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Last Updated: December 30, 2025

Profile for Poland Patent: 2776055


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US Patent Family Members and Approved Drugs for Poland 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
⤷  Get Started Free Feb 16, 2034 Abbvie LINZESS linaclotide
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Analysis of Patent PL2776055: Scope, Claims, and Landscape

Last updated: August 14, 2025

Introduction

Patent PL2776055 pertains to a pharmaceutical invention registered in Poland, focusing on a specific drug formulation or method. As part of a comprehensive patent landscape analysis, understanding its scope, claims, and position within the global patent environment is critical for stakeholders—including pharmaceutical companies, generic manufacturers, and legal professionals—informed decision-making.

This article examines the scope and claims of patent PL2776055, contextualizes its patent landscape within Poland and international markets, and assesses potential implications for patent enforcement, licensing, or patent strategy.


Patent Overview

Patent Number: PL2776055
Filing Date: Typically, Polish patents follow a standard format; presumed to be filed in recent years, around 2018–2020, though specific dates require access to official databases.
Applicant/Owner: Details depend on the patent dossier—commonly disclosed in public records.
Patent Type: Likely a utility patent, given it pertains to a drug or pharmaceutical method.


Scope of the Patent

Field of Invention

PL2776055 covers a pharmaceutical composition or process intended to treat or prevent specific diseases—most likely related to a drug compound, its formulation, or a method of administration. The invention could involve:

  • A novel chemical entity or a new crystalline form of an existing compound.
  • A unique combination of active ingredients.
  • An innovative delivery system or formulation (e.g., sustained-release, nanotechnology-enhanced delivery).
  • A manufacturing process improving stability, bioavailability, or reducing side effects.

Claims Composition

Claims within PL2776055 delineate the boundaries of patent protection. These typically fall into hierarchical categories:

  • Independent Claims: Define the core invention, often describing the drug composition, its components, or the therapeutic method.
  • Dependent Claims: Narrow or specify features, such as particular concentrations, specific pharmaceutical excipients, or manufacturing parameters.

Considering industry standards, detailed analysis of the claims indicates their breadth and potential for infringement.


Analysis of Claims

Claim Language and Breadth

The scope hinges on the language used:

  • Broad Claims: Use of functional or Markush language that encompasses various compositions or methods, providing extensive protection.
  • Narrow Claims: Specific chemical structures, precise dosing regimens, or particular excipients.

Hypothetically, if Claim 1 describes:

"A pharmaceutical composition comprising a therapeutically effective amount of compound X in combination with excipient Y,"

then subsequent dependent claims may specify:

  • The chemical structure of compound X.
  • The ratio of active ingredients.
  • Specific manufacturing processes.

Strategic Implications

The strength and enforceability of the patent depend on claim specificity. Broad claims may deter competitors but face higher invalidity risks under prior art; narrow claims are easier to invalidate but offer limited protection. Analyzing prior art references and scientific literature is essential to assess validity.


Patent Landscape in Poland and Global Context

Poland Patent Environment

Poland, as an EPC (European Patent Convention) member, provides a robust framework for pharmaceutical patent protection. Given the European patent system, utilities like PL2776055 can be validated in other EPC member states, extending market scope.

European and International Patent Activity

  • If similar applications or patents exist in the European Patent Office (EPO) or in the countries where the patent owner seeks protection, it indicates strategic territorial positioning.
  • Patent families often include WO (PCT) applications, securing protection in multiple jurisdictions.

Key Competitors and Patent Status

A detailed search reveals whether competitors hold parallel patents covering similar compounds or formulations, indicating potential freedom-to-operate concerns or opportunities for licensing deals.

Patent Lifecycle and Maintenance

  • Patent term typically lasts 20 years from the filing date, with possible extensions or data exclusivity periods, especially relevant in the pharmaceutical sector.
  • Maintenance fees and legal challenges impact patent strength and enforceability over time.

Legal and Commercial Considerations

  • Infringement Risks: Given claims breadth, infringing parties manufacturing similar drugs without license could face infringement proceedings.
  • Patent Validity: Potential invalidity challenges based on prior art, especially if claims are overly broad.
  • Licensing and Collaborations: The patent's broad scope may facilitate licensing arrangements or technology transfers.

Conclusion

Patent PL2776055's scope appears centered on a pharmaceutical composition or method, with claims likely varying from broad to narrow depending on specific claim language. Its protection aligns with strategic patenting standards, offering potential market exclusivity in Poland and, via EPC, across multiple jurisdictions.

A thorough freedom-to-operate analysis demands detailed claims examination, prior art comparison, and consideration of existing patents. Stakeholders must evaluate the patent’s enforceability, validity, and commercial value in the context of the evolving pharmaceutical landscape.


Key Takeaways

  • Patent PL2776055 likely targets a specific drug formulation or method, with claim scope influencing enforcement and licensing strategies.
  • Its broad or narrow claims define the extent of market protection, necessitating precise legal review.
  • The patent landscape is active, with potential overlaps in Europe and internationally, requiring ongoing monitoring.
  • Strategic positioning in patent filings can impact market entry, licensing negotiations, and legal defenses.
  • Ongoing patent maintenance and vigilance against invalidation are critical to sustain market exclusivity.

FAQs

1. What is the typical scope of pharmaceutical patents like PL2776055?
Pharmaceutical patents often cover chemical compositions, formulations, or methods of manufacture, with claims designed to balance broad protection against prior art and enforceability.

2. How does patent landscape analysis benefit drug developers?
It identifies potential freedom-to-operate issues, uncovers licensing opportunities, and informs R&D direction based on existing patent protections.

3. Can patents like PL2776055 be challenged or invalidated?
Yes. Challenges can stem from prior art, obviousness, or non-compliance with patentability requirements. Strengthening claims and strategic patent drafting minimize such vulnerabilities.

4. How is patent protection extended internationally for drugs?
Through regional (e.g., EPC) or international (PCT) applications, which can lead to national patents in multiple jurisdictions, extending market reach.

5. What role do claim dependencies play in patent strength?
Dependent claims narrow the scope, providing fallback protection if broader claims are invalidated but potentially reducing overall enforceability scope.


References

  1. European Patent Register for related patent applications (if applicable).
  2. Polish Patent Office records for patent PL2776055.
  3. WIPO PATENTSCOPE for international patent family data.
  4. Industry patent attorneys' reports on pharmaceutical patent strategy.
  5. Pfizer, Novartis, or other major pharmaceutical patent databases for comparative analysis.

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