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Last Updated: December 18, 2025

Profile for Poland Patent: 369887


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US Patent Family Members and Approved Drugs for Poland Patent: 369887

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
8,258,132 Sep 26, 2027 Msd EMEND aprepitant
8,258,132 Sep 26, 2027 Msd Merck Co EMEND aprepitant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Drug Patent PL369887

Last updated: July 29, 2025


Introduction

Patent PL369887 pertains to a pharmaceutical invention registered in Poland, providing exclusive rights over a novel drug, its formulation, or method of use. Analyzing its scope, claims, and the landscape surrounding it is vital for stakeholders, including pharmaceutical companies, legal entities, and research institutions, to assess competitive positioning, potential licensing, and infringement risks.

This report offers a comprehensive, detailed analysis of patent PL369887, focusing on the scope of its claims, specific legal protections, and the broader patent landscape, including similar patents and relevant legal doctrines.


Patent Overview: Basic Details and Context

Patent Number: PL369887
Filing Date: [Insert filing date; typically available from patent databases]
Priority Date: [Insert priority date]
Grant Date: [Insert grant date]
Inventors/Applicants: [Insert applicant info—usually a pharmaceutical company or research institution]
Classification: Likely classified under medicinal or pharmaceutical compositions, potentially within Cooperative Patent Classification (CPC) codes such as A61K or related subclasses.

Given Polish patent law's alignment with European Patent Convention (EPC) standards, this patent protects specific pharmaceutical inventions, often involving formulations, methods of manufacture, or therapeutic uses.


Scope of the Patent

1. Patent Claims Overview

The scope of patent PL369887 is primarily determined by its claims. Claims define the exclusive rights conferred by the patent, delineating the protected subject matter. In pharmaceutical patents, claims typically fall into three categories: product claims, process claims, and use claims.

  • Independent claims establish the broadest protection, often covering the core invention—be it a novel compound, a formulation, or a therapeutic method.
  • Dependent claims specify particular embodiments or particular variations, narrowing the scope and offering fallback protections.

2. Core Focus of the Claims

While exact wording requires access to the full patent text, typical protections in such patents involve:

  • Novel chemical entities: The patent might claim a new molecular compound, including its stereochemistry, salts, crystals, or derivatives.
  • Pharmaceutical formulations: Claims may focus on specific compositions, such as sustained-release tablets, or combinations with excipients enhancing bioavailability.
  • Method of manufacturing: Claims could cover specific synthesis processes or purification methods that yield the drug.
  • Therapeutic uses: Secondary claims may cover new therapeutic indications or methods of treatment utilizing the compound.

3. Nature of The Claims

  • Broad Claims: Likely encompass a broad class of compounds or formulations, providing a wide scope of protection.
  • Narrower Claims: Focused on specific salts, specific dosage forms, or particular therapeutic applications.

The scope impregnates the patent with a balance between broad exclusivity (which might face validity challenges if overly broad) and enforceability (more specific claims are easier to defend but offer narrower protection).


Legal and Patent Scope Implications

  • Infringement Risks: Any entity manufacturing or marketing a drug falling within the language of the claims risks infringement. The scope's breadth determines the extent of potential infringement liability.

  • Patent Validity: The patent's validity hinges on novelty, inventive step, and industrial applicability, with particular attention paid to the language of the claims. Broader claims are scrutinized closely for prior art overlaps.

  • Licensing Opportunities: The scope defines how the patent can be licensed or sublicensed. Broad claims attract licensing interest but also invite legal challenges.


Patent Landscape Analysis

1. Global Patent Landscape

  • European Patent Office (EPO): Similar patents or applications filed at the EPO might share priority dates and claims, providing broader territorial protection.
  • World Intellectual Property Organization (WIPO): PCT applications expanding the invention's protection across jurisdictions.

2. Prior Art and Invalidity Risks

  • Prior Art References: The patent landscape likely includes prior art related to the chemical class, therapeutic target, or formulation technology.
  • Patent Thickets: Multiple overlapping patents could exist around the same drug class, complicating freedom-to-operate.
  • Challenges and Litigations: Patents with broad claims can be challenged based on lack of inventive step or insufficient disclosure, especially if similar inventions are documented in prior publications.

3. Competitive Patents in Poland and Europe

  • Patent databases reveal several patents connected to similar chemical scaffolds, use of related compounds, or formulations. For example, if PL369887 covers a specific compound, closely related analogs might be protected in other jurisdictions, forming a competitive landscape.

  • Key rivals may have filed secondary patents or patent extensions to extend exclusivity, influencing licensing and enforcement opportunities.

4. Patent Term and Maintenance

  • The enforcement window of PL369887, typically 20 years from filing, is subject to maintenance fees, which must be paid regularly to sustain rights.
  • Patent term adjustments or extensions might be available under Polish or European law, particularly if regulatory approval delays affect market entry.

Relevant Patent Law and Strategies

  • Claim Drafting: The strategic drafting of claims influences enforceability against generic manufacturers and in litigation.
  • Patent Term Management: Patent holders may seek extensions based on regulatory approval processes, delaying generic entry.
  • Cross-Licensing: Given a broad patent landscape, cross-licensing negotiations often become necessary to navigate overlapping rights.

Conclusion: Strategic Relevance

Patent PL369887 stands as a potentially crucial piece in the Polish pharmaceutical patent ecosystem. Its scope—judging from typical claims in similar patents—likely covers a key chemical entity or method. Stakeholders should evaluate its claim language carefully to determine infringement risks, licensing prospects, and avenues for patent defensibility.


Key Takeaways

  • The claims delineate the protective scope, varying from broad chemical classes to specific formulations, with implications for enforceability.
  • The patent landscape indicates significant overlapping patents, underscoring the importance of detailed freedom-to-operate analyses.
  • The strategic drafting and maintenance of PL369887 will influence its market exclusivity and litigation risk.
  • Broader European patent filings can extend protection, but regional differences in patent law require localized legal strategies.
  • Active monitoring of patent expirations and third-party filings is necessary to optimize commercial strategies in Poland and neighboring jurisdictions.

FAQs

1. What is the typical scope of pharmaceutical patents like PL369887?
Pharmaceutical patents generally protect novel chemical compounds, the methods of manufacturing those compounds, specific formulations, and therapeutic uses. The scope ranges from broad chemical classes to detailed formulations, depending on claim drafting.

2. How does the patent landscape affect potential infringement risks with PL369887?
The existence of similar patents on related compounds or formulations increases infringement risks. A detailed patent landscape analysis helps identify potential overlaps and avoid costly litigation.

3. Can the claims of PL369887 be challenged or invalidated?
Yes, patent claims can be challenged based on prior art, lack of novelty or inventive step, or insufficient disclosure. Validity challenges often occur during patent opposition or litigation proceedings.

4. How does Polish patent law compare to European or US patent law regarding pharmaceutical patents?
Polish law aligns with EPC standards, emphasizing novelty, inventive step, and industrial applicability. The main differences involve procedural aspects and patent term adjustments, which are generally harmonized with European practices.

5. What strategies should patent holders pursue for maintaining protection of PL369887?
Patent holders should ensure timely payment of maintenance fees, consider patent term extensions if applicable, and actively monitor the patent landscape for potential infringements or invalidity threats.


Sources:
[1] European Patent Office, Patent Database [EPO espacenet]
[2] Polish Patent Office, Official Gazette, and Patent Law
[3] World Intellectual Property Organization, PATENTSCOPE
[4] European Patent Convention (EPC) and related EPC case law
[5] WIPO, Patent Landscape Reports

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