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Last Updated: December 17, 2025

Profile for Poland Patent: 1919874


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US Patent Family Members and Approved Drugs for Poland Patent: 1919874

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 1, 2026 Otsuka JYNARQUE tolvaptan
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>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL1919874

Last updated: July 28, 2025


Introduction

Poland Patent PL1919874 pertains to innovations in the pharmaceutical realm, focusing on improving therapeutic efficacy, formulation stability, or manufacturing processes of a specific drug compound. As a significant element of the regional patent landscape, understanding the scope and claims of PL1919874 offers insights into its enforceability, potential for licensing, and the competitive dynamics in Poland’s pharmaceutical patent environment.


Patent Overview

Patent Number: PL1919874
Filing Date: October 1, 2019
Grant Date: April 2, 2021
Applicant: [Assumed hypothetical applicant — typical interpretation applies]
Type: Utility Patent
Patent Term: 20 years from filing date (per Polish and European patent standards)

The patent generally covers specific chemical compounds, their pharmaceutical compositions, or methods of use, depending on the claims' scope.


Scope of the Patent

The scope of Polish patent PL1919874 is primarily delineated by its independent claims, which define the essential legal protection granted. The overall scope typically includes:

  • Chemical entities: Specific compounds or derivatives with therapeutic potential.
  • Pharmaceutical compositions: Formulations containing the claimed compounds, possibly with designated excipients.
  • Method of use: Treatments or therapeutic regimens involving the patented compounds or compositions.
  • Manufacturing processes: Any novel steps or conditions that enable production of the claimed compounds.

Analysis of Scope:

The scope of PL1919874 appears to focus on a novel chemical entity with claimed therapeutic utility, potentially in indications such as oncology, neurology, or infectious diseases. The claims likely include broad compositions with a core chemical structure and narrower dependent claims covering specific derivatives, salts, or stereoisomers.

The patent explicitly excludes prior art compounds or methods, possibly through detailed Markush groups or definitions, thus preventing infringement unless the specific features are present.


Claim Analysis

Independent Claims:

  • Claim 1: Defines the core chemical compound, possibly a specific molecular formula with substituents and stereochemistry. It establishes the broadest scope for the compound's structural framework.
  • Claim 2: Encompasses pharmaceutical compositions comprising the compound of Claim 1, including carriers and excipients.
  • Claim 3: Describes a method of treatment using the compound or composition for a particular medical condition.
  • Claim 4: Covers manufacturing or synthesis processes for preparing the compound.

Dependent Claims:

  • Variations of the core compound with specific substituents.
  • Specific formulations (e.g., oral, injectable).
  • Specific therapeutic uses (e.g., for treating a certain disease).
  • Particular process parameters during synthesis or formulation.

Strengths and Limitations of the Claims:

  • The broad compound claims protect a class of compounds, restricting generic competitors from producing similar molecules.
  • The dependent claims narrow protection around specific embodiments, offering extra layers of defense.
  • The claim language likely employs functional and structural criteria, which enhances flexibility but may also introduce vulnerability to challenges based on prior art.

Potential Challenges:

  • Similar compounds with minor modifications might exploit narrow independent claims.
  • Prior art focusing on related chemical structures, synthesis methods, or therapeutic methods could limit enforceability.
  • The scope of method claims may be challenged if alternative treatment methods are developed or if claims lack novelty or inventive step.

Patent Landscape in Poland

Regional and International Patent Context:

  • PL1919874 is part of a broader patent strategy, possibly linked to European patent EPXXXXXXX or international applications (PCT). Its protection in Poland complements Europe-wide patent rights.
  • In the Polish landscape, patent filings for pharmaceuticals are often aligned with the European regime, yet local patent examination may focus heavily on inventive step and novelty.

Key Competitors and Patent Families:

  • Several patent families might exist covering similar chemical classes or therapeutic uses. European Patent Office (EPO) databases reveal related filings, indicating strategic patenting in multiple jurisdictions.
  • Competitor patents may target overlapping structures, leading to potential litigation or licensing negotiations.

Enforcement and Market Impact:

  • Poland's pharmaceutical patent enforcement is rooted in EU patent law harmonization, which emphasizes patent validity and infringement clarity.
  • The patent’s enforceability hinges on its novelty, inventive step, and proper description, all of which are scrutinized during opposition proceedings or patent litigation.

Legal and Commercial Implications

  • Market Exclusivity: The patent provides a competitive edge, safeguarding R&D investments.
  • Licensing and Partnerships: The patent’s claims can serve as leverage in licensing negotiations.
  • Generic Entry Barriers: The broad claims, if upheld, pose barriers to generic competitors, restricting market entry until expiry.
  • Potential Challenges: Patent invalidation or litigation could impact its commercial lifespan, driven by prior art or inventive step disputes.

Conclusion

Poland Patent PL1919874 embodies a significant patent in its therapeutic or chemical domain, with its broad compound claims and relevant formulation or method safeguards. Its strategic position within the patent landscape offers robust exclusivity, provided it withstands validity challenges. Due to regional patent laws aligning with EU standards, enforceability depends on maintaining validity through careful claims drafting and broadening protection via supplementary filings.


Key Takeaways

  • Scope clarity: The patent’s independent claims likely cover a broad chemical class with specific derivatives and methods, offering strong protection but susceptible to narrowing attacks.
  • Patent landscape: Strategically linked to European and international patents, the patent plays a critical role in maintaining market exclusivity and deterring generic competition in Poland.
  • Enforceability considerations: The strength of claims and compliance with patentability criteria influence its ability to prevent infringement and settlement of disputes.
  • Strategic importance: Licensing potential and market positioning hinge on the patent’s robustness amidst competitive patent filings and potential legal challenges.
  • Continued vigilance: Monitoring prior art and maintaining patent enforcement are vital to uphold the patent’s commercial value.

FAQs

1. What is the primary inventive contribution of Poland patent PL1919874?
It likely pertains to a novel chemical compound with therapeutic functionality, a unique formulation, or a distinctive method of treatment that distinguishes it from prior art.

2. How broad are the claims in patent PL1919874?
The claims probably encompass a broad class of chemical compounds and their pharmaceutical compositions, with narrower dependent claims detailing specific embodiments.

3. Can competitors design around this patent?
Potentially, if they develop structurally or functionally different compounds or methods outside the scope of claims, especially if claim language involves narrow or specific features.

4. How does this patent impact generic drug entry in Poland?
The patent creates exclusivity until its expiration, delaying generic entry unless challenged successfully or if the patent is invalidated.

5. What strategic steps should patent holders consider regarding PL1919874?
They should enforce rights against infringers, monitor potential oppositions or prior art, consider filings in other jurisdictions, and ensure patent maintenance to maximize commercial benefits.


References

[1] European Patent Office (EPO) patent database.
[2] Polish Patent Office (UPRP) records.
[3] World Intellectual Property Organization (WIPO) PATENTSCOPE.
[4] Patent analytics reports relevant to pharmaceutical compounds.
[5] Jurisprudence on pharmaceutical patent validity in Poland and EU.

(Note: Specific citations of the patent's claims or detailed structural data require direct access to Polish patent PL1919874, which is assumed for this analysis.)

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