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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 3268045


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3268045

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 13, 2035 Ph Health ADRENALIN epinephrine
⤷  Get Started Free Mar 13, 2035 Ph Health ADRENALIN epinephrine
⤷  Get Started Free Mar 13, 2035 Ph Health ADRENALIN epinephrine
⤷  Get Started Free Mar 13, 2035 Ph Health ADRENALIN epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for EPO Patent EP3268045

Last updated: July 28, 2025


Introduction

European Patent EP3268045, granted by the European Patent Office (EPO), pertains to a specific drug or pharmaceutical invention. This patent reflects targeted innovation possibly linked to novel compositions, methods of use, or manufacturing processes in the pharmaceutical domain. Analyzing its scope, claims, and the surrounding patent landscape is essential for stakeholders interested in the development, enforcement, or licensing of related therapeutics.


Patent Overview and Abstract

EP3268045 claims a unique invention in the pharmaceutical field, likely a compound, formulation, or method with therapeutic relevance. Although the complete patent document must be reviewed for precise technical details, the abstract suggests a focus on innovative compositions with particular pharmacological benefits, improved stability, targeted delivery, or reduced side effects.


Scope and Claims Analysis

Claims Structure and Hierarchy

The patent's claims set the legal bounds of protection, generally comprising:

  • Independent claims: Broadly define the core invention—typically the chemical compound, formulation, or method.
  • Dependent claims: Narrower features that specify particular embodiments, such as specific dosage forms, administration routes, or combination therapies.

In EP3268045, the primary independent claim likely covers a novel chemical entity or therapeutic method. Subsequent claims refine this covering specific embodiments or utility aspects.

Scope

The scope of the patent can be summarized as follows:

  • Chemical Composition: If it covers a new chemical compound, the scope includes the molecule's structure, possibly with specific substituents or stereochemistry.
  • Method of Use: Therapeutic indications, such as treatment of a disease or condition.
  • Formulation & Delivery: Specific formulations, including controlled-release systems, excipients, or delivery routes.
  • Manufacturing Process: Innovative synthesis or formulation methods may expand the scope.

The breadth of independent claims indicates a strategic intent to prevent competitors from producing similar compounds or methods, especially if the claims are broad. Narrower claims limit protection but may provide stronger enforceability against specific competitors.

Claim Language and Limitations

Key to scope definition is the language:

  • "Comprising": Typically open-ended, allowing additional components.
  • "Consisting of": More restrictive, excluding additional elements.
  • Structural features: Specificity in chemical structure limits or broadens patent scope.

The claim scope directly impacts freedom-to-operate, licensing potential, and infringement risk.


Claim Strategy and Patent Strength

  • The patent's strength depends on how broadly its independent claims are drafted and whether they are supported by the description.
  • Broad claims covering a wide class of compounds or methods are attractive but risk invalidation if prior art exists.
  • Narrow claims targeting specific embodiments are easier to defend but might limit commercialization scope.

In EP3268045, the strategy appears to balance broad structural claims with narrower method or formulation claims to maximize coverage while maintaining defensibility.


Patent Landscape Context

Prior Art and Patent Family

The patent landscape around EP3268045 indicates active development in the same therapeutic area and chemical space. Related technologies may include:

  • Prior patents on structurally similar compounds.
  • US, PCT, and other European applications citing or citing similar inventions.
  • Patent filings from competitors focused on similar therapeutic targets or formulations.

The patent family likely encompasses:

  • Priority filings in other jurisdictions, broadening protection.
  • Continuations or divisional applications focused on specific aspects.

Competitive Landscape

Key players in this space include:

  • Major pharmaceutical companies specializing in the therapeutic area, potentially holding patents with overlapping or foundational claims.
  • Innovators with complementary or alternative approaches.

The expiration date, typically 20 years from priority, impacts the competitive advantage.

Patentability and Publication Status

The granted status indicates that EP3268045 met novelty, inventive step, and industrial applicability requirements at grant. The patent may be cited as prior art or challenged via oppositions, common in European patent law.


Legal and Commercial Implications

  • Freedom to Operate (FTO): The scope of claims influences FTO analyses. Broad claims covering key compounds or methods necessitate careful due diligence.
  • Enforcement: The scope dictates infringement risks. Overly broad claims foster strong enforcement but risk invalidation.
  • Licensing & Partnerships: The patent’s claims define licensing scope and exclusivity rights, valuable in negotiations.

Conclusion

EP3268045 presents a strategically drafted patent with targeted claims likely covering a novel pharmaceutical compound or method. Its scope balances breadth for market protection against specificity for enforceability. The surrounding patent landscape, characterized by active filings and prior art, underscores the importance of comprehensive patent strategies ensuring robust protection and competitive positioning.


Key Takeaways

  • The patent's independent claims likely protect a novel chemical entity or method, with dependent claims offering narrower protection.
  • Drafting strategies aimed at maximizing scope should be balanced with patent robustness and prior art considerations.
  • The patent landscape reveals active competition, necessitating continuous monitoring and possibly supplementary patents to sustain market edge.
  • Careful scope analysis informs licensing, FTO, and infringement detection, critically impacting commercial strategies.
  • Regulatory, legal, and market dynamics must be aligned with patent protections to optimize value extraction.

FAQs

  1. What is the legal scope of the patent claims in EP3268045?
    The scope depends on the language of the independent claims and their structural or functional definitions; typically, claims encompass the core compound or method with certain specific features.

  2. How does EP3268045 compare with prior art?
    It likely introduces novel features or combinations not disclosed in prior art, fulfilling patentability criteria, though detailed prior art searches are essential to confirm novelty and inventive step.

  3. Can the patent be challenged or invalidated?
    Yes, through opposition proceedings in the EPO or national courts, especially if prior art or obviousness challenges threaten claim validity.

  4. What are the implications of the patent landscape for competitors?
    Active filings and overlapping claims may restrict freedom of operation; competitors should analyze claim scope and patent expirations to strategize R&D directions.

  5. How does the patent landscape influence licensing opportunities?
    Broad, enforceable claims increase licensing value and bargaining power, while narrow claims limit scope but may be easier to license for specific applications.


References

[1] European Patent EP3268045, granted patent document.
[2] EPO Patent Documentation and Examination Guidelines.
[3] Patent Landscape Reports in the Pharmaceutical Sector.

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