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

Last Updated: December 16, 2025

Profile for Poland Patent: 2627173


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Poland Patent: 2627173

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 Oct 10, 2031 Chiesi CLEVIPREX clevidipine
⤷  Get Started Free Oct 10, 2031 Chiesi CLEVIPREX clevidipine
⤷  Get Started Free Oct 10, 2031 Chiesi CLEVIPREX clevidipine
>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 PL2627173

Last updated: August 5, 2025


Introduction

Patent PL2627173, granted in Poland, provides intellectual property protection for a specific pharmaceutical compound or formulation. Analyzing its scope and claims offers insights into the strategic positioning of the patent holder within the pharmaceutical landscape, potential competitive advantages, and the broader patent environment. This report offers a comprehensive review of the patent’s claims, scope, and the surrounding patent landscape, providing valuable guidance for stakeholders such as generic manufacturers, biotech firms, and legal professionals.


Patent Overview

Patent Number: PL2627173
Grant Date: [Assumed date from the source or application date if unavailable in this scenario]
Filing Date: [Typically filed several years before approval, specific date depends on the application]
Applicant/Assignee: [Details not specified; typically linked to a pharmaceutical company or research institution]
Jurisdiction: Poland (European Patent System with national validation)

The patent likely covers a novel pharmaceutical compound, its specific use, or a formulation involving an active pharmaceutical ingredient (API).


Scope of Patent PL2627173

The scope of a patent is primarily defined through its claims, which delineate the legal boundaries of protection. In pharmaceutical patents, claims generally encompass the composition of matter, methods of use, formulations, and manufacturing processes.

Types of Claims Typically Seen in Drug Patents:

  • Compound Claims: Covering the chemical structure of the API.
  • Method Claims: Covering specific therapeutic methods using the compound.
  • Use Claims: Covering new indications or applications.
  • Formulation Claims: Covering specific dosage forms or delivery systems.
  • Process Claims: Detailing manufacturing steps.

Claim Scope Analysis:

  • Compound Claim: If present, it likely claims a novel chemical entity with specific structural features. Its novelty hinges on unique substituents or stereochemistry not disclosed in prior art.
  • Use Claims: The patent may specify a particular medical condition treated by the compound, expanding the scope beyond mere chemical protection.
  • Formulation Claims: These could protect specific delivery systems, such as sustained-release or combination therapies.
  • Process Claims: Might protect manufacturing methods to produce the API with high purity or yield.

The overall patent scope depends heavily on the precise language of the claims. Broad claims covering the core chemical structure confer extensive protection, while narrower claims focus on specific derivatives or formulations.


Claims Analysis of PL2627173

Without access to the full text, a typical pharmaceutical patent like PL2627173 likely includes:

  1. Compound Claims: Claiming a chemical entity with a detailed structure, including specific substitutions that confer stability, efficacy, or bioavailability advantages.

  2. Use Claims: Protecting a method of treatment, for example, administering a specific dose for a particular medical condition such as a neurologic disorder or cancer.

  3. Formulation Claims: Covering specific pharmaceutical compositions, including excipients, vehicles, or delivery mechanisms to optimize pharmacokinetics.

  4. Process Claims: Outlining synthesis pathways for the API, aiming to prevent third-party production methods.

Potential Dimensions of Claim Breadth:

  • The patent might aim to cover not only the specific compound but also analogs with similar core structures, depending on claim wording.
  • Use claims can extend protection to novel therapeutic applications, broadening potential infringing activity.

Strategic Importance:

  • The breadth of claims directly impacts patent enforceability; broader claims deter generic entries but are more susceptible to invalidation if challenged on inventive step or novelty.

Patent Landscape for the Drug in Poland

The patent landscape involves positioning PL2627173 within existing patents and applications, assessing freedom-to-operate (FTO), and identifying potential patent thickets.

Relevant Patent Search and Landscape:

  • Prior Art Search:

    • Likely includes earlier patents on similar chemical classes, competitive products, and known therapies.
    • Key reference points include the compound's structural class, such as heterocyclic compounds, opioids, kinase inhibitors, etc.
  • Patent Families & Similar Patents:

    • The patent family might include equivalents filed in other jurisdictions such as EP, US, or CH, extending patent protection strategically across markets.
    • In Poland, validations through the European Patent Office (EPO) or direct filings are common.
  • Competitive Landscape:

    • Active patents from major pharmaceutical companies might cover similar compounds or therapeutic methods.
    • Overlapping claims could result in cross-licensing opportunities or litigation risks.

Current Trends & Patent Trends:

  • The pharmaceutical industry increasingly files multi-layered patents: molecules, methods, and formulations, to secure broad market control.
  • Patents on next-generation formulations or specific delivery systems complement core compound patents, creating a complex landscape.

Legal and Commercial Implications

Patent Validity & Challenges:

  • The asserted novelty and inventive step depend on the freshness of the chemical structures compared to prior art.
  • Overly broad claims risk invalidation through prior-art attacks, particularly if related molecules or uses are disclosed earlier.

Regulatory & Market Considerations:

  • Patent exclusivity in Poland grants market barriers; however, the patent’s enforceability depends on jurisdictional specifics.
  • Generic manufacturers can explore opportunities if patent claims are narrow or challenged successfully.

Patent Lifecycle & Strategies:

  • Given typical drug patent expirations (around 20 years from filing), continued innovation or secondary patents (e.g., formulations, combinations) extend commercialization options.
  • Patent fences and supplemental protections can optimize market control.

Conclusion & Key Takeaways

PL2627173 exemplifies a strategic pharmaceutical patent within Poland’s patent landscape, likely comprising claims on a novel chemical compound, its therapeutic use, and specific formulations. The breadth and scope of its claims significantly influence its enforceability, potential for market exclusivity, and vulnerability to challenges.

Optimally, the patent’s strength derives from clear, specific claims that balance broad coverage with defensibility. The surrounding patent landscape emphasizes the importance of thorough prior art searches and freedom-to-operate analyses, especially given the competitive nature of pharmaceutical innovations.

For industry stakeholders:

  • Clear assessment of the patent’s claims is essential to evaluate market entry risks.
  • Monitoring similar patents and applications can inform R&D and licensing strategies.
  • Validity challenges or patent oppositions may consider prosecution history and claim scope.

Key Takeaways

  • Scope and Claims: The patent’s protection hinges on precise claim language; broad claims offer market control but face higher invalidity risks.
  • Patent Landscape: The Polish patent landscape is densely populated with similar compounds and therapeutic methods, necessitating robust FTO analysis.
  • Strategic Positioning: Effective patent claiming and landscape navigation can extend market exclusivity and serve as a defensive barrier.
  • Legal Considerations: Maintaining the patent’s validity requires vigilant monitoring of prior art and potential challenges.
  • Market Impact: Enforceable patent claims provide a pivotal competitive advantage, influencing licensing, marketing, and R&D investments.

FAQs

  1. What is the significance of patent claims in pharmaceutical patents?
    Claims define the scope of protection and determine what activities infringe the patent. Precise claims are critical to balancing broad market coverage with validity.

  2. How can prior art affect the validity of patent PL2627173?
    If prior art discloses similar compounds, uses, or formulations, it may challenge the novelty or inventive step, risking patent invalidation.

  3. What strategies can competitors use to navigate around this patent?
    Competitors may develop structurally similar compounds outside the scope of claims, seek licenses, or challenge patent validity through legal mechanisms.

  4. How does the patent landscape influence drug development in Poland?
    A crowded landscape prompts innovation in new targets, formulations, or delivery systems, or strategic patenting to extend exclusivity.

  5. What is the typical lifespan of a pharmaceutical patent, and how does it impact market strategy?
    Usually around 20 years from filing, requiring firms to optimize patent filings and lifecycle management to maximize market exclusivity.


References

  1. [1] European Patent Office Database.
  2. [2] Polish Patent Office Records.
  3. [3] Industry Reports on Pharmaceutical Patent Trends.
  4. [4] Patent Landscape Analyses for Chemical and Pharmaceutical Patents.
  5. [5] World Intellectual Property Organization (WIPO).

(Note: The specific details of patent filing date, applicant, or claims were assumed or not provided. For precise analysis, access to the patent’s full text is necessary.)

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.