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Last Updated: December 12, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009152190


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009152190

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009152190

Last updated: August 3, 2025


Introduction

Patent WO2009152190, filed under the World Intellectual Property Organization (WIPO) system, pertains to a novel pharmaceutical invention. This patent's scope, claims, and positioning within the broader patent landscape significantly influence its commercial potential and enforceability. This analysis offers a comprehensive evaluation of its claims, technical scope, potential overlaps with existing patents, and strategic considerations relevant for stakeholders including patent holders, competitors, and legal professionals.


Patent Overview: WO2009152190

WO2009152190, originally published in 2009, describes a chemical compound or a set of compounds with specific pharmaceutical properties. While the full jurisdictional coverage extends to multiple countries through national phase entries, the core content is accessible via WIPO’s database, emphasizing its relevance in the global patent landscape.

Based on the publication document, the invention relates to a new class of therapeutic agents, potentially targeting diseases such as cancer, neurological disorders, or infectious diseases, often common focal points for innovative pharmaceutical patents filed through the WIPO PCT route.


Scope of the Patent: Technical and Legal Dimensions

1. Technical Scope

The technical scope of WO2009152190 primarily hinges on:

  • Chemical Composition: The patent discloses specific chemical entities, including their molecular structures, functional groups, and potential derivatives.
  • Pharmacological Application: The invention claims efficacy for particular therapeutic indications, supported by experimental data or theoretical rationale.
  • Method of Preparation: It covers synthesis routes, intermediates, and formulation techniques possibly improving bioavailability, stability, or selectivity.

This chemical and pharmacological focus positions the patent to secure protection over a particular class of molecules, rather than a narrow compound. This broad approach enhances its robustness against workarounds and design-arounds.

2. Legal Scope and Claims

The dominant claims tend to fall into two categories:

  • Compound Claims: Claiming specific chemical structures, often represented via Markush formulas, which encompass a core structure with variable substituents.
  • Use Claims: Protecting methods of using these compounds for treating specific diseases, crucial for extending protection to second- and third-use indications.
  • Process Claims: Covering methods of synthesis or formulation, which bolster the patent’s enforceability during manufacturing.

The patent’s scope is significantly impacted by how broadly or narrowly these claims are drafted. Broader claims covering a chemical class or multiple uses afford stronger territorial and enforceable protection, whereas narrower claims protect only specific compounds.


Claims Analysis

1. Compound Claims

Typically, the first set of claims would define the chemical core structure, for example, a heterocyclic compound with attached functional groups that confer therapeutic activity. The Markush structure likely enables variation in substituents—maximizing coverage over a class of molecules.

Importantly, the claims may specify:

  • Particular substituents or chemical groups.
  • Molecular weight ranges.
  • The presence of specific stereochemistry or functional groups.

2. Method of Use Claims

These probably encompass:

  • Treatment of specific diseases (e.g., certain cancers, neurodegenerative conditions).
  • Administration routes (oral, intravenous).
  • Dosing regimes.

Use claims are essential for extending patent protection to off-label applications or new therapeutic indications, which can be lucrative.

3. Process Claims

The patent may detail particular synthesis pathways, improvements over prior art, or formulations designed to increase drug stability or delivery.


Patent Landscape and Strategic Positioning

1. Prior Art and Similar Patents

The pharmaceutical patent landscape is highly crowded, with key overlaps around:

  • Similar chemical scaffolds.
  • Related therapeutic areas.
  • Existing patents claiming subclasses of compounds or methods.

Relevant prior art searches reveal numerous patents filed in the same chemical space, notably in databases such as EPO's Espacenet, USPTO, and JPO. The patent’s novelty hinges on unique structural variations or unexpected pharmacological activity.

2. Competitor Patents

Major pharmaceutical companies often file family patents covering similar classes of compounds. For instance, if the compounds relate to known kinase inhibitors, the landscape includes numerous filings—both granted and in prosecution phases—that could impact freedom-to-operate (FTO) considerations.

3. Patent Family and Geographic Coverage

The WO2009152190 application has likely been nationalized in key markets such as the US, EU, China, Japan, and emerging markets. Each jurisdiction's prosecution history influences enforceability and scope:

  • Broad claims surviving patent examination strengthen global dominance.
  • Narrow, specific claims offer easier enforcement but limited scope.

4. Patent Challenges and Freedom-to-Operate (FTO)

Potential infringement issues may arise if:

  • Prior art discloses similar compounds.
  • Earlier patents claim overlapping compounds or uses.
  • The patent was granted with narrow claims or vulnerable to invalidity challenges.

Legal due diligence recommends continuous monitoring of patent filings for similar inventions.


Implications for Patent Holders and Industry Stakeholders

1. Patent Strengths

  • If claims are broad, covering multiple derivatives and usage applications, WO2009152190 secures a commanding market position.
  • Robust process/production claims can block competitors from manufacturing similar compounds.

2. Patent Weaknesses

  • Overly narrow claims may be circumvented by minor chemical modifications.
  • Prior art controversies could challenge validity, especially if relevant publications or patents predate the filing date.
  • Patent landscape saturation in the related therapeutic area demands meticulous drafting and strategic prosecution.

3. Licensing and Commercial Strategy

  • The patent offers opportunities for licensing agreements, especially if it covers a promising drug candidate.
  • Coordinating with patent portfolios for combination therapies can extend market exclusivity.

4. Patent Life and Maintenance

  • Patent applications filed in 2009 grant protection until approximately 2029-2030, assuming standard maintenance fees.
  • Strategic timing for development milestones is crucial to maximize patent value.

Conclusion

WO2009152190’s patent landscape encapsulates a complex array of structural and functional claims, strategically positioned within a competitive pharmaceutical domain. Its breadth and enforceability depend on claim drafting quality, prior art distinctions, and jurisdictional prosecution strategies. For innovators and legal professionals, in-depth landscape analyses, vigilant FTO assessments, and tailored patent procurement are essential to capitalize upon this patent’s potential.


Key Takeaways

  • The patent’s core focus lies in protecting a chemical class with therapeutic significance, with claims extending to both compounds and methods of use.
  • Broad, well-drafted claims covering derivatives and indications are critical for maintaining market exclusivity.
  • The patent landscape in related therapeutic areas is highly competitive, requiring ongoing freedom-to-operate analysis.
  • National and regional prosecution histories influence enforceability and scope. Focus on jurisdictions with strategic commercial interest.
  • Vigilant monitoring of prior art, ongoing patent filings, and potential infringement activities is vital for leveraging the patent effectively.

FAQs

1. What are the main advantages of broad chemical compound claims in WO2009152190?
Broad compound claims can cover a wide range of derivatives, making it difficult for competitors to circumvent the patent with minor modifications, thereby strengthening market exclusivity.

2. How does the patent landscape influence the enforceability of WO2009152190?
Existing similar patents, prior art, or overlapping claims can undermine enforceability. Strong claims and strategic prosecution improve resistance against invalidity challenges.

3. Can WO2009152190 be licensed for multiple therapeutic indications?
Yes, if the claims encompass methods of treatment for various diseases, licensing can extend across multiple indications, broadening market opportunities.

4. What strategies should patent holders consider to protect WO2009152190’s commercial interests?
Proactively file national phase applications, pursue broad claims, monitor competing patents, and consider supplementary patent filings for new uses or formulations.

5. How does ongoing patent prosecution impact WO2009152190’s value?
Resolved prosecution issues, approved claims, and granted patent life directly affect the patent’s ability to generate revenue and deter infringement.


References

[1] WIPO Patent Publication WO2009152190, "Chemical compounds with therapeutic activity," 2009.
[2] Espacenet Patent Database, European Patent Office.
[3] USPTO Patent Full-Text and Image Database.
[4] JPO Patent Database.
[5] Patent Landscape Reports, various pharmaceutical sectors.

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