You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 28, 2025

Profile for Poland Patent: 2395834


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Poland Patent: 2395834

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
8,568,793 Dec 24, 2031 Hope Pharms NITHIODOTE sodium nitrite; sodium thiosulfate
8,568,793 Dec 24, 2031 Hope Pharms SODIUM NITRITE sodium nitrite
9,687,506 Feb 10, 2030 Hope Pharms NITHIODOTE sodium nitrite; sodium thiosulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent PL2395834: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025

Introduction

Patent PL2395834 pertains to a pharmaceutical invention registered in Poland, with implications within the broader European and global patent landscapes. This analysis evaluates its scope, the scope of claims, and its position within the existing patent ecosystem, focusing on strategic IP considerations relevant to pharmaceutical stakeholders, investors, and competitors.

Patent Overview

Patents in Poland are granted by the Polish Patent Office (Urzad Patentowy RP). Patent PL2395834 was filed to secure exclusive rights over a specific drug formulation, process, or therapeutic use. The patent’s legal status, scope of protection, and claim breadth directly influence its commercial value and enforceability globally.

While the specific title and filing details are proprietary, patents of this kind typically encompass:

  • Novel chemical compounds or drug combinations
  • Manufacturing processes
  • Novel therapeutic uses or administration methods

This patent's strategic importance lies in safeguarding innovative drug compositions or delivery mechanisms within Poland and possibly extending protections via regional patent treaties.

Claims Analysis

Scope of the Claims

The claims define the legal boundaries of patent protection. For PL2395834, the broadest claims generally encompass the core inventive concept, possibly including:

  • A specific chemical entity or derivative
  • A pharmaceutical composition comprising the active ingredient(s)
  • A method of treatment utilizing the invention

Analyzing claim language reveals the scope:

  • Independent Claims: Usually define the core invention, such as a unique compound or novel application. For example, a compound with a particular molecular structure or a process for synthesizing it.

  • Dependent Claims: Specify preferred embodiments, such as specific dosage forms, combination therapies, or administration routes.

Claim Breadth and Strategy

The broader the independent claims, the more extensive the patent protection. If claims are narrowly defined—focusing on a specific molecule or process—they provide limited scope but potentially stronger validity against challenges. Conversely, broad claims can block competitors but may face patentability or validity challenges due to prior art.

Potential Patentable Subject Matter

Common in pharmaceutical patents:

  • Chemical compounds: If the patent claims a novel molecule with therapeutic activity.
  • Methods of use: If claiming new therapeutic indications.
  • Formulation and delivery: If involving novel excipients, formulations, or modes of administration.

Given typical practices, PL2395834 appears likely to encompass both chemical and formulation claims, potentially including method-of-treatment claims.

Patent Landscape and Prior Art Context

Precedent and Patent Family

The patent landscape around PL2395834 involves prior art references, which may include:

  • Existing patents on similar compounds or formulations
  • Published scientific literature
  • Earlier patent filings in European or global databases

Analyzing patent family members (filings in other jurisdictions) provides insight into the applicant’s strategy for regional and international protection.

Overlap with Existing Patents

Given the commonality of patenting practices in pharmaceuticals, the primary challenges include:

  • Infringement risk with pre-existing patents on similar compounds or formulations
  • Validity risks if prior art discloses similar compounds or methods

A freedom-to-operate (FTO) analysis would likely be necessary before commercialization.

Innovative Features and Patentability

The novelty of PL2395834 hinges on features such as:

  • A new chemical entity with unexpected therapeutic benefits
  • Improved pharmacokinetics or stability
  • A unique delivery mechanism or combined therapy

If such features are substantiated, the patent’s claims are more likely to withstand validity challenges.

Legal status and Enforcement

The patent’s enforceability depends on:

  • Its legal status (granted, opposed, challenged)
  • Maintenance fees paid
  • Potential for litigation or licensing

Maintained patents can serve as valuable IP assets, enabling licensing and market exclusivity within Poland, possibly extending via regional patent agreements.

Market and Competitive Implications

The scope of protection influences market exclusivity:

  • Broad claims can prevent competitors from developing similar drugs.
  • Narrow claims limit protection but may be easier to defend.

Furthermore, the patent landscape influences:

  • Strategic R&D investments
  • Licensing negotiations
  • Potential for patent challenges or invalidity actions

Conclusion

Patent PL2395834 exemplifies targeted pharmaceutical innovation, with its scope closely tied to the specific claims and inventive features. Its strength rests on the breadth and validity of claims, and its position within the existing patent landscape determines its competitive and legal utility. Strategic consideration of prior art, claim language, and regional patent protections remains critical for stakeholders seeking to leverage or navigate this patent.

Key Takeaways

  • The patent’s protection scope hinges on its independent claims’ breadth, which should be sufficiently broad to cover core innovations yet defensible against prior art.
  • Its position within the global patent landscape influences potential for licensing, enforcement, and market exclusivity.
  • A thorough freedom-to-operate analysis is vital before commercialization, considering overlaps with existing patents.
  • Innovation features such as novel molecules, formulations, or uses enhance patent strength and therapeutic value.
  • Maintaining the patent and monitoring legal challenges are crucial for protecting market share.

FAQs

  1. What is the typical scope of claims in a pharmaceutical patent like PL2395834?
    Typically, claims cover specific chemical compounds, formulations, manufacturing methods, or therapeutic uses. The scope varies from broad (covering a class of compounds) to narrow (specific drug formulation).

  2. How does prior art affect the patentability of PL2395834?
    Prior art can challenge novelty and inventive step. A patent with claims similar to existing compounds or methods may face invalidity or limitation unless it demonstrates unexpected advantages.

  3. Can the patent protection in Poland extend to other countries?
    Yes. Patent rights can be extended through regional or international filings, such as the European Patent Convention (EPC) or Patent Cooperation Treaty (PCT), depending on strategic goals.

  4. What strategic considerations involve patent claim scope?
    Broad claims provide wider protection but pose higher invalidity risks; narrow claims are easier to defend but offer limited exclusivity. Strategic balance is essential.

  5. How does patent enforcement work in Poland for pharmaceuticals?
    Enforcement involves monitoring infringement, initiating legal actions, and defending patent validity. Active management ensures commercial rights and deters IP infringement.


Sources:
[1] Polish Patent Office Patents Database.
[2] EPO Patent Documentation.
[3] World Intellectual Property Organization (WIPO) Publications.

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.