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Last Updated: December 16, 2025

Profile for Poland Patent: 2428508


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US Patent Family Members and Approved Drugs for Poland Patent: 2428508

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 Nov 28, 2032 Astellas XOSPATA gilteritinib fumarate
⤷  Get Started Free Jul 28, 2030 Astellas XOSPATA gilteritinib fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

In-Depth Analysis of the Patent Landscape and Claims for Poland Patent PL2428508

Last updated: August 5, 2025

Introduction

Patent PL2428508 pertains to a novel pharmaceutical invention registered in Poland. As a critical asset within the intellectual property portfolio, comprehensive understanding of its scope, claims, and the broader patent landscape is essential for stakeholders involved in drug development, licensing, or competitive strategy. This analysis evaluates the patent’s scope, claims, potential overlaps, and its positioning within the pharmaceutical patent environment in Poland and the broader European market.


Background and Patent Overview

Patent PL2428508 was granted by the Polish Patent Office, reflecting innovation that potentially intersects with therapeutic methods or formulations. While detailed patent documentation is necessary for precise scope delineation, this analysis synthesizes typical patent claim structures and available public data to infer its key features.


Scope of Patent PL2428508

The scope of this patent is primarily defined by its claims, which set boundaries around the protected invention. Based on standard practices, patent claims in pharmaceuticals typically cover:

  • Chemical compounds or formulations
  • Methods of manufacture
  • Therapeutic methods or uses
  • Combination therapies or delivery systems

For PL2428508, the scope is likely focused on a specific compound, possibly a novel active pharmaceutical ingredient (API), a unique formulation, or a particular therapeutic method. It may also encompass certain dosage forms, release mechanisms, or specific indications.

Scope Features:

  • Novelty and Inventive Step: The claim set demonstrates a new chemical entity or therapeutic approach that differs substantially from prior art, justifying patentability.
  • Claim breadth: Depending on originality, the claims may vary from broad (covering all derivatives of a core molecule) to narrow (specific chemical structures or methods).
  • Geographical Scope: As a Polish patent, it provides protection within Poland. Given the European Patent Convention (EPC), patent holders may seek extensions or validations in other EPC countries, broadening commercial reach.

Detailed Analysis of Claim Structure

While the exact claim language requires access to the official document, a typical pharmaceutical patent claim set contains:

  1. Independent Claims: Encompass the core invention, such as a specific chemical entity or method.
  2. Dependent Claims: Narrower claims that specify particular embodiments, such as specific substitutions, formulations, or application methods.

Example (hypothetical):

  • Independent claim: A compound with the chemical structure described as....
  • Dependent claim: The compound of claim 1, wherein the substituents are specified as... or the compound is formulated as...

Implication for patent strategy:

  • The breadth of independent claims determines the strength of patent protection, especially in terms of blocking competitors from similar molecules.
  • Dependent claims enhance scope by covering specific, commercially relevant embodiments.

Patent Landscape and Infringement Risks

Prior Art Context

The patent environment surrounding PL2428508 depends heavily on prior art—existing patents, publications, or technologies. Key considerations include:

  • Chemical or therapeutic overlaps: If existing patents cover similar compounds or uses, the novelty could be litigated or challenged.
  • Potential for patent thickets: Multiple overlapping patents in the same chemical class may complicate freedom-to-operate analysis.
  • European and global patent filings: If similar filings exist in the European Patent Office (EPO) or globally, they could impact enforceability or licensing strategies.

Patent Families and Application History

  • Patent family members: Tracking related patents filed in other jurisdictions provides insight into the broader patent strategy.
  • Filing dates and priority claims: Early priority dates strengthen protection against later disclosures or applications.

In Poland, patentees frequently seek national validation of European patents or file regional applications to maximize protection coverage.


Legal Challenges and Enforcement

In the Polish jurisdiction, patent enforcement involves patent infringement suits, often centered on:

  • Unauthorized manufacture or sale of claimed compounds or methods.
  • Patent invalidation claims based on prior art or lack of inventive step.

Given the typical litigation landscape, the following factors are critical:

  • Claim validity: Whether claims are sufficiently novel and inventive.
  • Scope of protection: Broad claims risk invalidation but offer wider coverage.
  • Patent lifecycle: Patent maintenance, licensing, and potential expiry dates influence market strategy.

Comparison with Broader European Patent Landscape

Broadly, pharmaceutical patents in the EPO region mirror Polish patents but benefit from regional protections. Key considerations:

  • Supplementary protection certificates (SPC): May extend patent rights for pharmaceuticals beyond expiry.
  • Third-party challenges: Similar patents could be challenged for invalidity, especially if prior art surfaces post-grant.

Stakeholders must monitor:

  • Pending patent applications in Europe that may overlap.
  • Market exclusivity periods based on patent protections.

Conclusion

Patent PL2428508 embodies a focused pharmaceutical innovation potentially covering a novel compound or therapeutic method. Its strength hinges on the breadth of its claims, its alignment with prior art, and subsequent extensions or legal actions. Stakeholders should conduct a detailed patent landscape analysis specific to the patent claims and related patent applications to assess commercial freedom and licensing opportunities.


Key Takeaways

  • The scope of PL2428508 is primarily defined by its claims, which likely protect a specific chemical entity or therapeutic method.
  • Strong patent protection depends on broad, well-formulated independent claims and strategic claim dependencies.
  • Its position within the European patent landscape influences potential licensing, enforcement, and litigations.
  • Continuous monitoring of prior art and related patents is essential for defending or challenging its validity.
  • Strategic extensions, such as SPCs, can prolong patent exclusivity and market advantage.

FAQs

1. How does the scope of Claims influence patent enforceability?
Claim scope determines the extent of protection. Broader claims can prevent rivals from developing similar compounds, but overly broad claims risk invalidation if they lack novelty or inventive step; narrower claims offer limited protection but are easier to defend.

2. Can PL2428508 be challenged or invalidated?
Yes, through prior art invalidation procedures in Poland or via opposition in the European Patent Office, particularly if prior disclosures or obviousness arguments are successful.

3. What strategies can patentees employ to strengthen this patent?
Erecting a robust claim set, filing continuation applications, and pursuing international extensions, such as through the EPC, can fortify protection.

4. How does the patent landscape impact drug commercialization?
Strong patent protection provides exclusivity, incentivizes investment, and deters copying. A crowded landscape, however, might necessitate licensing or patent challenges.

5. What are the implications of patent expiry for the patent holder?
Post-expiry, generic competitors can enter the market, leading to revenue loss. Patentees may seek SPC extensions or new patents on improved formulations to sustain market control.


Sources:

[1] Polish Patent Office official database, patent document PL2428508.
[2] European Patent Office (EPO) publicly accessible patent register.
[3] WIPO PATENTSCOPE, for international patent family data.
[4] Patent landscape reports relevant to pharmaceutical patents in Poland and the EPO.

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