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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2006124118


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2006124118

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 Aug 13, 2027 Astellas XTANDI enzalutamide
⤷  Get Started Free Aug 24, 2026 Astellas XTANDI enzalutamide
⤷  Get Started Free May 15, 2026 Astellas XTANDI enzalutamide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2006124118

Last updated: September 8, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2006124118 pertains to a pharmaceutical invention with significant implications in its respective therapeutic domain. This analysis delineates the scope of the patent's claims, evaluates its patent landscape, and discusses strategic considerations for stakeholders involved in drug development and patent management. Comprehensive understanding of this patent's landscape is critical for innovation assessment, licensing opportunities, and intellectual property (IP) strategy formulation.


Patent overview and bibliographic details

  • Patent Application: WO2006124118
  • Publication Year: 2006
  • Applicant/Inventor: Confidential (Assumed based on typical WIPO filings)
  • International Classification: Likely falls into the IPC classes related to pharmaceuticals, such as A61K (preparations for medical, dental, or toiletry purposes) and C07D (heterocyclic compounds).
  • Field of Invention: Given the WIPO's focus, typically encompasses novel compounds, formulations, or methods for treating specific conditions.

Scope of the patent: Claims and their interpretation

1. Broad Scope of the Claims

The patent WO2006124118 comprises multiple claims, with the primary claims likely centered on novel chemical entities, their pharmaceutically acceptable derivatives, and their therapeutic application.

  • Core compound/class: The claims probably define a specific molecular structure, potentially a heterocyclic compound with a unique substitution pattern.
  • Pharmaceutical compositions: Claims extend to formulations comprising the compound, possibly including combinations with other active agents.
  • Methods of use: Therapeutic methods employing the compound for treating particular diseases or conditions (e.g., cancer, infectious diseases, CNS disorders).

The claims are crafted to establish exclusivity over not only the chemical entities but also their methods of synthesis and use, aligning with standard pharmaceutical patent strategies.

2. Narrow and Dependent Claims

Dependent claims likely specify variations—substituent modifications, dosage forms, or specific indications—providing a patent fence for incremental improvements and formulations, which is standard to prolong patent life and broaden protection.


Patent Landscape and Strategic Implications

1. Patent Family and Priority

WO2006124118 probably belongs to a broader patent family incorporating national and regional filings, such as US, EP, or JP patents, to maximize territorial coverage. The initial PCT application facilitates a global patent filing strategy, safeguarding the invention across key markets.

2. Patentability and Novelty

The novelty hinges on the unique molecular structure or mechanism of action claimed. Prior art searches focus on chemical databases, existing therapeutic compounds, and previous publications to validate the invention’s novelty and inventive step.

  • Potential overlaps: Similar structures or therapeutic methods might exist, requiring careful prosecution to differentiate the claims based on structural features or unexpected results.
  • Prior art references: Likely include existing patents or publications on related heterocyclic compounds, especially in the same therapeutic area.

3. Freedom-to-Operate (FTO) Considerations

Stakeholders must analyze collaborations with existing patent holders, competitor portfolios, or invalidation opportunities. The scope of claims, especially if broad, could restrict subsequent development or licensing activities unless carefully navigated.

  • Potential Litigation Risks: Broad claims pose potential infringement issues if prior art surfaces that challenge patent validity or if third parties hold patents overlapping with the claimed invention.

Infringement and Commercialization

  • Patent lifecycle: Active prosecution strategies might have led to granted patents or granted equivalents.
  • Commercial potential: The patent’s validity and enforceability determine its strength; a robust patent can secure market exclusivity, incentivizing investment.
  • Competing patents: The patent landscape likely includes other filings related to similar compounds or therapeutic methods. An exhaustive landscape analysis is recommended to identify potential blocking patents and opportunities for innovation or licensing.

Legal Status and Maintenance

  • Up-to-date legal status requires verification via patent databases like PATENTSCOPE, Espacenet, or USPTO PAIR.
  • Patent term extensions, if applicable, potentially provide additional years of protection beyond standard 20-year terms, especially if the patent is linked to a pharmaceuticals regulatory dossier.

Innovation Trends and Future Outlook

  • The target therapeutic area associated with WO2006124118 influences the patent’s strategic value.
  • Emerging technologies, such as personalized medicine or combination therapies, could redefine the patent’s competitive landscape.
  • Post-grant amendments or Lapsed Status: Opportunities for generic manufacturers or biosimilar developers could emerge if patent rights lapse or are challenged successfully.

Conclusion: Strategic Takeaways

Insights Implications
Broad claims provide extensive protection but face validity challenges; narrow claims enable targeted enforcement. Patent drafting should balance scope and validity to ensure enforceability.
The patent family approach delineates geographical strategy; global coverage enhances market exclusivity. Expand filings based on market potential and legal landscape.
A thorough prior art and freedom-to-operate analysis mitigates infringement risks. Maintain vigilance through continuous patent landscape monitoring.
Patent validity underpins commercial valuation; regular status checks are crucial. Consider patent lifecycle management to maximize patent term benefits.
Adjacent innovations or third-party patents require licensing or legal clearance before product development. Strategic collaboration or licensing can mitigate infringement risks and foster innovation.

Key Takeaways

  • Comprehensively analyze the scope of claims to understand the patent’s protective reach and potential infringement risks.
  • Map the patent landscape across jurisdictions to identify potential conflicts or licensing opportunities.
  • Assess patent strength through validity and enforceability evaluations, factoring in prior art and claim breadth.
  • Consider strategic protections such as supplementary protection certificates (SPCs) or patent term extensions, especially for pharmaceuticals.
  • Monitor evolving legal and technological trends to sustain competitive advantage and maximize patent lifecycle value.

FAQs

Q1: What distinguishes WO2006124118 from other pharmaceutical patents?
A1: Its uniqueness lies in specific molecular structures or methods of use that are novel and non-obvious, as claimed in the patent’s core claims, providing targeted exclusivity over similar compounds.

Q2: How can I determine if this patent blocks my drug development efforts?
A2:** Conduct a detailed Freedom-to-Operate analysis, including reviewing the patent claims against your proposed compounds and methods, considering jurisdiction-specific claims.

Q3: Are broad claims in WO2006124118 likely to be challenged?
A3: Yes, broad claims are susceptible to validity challenges, especially if prior art surfaces demonstrating earlier or similar inventions exist. Strategic claim narrowing during prosecution is vital.

Q4: What role does patent family strategy influence this patent’s value?
A4: A well-structured patent family ensures comprehensive territorial coverage, reinforcing market exclusivity and reducing potential infringement issues.

Q5: How can I stay updated on legal status and potential expirations of this patent?
A5:** Regular monitoring via patent databases such as PATENTSCOPE or national patent offices provides timely updates on legal status, maintenance fees, and expiry dates.


References

  1. WIPO Patent Application WO2006124118.
  2. European Patent Office (EPO) Patent Landscape Reports.
  3. PatentScope, WIPO database.
  4. Espacenet, European Patent Office Database.
  5. USPTO Patent Full-Text and Image Database.

(Note: Detailed actual claims, inventors, and legal status should be obtained through official patent documents for precise analysis.)

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