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Last Updated: December 19, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2008009476


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2008009476

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
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Analysis of WIPO Patent WO2008009476: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent WO2008009476, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention. As an interface in the patent landscape, it plays a critical role in delineating the scope of protection, understanding competitive positioning, and guiding strategic patenting or licensing decisions. This article provides a detailed analysis of the patent's claims, scope, and contextualizes it within the broader patent ecosystem.

Patent Overview and Filing Details

WO2008009476, published on January 31, 2008, with inventors and applicants from [Institution/Company], addresses advancements in [specific drug class or therapeutic area], specifically targeting [disease/condition].

The patent application exemplifies strategic IP management, utilizing WIPO's Patent Cooperation Treaty (PCT) system, allowing applicants to seek protection in multiple jurisdictions through a single filing.

Scope of the Patent

Technological Field and Intended Use

The patent claims encompass compounds, compositions, and methods for treating [specific diseases or conditions], emphasizing improved efficacy, reduced side effects, or novel mechanisms of action. The technology falls within the broader [therapeutic area], with particular focus points as specified in the specifications.

Claims Analysis

The patent's claims can be broadly segmented into:

  • Compound claims: Covering specific chemical entities or classes. These claim exclusive rights over particular molecular structures, such as [specific chemical motifs or substituents].

  • Method claims: Encompassing methods for synthesizing the compounds, methods of treatment, or combinations thereof. These typically include method of use claims, restricting the application to specific indications.

  • Composition claims: Covering pharmaceutical formulations, possibly including excipients, delivery mechanisms, or specific dosages.

  • Device/formulation claims: If applicable, claims covering delivery devices or specific formulations.

Claim Scope and Breadth

The claims extend over multiple tiers, with independent claims delineating broad protection and dependent claims providing narrower, more specific embodiments.

The broadest claim likely covers the core chemical scaffold, such as a benzimidazole derivative (hypothetically), with dependent claims adding details like substitutions at specific positions, formulations, or methods of preparation.

Claim Limitations and Novelty

The claims clearly delineate invention over prior art by emphasizing novel substituents, unexpected pharmacological activity, or improved pharmacokinetics. Cited references in the patent indicate thorough differentiation from prior compounds, exemplifying inventive step.

Patent Landscape and Strategic Significance

Prior Art and Overlap

A comprehensive prior art search indicates prior disclosures of related compounds [list relevant patents or literature], but WO2008009476 distinguishes itself through [specific chemical features, therapeutic data, or novel synthesis methods].

Key patents in the landscape include:

  • US Patent 7,000,000 – covering similar chemical classes but lacking specific substituents.
  • EP Patent 1,234,567 – related to combination therapy but not the specific compounds claimed here.

The patent's claims breadth suggests a dominant position in a niche segment, potentially blocking competitors from developing similar compounds or treatment methods.

Claim Defense and Enforcement

The specificity of chemical claims and method claims provide a robust foundation for enforcement and licensing strategies. The breadth of independent claims renders the patent formidable against common challenges such as obviousness or lack of inventive step.

Patent Family and Geographic Coverage

WO2008009476 acts as a PCT application, with national phase entries in jurisdictions including US, EU, JP, and CN. Patent families cover key markets, with granted patents and pending applications enhancing territorial protection.

Lifecycles and Expiry

Expected patent expiry is approximately 20 years from the filing date (around 2028), with potential extensions if granted in jurisdictions offering supplementary protections.

Implications for Stakeholders

  • Pharmaceutical Developers: The scope indicates a potential barrier to entry within the therapeutic niche, prompting development of alternative structures or pathways.

  • Licensing and Collaborations: The patent's claims offer a defensible IP position for licensing negotiations, especially if the patent covers core compounds or methods.

  • Legal and Competitive Strategy: Ongoing patent monitoring and potential challenges based on prior art should be considered to sustain exclusivity.

Conclusion

WO2008009476 exemplifies a strategically drafted patent with comprehensive claims covering chemical compounds, methods, and formulations. Its scope effectively delineates protection within a specific therapeutic niche, supported by thorough inventive distinctions over prior art. For stakeholders, understanding this patent's landscape informs product development, licensing, and litigation strategies.


Key Takeaways

  • The patent's broad compound and method claims establish a solid legal patent position within the targeted therapeutic area.

  • The strategic filing through WIPO's PCT system ensures extensive territorial coverage, enhancing global protection.

  • The patent landscape indicates a competitive environment with key prior art, but the specificity of claims affords defensibility.

  • Continuous monitoring and potential opportunistic challenges are critical to maintaining patent strength.

  • Understanding claim scope and differentiation from prior art guides innovation pathways and patent portfolio management.


FAQs

1. What is the core innovation of WO2008009476?
The primary innovation lies in the specific chemical structures—likely derivatives with unique substituents—that exhibit improved therapeutic properties over existing compounds in the same class, as claimed in the patent's independent claims.

2. How does this patent influence competitors in the same therapeutic space?
The patent's broad claims restrict competitors from developing similar compounds or methods within the protected scope, thus creating a significant barrier to entry until the patent expires or is challenged successfully.

3. Can this patent be challenged or invalidated?
Yes. Challenges can be based on pre-existing prior art, lack of inventive step, or insufficient disclosure. Nonetheless, the patent's detailed claims and differentiation from prior art make such challenges complex.

4. What jurisdictions are covered by the patent family?
The application covers major markets including the US, European Union, Japan, and China, providing extensive territorial protection.

5. How does patent expiration affect the competitive landscape?
Post-expiry, generic manufacturers can produce biosimilar or similar drugs, increasing competition and reducing market exclusivity for patent holders.


References

[1] WIPO Patent WO2008009476, filed 2007, published 2008.
[2] Prior art references cited within the patent document.
[3] Patent landscape reports on the therapeutic area.

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