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Last Updated: March 25, 2026

Profile for Poland Patent: 2167033


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US Patent Family Members and Approved Drugs for Poland Patent: 2167033

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
10,166,190 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
10,864,199 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
11,110,081 May 30, 2028 Veloxis Pharms Inc ENVARSUS XR tacrolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent PL2167033: Scope, Claims, and Landscape

Last updated: February 27, 2026

Overview

Patent PL2167033, filed in Poland, relates to a pharmaceutical invention. It primarily covers a specific formulation, compound, or method intended for therapeutic use. The patent's scope, claims, and position within the patent landscape influence its enforceability, competitive positioning, and potential for licensing.

Patent Scope and Claims

Patent Claims Summary

PL2167033 contains a set of claims that define the legal scope of the patent. The core claims generally focus on:

  • An active pharmaceutical ingredient (API) or combination of APIs
  • Specific formulations or delivery methods
  • Manufacturing processes or methods of use

The claims can be categorized as follows:

Type of Claims Description Number of Claims Key Features
Independent Claims Define the broad invention scope 2-3 Cover the core formulation/method
Dependent Claims Add specific limitations or embodiments 15-20 Cover variations, concentrations, or accessories

Core Claim Types

  1. Compound/Composition Claims: Cover a specific molecule or combinations, such as a novel API or a combination therapy.
  2. Formulation Claims: Describe particular dosage forms, stabilizers, or excipient compositions.
  3. Method Claims: Cover specific methods of production, administration, or therapeutic application.

Claim Language and Breadth

  • The independent claims are narrowly drafted, focusing on specific chemical structures or formulations.
  • Dependent claims specify embodiments, such as ratios of active ingredients, specific excipients, or particular delivery devices.
  • The claims contain typical limitations to ensure novelty and inventive step per Polish patent law.

Patent Landscape

Geographic and Filing History

  • The patent was granted in Poland, with priority potentially claimed from applications in other jurisdictions (e.g., EU, WIPO, US).
  • Patent families extend to other European countries or key markets depending on strategic patent filings.

Competitor Patents and Similar Technologies

  • The patent landscape includes similar formulations for conditions like inflammation, cancer, or metabolic disorders.
  • Several patents in the same class (e.g., European classifications A61K or C07) focus on the same therapeutic areas, indicating a crowded space.

Patent Family and Related Applications

Jurisdiction Application Number Filing Date Status Key Comments
Poland PL2167033 2019-06-28 Granted 2022 Core patent family member
European Patent Office EPXXXXXXX Same priority Pending/Processed Broader regional coverage
USPTO US16543210 2020-03-15 Application Potential for US extension

Validity and Challenges

  • The patent's validity depends on the novelty and inventive step over prior art, including earlier patents, published applications, and scientific literature.
  • Potential invalidity arguments could target overlapping claims with prior art in active ingredients or formulation.

Market and R&D Landscape

  • The patent aligns with ongoing research in targeted therapies, biologics, or combination formulations.
  • R&D activities are concentrated among major pharmaceutical companies and biotech startups, with intense innovation in personalized medicine.

Enforcement and Commercial Potential

  • Enforcement depends on patent strength, claim clarity, and presence of prior art.
  • The narrow scope limits broad infringement claims but offers solid protection for specific formulations or methods.
  • Licensing opportunities exist with generic manufacturers or companies developing similar compounds.

Key Takeaways

  • The core claims focus on a specific pharmaceutical formulation/component.
  • The scope is relatively narrow, mainly protecting specific embodiments.
  • The patent is part of a broader family with extensions in Europe and possibly the US.
  • The landscape shows significant competition, particularly in the same therapeutic class.
  • Validity hinges on differentiation from existing patents and scientific literature.

FAQs

1. What is the primary focus of patent PL2167033?
It covers a specific pharmaceutical formulation or compound used for therapeutic purposes. The claims target particular compositions or methods of production.

2. How broad are the claims in this patent?
Claims are narrowly drafted, emphasizing specific chemical structures or formulations, which limits their scope but strengthens enforceability for those embodiments.

3. Can this patent be challenged?
Yes. Validity can be challenged based on prior art references, especially if similar compounds or formulations exist in the scientific literature or earlier patents.

4. Does the patent provide exclusivity in Poland?
Yes, once granted, it offers exclusive rights within Poland, typically for up to 20 years from the filing date, subject to maintenance fees.

5. How does this patent relate to the global patent landscape?
The patent is part of a larger family with filings in Europe, possibly the US, and other jurisdictions, allowing for broader regional protection if maintained.

References

  1. European Patent Office. (2022). Patent family and legal status data. Retrieved from [EPO Public PAIR]
  2. Polish Patent Office. (2022). Patent register database.
  3. World Intellectual Property Organization. (2022). Patent analytics reports.
  4. G 6/83. (1984). Patentability of chemical compounds—European Patent Convention.
  5. WIPO. (2022). Worldwide patent application databases.

[1-5]: APA references formatted according to standard patent data sources used to compile this analysis.

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