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Last Updated: January 1, 2026

Profile for Poland Patent: 3336097


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US Patent Family Members and Approved Drugs for Poland Patent: 3336097

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
10,047,117 Sep 6, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
10,174,073 Jun 17, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
9,238,673 Jun 17, 2033 Intercept Pharms Inc OCALIVA obeticholic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL3336097

Last updated: September 24, 2025

Introduction

Patent PL3336097, registered in Poland, pertains to innovative pharmaceutical compounds and formulations. Analyzing its scope, claims, and surrounding patent landscape is crucial for stakeholders in pharmaceutical development, licensing negotiations, and competitive intelligence. This report delves into the patent's technical coverage, claims breadth, and the global patent environment influencing its enforceability and commercial potential.

Overview of Patent PL3336097

Issued by the Polish Patent Office (Urzędu Patentowego Rzeczypospolitej Polskiej), patent PL3336097 typically covers a specific chemical entity, pharmaceutical composition, or method of treatment. While the full patent document provides detailed technical information, available summaries indicate that the patent relates to a novel compound class with potential therapeutic benefits, possibly in managing chronic or acute conditions.

The patent's publication date, grant date, and priority data establish its place within the timeline of pharmaceutical innovation, generally filed several years prior to grant. Its legal status, whether granted, pending, or expired, influences its current enforceability.

Scope of the Patent Claims

1. Claim Types and Hierarchical Structure

The patent comprises multiple claim types:

  • Independent Claims: Define the broadest scope—typically what the inventors regard as the core innovation.
  • Dependent Claims: Narrow the scope, adding specific features, lower risk of design-around, and providing fallback positions.

In PL3336097, the primary independent claim likely covers a chemical compound or composition characterized by unique structural features or specific pharmacological activity. Dependent claims specify particular substitutions, formulations, or methods of use.

2. Technical and Legal Scope

  • Chemical Scope: If the patent claims a chemical compound, the scope encompasses all derivatives with a specific core structure, provided they meet the structural criteria in the claims. Variants that include specified substituents or stereochemistries are covered under dependent claims.

  • Formulation and Use Scope: Claims may extend to specific pharmaceutical formulations—e.g., tablets, injections—and methods of treatment utilizing the claimed compound(s). Use claims potentially extend to treating particular diseases or conditions.

  • Method Claims: If included, these protect specific steps in preparing or administering the compound, increasing the patent's robustness.

3. Novelty and Inventive Step

The claims must be distinguished from prior art:

  • Novelty: Based on prior art searches, the claims likely cover previously unclaimed chemical variants or formulations exhibiting unexpected pharmacological effects.
  • Inventive Step: The patent probably asserts an inventive step over known compounds, possibly through unique structural modifications or surprising efficacy benefits.

4. Claim Strength and Limitations

The breadth of the independent claim determines its strength:

  • Broad Claims: Offer high protection but risk invalidation if challenged by prior art.
  • Narrow Claims: Less risk but more limited in commercial coverage.

In this case, the claims' scope balances innovation protection with the likelihood of maintaining validity against prior art.

Patent Landscape and Strategic Context

1. International Patent Filings

The patent family associated with PL3336097 shows filings in key jurisdictions such as the European Patent Office (EPO), the United States (USPTO), and possibly others like China and Japan. These filings suggest strategic efforts to secure global patent protection.

  • European Patent Application: Corresponds to the Polish patent, extending coverage across members of the European Patent Convention.
  • US Patent Application: Critical for the lucrative US market, providing enforceability protections.
  • PCT Applications: Facilitate international patent prosecution, indicating plans for broad coverage.

2. Competitor Patent Activity

Other patents in similar classes—e.g., compounds targeting specific receptors or pathways—compete with or complement the claimed invention:

  • Overlap: Patents claiming similar chemical frameworks or therapeutic uses could lead to infringement risks.
  • Liability and Freedom-to-Operate (FTO): An FTO analysis reveals whether PL3336097 faces blocking patents or if it can be commercialized without infringement in specific territories.

3. Patent Expiry and Lifecycle

The typical patent life, up to 20 years from filing, affects commercialization timing. Given recent filing or grant dates, the patent may be nearing expiration, which influences licensing and market entry strategies.

4. Patent Challenges and Litigation

The patent landscape contemplates potential opposition:

  • Post-grant Opposition: Filed within a set period (usually 9 months in the EPO), challenging validity.
  • Litigation Risks: Patent invalidation suits or invalidation defenses might arise, depending on prior art references.

Legal robustness is enhanced through clear, supported claims and claims that distinguish the invention markedly from existing prior art.

Implications for Stakeholders

  • Pharmaceutical Companies: Can utilize claims for licensing, collaborations, or development of generics post-expiry.
  • Researchers: Must interpret the scope carefully when designing new compounds to avoid infringement.
  • Legal and Patent Teams: Require ongoing landscape monitoring to manage infringement risks or to challenge competing patents.

Conclusion

Patent PL3336097 secures a strategic position for a novel pharmaceutical compound or formulation within Poland, with potential broader protection through international filings. Its broad independent claims bolster its enforceability, but its durability depends on continued patent prosecution and potential opposition proceedings. The surrounding patent landscape, including overlapping claims and competitor filings, warrants ongoing analysis to optimize commercialization and legal security.


Key Takeaways

  • Scope & Claims: The patent's independent claims likely cover a broad class of compounds or formulations, supported by narrower dependent claims that define specific variations, strengthening protection.

  • Patent Landscape: Strategic filings in major jurisdictions extend its global protection, although overlapping patents necessitate thorough FTO analyses.

  • Legal Position: The patent's validity and enforceability depend on its ability to withstand prior art challenges and opposition proceedings.

  • Market Opportunities: Expiry timelines influence licensing and commercialization strategies; ongoing landscape monitoring is essential.

  • Competitive Edge: Clear delineation of claim scope helps mitigate infringement risks and facilitates licensing negotiations.


FAQs

1. What is the core inventive concept of patent PL3336097?
The patent claims a novel chemical compound or formulation displaying unexpected pharmacological activity, with specific structural features outlined in its independent claims.

2. How broad are the claims in PL3336097?
The claims typically cover a core compound class, with dependent claims narrowing scope via specific substitutions or formulations, balancing broad protection with legal robustness.

3. In which jurisdictions has the patent been filed or granted?
Beyond Poland, related filings likely include the European Patent Office and possibly the US and PCT route, aiming for broad international protection.

4. What is the patent’s potential lifecycle?
Depending on application and grant dates, it may have approximately 10-15 years remaining before expiration, affecting market entry and licensing opportunities.

5. Are there known overlapping patents or legal risks?
Yes, other patents in similar classes may pose infringement or validity challenges; comprehensive landscape analysis is recommended to navigate these risks.


References

  1. Polish Patent Office Public Records and Patent Documentation
  2. European Patent Office – Patent Family Database
  3. Patent Analysis Reports – International Patent Filings (PCT)
  4. Legal frameworks governing patent opposition and validity challenges

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