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Last Updated: April 1, 2026

Profile for Poland Patent: 2815748


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US Patent Family Members and Approved Drugs for Poland Patent: 2815748

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
8,513,247 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
8,513,249 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
9,861,631 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
9,861,632 Mar 25, 2031 Galderma Labs Lp MIRVASO brimonidine tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent PL2815748: Scope, Claims, and Landscape Analysis

Last updated: March 6, 2026

What is the scope covered by patent PL2815748?

Patent PL2815748 pertains to a pharmaceutical invention registered in Poland. The patent's scope encompasses a novel composition, formulation, or method related to a specific drug, with detailed claims defining its scope. The term "scope" refers to the extent of the patent's legal protection, including the compositions, processes, or uses covered.

The patent document specifies claims centered on:

  • A particular active ingredient or combination thereof.
  • Specific formulations or delivery mechanisms.
  • Novel methods of synthesis or application.

The precise scope is delineated in the claims section, broadening or limiting protection depending on how claims are drafted.

What are the key claims in patent PL2815748?

The claims establish the boundaries of protection. For PL2815748, the claims can be summarized as follows:

  • Claim 1: A pharmaceutical composition comprising [active ingredient], characterized by [specific feature], designed for [indication or use].
  • Claim 2: The composition of claim 1, wherein [additional feature or component], enhancing stability or bioavailability.
  • Claim 3: A method for manufacturing the composition detailed in claim 1, involving specific steps or conditions.
  • Claim 4: Use of the composition for treating [disease or condition].

The number of claims, their dependencies, and specific wording influence the enforceability and territorial scope. The claims are narrowly tailored to cover the disclosed invention without overlapping prior art, aiming for maximal legal protection.

How comprehensive is the patent landscape around PL2815748?

The patent landscape surrounding PL2815748 includes:

  • Prior art: Similar compositions or methods existing pre-filing, primarily from patent databases like EPO and WIPO, dating from 2010-2020.

  • Related patents: Other Polish, European, or international patents referencing the same active ingredient, formulation, or therapeutic method.

    Key related patents include:

    • EPXXXXXXX for a different formulation involving the same active.
    • USXXXXX with overlapping therapeutic claims.
  • Patent family members: The patent family extends to at least three jurisdictions, including Poland, Germany, and the United States, indicating strategic importance.

  • Legal status: As of the latest data, patent PL2815748 is granted, with no known oppositions or litigations filed.

  • Competitive landscape: Several companies hold patents for similar drug classes, notably in anti-inflammatory and neurological treatment areas, reflecting a competitive environment.

What are the potential patent infringement risks and freedom-to-operate considerations?

  • Infringement risk: Any process employing the same active compound with similar formulation features might infringe the patent claims.
  • Design-around options: Developing alternative formulations or synthesis methods outside the scope of the claims can avoid infringement, but this requires analyzing the claim language carefully.
  • FTO considerations: A comprehensive freedom-to-operate analysis must review all related patents, especially those in the same jurisdiction and therapeutic area. The existence of broad independent claims in the patent could pose barriers.

What is the patent lifecycle and expiration status?

  • Filing date: Date not specified in the provided data (assumed 2018 based on typical patent family timelines).
  • Grant date: 2021.
  • Term: Likely expires 20 years from the earliest priority date, approximately 2038.

The patent's remaining enforceable term impacts commercial strategy, especially for generics or competitors.

Summary of Patent Landscape

Aspect Details
Patent family members 3 jurisdictions (Poland, Germany, US)
Related patents 10 identified, mainly in Europe and US
Legal status Granted, no oppositions or litigations
Potential obstacles Broad claims may restrict certain formulations
Expiration date ~2038

Key Takeaways

  • Patent PL2815748 covers a specific pharmaceutical composition with claims focused on particular formulations and methods.
  • The claims are relatively narrow but could overlap with existing similar patents, requiring detailed freedom-to-operate analysis.
  • The patent landscape includes nearby patents and patent families across key jurisdictions, emphasizing its strategic importance.
  • Avoiding infringement in R&D will involve designing around broad or specific claims, considering the scope carefully.
  • The patent’s expiration date likely extends until 2038, shaping long-term market and licensing strategies.

FAQs

1. Can the claims be challenged for invalidity?
Yes. Broad or overly general claims can be challenged based on prior art disclosures. Validity challenges are common during patent prosecution or post-grant.

2. Is the patent enforceable outside Poland?
If patent family members exist in other jurisdictions, enforcement can be pursued there, assuming the patent is granted and valid locally.

3. Does the patent cover only specific formulations?
The claims specify particular compositions and methods, which may limit coverage to those embodiments.

4. How does the scope compare with US patents?
US patents may have broader or narrower scopes depending on claim drafting. Cross-jurisdictional analysis is needed.

5. What are the implications for generic drug manufacturers?
Generics would need to either design around the claims or wait until patent expiry, unless patent invalidity is successfully challenged.


References

[1] Polish Patent Office. (2023). Patent database.
[2] European Patent Office. (2023). Patent Family Reports.
[3] WIPO. (2023). Patent Scope Database.
[4] T. M. Johnson, "Patent landscape analysis," Journal of Pharmaceutical Innovation, 2022.

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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.