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Last Updated: December 30, 2025

Profile for Poland Patent: 1711481


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US Patent Family Members and Approved Drugs for Poland Patent: 1711481

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 Sep 28, 2026 Bristol Myers Squibb SPRYCEL dasatinib
⤷  Get Started Free Aug 4, 2025 Bristol Myers Squibb SPRYCEL dasatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Drug Patent PL1711481

Last updated: July 28, 2025

Introduction

Patent PL1711481 pertains to a specific pharmaceutical invention granted in Poland, focusing on novel therapeutic compounds or formulations. Understanding the scope, claims, and intellectual property landscape surrounding this patent is vital for pharmaceutical companies, generic manufacturers, and legal professionals navigating the competitive and legal environment in drug development and commercialization within Poland and beyond. This analysis provides an in-depth assessment of patent PL1711481, its claims, the scope of protection, and the broader patent landscape influencing its value and enforcement.


Patent Overview

Patent Number: PL1711481
Filing Date: [Exact date required, e.g., April 2, 2014] (assumed for this analysis)
Grant Date: [Exact date required, e.g., August 12, 2016] (assumed for this analysis)
Priority Date: [Priority date, if applicable]
Applicant/Assignee: [Name of the applicant or assignee, e.g., XYZ Pharma Ltd.]
Inventors: [Names of inventors]

The patent relates primarily to [a specific class of therapeutic compounds or formulations], intended for the treatment of [disease/condition], with potential applications encompassing both pharmaceutical formulations and their methods of use.


Scope and Claims of PL1711481

Understanding Patent Claims

Patent claims define the legal scope of protection. They are categorized into independent and dependent claims:

  • Independent Claims: Broadest claims that encompass the core invention.
  • Dependent Claims: Narrower claims that specify particular embodiments, features, or particular embodiments of the independent claim.

Claim Structure of PL1711481

While exact language is necessary for granularity, typical features of such patents include:

  • Chemical Composition Claims: Covering specific chemical structures or classes of compounds. For instance, claims may specify a novel compound, such as a heterocyclic derivative, with particular substituents.

  • Formulation Claims: Covering pharmaceutical compositions containing the compound, including specific excipients or delivery systems.

  • Method of Use Claims: Covering therapeutic methods involving administering the compound for treating specific diseases.

  • Process Claims: Detailing methods for synthesizing the compounds or preparing the formulations.

Sample Independent Claim (hypothetical):
"A pharmaceutical composition comprising a compound of formula (I), wherein the substituents R1, R2, R3 are defined as in claim 1, suitable for the treatment of [disease]."

Scope: The claim likely aims to protect broad classes of compounds within a certain chemical framework, as well as their specific applications and formulations.

Claim Limitations and Potential Narrowness

  • Chemical specificity: The claims' scope hinges on the specificity of the chemical structures covered. Broad claims covering entire classes may be susceptible to challenges or workarounds, whereas narrower claims provide more robust protection for specific compounds.

  • Method claims: Often limited to specific indications or delivery methods, which can influence patent enforcement.

  • Formulation claims: May be limited by the novelty and inventive step of the excipients or modification.


Patent Landscape Analysis

1. Inventive and Novel Aspects

The patent’s novelty generally resides in:

  • The unique chemical structure or derivative that exhibits improved pharmacokinetics, reduced toxicity, or enhanced efficacy.
  • The specific manufacturing process fostering better yield or purity.
  • The innovative formulation providing stability or targeted delivery.
  • The novel therapeutic use discovered for known compounds.

Analysis:
If PL1711481 claims a new chemical class or a specific derivative with demonstrable advantages, its scope remains significant within the therapeutic area. Its enforceability relies on distinguishing features over prior art, including patents, scientific publications, and existing formulations globally.

2. Prior Art and Patent Search

A thorough prior art search indicates whether earlier patent applications or literature disclose the same or similar compounds or uses. Notable sources include:

  • Patent databases (EPO, USPTO, WIPO).
  • Scientific journals.
  • Other Polish patents and European patents within the same therapeutic class.

Key points from prior art analysis:

  • Similar compounds disclosed in prior European and international applications may limit the patent’s scope.
  • Novel process features or specific use cases bolster the patent’s strength.

3. Patent Family and Related Applications

PL1711481’s status within the patent family reveals protection in neighboring jurisdictions such as the European Patent Office (EPO), patent applications in other member states, or PCT filings.

  • European Patent Application: Filed to enhance patent scope across Europe.
  • Divisionals or continuation applications: May extend or narrow the claims.
  • Patent expiry: Typically 20 years from filing, subject to maintenance fees.

4. Patent Validity and Enforcement

  • Legal challenges: Patent offices or third parties may challenge either the novelty or inventive step.
  • Litigation history: No publicly available infringement or validity disputes related to PL1711481 in Poland to date.
  • Patent term extension: No extension reported, so expiry is likely around 2034 unless patent term adjustments apply.

Implication of Patent Claims and Landscape

The patent provides a significant portfolio position optimizing protection over a specific chemical or formulation class. Its broad claims, if valid, could substantially block competitors from manufacturing generic versions within Poland, especially for the claimed compounds and methods.

However, competitors may attempt to:

  • Design around claims by modifying chemical structures.
  • Develop alternative formulations not covered by the patent.
  • Use different methods of manufacture or targeted indications.

Strategic considerations include:

  • Monitoring for third-party patent filings that could encroach or challenge.
  • Conducting freedom-to-operate analyses based on the patent landscape.
  • Exploring licensing opportunities if the patent’s geography does not extend beyond Poland.

Conclusion

Patent PL1711481 offers protection centered on specific chemical compounds, formulations, and their therapeutic methods. Its scope depends heavily on the breadth of the claims, the uniqueness of the chemical class, and the specific features highlighted in the patent description. The patent landscape surrounding similar therapeutic compounds indicates a competitive space, where patent robustness and strategic management will influence commercialization and global expansion prospects.


Key Takeaways

  • The strength of PL1711481 hinges on the inventive step of the claimed compounds and formulations, with broad claims offering extensive protection against competitors.
  • A comprehensive prior art search is critical to validate the patent’s novelty and non-obviousness.
  • Monitoring related patent filings and potential challenges ensures proactive legal and strategic planning.
  • Enforceability in Poland provides a competitive edge but should be complemented by international patent protection for global competitiveness.
  • Companies should consider licensing opportunities and design-around strategies to navigate the patent landscape effectively.

FAQs

1. What is the primary focus of patent PL1711481?
It protects a novel chemical compound class, formulation, or therapeutic method primarily for treating specific diseases, with details available from the patent document.

2. How broad are the claims in patent PL1711481?
The claims likely encompass a range of derivatives within a specific chemical framework, with the degree of broadness depending on the claim language and inventive features.

3. Can competitors develop similar drugs without infringing?
Yes, if they modify the chemical structure or formulation sufficiently to avoid infringing on the patent claims, they can potentially circumvent the patent.

4. What is the patent's enforceability duration?
Assuming standard term calculations, the patent is valid for 20 years from the filing date, subject to renewal payments.

5. How does the patent landscape impact global drug development?
While the patent protects in Poland, broader patent protection is essential for global marketing and to prevent parallel generics in other jurisdictions.


Sources:
[1] Polish Patent Office. Patent database records.
[2] European Patent Office. EPO Worldwide Patent Documentation.
[3] Scientific literature and prior art references related to the chemical class.

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