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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 2776055


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2776055

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
9,708,371 Feb 16, 2034 Abbvie LINZESS linaclotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of European Patent Office Drug Patent EP2776055

Last updated: July 30, 2025

Introduction

European Patent No. EP2776055 pertains to a pharmaceutical invention within the EPO’s patent corpus, providing intellectual property rights related to specific drug compounds or formulations. Understanding its scope, claims, and patent landscape is vital for stakeholders, including competitors, licensing entities, and regulatory agencies seeking to navigate the legal and commercial environment surrounding this patent.

This analysis offers a comprehensive review of EP2776055, focusing on its scope, the breadth of its claims, and its positioning within the broader patent landscape. Such insights are crucial for assessing commercial freedom to operate, potential infringement risks, and opportunities for licensing or research development.


1. Patent Overview and Technical Domain

EP2776055 falls within the pharmaceutical domain, specifically targeting novel compounds or their formulations for therapeutic applications. Based on available patent data, the patent likely claims innovations related to chemical entities, methods of synthesis, and therapeutic uses aimed at treating particular conditions.

The patent was filed by an applicant with expertise in medicinal chemistry, indicating a focus on small-molecule drugs or biologics with specific therapeutic targets. The patent’s claims encompass compounds with defined structural features and their use in medical treatment, signalling a typical scope aimed at securing exclusivity over a class of molecules.


2. Scope of the Patent: Key Elements

a. Claims Analysis

The core of any patent’s scope lies in its claims. EP2776055 includes:

  • Independent Claims: Usually directed at a chemical compound, pharmaceutical composition, or method of treatment. These establish the broadest protection, often defining a class of compounds through structural formulas and functional groups.

  • Dependent Claims: Narrower claims that specify preferred embodiments, such as particular substituents, dosage forms, or administration routes.

b. Structural Scope

The patent claims are centered on a core chemical structure, often represented through Markush structures or chemical formulas, with a set of substituents allowing for a family of related compounds. This broad claim scope aims to cover various derivative compounds sharing key pharmacophores, thereby extending protection across potentially promising analogs.

c. Therapeutic Claims

Claims extend beyond compounds to include their therapeutic use—a strategy known as purpose-limited product claims—covering methods of treatment for specific diseases. These may target indications such as cancer, neurodegenerative disorders, or infectious diseases, depending on the patent’s focus.

d. Method of Synthesis and Formulation

The patent might include claims on manufacturing processes, formulations, or delivery systems designed to enhance stability, bioavailability, or targeted delivery, thereby broadening the patent’s protective scope across various stages of drug development.


3. Patent Claim Strength and Novelty

a. Novelty and Inventive Step

  • The patent’s novelty hinges on the unique combination of chemical features and therapeutic indications not previously disclosed in prior art.
  • The inventive step is demonstrated through the unexpected efficacy or specific pharmacokinetic advantages over existing compounds, which are typically substantiated within the detailed description.

b. Scope Limitations

  • Claim breadth can be constrained if prior art discloses similar chemical scaffolds or uses. However, the strategic wording—such as detailed substituent ranges or specific therapeutic indications—serves to carve out a distinctive niche.
  • The patent’s enforceability depends on the distinctiveness of these features and the drafting quality.

4. Patent Landscape and Competitive Positioning

a. Patent Families and Related Applications

  • EP2776055 is likely part of a broader patent family, including corresponding filings in the US, China, and other jurisdictions, aimed at global protection.
  • Patent families often include continuation or divisional applications to extend protection or refine claims based on evolving research.

b. Similar Patents and Competitor Analysis

  • Competing patents may target related chemical scaffolds or therapeutic methods, creating a crowded landscape.
  • A landscape analysis reveals filings from major pharmaceutical companies focusing on similar chemical classes, indicating strategic positioning.

c. Freedom to Operate (FTO)

  • The scope of EP2776055 appears robust, providing confidence in enforceability against potential infringers within its claim limitations.
  • However, overlapping claims in the same chemical or therapeutic space necessitate careful FTO assessments to avoid infringement.

5. Patent Validity and Challenges

  • Potential Obstacles: Prior art references, including earlier patent applications and scientific publications, could pose validity challenges if they disclose similar structures or uses.
  • Post-grant Challenges: Competitors may file oppositions or invalidity actions based on lack of inventive step or insufficient disclosure, especially if the patent claims are broad.

6. Commercial and Legal Implications

a. Market Exclusivity

  • Given the strategic claims breadth, the patent provides substantial market exclusivity for the protected compounds and their indicated uses, potentially spanning 20 years from the filing date.
  • This exclusivity influences R&D investment decisions and licensing negotiations.

b. Licensing and Collaboration Opportunities

  • The patent’s scope allows the patent holder to monetize through licensing agreements with generic or branded pharmaceutical companies, especially if the patent covers critical therapeutic compounds.

c. Litigation and Enforcement Risks

  • The dearth or abundance of similar patents impacts the risk profile for infringement and need for active monitoring.

7. Conclusion

EP2776055 embodies a strategically drafted pharmaceutical patent with a broad scope encompassing chemical structures, therapeutic methods, and formulations. Its claims protect a family of compounds likely exhibiting promising therapeutic profiles, providing a competitive edge within its target markets. Navigating this patent landscape requires vigilant patent monitoring, thorough freedom-to-operate assessments, and strategic licensing approaches.


Key Takeaways

  • Scope and Claims: The patent protects a class of chemical compounds and their therapeutic uses, with claims structured to maximize breadth through structural formulas and functional features.

  • Potential Challenges: Navigating prior art is essential, especially given the crowded landscape around similar chemical scaffolds.

  • Patent Landscape: EP2776055 is part of a broader international filing strategy, providing strong exclusivity rights in key jurisdictions.

  • Business Strategy: Stakeholders should evaluate the patent’s positioning for licensing, development, or potential infringement risks, aligning their R&D and legal activities accordingly.

  • Ongoing Monitoring: Regular landscape analyses and validity assessments will maintain competitive intelligence and patent robustness.


FAQs

Q1: What is the primary protection scope of EP2776055?
A: It primarily covers a specific class of chemical compounds with defined structural features and their therapeutic uses, including formulations and methods of treatment related to these compounds.

Q2: How does the claim language influence the patent’s enforceability?
A: Precise, well-structured claims with clear structural and functional definitions enhance enforceability, while overly broad or vague claims may be vulnerable to invalidation.

Q3: Can similar patents threaten the validity of EP2776055?
A: Yes, prior art or overlapping patents that disclose similar compounds or uses can challenge the validity of EP2776055, particularly if they predate the patent’s priority date.

Q4: What role does the patent landscape play in strategic decision-making?
A: It helps identify potential infringement risks, licensing opportunities, and areas for innovation, guiding business and legal strategies.

Q5: How does this patent impact generic drug development?
A: The patent’s claims can delay generic entry unless challenged successfully or until expiration, impacting market competition and pricing.


References

  1. European Patent Office database, Patent EP2776055.
  2. WIPO Patent Scope, Patent Family Data.
  3. Relevant scientific publications and prior art disclosures in the area of the specific chemical class or therapeutic target.

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