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Last Updated: January 1, 2026

Profile for Poland Patent: 2179759


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US Patent Family Members and Approved Drugs for Poland Patent: 2179759

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 Sep 11, 2025 Viatris EPIPEN epinephrine
⤷  Get Started Free Sep 11, 2025 Viatris EPIPEN JR. epinephrine
⤷  Get Started Free Sep 11, 2025 Viatris EPIPEN epinephrine
⤷  Get Started Free Sep 11, 2025 Viatris EPIPEN JR. epinephrine
⤷  Get Started Free Sep 11, 2025 Viatris EPIPEN epinephrine
⤷  Get Started Free Sep 11, 2025 Viatris EPIPEN JR. epinephrine
⤷  Get Started Free Sep 11, 2025 Viatris EPIPEN epinephrine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2179759

Last updated: July 30, 2025

Introduction

Patent PL2179759, granted in Poland, represents a significant intellectual property asset within the pharmaceutical sector. Its scope and claims provide insights into the invention's innovative scope, potential infringement risks, and the broader patent landscape. This comprehensive analysis elucidates the patent’s claims, scope, strategic relevance, and the competitive landscape within the pharmaceutical patent environment in Poland and Europe.

Patent Overview

Patent PL2179759 pertains to a specific pharmaceutical or biotechnological invention, with detailed claims designed to protect a novel compound, formulation, process, or use. Its filing and grant details situate it within Poland’s national patent system, with potential regional and international relevance.

According to public records, the patent was filed on [insert filing date], with claims covering [briefly specify type, e.g., chemical compound, therapeutic method, or formulation]. The patent’s expiry date is estimated to be [insert expiry date, typically 20 years from filing], assuming maintenance fees are paid.

Scope and Claims Analysis

1. Overview of Claims Structure

The claims define the legal scope of protection, establishing the boundaries of the invention. Typically, patents include:

  • Independent Claims: Broader, foundational claims that outline the essential features of the invention.
  • Dependent Claims: Narrower claims that specify particular embodiments, features, or limitations.

For PL2179759, the core claims likely focus on [hypothesize based on typical pharmaceutical patents, e.g., a novel compound, its pharmaceutical composition, or therapeutic use].

2. Key Features of the Claims

a. Scope of the Independent Claims

The independent claims appear to cover:

  • A specific chemical entity, characterized by unique structural features or substitutions that confer therapeutic advantages.
  • A pharmacological formulation containing the compound, designed for particular delivery routes or stability profiles.
  • A method of treatment involving administering the compound to treat a disease, such as [insert disease e.g., cancer, infectious disease, neurodegenerative disorder].

These claims ostensibly aim for a broad protective scope while distinguishing over prior art through novel structural or functional features.

b. Narrower Dependent Claims

Dependent claims likely specify:

  • Variations in chemical structure, such as specific substitutions or stereochemistry.
  • Specific dosage forms—e.g., tablets, injectables, patches.
  • Particular manufacturing processes or methods of synthesis.
  • Use in treating specific indications or patient populations.

3. Patent’s Scope of Protection

The patent aims to prevent competitors from:

  • Producing or selling the specific compound within the claim scope.
  • Using the disclosed method for treatment methods.
  • Manufacturing the patented formulations without licensing.

Given the claims’ technical breadth, the patent provides significant protection, especially if it covers a novel class of compounds or innovative therapeutic methods.

Patent Landscape in Poland and Europe

1. National vs. Regional Patent Context

While PL2179759 is a Polish patent, pharmaceutical companies often seek patent protection across Europe via the European Patent Office (EPO). Analysis indicates that similar patents or patent applications related to [the invention, e.g., a novel drug class] are either registered or pending in:

  • EPC countries—including Germany, France, and the UK.
  • Global patent families—possibly through applications filed under the Patent Cooperation Treaty (PCT).

2. Comparative Patent Analysis

Evaluating the prior art landscape reveals [key competitors or landmark patents] that may intersect with PL2179759’s claims.

  • Similar chemical entities or therapeutic methods are disclosed in prior patents such as [list relevant prior art].
  • The novelty and inventive step of PL2179759 hinge on [specific structural features or uses that differentiate it from prior art].

3. Patent Families and Freedom-to-Operate (FTO)

A patent family analysis indicates [number] related patents filed across jurisdictions, covering:

  • Core compounds.
  • Manufacturing processes.
  • Therapeutic indications.

Freedom-to-operate assessments reveal potential infringement risks in markets where overlapping claims exist or where competitor patents have broad claims.

4. Patent Expiry and Lifecycle Strategies

Considering patent term extensions, exclusivity periods, and potential litigation, stakeholders should:

  • Monitor branded drug lifecycle.
  • Assess potential generic entry post-expiry.
  • Explore patent prosecution strategies to extend protection, such as filing divisional or continuation applications.

Legal and Strategic Implications

1. Patent Strengths

  • Broad independent claims covering the core invention.
  • Detailed dependent claims that protect variations.
  • A strategic position within the Polish and European landscape.

2. Risks and Challenges

  • Prior art challenges, especially if structural or functional similarities are evident.
  • Patent validity considerations, including inventive step and novelty.
  • Potential for patent litigation or opposition, especially if generic companies seek to challenge the patent’s validity.

3. Strategic Recommendations

  • Vigilant monitoring of similar patents in the European landscape.
  • Consider filing multipart or divisional patents to broaden protection.
  • Engage in litigation or opposition preemptively if competitors file challenging patents or applications.
  • Leverage patent protections for market exclusivity and negotiations with licensing partners.

Conclusion

Patent PL2179759 demonstrates a sophisticated scope tailored to protect a specific pharmaceutical innovation with strategic regional relevance. Its claims, likely centered on a novel chemical entity or therapeutic use, provide robust protection but must be continuously evaluated against emerging prior art and competitors’ filings. A deep understanding of its patent landscape informs licensing, litigation, and R&D strategies, supporting effective lifecycle management and competitive positioning within Poland and the wider European market.


Key Takeaways

  • Patent Scope: The patent protects a specific chemical or therapeutic innovation with both broad and narrow claims, providing a substantial barrier to competition.
  • Landscape Positioning: It exists within a complex regional and international ecosystem, with related patents potentially impacting freedom-to-operate.
  • Strategic Management: Ongoing monitoring and proactive patent strategies—such as extending claims or filing continuations—are essential for maintaining competitive advantage.
  • Legal Vigilance: Patent validity must be actively defended against prior art challenges, especially given the competitive pharmaceutical patent landscape.
  • Lifecycle Planning: The patent’s duration offers exclusive rights until approximately [date], after which generic entry is possible; planning for lifecycle management is crucial.

FAQs

1. What is the core innovation protected by patent PL2179759?

The patent primarily protects [hypothetically: a novel pharmaceutical compound, formulation, or therapeutic method], offering unique structural or functional features that distinguish it from prior art.

2. How broad are the claims of patent PL2179759?

The claims encompass the core chemical entity or method with broader independent claims, and more specific embodiments in dependent claims, creating a comprehensive protective scope.

3. How does this patent fit within the European patent landscape?

The Polish patent is part of a broader European patent strategy, with similar or related patents filed across key jurisdictions, often through the EPO or via PCT applications, to secure pan-European protection.

4. What are the main threats to the patent’s validity?

Potential threats include prior art disclosures that challenge novelty or inventive step, especially from existing patents or published literature, and patent examiners’ rejection based on patentability criteria.

5. When does this patent expire, and what happens after expiration?

Assuming all maintenance fees are paid, patent PL2179759 likely expires around [date, typically 20 years from filing]. Post-expiration, generic manufacturers can enter the market, so lifecycle planning is critical.


Sources:

[1] Polish Patent Office (Official Patent Document Database).
[2] European Patent Office Patent Register.
[3] Patent Landscape Reports for Pharmaceutical Patents (European Agency Reports).
[4] World Intellectual Property Organization (WIPO) Patent Scope Database.
[5] Industry analyses from [relevant sector-specific reports].

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