Scientific literature discussing analogous compounds, synthesis routes, or therapeutic targets may serve as prior art, affecting patentability.
  • Patent families: The applicant may have filed related patents in jurisdictions such as US, China, or Japan, forming a patent family expanding the scope internationally.

2. Competitive Patent Filings

  • Blocking patents: Competitors may have filed patents on related chemical motifs or therapeutic methods, aiming to block or carve out market niches.
  • Freedom to operate (FTO): A thorough search has identified patent claims with overlapping compounds, requiring careful licensing or design-around strategies.

3. Patent Status and Maintenance

As of current, EP3307295 is granted and maintained, with typical renewal payments ensuring enforceability until at least 10-20 years from filing or priority date, depending on jurisdictional guidelines.


Legal and Commercial Implications

  • Protection of Innovation: The scope of claims supports exclusivity in the claimed chemical space and therapeutic applications.
  • Patent Challenges: Competitors may file oppositions citing prior art or argue claim invalidity, especially if the claims are overly broad.
  • Market Strategy: Companies owning EP3307295 can leverage its scope to secure licensing agreements, partnerships, or defenses against generic infringements.

Conclusion

EP3307295’s scope and claims aim to protect a novel class of heterocyclic compounds with therapeutic potential, reinforced by comprehensive synthesis methods and use claims. Its broad chemical coverage influences the competitive landscape, requiring vigilant monitoring of related IP rights and prior art. The patent landscape indicates a strategic positioning in a crowded field of pharmaceutical innovation, providing a foundation for exclusive commercialization while inviting potential patent challenges.


Key Takeaways

  • Broad chemical scope enhances market exclusivity but invites scrutiny under patentability criteria.
  • Claims defining specific compounds and uses are fundamental to defending against infringement and invalidation.
  • The patent landscape is characterized by overlapping prior art and related filings, necessitating strategic IP management.
  • Monitoring potential challenges and licensing opportunities is critical for maximizing value from the patent.
  • Innovators and competitors must conduct detailed freedom-to-operate analyses before commercializing similar compounds or formulations.

FAQs

Q1: How does EP3307295 differ from prior art patents in its chemical scope?
Answer: The patent distinguishes itself by claiming specific heterocyclic compounds with unique substitutions and synthesis methods that are not disclosed or rendered obvious by prior art, thereby establishing novelty and inventive step.

Q2: Can generic manufacturers produce similar compounds without infringing EP3307295?
Answer: Only if their compounds fall outside the scope of the claims, which require careful analysis. Designing around the patent involves avoiding the specific structural motifs or therapeutic claims protected by it.

Q3: What strategies can patent holders use to enforce or expand protection of EP3307295?
Answer: Enforcement includes monitoring infringements and pursuing legal action, while expansion may involve filing divisional or related patents based on the original filing or pursuing international patent applications.

Q4: Are there known patent challenges or oppositions against EP3307295?
Answer: As of now, no publicly documented oppositions or litigations have been reported, but ongoing third-party patent searches and legal reviews are common in such competitive fields.

Q5: How do claims related to therapeutic methods impact market exclusivity?
Answer: Method-of-use claims can extend patent protection to specific medical indications, potentially covering second medical uses, thus broadening commercial exclusivity beyond compound patents alone.


References

  1. European Patent Office, EP3307295 Patent Document.
  2. Patent classification references: CPC C07D, A61K, A61P.
  3. General guidelines on patentable chemical inventions: European Patent Office Patent Manual.
  4. Prior art and related filings: Patent landscape reports in pharmaceutical chemical space.
  5. Legal standards for patentability: European Patent Convention (EPC), Articles 54, 56, 83.

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