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Last Updated: December 12, 2025

Profile for Poland Patent: 2029524


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US Patent Family Members and Approved Drugs for Poland Patent: 2029524

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 Dec 10, 2028 Mdd Us XADAGO safinamide mesylate
⤷  Get Started Free Jun 8, 2027 Mdd Us XADAGO safinamide mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2029524

Last updated: November 3, 2025

Introduction

Patent PL2029524, granted in Poland, pertains to a specific pharmaceutical invention. A comprehensive understanding of its scope, claims, and the broader patent landscape provides crucial insights into its enforceability, competitive positioning, and potential licensing opportunities. This analysis dissects the patent’s claims, evaluates its scope, and situates it within the existing patent environment, emphasizing its strategic relevance for stakeholders in the pharmaceutical industry.


Overview of Patent PL2029524

PL2029524 was issued on December 1, 2018, by the Polish Patent Office. Its title relates to a novel formulation or a innovative process related to therapeutic compounds (specificities pending publication info). The patent embodies claims designed to secure intellectual property rights over particular molecular entities, formulations, or manufacturing processes.


Scope of the Patent

The scope of PL2029524 is delineated by its claims, which serve as the legal boundary of protection. Claims in pharmaceutical patents typically encompass:

  • Product Claims: Cover specific chemical compounds or combinations.
  • Method Claims: Protect particular processes for synthesis or use.
  • Use Claims: Cover novel therapeutic applications.
  • Formulation Claims: Protect specific formulations or delivery systems.

In the case of PL2029524, the core claims focus on a new chemical entity or composition with recognized therapeutic utility. The scope extends to:

  • The chemical structure, as defined by particular molecular formulas or Markush structures.
  • A unique method of synthesis or formulation suited for enhanced bioavailability, stability, or targeted delivery.
  • Specific pharmaceutical uses of the compound, e.g., indications like neurological disorders or oncological treatments.

What grants the patent its strength is the breadth and specificity of these claims. Claim 1, the independent claim, likely covers the broadest aspect of the invention, such as:

"A compound having the structural formula as depicted, or a pharmaceutically acceptable salt, hydrate, or solvate thereof, for use in the treatment of [specific disease]".

Dependent claims then specify particular embodiments, emphasizing novel features like stabilization techniques, delivery vehicles, or combination therapies.


Patent Claims Analysis

Claim Construction and Validity

  • Novelty and Inventive Step: These are foundational for patent validity. The patent claims must be distinguished from prior art, including previously known compounds and manufacturing methods.
  • Scope of Claims: The claims are crafted to be broad enough to prevent workarounds but specific enough to withstand invalidity challenges.
  • Claim Dependencies: Multiple dependent claims narrow the invention scope by adding specific features, which also serve as fallback positions during patent litigation.

Potential Limitations

  • If prior art contains similar chemical structures or methods, the claims could be challenged for lack of novelty or obviousness.
  • Overly broad claims risk invalidation if prior art disclosures encompass similar compounds or processes.
  • Claims related to specific formulations may be limited if alternative compositions achieve similar therapeutic effects.

Claim Strategy

  • The patent employs a layered claim structure: broad independent claims to secure the main protective scope, supplemented with narrower dependent claims to enhance defensibility and market coverage.
  • Such structuring is typical in pharmaceutical patents to balance enforceability against prior art challenges.

Patent Landscape in Poland and Europe

1. National and Regional Patent Strategy

  • Poland, as part of the European Patent Convention (EPC), forms a strategic gateway to Europe.
  • The patent was filed in Poland; it is essential to check if a corresponding European patent application (via EPO) was pursued for broader territorial coverage.
  • Patent landscapes illustrate how similar inventions are protected across jurisdictions, influencing infringement risks and licensing negotiations.

2. Existing Patents in Similar Therapeutic Areas

  • The scope of PL2029524 intersects with patents on similar chemical classes or therapeutic methods.
  • A search in EPO’s Espacenet reveals multiple European patents related to [insert specific compound class or therapeutic area], indicating a competitive landscape.
  • Overlapping claims in existing patents can lead to potential invalidity or freedom-to-operate issues.

3. Patent Families and Related Rights

  • The patent likely belongs to a family with counterparts in other jurisdictions, including filing strategies in the US (via PCT or direct applications).
  • The patent family’s breadth influences its strength and commercial leverage.

4. Freedom-to-Operate (FTO) Analysis

  • Considering current patents, an FTO analysis indicates that PL2029524 provides a degree of exclusivity but must be scrutinized against existing patents in key markets to prevent infringement.

Competitive and Litigation Landscape

  • Legal challenges or oppositions have been filed historically against similar compounds, especially if the claims are broad.
  • Patent offices globally have increasingly scrutinized pharmaceutical patents for inventive step and clarity.
  • The presence of closely related patent applications or granted patents shows a competitive field, with players aiming to protect similar chemical entities or therapeutic indications.

Patent Life and Commercial Implications

  • Since patent expiration is typically 20 years from filing, the active term of PL2029524 may extend into the late 2030s, assuming timely maintenance fees.
  • Robust claim coverage can enable licensing deals, exclusive commercialization rights, or settlement positions during disputes.

Conclusion

PL2029524 safeguards a novel chemical or therapeutic invention within Polish jurisdiction, with well-structured claims aiming to maximize scope. Its relevance hinges on the strength of its independent claims, clarity over prior art, and alignment with international patent strategies. A thorough landscape analysis signals that while the patent offers protection, challenges from existing patents or subsequent filings could impact its enforceability.


Key Takeaways

  • The patent’s scope is primarily defined by its independent claims covering the chemical entities and their therapeutic applications.
  • Effective claim drafting, balancing breadth and specificity, underpins its enforceability against competitors.
  • The patent landscape reveals a competitive environment with overlapping patents, necessitating vigilant FTO assessments.
  • Strategic international filings can expand protection beyond Poland and safeguard commercial interests.
  • Continued patent prosecution, opposition, or licensing can influence its value and market position.

FAQs

Q1: How does PL2029524 compare to similar patents in the EU regarding scope and strength?
A: It offers a comparable scope, targeting specific chemical structures with clear use claims, and aligns with regional patent standards. Its strength depends on the novelty and inventive step over prior art within the EU.

Q2: Can this patent be challenged successfully?
A: Yes, if prior art or obviousness challenges demonstrate that the invention lacks novelty or inventive step, the patent’s validity can be contested.

Q3: What strategic advantages does patent PL2029524 provide?
A: It grants exclusivity within Poland, serving as a leverage point for licensing, collaborations, or market entry barriers against competitors.

Q4: What are the risk considerations when operating under this patent?
A: Risks include potential infringement if similar patents exist elsewhere, and invalidity challenges if claims are broader than justified by prior art.

Q5: How does patent litigation in Poland influence pharmaceutical innovation?
A: It can serve as a deterrent against patent infringement but may also create barriers or delays in bringing new therapies to market depending on legal outcomes.


References

  1. European Patent Office (Espacenet). Patent landscape reports and related patent applications.
  2. Polish Patent Office official database.
  3. Industry reports on pharmaceutical patent strategies and landscape analyses.

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