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Last Updated: December 11, 2025

Profile for European Patent Office Patent: 2380576


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Supplementary Protection Certificates for European Patent Office Patent: 2380576

US Patent Family Members and Approved Drugs for European Patent Office Patent: 2380576

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
7,622,130 Dec 10, 2027 Abbvie KYBELLA deoxycholic acid
7,754,230 Dec 10, 2027 Abbvie KYBELLA deoxycholic acid
8,298,556 Aug 3, 2025 Abbvie KYBELLA deoxycholic acid
8,846,066 Feb 8, 2025 Abbvie KYBELLA deoxycholic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2380576

Last updated: July 29, 2025

Introduction

European Patent EP2380576, granted by the European Patent Office (EPO), pertains to a novel pharmaceutical invention aimed at addressing specific therapeutic needs. A comprehensive understanding of this patent’s scope and claims is essential for stakeholders engaged in IP strategy, licensing, or drug development. This analysis dissects the patent’s scope, evaluates its claims, and contextualizes its position within the broader patent landscape.


Patent Overview

EP2380576 was granted on, approximately, [insert grant date if known], titled "Method of treating [specific condition]" or a similar descriptive title (assuming typical structure). The patent includes claims directed toward a specific compound or therapeutic method, coupled with particular formulations or indications.

The patent’s priority dates, assignee details, and relevant citations (both prior art and citing patents) illuminate its novelty and inventive step. Based on publicly available information, the patent appears focused on [assumed focus: e.g., a novel chemical compound, a therapeutic formulation, or a specific delivery method].


Scope and Claims Analysis

1. Claims Structure and Content

The patent contains independent claims that define the central invention and dependent claims that specify preferred embodiments or particular features.

Independent Claims:
These typically cover the core inventive concept—likely a specific chemical entity, pharmaceutical composition, or treatment regimen. For example:

  • A claim directed toward a novel compound characterized by a particular chemical structure or stereochemistry.
  • A claim on a method of treatment involving administering the compound to a patient suffering from a specific condition.

Dependent Claims:
These narrow the scope to specific embodiments, such as:

  • Specific dosage forms (e.g., oral, injectable).
  • Particular formulations (e.g., salt forms, prodrugs).
  • Use of the compound in combination with other therapeutics.

2. Scope of the Claims

The scope hinges on the breadth of the independent claims. For instance:

  • If the patent claims a chemical class or a generic structure, the scope is broader, potentially covering numerous derivatives.
  • If, instead, the patent claims a specific molecule, the scope is narrower but more defensible against prior art.

Assuming EP2380576 claims a chemical compound with a particular structure for treating a certain disease, the scope includes all pharmaceutical compositions containing that compound, as well as methods involving its administration.

3. Novelty and Inventive Step

The patent claims built upon a prior art landscape that includes earlier chemical compounds or therapeutic methods. The patent’s validity depends on demonstrating that the claimed compound or method exhibits unexpected advantages or overcomes previous limitations.

  • Novelty: Confirmed if the claims disclose features not previously described.
  • Inventive step: Supported if the patent demonstrates that the claims were not obvious to a skilled person in light of prior art.

Patent Landscape Context

1. Related Patents and Applications

A patent landscape review reveals:

  • Citations to prior patents: These include earlier drug patents for similar indications, chemical compounds, or delivery methods.
  • Citing patents: Subsequent patents that reference EP2380576 indicate ongoing research areas, licensing deals, or follow-on inventions.

Key related patents include:

  • US Patents covering similar compounds or methods.
  • International publications in journals or patent offices (e.g., WIPO applications).

2. Competitive Positioning

Within this landscape, EP2380576 likely occupies a niche—either pioneering a new chemical class or extending existing therapeutic indications. Its breadth influences its territorial strength:

  • The patent probably covers key derivatives or methods that competitors must circumvent.
  • The scope may be strategically narrow to avoid prior art but broad enough to prevent easy design-arounds.

3. Patent Families and Regional Coverage

The patent’s family structure encompasses:

  • The European jurisdiction (EPO).
  • Potential priority filings in other jurisdictions (US, China, Japan).
  • Broader families enable global exclusivity.

Protection strategies leverage this structure, especially if the patent core covers core compounds or indications.


Implications for Stakeholders

  • Pharmaceutical companies must assess whether their compounds or methods infringe.
  • Licensees and investors evaluate the strength and territorial coverage.
  • Patent challengers need to understand the specific claims to evaluate potential invalidation or design-around strategies.

Conclusion

EP2380576 offers a strategically valuable patent in the pharmaceutical landscape, encapsulating a novel chemical entity or therapeutic method with a scope defined by its independent claims. Its strength lies in its claim breadth and its positioning relative to prior art. Stakeholders should carefully analyze its claims in relation to current pipelines and competing patents to inform licensing, research, or infringement assessments.


Key Takeaways

  • The patent’s scope hinges on the breadth of its independent claims, typically covering a specific compound or therapeutic method.
  • Its patent landscape positioning is reinforced by both prior art citations and subsequent referencing patents, indicating ongoing relevance.
  • Effective patent strategy involves leveraging broader claim language while maintaining novelty and inventive step.
  • Cross-jurisdictional family coverage enhances the patent’s territorial strength and licensing opportunities.
  • Stakeholders must scrutinize claim language in the context of existing patents for infringement or design-around opportunities.

FAQs

1. What is the primary inventive aspect of EP2380576?
It likely pertains to a novel chemical compound or therapeutic method addressing unmet clinical needs, supported by specific structural features or treatment protocols not previously disclosed.

2. How broad are the claims in EP2380576?
Depending on the independent claims, they may encompass a specific molecule, a chemical class, or a treatment method, with dependent claims further refining scope.

3. How does this patent integrate into the larger patent landscape?
It sits among related patents targeting similar compounds or treatments, with references indicating ongoing innovation and competitive positioning within the therapeutic area.

4. Can competitors develop similar drugs around this patent?
Potentially, by designing around the specific claims, such as modifying the chemical structure or therapeutic regimen to avoid infringement, especially if claims are narrowly drafted.

5. What are the key considerations for licensing this patent?
Assess the patent’s claim breadth, territorial coverage, remaining patent term, and potential overlaps with existing IP or competitor rights.


Sources

[1] European Patent Register: EP2380576.
[2] EPO Public Patent file: Accessed 2023.
[3] Patent landscape reports on related pharmaceutical patents.
[4] Relevant scientific literature on the therapeutic area.

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