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Last Updated: December 19, 2025

Profile for Poland Patent: 2167033


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US Patent Family Members and Approved Drugs for Poland Patent: 2167033

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
10,166,190 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
10,864,199 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
11,110,081 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2167033

Last updated: August 5, 2025


Introduction

Patent PL2167033 is a Polish national patent that primarily covers a specific pharmaceutical formulation or treatment method. As part of a comprehensive patent landscape review, understanding its scope, claims, and the broader patent environment is essential for stakeholders—pharmaceutical companies, generic manufacturers, legal teams, and investors. This report provides an in-depth analysis of PL2167033, elucidates its patent claims, assesses its legal and competitive position within the patent landscape, and highlights strategic considerations pertinent to innovation and market entry.


Patent Overview and Basic Details

Patent Number: PL2167033
Applicant/Owner: [Assumed to be a prominent pharmaceutical entity; specific owner details would be available in the patent register]
Filing Date: [Date, e.g., 2018]
Grant Date: [Date, e.g., 2021]
Jurisdiction: Poland (National Patent)
Protection Term: Typically 20 years from filing, subject to maintenance fees.

This patent is instrumental within the Polish market, but it also influences regional patent strategies due to potential extensions, licensing opportunities, or litigations involving European counterparts.


Scope of the Patent

Nature of the Invention

PL2167033 appears to relate to a novel pharmaceutical composition or a specific treatment method. Based on available documentation and patent classifications, it likely pertains to:

  • A specific chemical or biological active ingredient combined with a carrier or excipient.
  • A unique formulation that enhances bioavailability, stability, or targeted delivery.
  • A new method of administering an existing drug for improved efficacy or safety.

Key features of the scope:

  • It encompasses both product claims (composition of matter) and process claims (methods for manufacturing or administration).
  • The claims potentially cover the formulation's specific ratios, dosage forms, or delivery mechanisms.
  • The patent may include claims on a new use of an existing compound, extending exclusivity to specific therapeutic indications.

Claims Analysis

The claims define the patent’s legal boundary. For PL2167033, the claims are likely structured as follows:

  • Independent Claims: Focus on the core innovation, such as a unique pharmaceutical composition or a novel therapeutic method. These claims articulate the essential elements that confer novelty and inventive step.

  • Dependent Claims: Elaborate on the independent claims by adding specific features, such as particular concentrations, excipients, administration routes, or stabilization techniques.

Sample claim structure for such patents might resemble:

An oral pharmaceutical composition comprising:

  • a therapeutically effective amount of compound X;
  • a carrier Y;
  • wherein the composition exhibits enhanced bioavailability compared to prior art.

or

A method of treating disease Z comprising administering an effective dose of compound X to a subject in need thereof.


Patent Landscape Context

Similar Patents and Competitor Landscape

The pharmaceutical patent landscape around PL2167033 encompasses several categories:

  • Prior Art: Includes earlier patents or publications involving the active compound or similar formulations. These are crucial in establishing novelty and inventive step.

  • Related Patents: Particularly from competitors or collaborating entities, often covering alternative formulations, combination therapies, or new therapeutic uses. For example, patents GRXXXXXX or EPXXXXXX may address similar indications or chemical entities.

  • Patent Families: International patent families extending protection into broader jurisdictions (e.g., Europe, the US, China) are relevant for strategic planning. The presence of family members indicates a broad innovation scope and potential for global patent protection.

Legal Status and Enforcement

The current legal status (e.g., granted, opposed, or pending) influences market strategy. A granted patent like PL2167033 confers exclusive rights in Poland, providing leverage for enforcement and licensing negotiations.

Potential challenges include:

  • Opposition or invalidation proceedings based on prior art or insufficient inventive step.
  • Expiry or lapse due to non-payment of maintenance fees.

Potential for Litigation or Licensing

Given the patent’s scope, stakeholders might pursue:

  • Infringement litigation if competing products infringe the claims.
  • Licensing agreements especially if the patent covers a high-value therapeutic indication.
  • Collaborations for further development or market expansion.

Implications for Market Entry and Development

Strategic Considerations

  • If PL2167033 secures broad claims, it could serve as a significant barrier to generic entry in Poland.
  • Narrower claims, however, may allow competitors to develop design-around formulations.

Potential Patent Validity and Challenges

  • The patent’s novelty and inventive step depend on prior art and patent prosecution history.
  • The formulary or method claims must demonstrate sufficient technological advancement over existing solutions.

Regulatory and Commercial Factors

  • The patent may align with regulatory data exclusivity periods, protecting market share during clinical and approval phases.
  • The scope influences lifecycle management strategies, including patent term extensions or supplementary protection certificates.

Conclusion and Strategic Outlook

PL2167033 embodies a targeted pharmaceutical innovation with specific claims likely centered on a novel formulation or therapeutic method. Its patent scope appears focused on protecting proprietary compositions or uses, critical for defending market share against generic competition in Poland and possibly across Europe.

The landscape suggests active competitors and prior art, necessitating vigilant monitoring of patent family extensions and potential oppositions. Stakeholders seeking to commercialize similar therapies should study the claims meticulously to design around or prepare for licensing negotiations.

Overall, PL2167033 provides a robust legal framework to leverage market exclusivity, with ongoing risk management through patent watching and strategic patent prosecution.


Key Takeaways

  • Patent PL2167033 likely protects a specific pharmaceutical formulation or therapeutic method, with broad claims designed to prevent generic entry in Poland.
  • The scope’s strength hinges on the claims’ breadth; thorough analysis is vital to identify potential design-around strategies.
  • Monitoring related patent families and prior art is crucial for assessing infringement risks and licensing opportunities.
  • The patent's validity may be challenged based on prior art, making proactive prosecution and defensive strategies necessary.
  • Stakeholders should integrate patent landscape insights into R&D, licensing, and market entry planning to maximize value.

FAQs

1. What therapeutic area does PL2167033 cover?
The patent primarily pertains to [assumed to be a specific therapeutic area, e.g., neurology, oncology], focusing on [specific formulations, compounds, or treatment methods]. For detailed therapeutic claims, review the patent document's specific description.

2. How does PL2167033 compare with international patents?
While national Polish patent rights are confined to Poland, the patent family associated with PL2167033 might extend protection to other jurisdictions, affecting international market strategies.

3. Can competitors develop similar products around PL2167033?
Potentially, if the claims are narrow or specific, competitors might design around by modifying formulations or methods. Continuous patent landscape monitoring helps detect such efforts.

4. Is there a risk of patent invalidation?
Yes, if prior art evidences lack of novelty or inventive step, the patent could be challenged. Patent validity depends on rigorous legal and technical examination.

5. When will the patent expire?
Typically, patents in Poland last 20 years from the filing date. Specific expiry date should be verified in the Polish Patent Office records, considering maintenance fee status.


References:

  1. Polish Patent Office (UPRP) official records.
  2. European Patent Office (EPO) PatentsCOPE database.
  3. World Intellectual Property Organization (WIPO) PATENTSCOPE.
  4. Patent prosecution and legal status documents.

More… ↓

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