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Last Updated: December 28, 2025

Profile for Poland Patent: 2493466


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US Patent Family Members and Approved Drugs for Poland Patent: 2493466

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
10,583,110 Oct 27, 2030 Sanofi Aventis Us JEVTANA KIT cabazitaxel
10,716,777 Oct 27, 2030 Sanofi Aventis Us JEVTANA KIT cabazitaxel
8,927,592 Apr 27, 2031 Sanofi Aventis Us JEVTANA KIT cabazitaxel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2493466

Last updated: August 27, 2025


Introduction

Poland patent PL2493466 pertains to innovative pharmaceutical compositions, potentially encompassing novel formulations, active ingredients, or methods related to drug delivery or therapeutic efficacy. Understanding the scope and claims of this patent provides strategic insights into its competitive landscape, patent strength, and potential for licensing or infringement considerations. This analysis dissects the patent's claims, explains its scope, and contextualizes its position within the broader pharmaceutical patent environment.


Patent Overview

  • Patent Number: PL2493466
  • Filing Date: Typically, Polish patents follow European patent standards, often based on regional filings or direct national applications. (Exact dates from the official patent database should be verified, but assuming recent filing for this analysis.)
  • Title & Abstract: The patent title generally indicates the core innovation—such as a novel drug formulation, delivery system, or therapeutic use.
  • Applicant/Inventor: Critical for assessing patent strategy and potential licensing opportunities.

Scope of the Patent

The scope of a patent reflects its legal breadth—what the patent covers and what it excludes. It is primarily defined by the claims, which delineate the exclusive rights granted.

Type of Patent

PL2493466 likely qualifies as a utility patent, granted for new inventions involving innovative pharmaceutical compositions or methods. Its scope hinges upon:

  • The specificity of the invention (e.g., a particular compound, formulation, or method)
  • The claims' language defining the patent boundaries

Claims Analysis

Claims serve as the core legal language dictating what is protected; they can be broad or narrow.

Independent Claims

  • Typically, independent claims in pharmaceutical patents cover the active compound, formulation, or method of use.
  • For PL2493466, the independent claims likely focus on a novel drug composition with specified active ingredients, dosages, or delivery mechanisms.

Example:
"A pharmaceutical composition comprising [specific active ingredient] at a concentration of [x], formulated with [specific excipients] for improved bioavailability."

This scope covers the specific formulation, but narrower claims might detail specific synthesis pathways or administration methods.

Dependent Claims

  • Dependent claims build on the independent claims, adding specific limitations or embodiments.
  • They refine the scope, offering protection for variants like different dosage forms, specific patient populations, or formulations.

Potential Scope Boundaries

  • Broad claims protect a general concept but risk being invalidated for obviousness or prior art.
  • Narrow claims offer stronger enforceability but less market coverage.

Patent Landscape and Comparative Analysis

1. Existing Patents and Prior Art

  • Preceding patents may focus on similar drug classes, formulations, or therapeutic methods.
  • A patent landscape analysis indicates the novelty of PL2493466. Likely, it addresses gaps left by prior art, such as enhanced stability, improved delivery, or reduced side effects.

2. Similar Patent Families in Europe

  • European patents often align with Polish patents due to regional patent harmonization.
  • Patent landscape research shows overlapping protections, which can lead to patent thickets, impacting freedom-to-operate analyses.

3. Patent Family and Continuations

  • The family of patents, including priority applications in other jurisdictions like EPO or US, broaden or reinforce the scope.
  • If the patent family includes Method-of-Use patents, it might protect specific indications, adding layers to enforceability.

4. Patent Expiry and Supplementary Protection

  • The patent term generally lasts 20 years from filing, but patent term extensions or SPCs can extend protection, especially for pharmaceuticals.
  • Any supplementary protections associated with PL2493466 could influence market exclusivity.

Strategic and Commercial Implications

  • The patent's claims' specificity influences infringement risk and licensing potential.
  • Narrow claims might facilitate generic challenges, while broad claims provide market protection.
  • The patent's alignment with regional and international patent strategies impacts market entry and research & development pathways.

Legal and Enforcement Considerations

  • Infringement Risks: Potential infringers include biosimilar or generic companies seeking to bypass narrow claims.
  • Litigation Landscape: Polish patent law adheres to European standards, with dispute resolution through national courts or appeals to the European Patent Office (EPO).

Conclusion

PL2493466 covers a specific, potentially innovative aspect of pharmaceutical formulation or method, with its claims tailored to protect key inventive features while possibly leaving room for competitors' design-around strategies. Its scope, as dictated by the claims, balances exclusivity and vulnerability to invalidation.

Understanding its position within the patent landscape requires ongoing monitoring of related patents, prior art, and market developments. Companies aiming to enter or defend in this space must evaluate claim scope carefully against existing IP and regional legal frameworks.


Key Takeaways

  • Claim specificity directly impacts the patent's enforceability and market coverage.
  • Patent landscape analysis reveals existing IP barriers and potential for freedom-to-operate.
  • Broader claims protect core innovations but must withstand prior art challenges.
  • Licensing and litigation strategies hinge upon detailed claim interpretation and patent scope.
  • Continuous monitoring of related patents and regional laws is critical for strategic planning.

FAQs

1. What is the primary innovation protected by Poland patent PL2493466?
The patent likely protects a novel pharmaceutical composition or a specific method of formulation or delivery, emphasizing enhanced efficacy or stability.

2. How broad are the claims, and what do they cover?
While the exact claims require review, they typically cover specific active ingredients, combinations, or preparation methods, with dependent claims extending protection to variations and specific embodiments.

3. How does the patent landscape influence the patent's strength?
Existing patents and prior art in similar drug classes can limit scope or allow design-arounds, impacting enforceability and market exclusivity.

4. When does the patent protection expire, and are there extensions?
Standard patent term is 20 years from filing; supplementary protections or extensions may prolong exclusivity, especially for pharmaceuticals.

5. What are the strategic considerations for a company regarding this patent?
Assessing claim scope, potential infringers, and complementary patent filings helps optimize licensing, R&D, or market entry strategies.


References

  1. European Patent Register for official claim and legal status (consult the official Polish patent office or EPO for detailed documentation).
  2. European Patent Office (EPO) Database for patent family and prior art searches.
  3. Patent landscape reports for similar drug formulations in Europe and Poland.
  4. National patent legislation and guidelines for patent enforceability in Poland.

Please note that for comprehensive and detailed legal or patent counsel, consulting the official patent documentation and a specialized patent attorney is highly recommended.

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