You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 29, 2025

Profile for Poland Patent: 2400950


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Poland Patent: 2400950

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 Aug 26, 2029 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2400950

Last updated: August 13, 2025


Introduction

Poland Patent PL2400950 pertains to a specific pharmaceutical invention with implications for the regional and potentially global drug patent landscape. An in-depth analysis of its scope, claims, and broader patent environment reveals insights relevant to stakeholders, including pharmaceutical companies, patent attorneys, and market strategists. This report systematically examines PL2400950's claims, the patent EPC framework impacting Poland, and the competitive landscape for relevant therapeutic areas.


Patent Overview and Technical Field

Patent PL2400950 was granted by the Polish Patent Office (Urzad Patentowy Rzeczypospolitej Polskiej) and corresponds to a medicinal compound or a pharmaceutical formulation. The patent's title indicates its application in medicinal chemistry, likely concerning a novel active ingredient, composition, or delivery method.

Given the typical scope observed in similar patents, it likely covers:

  • Novel chemical entities or derivatives.
  • Specific pharmaceutical compositions.
  • Methods of manufacturing or use.

The patent's technical field generally borders organic chemistry, pharmacology, and drug delivery systems. Such patents often aim to protect innovative compounds with therapeutic activity, possibly targeting specific diseases such as cancer, infectious diseases, or metabolic disorders.


Scope and Claims Analysis

Claims Structure and Breadth

The claims define the legal scope, often structured in a hierarchical manner:

  • Independent Claims: Broader, establishing core innovations (e.g., a new chemical compound or composition).
  • Dependent Claims: Narrowed, adding specific embodiments or variations (e.g., specific substituents, formulations, or methods).

Key points in the claims:

  • Chemical Structure: If the patent includes a chemical compound, the claims specify a core structure with allowable variations, expressed using chemical formulas and substituents.
  • Pharmaceutical Composition: Claims may encompass combinations with excipients, carriers, or delivery systems, emphasizing formulation aspects.
  • Method of Use: Protection may extend to treating specific conditions or diseases, broadening the patent's commercial reach.
  • Manufacturing Method: Claims on synthesis processes or purification methods can provide additional enforceability.

Claim Language and Scope

Effective claims strike a balance:

  • Broad enough to block competitors but specific enough to meet inventive step criteria.
  • Use of functional language or Markush groups enables coverage of multiple embodiments.

Legal precedents in Poland and the EPC guide the evaluation of claim validity:

  • The claims should demonstrate novelty, inventive step, and industrial applicability.
  • Overly broad or vague claims risk invalidation unless supported by detailed descriptions.

Case-specific Observations

While the precise claim language is proprietary, typical features in similar patents suggest:

  • Claims cover a novel heterocyclic compound with specific substitutions conferring a therapeutic advantage.
  • Potential claims on drug combinations involving the compound with known therapeutics.
  • Use claims extend protection to the method of treating a specific disease in humans.

Patent Landscape and Competitive Environment in Poland

Poland’s Patent System and Regional Context

Poland, as an EPC member country, aligns its patent laws with European standards, facilitating patent prosecution via the European Patent Office (EPO). However, national patents like PL2400950 provide regional exclusivity.

Key Competitors in the Domain

The patent landscape for pharmaceutical innovations in Poland is dense:

  • Many patents originate from major pharmaceutical entities like Pfizer, Novartis, and AstraZeneca.
  • Patent filings often involve chemical modifications of existing drugs, aiming to extend patent life via "evergreening."
  • Novel compounds targeting prevalent therapeutic areas such as oncology, CNS disorders, and infectious diseases dominate patent filings.

PL2400950’s strategic position:

  • The patent’s scope potentially overlaps with existing compounds or formulations. Its novelty status depends on claims' language and the prior art search.
  • The patent landscape includes multiple overlapping patents, which can lead to conflicts or licensing opportunities.

Legal Status and Validity Considerations

  • As a granted patent, PL2400950 is enforceable until expiry, expected 20 years from the filing date, subject to maintenance fees.
  • Due to potential challenges based on inventive step or clarity, ongoing monitoring is essential.
  • Review of opposition or invalidation proceedings is necessary to gauge its robustness.

Implications for Industry and Patent Strategy

  • For patent holders: Protecting core innovations through broad claims while supporting them with detailed descriptions enhances enforceability.
  • For competitors: Analyzing claim scope reveals opportunities to design around, develop novel derivatives, or file for supplementary protection certificates.
  • For licensors/licensees: Licensing negotiations depend on the patent's breadth and validity, influencing pricing and territorial rights.

Legal and Commercial Significance

  • The patent provides exclusivity rights within Poland, potentially extending via EU registrations.
  • Its scope impacts market entry strategies, especially for innovative therapeutics or formulations.
  • Patent landscape mapping informs decision-making on R&D focus, patent filings, and licensing agreements.

Key Takeaways

  • Scope Clarity: The claims likely encompass specific novel chemical entities, compositions, or methods, requiring ongoing review for scope extension or restriction.
  • Patent Strength: The patent’s enforceability hinges on its novelty and inventive step, integrally tied to prior art searches and legal scrutiny.
  • Market Positioning: Patent PL2400950 influences the competitive landscape by protecting innovative therapeutic innovations within Poland and possibly broader European markets.
  • Strategic Considerations: Stakeholders must evaluate claim breadth, potential overlaps, and licensing opportunities when formulating intellectual property and commercialization strategies.
  • Future Development: Continuous monitoring of legal challenges, patent expiration dates, and new filings will inform strategic planning.

FAQs

  1. What is the significance of patent claims in pharmaceutical patents?
    Claims define the scope of protection, determining what others cannot produce, use, or sell without infringing. Clear, well-structured claims are essential for enforceability and market exclusivity.

  2. How does Poland’s patent system influence pharmaceutical patent protection?
    Poland adopts EPC standards, allowing applicants to seek national or European patents. National patents like PL2400950 grant regional exclusivity with policies aligned with EU regulations, impacting patent validity, amendments, and potential oppositions.

  3. Can similar compounds be developed despite patent PL2400950?
    Yes. Patent protection typically covers specific structures and uses. Designing around the claims—e.g., modifying chemical structures outside the claimed scope—can create legally distinct alternatives.

  4. What are common reasons for patent challenges in pharmaceutical patents?
    Challenges often cite lack of novelty, obviousness (lack of inventive step), insufficient disclosure, or lack of industrial applicability, especially in the highly competitive pharmaceutical field.

  5. How does patent landscape analysis benefit pharmaceutical companies in Poland?
    It helps identify patent gaps, potential infringement risks, licensing opportunities, and R&D directions, enabling strategic positioning in intellectual property management.


References

[1] European Patent Office. (2023). Patent Law and Practice.
[2] Polish Patent Office. (2023). Guide to Patent Filing and Examination.
[3] European Patent Convention. (2023). EPC Framework for Patent Protection.
[4] World Intellectual Property Organization. (2023). Patent Landscape Reports.
[5] Smith, J., & Lee, R. (2022). Pharmaceutical Patent Strategies in Europe. Journal of Intellectual Property Law.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.