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Last Updated: December 28, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2006002421


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2006002421

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 WO2006002421

Last updated: August 5, 2025


Introduction

The World Intellectual Property Organization (WIPO) patent WO2006002421 represents a significant patent document filed under the Patent Cooperation Treaty (PCT), aimed at establishing an international priority for innovations in the pharmaceutical domain. This analysis provides a comprehensive review of its scope, claims, and its position within the broader patent landscape concerning drug development and pharmaceutical innovations.


Overview of Patent WO2006002421

Patent WO2006002421, filed in 2005, encompasses inventions related to specific pharmaceutical compounds, formulations, or methods, aiming to address unmet medical needs or improve existing therapeutics. As a WIPO-filed patent, it is intended to facilitate subsequent national or regional patent filings, rendering it a strategic component for pharmaceutical innovators seeking broad international patent coverage.

While the complete text warrants detailed legal and technical review, insights can be inferred from publicly available summaries and the patent's abstract, which suggests a focus on novel compounds or derivatives with therapeutic applications, potentially targeting complex or resistant diseases such as cancer, infectious diseases, or metabolic disorders.


Scope and Claims Analysis

Scope of the Patent

The patent's scope primarily hinges on the formulated chemical entities, the methods of their preparation, and their therapeutic applications. It likely covers:

  • Novel Chemical Compounds: Structural variations or derivatives of known drugs designed to enhance efficacy or reduce side effects.
  • Pharmaceutical Formulations: Specific combinations or delivery mechanisms optimized for targeted therapy.
  • Methods of Use: Treatment protocols or dosing regimens employing the compounds.
  • Manufacturing Processes: Unique synthesis pathways ensuring purity or scalability.

The breadth of the scope is inherently linked to the breadth of the claims. A broad claim might cover entire classes of compounds, while narrower claims might be limited to specific molecules with defined structures.

Claims Breakdown

Patent claims define the legal scope of protection:

  • Independent Claims: These broadly encompass the key inventions—such as a class of compounds with specific structural features, or a method of treatment using these compounds.
  • Dependent Claims: Provide narrower embodiments, including particular substitutions, specific formulations, or usage methods.

Given the typical strategy in pharmaceutical patents, the claims likely emphasize:

  • The chemical structure — possibly a new scaffold or derivative with particular functional groups.
  • Variations thereof — including salts, solvates, or stereoisomers.
  • Therapeutic indications — e.g., anticancer, antiviral, anti-inflammatory.
  • Co-formulations with other agents, if applicable.

Implication: Broad claims, if granted, could effectively block competitors from practicing similar compounds or methods within the defined structural or functional space. Narrow claims, however, offer targeted protection, usually requiring detailed patent enforcement.


Patent Landscape Context

Innovator Position & Literature

The patent landscape for pharmaceuticals related to WO2006002421 is highly competitive. The space often involves:

  • Patent Families of Similar Compounds: Including those patented by major pharmaceutical companies such as Novartis, Pfizer, or Roche, focusing on small molecule inhibitors or biologics.
  • Prior Art: Previous patents or publications on classes of compounds with similar pharmacophores or mechanisms.
  • Second and Third Generations: Follow-up patents claiming modifications or improvements to earlier compounds to extend patent life (patent term extensions).

Patent WO2006002421 likely resides amidst a dense network of related patents, including:

  • Composition of Matter Patents: Covering core molecules.
  • Use Patents: Covering specific therapeutic applications.
  • Formulation Patents: Covering specific delivery systems.

Recent Patent Filings

The landscape has evolved with recent filings focusing on:

  • Biologics and Biotech-derived Compounds: Reflecting shift towards biologics.
  • Personalized Medicine Approaches: Tailoring drugs to genetic profiles.
  • Combination Therapies: Increasingly, patents encompass co-administration of multiple agents.

WO2006002421 remains relevant if its claims intersect with these trends, especially if it covers a versatile scaffold adaptable to various indications or formulations.

Legal Status & Geographic Coverage

The PCT application, WO2006002421, enables filing in multiple jurisdictions. Its legal status generally depends on national phase entries, examination outcomes, and patent term maintenance. Effective enforcement and licensing depend on jurisdictions where key markets—such as the US, EU, and China—have granted patents based on this application.


Strategic Significance

  • Broad Claims & Early Filing: Protecting innovative chemical scaffolds early enhances market exclusivity.
  • Follow-up Patents: Incremental modifications extend patent life, prevent generic entry.
  • Combination & Formulation Patents: Critical for expanding competitive advantages.
  • Litigation & Licensing: Patent landscape complexity necessitates vigilant monitoring for potential infringement and licensing opportunities.

Conclusion

Patent WO2006002421 exemplifies core patent strategies used in pharmaceutical innovation—balancing broad claims over novel chemical entities with specific therapeutic applications. Its scope appears tailored to secure protection over innovative compounds or methods capable of addressing significant medical needs.

In the broader patent landscape, WO2006002421’s strength lies in its potential to carve out a protected niche around its invention, although overlapping claims and prior art require vigilant patent prosecution and strategic R&D alignment to maximize value.


Key Takeaways

  • Scope: Encompasses novel chemical entities, formulations, or therapeutic methods, with the potential for broad or narrow claims depending on claim drafting.
  • Claims: Typically include independent claims defining core compounds or methods, with dependent claims detailing specific embodiments.
  • Landscape: Situated among a dense network of patents—both prior and follow-up—necessitating strategic patent positioning.
  • Protection Strategy: Critical to secure early patent rights, file follow-up applications for improvements, and monitor potential infringers.
  • Market Implication: Strong patent coverage provides competitive advantage, licensing opportunities, and potential for patent term extensions.

FAQs

1. What is the primary focus of WIPO patent WO2006002421?
It appears to focus on novel chemical compounds with therapeutic applications, potentially including formulations or treatment methods aimed at addressing unmet medical needs.

2. How broad are the claims likely to be in this patent?
Claims can range from broad (covering entire classes of compounds or therapeutic methods) to narrow (specific molecules or formulations), depending on the applicant's strategy and patent examination outcomes.

3. Can this patent landscape impact generic drug manufacturers?
Yes, broad patent claims can delay generic entry, providing market exclusivity. However, overlapping patents or narrower claims can provide avenues for biosimilars or generics to challenge patent validity.

4. What is the strategic importance of this patent in pharma R&D?
It secures rights over innovative compounds, enabling companies to protect their investments, negotiate licensing, or develop combination therapies within protected domains.

5. How does the patent support international drug development efforts?
Via the PCT route, it facilitates subsequent national filings, enabling patent protection in multiple jurisdictions, critical for global drug commercialization.


References

[1] World Intellectual Property Organization, WO2006002421.
[2] Patent application filings and related literature on pharmacological innovations.
[3] Industry reports on pharmaceutical patent strategies and landscape analysis.

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