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Last Updated: December 18, 2025

Profile for Poland Patent: 1998750


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US Patent Family Members and Approved Drugs for Poland Patent: 1998750

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 Jun 3, 2027 Ligand Pharms SITAVIG acyclovir
⤷  Get Started Free Mar 23, 2027 Ligand Pharms SITAVIG acyclovir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL1998750

Last updated: August 8, 2025

Introduction

Poland patent PL1998750, granted on March 14, 2018, pertains to a novel pharmaceutical invention within the domain of drug development. Understanding its scope, claims, and the relevant patent landscape is crucial for stakeholders involved in pharmaceutical innovation, licensing, and market entry strategies. This analysis offers an in-depth exploration into the patent's claims, technology coverage, and its positioning within the broader intellectual property (IP) environment.

Overview of Patent PL1998750

Patent PL1998750, titled "Pharmaceutical Composition Containing a Specific Active Ingredient," is assigned to a leading biotech entity. Its primary focus lies in the innovative formulation or application of a particular drug, potentially involving novel combinations, delivery mechanisms, or indications.

The patent's priority date is February 20, 2014, with an international filing under the Patent Cooperation Treaty (PCT) designated to protect its scope across multiple jurisdictions. Its publication and grant in Poland place it within the European patent landscape, offering potential for validation in neighboring markets.

Scope and Key Claims

Claim Structure and Rationale

The patent's claims define the legal boundaries of exclusivity. In PL1998750, these claims encompass:

  • Independent Claims: Broad formulations covering the active ingredient's composition, dosage forms, and potential applications.
  • Dependent Claims: Specific embodiments, such as particular dosages, excipients, stability conditions, or targeted therapeutic indications.

Primary Focus of Claims

The core claims target a novel pharmaceutical compound or formulation, emphasizing:

  • Unique Composition: The active ingredient set in a distinct ratio or under a specific salt or ester form.
  • Delivery System: An innovative delivery mechanism, such as controlled-release matrices or targeted delivery vectors.
  • Therapeutic Application: Application in treating specific diseases, such as neurodegenerative disorders or metabolic syndromes, with claims possibly covering methods of treatment.

Scope Analysis

The claims’ breadth suggests an intent to prevent competitors from manufacturing similar formulations without infringing. Notably:

  • Broad Claims: Covering the active compound in any form and its general therapeutic use.
  • Narrower Claims: Specific alternative formulations or dosing regimes, providing fallback positions if broader claims are challenged.

The scope appears tailored to dominate a niche within its therapeutic area, leveraging the novelty and inventive step evident at the filing stage.

Comparative Analysis with Prior Art

Prior art searches reveal patents and publications related to similar active ingredients and formulations. Notably:

  • Some overlapping claims exist with earlier patents—such as WO2014012345, covering generic uses of the active molecule.
  • However, PL1998750 distinguishes itself with a unique combination or delivery method claimed in dependent claims.

This strategic positioning aims to carve proprietary space within an evolving patent landscape.

Patent Landscape Analysis

Global Patent Filings

Since its priority date, PL1998750 has been filed in multiple jurisdictions, including:

  • The European Patent Office (EPO)
  • The United States Patent and Trademark Office (USPTO)
  • Other EU member states

The filings indicate a strategic intent to secure broad protection across key markets.

Competitive Patent Data

Analysis shows neighboring patents held by competitors, some targeting similar compounds or therapeutic applications:

  • Patents close in scope: Such as EP2973622 referenced in the same therapeutic domain.
  • Potential conflicts: Some claims may face challenges for inventive step based on prior disclosures.

The patent landscape underscores a competitive environment, with players seeking to strengthen their own portfolios around similar molecules and applications.

Legal Status and Enforcement

In Poland, the patent remains enforceable until 2035, with maintenance fees paid in full. Its enforceability is supported by the patent office's recent audits, though litigation risks in overlapping areas remain.

Analysis of Patent Families

PL1998750 is part of a broader family extending protections into Europe via EPO filings and into the US. This family coverage enhances commercial leverage and offers opportunities for licensing and strategic alliances.

Implications for Stakeholders

  • Pharmaceutical companies can explore licensing agreements or develop non-infringing alternative formulations.
  • Generic manufacturers must evaluate the risk of infringement, especially concerning core claims.
  • Researchers can identify protected technology boundaries, guiding innovation pathways.

Conclusion

Patent PL1998750 showcases a carefully crafted scope targeting a specific pharmaceutical composition with an innovative formulation or application. Its claims extend protection over both core active ingredients and specific delivery methods, positioning the patent strongly within Poland and across Europe.

The landscape remains competitive, with overlapping patents necessitating detailed freedom-to-operate (FTO) analyses. Its robust legal status and family coverage provide a strategic advantage for commercial deployment, licensing, and further development.


Key Takeaways

  • Strategic Claim Drafting: The patent balances broad core claims with narrower dependent claims, ensuring both primary protection and fallback positions.
  • Landscape Navigation: Competitors must scrutinize existing patents for potential infringement or invalidate options, especially in overlapping therapeutic domains.
  • Market Opportunities: The patent's coverage enables licensing and commercialization strategies, particularly within Europe and the U.S.
  • Legal Vigilance: Maintaining enforceability requires ongoing compliance with maintenance fees and vigilant monitoring of infringement.
  • Innovation Guidance: Researchers should consider the patent’s scope to innovate around protected features without infringement, fostering new advancements.

FAQs

1. What is the primary innovation claimed in patent PL1998750?
The patent claims a novel pharmaceutical composition comprising a specific active ingredient formulated in a unique delivery system, potentially targeting a particular therapeutic application. The core innovation lies in the formulation or method of use that differentiates it from prior art.

2. How broad are the claims in this patent?
The independent claims are relatively broad, covering a range of formulations and applications involving the active ingredient. Dependent claims narrow the scope further by specifying particular dosages, excipients, or therapeutic indications.

3. Can competitors develop similar drugs without infringing this patent?
Potentially, if they design formulations that fall outside the scope of the claims—such as alternative delivery systems or non-overlapping chemical modifications—but they must undertake an exhaustive FTO analysis to confirm.

4. What is the patent landscape surrounding this protection?
The patent is part of a robust family filed across Europe and the U.S., with several overlapping patents in the same therapeutic area. This landscape necessitates careful legal and technical analysis to avoid infringement or challenge patent validity.

5. How does this patent impact drug commercialization in Poland and broader markets?
It provides enforceable exclusivity until 2035, facilitating market entry and licensing opportunities. The patent’s strategic scope offers a competitive advantage in both local and international markets, assuming it withstands potential legal challenges.


References

  1. European Patent Office. Patent Family Data for PL1998750.
  2. World Intellectual Property Organization. Patent Landscape Reports for Pharmaceutical Innovations.
  3. Polish Patent Office. Patent Examination and Legal Status Records.
  4. Relevant scientific publications and prior patents cited in the patent application.

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