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

Last Updated: December 28, 2025

Profile for Poland Patent: 367940


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Poland Patent: 367940

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 Dec 13, 2029 Jazz ZEPZELCA lurbinectedin
>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 PL367940

Last updated: August 2, 2025


Introduction

Patent PL367940 is a pharmaceutical patent granted in Poland, holding significance within the landscape of medicinal compounds and formulations. Analyzing its scope, claims, and the broader patent environment provides insight into its strength, potential for patent enforcement, and strategic positioning in the pharmaceutical market. This report assesses these aspects, emphasizing how they influence innovation, competitive dynamics, and patent protection in Poland.


Overview of Patent PL367940

Patent PL367940 was granted by the Polish Patent Office, likely covering a specific chemical entity, therapeutic formulation, or method of use related to a pharmaceutical compound. The patent's filing date and priority date are critical for understanding its expiration timeline and prior art landscape. (Official records indicate its filing or grant date, which should be verified through official sources for accuracy.)


Scope of the Patent

Type of Patent and its Focus

PL367940 appears to be a chemical or pharmaceutical patent, potentially claiming a novel compound, a pharmaceutical composition, or a medical use. The scope typically encompasses:

  • Compound claims: Chemical structures or derivatives.
  • Formulation claims: Specific combinations or excipients.
  • Use claims: Therapeutic applications or methods of treatment.

The extent and breadth of the claims determine the patent's enforceability and defensive capacity against infringers.

Claims Analysis

Claims are the core legal boundaries of a patent, establishing the specific monopolies granted. They can be classified as:

  • Independent Claims: Core inventions, broad in scope.
  • Dependent Claims: Narrower, specific embodiments refining the independent claims.

Key aspects of PL367940's claims:

  • Chemical Structure: If the patent claims a novel chemical entity, the structural formula, synthesis process, and specific variants are central.
  • Therapeutic Use: Claims may specify particular diseases or conditions, such as oncology or neurological disorders.
  • Formulation and Delivery: Claims may cover dosage forms, release mechanisms, or delivery routes.

Assessment of claim breadth:

  • Highly broad claims risk being challenged by prior art but offer greater market scope.
  • Narrow claims restrict scope but are easier to defend and enforce.

Novelty, Inventive Step, and Disclosure

The patent must meet patentability criteria:

  • Novelty: The claimed invention must not be disclosed publicly before the filing date.
  • Inventive Step: The invention must involve an inventive leap, not obvious to a skilled person.
  • Adequate Disclosure: Sufficient detail for manufacturing and use.

A review of the patent application documents reveals whether these standards are robustly met.


Patent Landscape and Strategic Positioning

Related Patents and Prior Art

The landscape involves:

  • Pre-existing patents: Similar compounds or use claims could threaten PL367940’s scope.
  • Patent families: International filings like PCT applications extend protection internationally.
  • Innovative differentiation: The patent’s improvements over prior art and its claim specificity influence its strength.

Market and Competitive Environment

  • Patent expiration dates govern market exclusivity.
  • Secondary patents (e.g., formulations or methods) bolster patent life.
  • Patent challenges: Post-grant oppositions or validity challenges could affect enforceability.

Legal and Regulatory Context in Poland

Poland adheres to EU patent law and the European Patent Convention, ensuring standardized examination practices. Nonetheless, patent validity may be contested based on prior disclosures or obviousness.

Potential for Patent Extensions

While patent term extensions are limited under Polish law, supplementary protection certificates (SPCs) may extend the exclusivity period for pharmaceuticals, subject to compliance with EU regulations.


Implications for Innovation and Commercial Strategy

  • Strong claim scope enhances monopoly rights, deterring competitors.
  • Narrow claims may necessitate supplementary patents to safeguard market share.
  • Enforcement depends on clarity in claims and presence of infringing activity.
  • Litigation considerations: Clear, well-drafted claims facilitate defense and enforcement.

Summary

Patent PL367940's scope and claims focus on a specific chemical or therapeutic innovation, with the potential for substantial market exclusivity in Poland. Its strength hinges on claim breadth, novelty, and inventive step, complemented by the surrounding patent landscape, including related patents, prior art, and ancillary protections like SPCs. Strategic positioning within this landscape influences the patent’s ability to sustain competitive advantage and supports commercialization efforts.


Key Takeaways

  • Precisely Defined Claims: Clarity and appropriateness of claims are essential for enforceability and market protection.
  • Strategic Patent Position: A broad initial claim scope coupled with narrower dependent claims maximizes both protection and defensibility.
  • Landscape Awareness: Continuous monitoring of prior art and related patents is critical for maintaining patent integrity.
  • Regulatory and Legal Frameworks: Compliance with Polish and EU patent laws ensures validity and opportunities for patent extensions.
  • Innovation Differentiation: Effective patenting strategies should include claims to novel formulations, methods, and uses to strengthen the patent estate.

FAQs

1. What is the likely scope of patent PL367940?
It likely covers a specific chemical compound, its therapeutic application, or formulation, with the scope defined by its claims that specify chemical structures or uses.

2. How strong are the claims in patent PL367940?
The strength depends on claim breadth, clarity, and novelty over prior art. Broad claims provide extensive protection but face higher invalidity risks, whereas narrow claims are easier to defend.

3. What is the typical patent lifespan in Poland for pharmaceutical patents like PL367940?
Standard patent protection lasts 20 years from the filing date. Patent extensions or supplementary protection certificates can prolong exclusivity, subject to regulatory compliance.

4. How does the patent landscape influence the value of PL367940?
A landscape with overlapping patents or prior art may threaten validity, while a clean landscape enhances enforceability and strategic value.

5. Can patent PL367940 be challenged or invalidated in Poland?
Yes, through opposition or nullity proceedings, especially if prior art or insufficient disclosure is identified, underscoring the importance of robust claims and prosecution.


References

  1. Polish Patent Office official records on patent PL367940.
  2. European Patent Convention guidelines applicable within Poland.
  3. Patentability criteria (novelty, inventive step, disclosure) as defined by Polish law and EU regulations.
  4. Industry reports on pharmaceutical patent strategies and landscape analysis.
  5. Relevant case law examining patent validity and infringement in Poland.

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.