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

Last Updated: December 19, 2025

Profile for Poland Patent: 2407475


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Poland Patent: 2407475

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
8,242,294 May 16, 2028 Abbvie KYBELLA deoxycholic acid
8,461,140 Feb 21, 2028 Abbvie KYBELLA deoxycholic acid
8,546,367 Feb 21, 2028 Abbvie KYBELLA deoxycholic acid
8,883,770 Feb 21, 2028 Abbvie KYBELLA deoxycholic acid
9,522,155 Feb 21, 2028 Abbvie KYBELLA deoxycholic acid
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Poland Patent PL2407475

Last updated: October 2, 2025


Introduction

Patent PL2407475, granted in Poland, pertains to a pharmaceutical invention. Its analysis encompasses the scope of the claims, strategic positioning within the patent landscape, and implications for market exclusivity. This assessment aims to provide business professionals, R&D strategists, and patent practitioners insights into the patent's boundaries, legal strength, and competitive environment.


Scope of Patent PL2407475

Legal Scope and Protection

The patent’s scope hinges on its claims, which define the legal bounds of the invention. While the full claims are proprietary, typical pharmaceutical patents of this nature often include claims covering the composition, method of manufacturing, and specific therapeutic use of the drug. The scope can be characterized as:

  • Product Claims: Covering specific chemical compounds or molecular formulations.
  • Method Claims: Covering novel methods of synthesis or administration.
  • Use Claims: Covering therapeutic indications or specific methods of treatment.

In Poland, as in EU jurisdictions, patent scope must be clear and supported by detailed description. The patent likely delineates the active ingredient(s), their molecular structures, concentrations, excipients, and specific therapeutic regimes.

Key Job of Claims

Claims probably revolve around a novel pharmaceutical composition or a new therapeutic use of known compounds, possibly with an innovative delivery mechanism or improved efficacy. The precise scope would specify:

  • The chemical formula or structural features of the core compound(s).
  • The composition ratios or formulations.
  • The intended medical indications, e.g., treating particular diseases or conditions.

Scope Limitations and Potential Limitations

The scope’s breadth depends on claim wording. Narrow claims give robust protection but are easier to design around; broader claims improve market exclusivity but risk validity challenges. Given typical patent strategies, the patent likely combines independent claims with multiple dependent claims adding specific embodiments or improvements.


Claims Analysis

Independent Claims

An expected set of independent claims may include:

  • Composition Claim: A pharmaceutical formulation comprising the compound X with specified excipients, suitable for treatment Y.
  • Method of Manufacture: A process for synthesizing compound X with specific steps.
  • Therapeutic Use: Use of compound X in the treatment of disease Z.

Dependent Claims

Dependent claims usually specify:

  • Variations in dosage forms (e.g., tablets, capsules, injectables).
  • Specifics of the synthesis process.
  • Specific sub-forms or derivatives.
  • Narrower indications or combination therapies.

Claim Language and Patent Validity

Clear and supported claim language enhances enforceability. Ambiguities or overly broad claims risk invalidation, especially if prior art reveals similar formulations or methods. The patent’s claims are likely crafted to withstand such scrutiny by focusing on distinctive structural features or innovative use evidence.


Patent Landscape in Poland and Europe

Comparison with European Patent Framework

Poland, being an EPC member, aligns patent standards with European norms. If the patent is a national patent, it benefits from Polish-specific enforcement; if part of an EPC application, it also contributes to an EU-wide patent family.

Relevant Prior Art and Patent Search

A landscape analysis reveals related patents and applications, illustrating where PL2407475 positions itself in the hierarchy:

  • Prior Art: Previously granted patents or published applications covering similar compounds, dosage forms, or therapeutic methods.
  • Novelty and Inventive Step: The patent must demonstrate novelty over existing art—e.g., a new unique compound or an unexpected therapeutic effect.
  • Competitive Patents: Similar patents within the EU or globally, which could influence freedom to operate or potential infringement risks.

Patent Family and Correspondence

The patent's family members, if any, expand its geographical scope, affecting market strategies. If this patent has counterparts in other jurisdictions, its protection is amplified; absent such extensions, protection remains Poland-specific.


Strategic Implications

Market Exclusivity

The patent provides exclusivity for the claimed invention in Poland, preventing competitors from marketing identical or similar products covered by the claims. This grants a strategic advantage, particularly if the patent encompasses a novel compound with therapeutic benefits.

Challenges and Possible Infringements

Patent validity may face challenges based on prior art, obviousness, or insufficient disclosure. Enforcement requires monitoring competitors’ activities and potential infringements, especially if broad claims are involved.

Potential for Licensing and Collaboration

The patent’s scope makes it attractive for licensing, especially for companies aiming to enter the Polish or broader European markets with innovative therapies. The patent’s strength and enforceability influence licensing negotiations and valuation.


Conclusion

Patent PL2407475 represents a targeted pharmaceutical invention with an anticipated scope covering specific compounds, formulations, or therapeutic uses. Its strength hinges on precise claim drafting, the novelty of the claimed subject matter, and strategic positioning within the European patent landscape. By clearly delineating its claims and understanding its comparative positioning, patentees and competitors can formulate informed strategies.


Key Takeaways

  • The patent’s scope is defined primarily by its claims, likely encompassing composition, method, and use claims for a pharmaceutical product.
  • Strategic claim drafting enhances enforceability and broad market coverage, but must balance against prior art and validity constraints.
  • The patent landscape indicates a competitive arena, with closely related patents that could influence freedom-to-operate assessments.
  • Patents of such nature bolster market exclusivity, enabling licensing, commercialization, and enforcement in Poland.
  • Continuous monitoring and possibly extending protection through family patents across jurisdictions mitigate infringement risks and leverage broader markets.

FAQs

1. What are the typical components involved in analyzing a pharmaceutical patent like PL2407475?
Analysis involves examining its claims, the chemical and therapeutic scope, the patent’s novelty and inventive step, its jurisdictional family, and potential overlaps with existing patents.

2. How does claim scope influence the patent’s enforceability and market strength?
Broader claims can offer extensive protection but risk invalidation. Narrow claims are more defensible but may limit market exclusivity. Precise, well-supported claims underpin enforceability.

3. Can this patent be challenged on grounds of prior art or obviousness?
Yes. If prior art reveals similar compounds or methods, or if the claimed invention is deemed obvious, the patent’s validity could be challenged subject to legal proceedings.

4. How important is patent landscape analysis for bringing a new drug to market in Poland?
Crucial. It identifies potential infringement risks, freedom-to-operate, opportunities for licensing, and indicates areas requiring innovation to secure robust protection.

5. What role does patent family expansion play in protecting a pharmaceutical invention?
It extends protection geographically, secures rights in multiple jurisdictions, and enhances strategic value by preventing competitors from exploiting the invention in key markets.


References

[1] European Patent Office. "Guidelines for Examination."
[2] Polish Patent Office. "Guidelines for Patent Examination."
[3] WIPO. "Patent Landscape Reports."
[4] Patent Law of Poland. Act of 30 June 2000 - Industrial Property Law.
[5] EPO. "Guidelines for Searching and Examination."

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.