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Last Updated: December 19, 2025

Profile for Poland Patent: 2916856


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US Patent Family Members and Approved Drugs for Poland Patent: 2916856

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 Nov 5, 2033 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
⤷  Get Started Free Nov 5, 2033 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
⤷  Get Started Free Nov 5, 2033 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent PL2916856: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025

Introduction

Patent PL2916856, issued in Poland, pertains to an innovative pharmaceutical invention. Its scope, claims, and positioning within the patent landscape influence its value, enforceability, and strategic importance for stakeholders involved in drug development, licensing, or commercialization. This analysis provides a comprehensive evaluation of the patent's scope, specific claims, and its standing amid the global and local patent landscape.


1. Patent Overview

Patent Number: PL2916856
Filing and Grant Dates: Filed [date], Granted [date] (exact dates pending or assumed based on available data)
Applicant: [Applicant Name] (likely a pharmaceutical or biotech entity)
Priority Date: [date], establishing the earliest filing date, critical for determining novelty and inventiveness
Patent Term: Typically 20 years from filing, subject to maintenance fees and national regulations

PL2916856 covers a pharmaceutical invention, possibly related to a novel drug compound, formulation, or use thereof. The patent is designed to secure exclusive rights within Poland, with potential extensions or equivalents in other jurisdictions through PCT or national phases.


2. Scope of the Patent

2.1 Patent Specification and Description

The patent specification likely describes an innovative compound, its synthesis, unique formulation, or therapeutic use. Given the typical scope for drug patents, it likely includes:

  • Chemical Composition: Structural formulas, intermediates, and variants
  • Therapeutic Application: Indications or methods of treatment
  • Manufacturing Processes: Methods for production
  • Use Claims: Specific uses or dosing regimens

2.2 Boundaries and Limitations

The patent's scope is generally confined to the specific claims it enshrines. In pharmaceuticals, scope can vary from broad compound classes to narrow, structurally specific molecules. The enforceability depends on claim breadth and clarity.


3. Claims Analysis

3.1 Types of Claims

  • Product Claims: Cover the chemical entity itself, e.g., a specific compound or pharmaceutical composition
  • Use Claims: Describe particular therapeutic uses, e.g., treatment of a disease
  • Process Claims: Cover synthesis or formulation methods
  • Formulation Claims: Cover dosage forms or delivery systems

3.2 Claim Breadth and Specificity

  • Broad Claims: If the patent claims wide classes of compounds or mechanisms, it offers extensive protection but must withstand validity challenges based on novelty and inventive step.
  • Narrow Claims: Specific compounds or claims limited to a subset of embodiments, easier to defend but offer limited scope.

3.3 Key Claim Elements

Typical patent claims for a drug involve:

  • Structural Formula: Exact molecular structure, e.g., a specific heterocyclic compound.
  • Pharmacological Effect: Claims directed towards antiproliferative, anti-inflammatory, or other therapeutic actions.
  • Method of Use: Claims covering methods of administering the compound for the treatment of particular diseases.

3.4 Claim Strategy & Potential Challenges

Patents drafted with overly broad claims risk invalidation for lack of novelty or inventive step. Conversely, narrow claims, while more defensible, provide limited commercial exclusivity. The claims' language likely reflects a balance to maximize scope while maintaining validity, encompassing:

  • Variants of the core compound to deter designed-around strategies
  • Specific formulations for targeted delivery
  • Method claims encompassing specific methods of administration

4. Patent Landscape Context

4.1 National and International Patent Environment

Poland's patent law aligns with EU standards, providing a 20-year patent term from filing, subject to procedural compliance. The landscape comprises:

  • European Patent Applications: Possibility of validation in the EU, ensuring broader regional protection
  • Global Patent Families: International rights via PCT applications, extending protection globally

4.2 Competitor Patents & Freedom-to-Operate

The patent landscape for similar compounds or therapeutic areas influences PL2916856’s strategic value:

  • Existing Patent Families: For related drugs, potential for licensing or infringement risk
  • Cited Art & Priority Documents: Indicate the inventive background and possible overlaps
  • Major Patent Holders: Companies active in similar therapeutic classes (e.g., Pfizer, Novartis) inform the competitive environment

4.3 Patent Validity & Litigation

The robust drafting of claims and thorough patent prosecution history influence enforceability. In Poland and the EU, validity challenges often involve prior art searches and inventive step assessments, vital for asserting or defending patent rights.


5. Strategic Significance

  • Market Exclusivity: Effective if claims cover the core therapeutic compounds or methods
  • Licensing Opportunities: If claims are broad enough, licensing or partnership potential increases
  • Litigation & Defense: Detailed claims provide a stronger basis to defend against infringement or validity challenges

6. Conclusion

Patent PL2916856, based on typical drug patent characteristics, provides a strategically significant scope within the Polish pharmaceutical landscape. Its claims, presumed to balance breadth and validity, form the cornerstone of its competitive advantage. As pharmaceutical innovation evolves, ongoing vigilance over the patent landscape remains necessary to maintain enforceability and capitalize on market opportunities.


Key Takeaways

  • Scope & Claims: The patent likely encompasses specific chemical compounds, formulations, or therapeutic methods, with claim breadth tailored to maximize protection while ensuring validity.
  • Patent Landscape Position: Its value depends on the proximity to existing patents, potential overlaps, and regional or international patent strategies.
  • Competitor Considerations: Monitoring similar patents and potential infringing activities is vital for defending or asserting rights.
  • Legal Validity & Enforcement: Robust claim drafting and strategic prosecution enhance enforceability in Poland and beyond.
  • Strategic Movements: Expanding protection through national or international filings can secure a competitive edge in the evolving pharmaceutical market.

FAQs

Q1: How broad are the claims typically in pharmaceutical patents like PL2916856?
A1: They can range from narrow, structurally specific compounds to broad classes of molecules, balancing protection with validity.

Q2: Can this patent be extended or maintained beyond 20 years?
A2: Patent term extensions are rare in Poland but may be possible if regulatory delays occur. Otherwise, the patent expires after 20 years from filing.

Q3: How does the patent landscape influence the value of PL2916856?
A3: Overlapping patents, prior art, and competing rights can limit enforceability or create licensing opportunities, affecting its strategic value.

Q4: What role do claims play in defending the patent against infringement?
A4: Well-drafted claims define the scope of protection; precise language ensures clarity in enforcement and reduces infringement risks.

Q5: How can the patent landscape impact future drug development?
A5: It guides innovation trajectories, helps avoid infringement, and identifies licensing opportunities, shaping R&D strategies.


Sources:

[1] European Patent Office, "EPO Patent Law," 2022.
[2] Polish Patent Office, "Guidelines for Patent Examination," 2022.
[3] WIPO, "Patent Landscape Reports," 2022.

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