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Last Updated: December 19, 2025

Profile for Poland Patent: 1940817


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US Patent Family Members and Approved Drugs for Poland Patent: 1940817

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
9,763,953 Dec 1, 2026 Alpha Cognition ZUNVEYL benzgalantamine gluconate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL1940817

Last updated: July 29, 2025


Introduction

Poland patent PL1940817 pertains to a pharmaceutical invention aimed at securing exclusive rights within the Polish patent landscape. Its scope, claims, and surrounding patent ecosystem are critical for stakeholders interested in the development, commercialization, or legal navigation of the patented technology. This analysis delineates the patent's scope, examines its claims in detail, and contextualizes its position within the broader patent landscape.


Patent Overview and Basic Details

Patent PL1940817, filed or granted in Poland, appears to focus on a novel pharmaceutical composition or method — though specifics require direct review of the official patent document. The patent's scope is defined predominantly through its claims, which delineate the boundaries of exclusivity. The patent’s priority date, filing date, title, and assignee (if available) are essential for assessing the IP's novelty and scope.

(Note: For this analysis, available public records, patent databases, and the patent’s official documentation are considered. The following presentation is based on assumed standard patent structures for pharmaceuticals.)


Scope of the Patent

1. Patent Scope Characteristics

The scope encapsulates the scope of protection conferred by the patent — predominantly reflected through independent claims. Typically, patent scope in pharmaceutical patents involves:

  • Compound or Composition Claims: Covering a specific chemical entity or its pharmaceutically acceptable formulations.
  • Method Claims: Encompassing novel methods of synthesis, formulation, or therapeutic use.
  • Use Claims: Covering the specific therapeutic application of the compound.

Given typical scenarios, PL1940817 likely contains:

  • Independent Claims: Covering the core inventive compound or composition, and potentially, its method of preparation or administration.
  • Dependent Claims: Detailing specific embodiments, dosage forms, patentable modifications, or particular therapeutic indications.

2. Breadth and Limitations

The scope’s breadth determines its enforceability and competitive relevance. A broad claim might encompass related compounds or formulations, while narrow claims target specific embodiments. The clarity and definiteness of the claims are critical for defending the patent against invalidation or patent workarounds.

3. Patent Term and Geographic Scope

Although specific to Poland, the patent's claims may influence regional or European patent strategies if extensions or national phase entries exist. The patent term generally lasts 20 years from the filing date, subject to maintenance fees.


Analysis of the Claims

1. Independent Claims

The independent claims form the backbone of the patent's scope. For PL1940817, these likely specify:

  • The chemical structure of the novel compound, possibly with Markush structures specifying variants.
  • The pharmaceutical composition comprising the claimed compound.
  • A particular medical use or therapeutic method.

2. Claim Language and Specificity

Claims should be precisely drafted to balance breadth with clarity. Overly broad claims risk invalidation for lack of novelty or inventive step, while narrow claims might be circumvented more straightforwardly.

3. Claim Dependencies

Dependent claims probably specify alternative substituents, dosage forms, or synthesis routes. These serve to fortify the patent’s scope by covering multiple embodiments related to the core invention.

4. Novelty and Inventiveness

The substantiveness of the claims relies on demonstrating novelty over prior art and inventive step — a critical consideration for patent validity and enforcement.

5. Potential Claim Set (Hypothetical Example)

An example independent claim might read:

"A pharmaceutical composition comprising a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of [specific disease]."

Dependent claims might specify:

  • Specific substituents on the core structure.
  • Doses and formulations.
  • Methods of preparation.

Patent Landscape Context

1. Related Patents and Patent Families

The patent family likely includes Asian, European, or US counterparts, especially if the invention is commercially relevant globally. Similar or overlapping patents may exist, covering related compounds, formulations, or uses, leading to a complex landscape.

2. Prior Art and Patent Challenges

Prior art searches reveal precedence in chemical structures or therapeutic indications. Challenges such as patentability rejections or prior art invalidations emphasize the importance of claim specificity.

3. Competitor Landscape

Competitors may hold patents on similar compounds or therapeutic methods, leading to potential infringement risks or licensing opportunities. The patent’s scope here influences freedom-to-operate analyses.

4. Patent Expiry and Market Implications

The expiry date (typically 20 years from filing) is crucial in assessing market exclusivity timelines. Patent life extension strategies, such as supplementary protection certificates (SPCs) in Europe, may also be relevant.


Legal and Commercial Implications

1. Enforcement and Litigation

The strength of the claims determines enforceability. Narrow claims are easier to circumvent but harder to invalidate, whereas broad claims provide more comprehensive protection.

2. Licensing and Partnerships

Robust claims attract licensing deals, especially if they cover key therapeutic improvements or targeted diseases. Narrow claims can still generate licensing revenue if they cover niche markets.

3. Innovation Climate in Poland

Poland’s pharmaceutical patent environment favors strong, clear claims aligned with European patent standards. The patent landscape is also shaped by EU regulations, particularly regarding biotech and pharma.


Summary Table of Key Aspects

Aspect Observations Implications
Scope Likely includes pharmaceutical composition and use claims Defines the breadth of protection, influences enforcement
Claims Core compounds, formulations, methods Clarity and novelty critical for validity
Patent Family Possibly international filings Affects global competitive positioning
Market Life 20-year term from filing Timing for market entry or generic challenges
Landscape Competing patents and prior art Necessitates strategic freedom-to-operate analyses

Key Takeaways

  • Claim Precision Is Critical: The depth and drafting quality of the claims determine the patent’s enforceability and strategic value.
  • Scope Balances Breadth and Validity: Broader claims enhance protection but risk invalidation; narrower claims provide specific coverage but less market exclusivity.
  • Patent Landscape Nuance: The presence of overlapping patents or prior art necessitates comprehensive landscape analysis, particularly in European and international contexts.
  • Market Strategy Linkage: The patent’s standing influences licensing, partnership, and commercialization plans within Poland and beyond.
  • Proactive Legal Monitoring: Regular review of patent status, legal disputes, and licensing activities is essential for safeguarding assets and optimizing commercial outcomes.

FAQs

Q1: What is the typical duration of patent protection for pharmaceutical inventions in Poland?
A: The standard patent term in Poland is 20 years from the filing date, subject to maintenance fees.

Q2: Can claims in PL1940817 be challenged or invalidated?
A: Yes, through opposition proceedings, nullity actions, or by proving lack of novelty or inventive step, especially if prior art evidence emerges.

Q3: How does the scope of claims affect the ability to enforce the patent?
A: Broader claims provide wider protection but are more vulnerable to invalidation; narrow claims may be easier to defend but offer limited protection.

Q4: What is the benefit of filing patent applications in multiple jurisdictions for the same invention?
A: It broadens territorial protection, reduces infringement risk across markets, and increases leverage in licensing or litigation.

Q5: How do patent landscapes influence R&D investment decisions?
A: Recognizing overlapping patents and freedom-to-operate issues enables strategic planning, risk mitigation, and innovation targeting.


References:

  1. Polish Patent Office (UPRP) Database. [Official patent registrations]
  2. European Patent Office (EPO). Patent documents and legal status reports.
  3. WIPO PATENTSCOPE. International patent filings and family data.
  4. Patent Law of Poland (Official Gazette). Legal framework and procedural guidelines.
  5. Industry reports on pharmaceutical patent strategies in Poland and Europe.

Conclusion

The Polish patent PL1940817 exemplifies a targeted approach to pharmaceutical IP, with scope predominantly defined through its claims. Its value hinges on claim clarity, legal robustness, and strategic positioning within the patent landscape. Business leaders and innovators must continuously monitor the patent’s legal status and surrounding patent environment to optimize its commercial potential and safeguard their innovations.

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